Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 165055 |
| ensemblid | ENSG00000163006.12 |
| hgncid | 26531 |
| symbol | CCDC138 |
| name | coiled-coil domain containing 138 |
| refseq_nuc | NM_144978.3 |
| refseq_prot | NP_659415.1 |
| ensembl_nuc | ENST00000295124.9 |
| ensembl_prot | ENSP00000295124.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 108786771 |
| end | 108876578 |
| strand | + |
| ver | v1.2 |
| region | chr2:108786771-108876578 |
| region5000 | chr2:108781771-108881578 |
| regionname0 | CCDC138_chr2_108786771_108876578 |
| regionname5000 | CCDC138_chr2_108781771_108881578 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 665 | 140 | 59 | 23 | 39 | 7 | 10 | 36 | CCDC138_chr2_108781771_108881578 | CCDC138 | MEPRV others(660): Show |
chr2 | 108781771 | 108881578 |
| a0002 | 0/0 | 665 | 36 | 20 | 5 | 5 | 1 | 5 | 4 | CCDC138_chr2_108781771_108881578 | CCDC138 | MEPRV others(660): Show |
chr2 | 108781771 | 108881578 |
| a0003 | 0/0 | 665 | 35 | 3 | 8 | 17 | 2 | 5 | 16 | CCDC138_chr2_108781771_108881578 | CCDC138 | MEPRV others(660): Show |
chr2 | 108781771 | 108881578 |
| a0004 | 0/0 | 665 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | MEPRV others(660): Show |
chr2 | 108781771 | 108881578 |
| a0005 | 0/0 | 665 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | MEPRV others(660): Show |
chr2 | 108781771 | 108881578 |
| a0006 | 0/0 | 665 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | MEPRV others(660): Show |
chr2 | 108781771 | 108881578 |
| a0007 | 0/0 | 665 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | MEPRV others(660): Show |
chr2 | 108781771 | 108881578 |
| a0008 | 0/0 | 665 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | MEPRV others(660): Show |
chr2 | 108781771 | 108881578 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1995 | 86 | 19 | 17 | 32 | 7 | 10 | CCDC138_chr2_108781771_108881578 | CCDC138 | ATGGA others(1990): Show |
chr2 | 108781771 | 108881578 | ||
| a0001c0004 | 1/0 | 1995 | 23 | 21 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | ATGGA others(1990): Show |
chr2 | 108781771 | 108881578 | ||
| a0001c0005 | 0/0 | 1995 | 20 | 18 | 2 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | ATGGA others(1990): Show |
chr2 | 108781771 | 108881578 | ||
| a0001c0006 | 0/0 | 1995 | 7 | 0 | 1 | 6 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | ATGGA others(1990): Show |
chr2 | 108781771 | 108881578 | ||
| a0001c0010 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | ATGGA others(1990): Show |
chr2 | 108781771 | 108881578 | ||
| a0001c0011 | 0/0 | 1995 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | ATGGA others(1990): Show |
chr2 | 108781771 | 108881578 | ||
| a0001c0012 | 0/0 | 1995 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | ATGGA others(1990): Show |
chr2 | 108781771 | 108881578 | ||
| a0001c0013 | 0/0 | 1995 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | ATGGA others(1990): Show |
chr2 | 108781771 | 108881578 | ||
| a0002c0002 | 0/0 | 1995 | 36 | 20 | 5 | 5 | 1 | 5 | CCDC138_chr2_108781771_108881578 | CCDC138 | ATGGA others(1990): Show |
chr2 | 108781771 | 108881578 | ||
| a0003c0003 | 0/0 | 1995 | 35 | 3 | 8 | 17 | 2 | 5 | CCDC138_chr2_108781771_108881578 | CCDC138 | ATGGA others(1990): Show |
chr2 | 108781771 | 108881578 | ||
| a0004c0007 | 0/0 | 1995 | 5 | 5 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | ATGGA others(1990): Show |
chr2 | 108781771 | 108881578 | ||
| a0005c0014 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | ATGGA others(1990): Show |
chr2 | 108781771 | 108881578 | ||
| a0006c0008 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | ATGGA others(1990): Show |
chr2 | 108781771 | 108881578 | ||
| a0007c0009 | 0/0 | 1995 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | ATGGA others(1990): Show |
chr2 | 108781771 | 108881578 | ||
| a0008c0015 | 0/0 | 1995 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | ATGGA others(1990): Show |
chr2 | 108781771 | 108881578 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2375 | 4 | 2 | 0 | 1 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0001c0001t0002 | 0/1 | 2375 | 82 | 17 | 17 | 31 | 7 | 9 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0001c0004t0001 | 0/0 | 2375 | 18 | 17 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0001c0004t0002 | 0/0 | 2375 | 4 | 4 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0001c0004t0003 | 1/0 | 2375 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0001c0005t0001 | 0/0 | 2375 | 19 | 18 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0001c0005t0002 | 0/0 | 2375 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0001c0006t0001 | 0/0 | 2375 | 7 | 0 | 1 | 6 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0001c0010t0002 | 0/0 | 2375 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0001c0011t0002 | 0/0 | 2375 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0001c0012t0001 | 0/0 | 2375 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0001c0013t0002 | 0/0 | 2375 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0002c0002t0001 | 0/0 | 2375 | 26 | 17 | 1 | 5 | 0 | 3 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0002c0002t0002 | 0/0 | 2375 | 4 | 1 | 2 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0002c0002t0003 | 0/0 | 2375 | 5 | 2 | 1 | 0 | 0 | 2 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0002c0002t0004 | 0/0 | 2375 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0003c0003t0001 | 0/0 | 2375 | 35 | 3 | 8 | 17 | 2 | 5 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0004c0007t0002 | 0/0 | 2375 | 5 | 5 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0005c0014t0001 | 0/0 | 2375 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0006c0008t0001 | 0/0 | 2375 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0007c0009t0001 | 0/0 | 2375 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| a0008c0015t0001 | 0/0 | 2375 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | GCGGG others(2370): Show |
chr2 | 108781771 | 108881578 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0004t0003g0089 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0005t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0006t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0006t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0006t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0006t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0006t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0006t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0006t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0010t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0011t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0012t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0001c0013t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0002c0002t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0003c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0004c0007t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0004c0007t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0004c0007t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0004c0007t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0004c0007t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0005c0014t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0006c0008t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0007c0009t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| a0008c0015t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0066 | EUR | GBR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG00099 | hp2 | a0003 | c0003 | t0001 | g0152 | EUR | GBR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG00408 | hp2 | a0003 | c0003 | t0001 | g0138 | EAS | CHS | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG00738 | hp1 | a0003 | c0003 | t0001 | g0149 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG00738 | hp2 | a0003 | c0003 | t0001 | g0141 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG00741 | hp1 | a0003 | c0003 | t0001 | g0180 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01081 | hp2 | a0001 | c0004 | t0001 | g0105 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01099 | hp1 | a0002 | c0002 | t0003 | g0186 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01109 | hp1 | a0001 | c0013 | t0002 | g0075 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01109 | hp2 | a0003 | c0003 | t0001 | g0136 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01167 | hp2 | a0003 | c0003 | t0001 | g0163 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0143 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01169 | hp2 | a0003 | c0003 | t0001 | g0151 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01175 | hp1 | a0001 | c0005 | t0002 | g0214 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0189 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01243 | hp1 | a0001 | c0012 | t0001 | g0013 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01243 | hp2 | a0001 | c0005 | t0001 | g0112 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0185 | AMR | CLM | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | CLM | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01261 | hp1 | a0001 | c0006 | t0001 | g0204 | AMR | CLM | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0191 | AMR | CLM | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01358 | hp1 | a0003 | c0003 | t0001 | g0153 | AMR | CLM | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | CLM | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0054 | EUR | IBS | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0085 | EUR | IBS | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0184 | EUR | IBS | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0080 | EUR | IBS | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01884 | hp1 | a0002 | c0002 | t0001 | g0129 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01891 | hp1 | a0005 | c0014 | t0001 | g0135 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0177 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG01993 | hp2 | a0002 | c0002 | t0004 | g0187 | AMR | PEL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | KHV | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | KHV | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02055 | hp1 | a0006 | c0008 | t0001 | g0165 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0131 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02145 | hp1 | a0001 | c0005 | t0001 | g0210 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02257 | hp1 | a0001 | c0005 | t0001 | g0216 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0173 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02258 | hp2 | a0001 | c0004 | t0001 | g0106 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02280 | hp1 | a0001 | c0005 | t0001 | g0217 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0132 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0174 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02523 | hp1 | a0007 | c0009 | t0001 | g0164 | EAS | KHV | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02572 | hp1 | a0001 | c0004 | t0001 | g0016 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0133 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02615 | hp1 | a0001 | c0005 | t0001 | g0119 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0166 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02647 | hp1 | a0001 | c0005 | t0001 | g0207 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02647 | hp2 | a0001 | c0004 | t0002 | g0096 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0196 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0194 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0178 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0160 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02735 | hp2 | a0003 | c0003 | t0001 | g0179 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02738 | hp2 | a0002 | c0002 | t0003 | g0192 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02818 | hp1 | a0001 | c0005 | t0001 | g0115 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02886 | hp1 | a0001 | c0004 | t0001 | g0104 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02886 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0130 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02895 | hp2 | a0001 | c0004 | t0001 | g0100 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02896 | hp1 | a0001 | c0004 | t0001 | g0103 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02896 | hp2 | a0001 | c0005 | t0001 | g0118 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02897 | hp1 | a0001 | c0004 | t0001 | g0101 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02897 | hp2 | a0001 | c0005 | t0001 | g0117 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0107 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0172 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02965 | hp2 | a0001 | c0005 | t0001 | g0215 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02970 | hp1 | a0001 | c0004 | t0001 | g0011 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03041 | hp1 | a0001 | c0004 | t0001 | g0014 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03041 | hp2 | a0001 | c0005 | t0001 | g0111 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0127 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03098 | hp2 | a0003 | c0003 | t0001 | g0159 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0126 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0110 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03195 | hp2 | a0001 | c0004 | t0002 | g0099 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03209 | hp1 | a0001 | c0004 | t0001 | g0012 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03225 | hp1 | a0001 | c0005 | t0001 | g0211 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0108 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03453 | hp1 | a0001 | c0004 | t0001 | g0109 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03453 | hp2 | a0002 | c0002 | t0002 | g0182 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03486 | hp1 | a0001 | c0005 | t0001 | g0208 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03486 | hp2 | a0004 | c0007 | t0002 | g0122 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03516 | hp1 | a0001 | c0004 | t0001 | g0010 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03516 | hp2 | a0001 | c0005 | t0001 | g0209 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03540 | hp1 | a0001 | c0005 | t0001 | g0212 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0094 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03579 | hp2 | a0004 | c0007 | t0002 | g0125 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03654 | hp1 | a0003 | c0003 | t0001 | g0157 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0170 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03688 | hp1 | a0002 | c0002 | t0003 | g0195 | SAS | STU | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | STU | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0076 | SAS | BEB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03927 | hp2 | a0003 | c0003 | t0001 | g0183 | SAS | BEB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG04115 | hp1 | a0003 | c0003 | t0001 | g0134 | SAS | STU | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | STU | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | STU | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG04199 | hp2 | a0003 | c0003 | t0001 | g0156 | SAS | STU | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0057 | SAS | STU | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18522 | hp1 | a0001 | c0005 | t0001 | g0213 | AFR | YRI | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | YRI | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18941 | hp1 | a0001 | c0006 | t0001 | g0198 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18945 | hp1 | a0003 | c0003 | t0001 | g0162 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18946 | hp2 | a0001 | c0006 | t0001 | g0199 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18954 | hp2 | a0001 | c0006 | t0001 | g0202 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18959 | hp1 | a0001 | c0006 | t0001 | g0203 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18968 | hp2 | a0003 | c0003 | t0001 | g0146 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18970 | hp1 | a0001 | c0006 | t0001 | g0200 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18970 | hp2 | a0003 | c0003 | t0001 | g0150 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18974 | hp2 | a0003 | c0003 | t0001 | g0120 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18977 | hp2 | a0003 | c0003 | t0001 | g0140 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18984 | hp2 | a0003 | c0003 | t0001 | g0148 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18993 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18994 | hp1 | a0003 | c0003 | t0001 | g0144 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18994 | hp2 | a0001 | c0011 | t0002 | g0031 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18998 | hp1 | a0003 | c0003 | t0001 | g0158 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18999 | hp1 | a0003 | c0003 | t0001 | g0147 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19011 | hp1 | a0003 | c0003 | t0001 | g0154 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19030 | hp1 | a0003 | c0003 | t0001 | g0139 | AFR | LWK | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19030 | hp2 | a0001 | c0005 | t0001 | g0114 | AFR | LWK | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19043 | hp1 | a0004 | c0007 | t0002 | g0124 | AFR | LWK | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19043 | hp2 | a0001 | c0004 | t0001 | g0197 | AFR | LWK | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19056 | hp2 | a0003 | c0003 | t0001 | g0145 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19070 | hp2 | a0003 | c0003 | t0001 | g0155 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19081 | hp2 | a0003 | c0003 | t0001 | g0142 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19082 | hp2 | a0003 | c0003 | t0001 | g0003 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19087 | hp2 | a0003 | c0003 | t0001 | g0161 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19088 | hp2 | a0001 | c0006 | t0001 | g0201 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19240 | hp1 | a0001 | c0005 | t0001 | g0116 | AFR | YRI | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | YRI | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA20129 | hp1 | a0004 | c0007 | t0002 | g0123 | AFR | ASW | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA20129 | hp2 | a0001 | c0004 | t0001 | g0102 | AFR | ASW | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA20752 | hp1 | a0003 | c0003 | t0001 | g0137 | EUR | TSI | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0083 | EUR | TSI | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0062 | EUR | TSI | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02486 | hp1 | a0001 | c0004 | t0002 | g0098 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02486 | hp2 | a0001 | c0010 | t0002 | g0067 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02559 | hp1 | a0002 | c0002 | t0003 | g0190 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG02559 | hp2 | a0001 | c0005 | t0001 | g0113 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03471 | hp1 | a0004 | c0007 | t0002 | g0121 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG06807 | hp1 | a0001 | c0004 | t0002 | g0097 | AFR | USA | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0176 | AFR | USA | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0128 | AFR | USA | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0181 | AFR | USA | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA21309 | hp1 | a0002 | c0002 | t0003 | g0188 | AFR | LWK | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| NA21309 | hp2 | a0008 | c0015 | t0001 | g0193 | AFR | LWK | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0088 | REF | REF | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| homoSapiens | grch38p0 | a0001 | c0004 | t0003 | g0089 | REF | REF | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:108788965 | T | C | 1 | a0004 | 5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.265T>C | p.Cys89Arg | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/15 | 317/2375 | 265/1998 | 89/665 | chr2 | 108788965 | |||
| chr2:108791703 | G | T | 3 | a0003 a0005 a0008 |
37 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(34): Show |
missense_variant | MODERATE | c.295G>T | p.Asp99Tyr | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/15 | 347/2375 | 295/1998 | 99/665 | chr2 | 108791703 | |||
| chr2:108791752 | G | A | 7 | a0002 a0003 a0004 others(4): Show |
80 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(77): Show |
missense_variant | MODERATE | c.344G>A | p.Arg115Lys | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/15 | 396/2375 | 344/1998 | 115/665 | chr2 | 108791752 | |||
| chr2:108812821 | G | C | 1 | a0006 | 1 | HG02055.hp1 | missense_variant&splice_region_variant | MODERATE | c.935G>C | p.Arg312Thr | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/15 | 987/2375 | 935/1998 | 312/665 | chr2 | 108812821 | |||
| chr2:108815996 | C | T | 1 | a0007 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1097C>T | p.Ser366Leu | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/15 | 1149/2375 | 1097/1998 | 366/665 | chr2 | 108815996 | |||
| chr2:108846814 | A | G | 1 | a0008 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1400A>G | p.Asp467Gly | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/15 | 1452/2375 | 1400/1998 | 467/665 | chr2 | 108846814 | |||
| chr2:108876166 | T | G | 1 | a0005 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.1911T>G | p.His637Gln | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 15/15 | 1963/2375 | 1911/1998 | 637/665 | chr2 | 108876166 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:108788928 | A | G | 1 | a0001c0006 | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
synonymous_variant | LOW | c.228A>G | p.Thr76Thr | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/15 | 280/2375 | 228/1998 | 76/665 | chr2 | 108788928 | |||
| chr2:108794691 | C | T | 2 | a0001c0005 a0001c0013 |
21 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(18): Show |
synonymous_variant | LOW | c.546C>T | p.Asp182Asp | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/15 | 598/2375 | 546/1998 | 182/665 | chr2 | 108794691 | |||
| chr2:108812645 | T | C | 1 | a0001c0010 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.870T>C | p.Ser290Ser | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 8/15 | 922/2375 | 870/1998 | 290/665 | chr2 | 108812645 | |||
| chr2:108812690 | T | A | 4 | a0001c0001 a0001c0010 a0001c0011 others(1): Show |
88 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(85): Show |
synonymous_variant | LOW | c.915T>A | p.Ala305Ala | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 8/15 | 967/2375 | 915/1998 | 305/665 | chr2 | 108812690 | |||
| chr2:108816096 | G | A | 1 | a0001c0012 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.1197G>A | p.Lys399Lys | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/15 | 1249/2375 | 1197/1998 | 399/665 | chr2 | 108816096 | |||
| chr2:108846839 | G | A | 1 | a0001c0011 | 1 | NA18994.hp2 | synonymous_variant | LOW | c.1425G>A | p.Glu475Glu | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/15 | 1477/2375 | 1425/1998 | 475/665 | chr2 | 108846839 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:108876275 | G | A | 1 | a0002c0002t0004 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*22G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 15/15 | 22 | chr2 | 108876275 | ||||||
| chr2:108876451 | A | G | 19 | a0001c0001t0001 a0001c0001t0002 a0001c0004t0001 others(16): Show |
212 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*198A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 15/15 | 198 | chr2 | 108876451 | ||||||
| chr2:108876546 | T | A | 8 | a0001c0001t0002 a0001c0004t0002 a0001c0005t0002 others(5): Show |
98 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*293T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 15/15 | 293 | chr2 | 108876546 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:108786919 | A | C | 11 | a0001c0005t0001g0207 a0001c0005t0001g0208 a0001c0005t0001g0209 others(8): Show |
11 | HG01175.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.93+4A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108786919 | |||||||
| chr2:108786941 | G | C | 2 | a0001c0005t0001g0207 a0001c0005t0001g0208 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.93+26G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108786941 | |||||||
| chr2:108786999 | G | A | 11 | a0001c0005t0001g0207 a0001c0005t0001g0208 a0001c0005t0001g0209 others(8): Show |
11 | HG01175.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.93+84G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108786999 | |||||||
| chr2:108787034 | C | G | 1 | a0002c0002t0001g0206 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.93+119C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108787034 | |||||||
| chr2:108787461 | A | G | 1 | a0001c0001t0002g0205 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.93+546A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108787461 | |||||||
| chr2:108787482 | G | T | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-550G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108787482 | |||||||
| chr2:108787500 | C | T | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-532C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108787500 | |||||||
| chr2:108787608 | C | T | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.94-424C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108787608 | |||||||
| chr2:108787610 | A | ATAAAATT others(12): Show |
1 | a0002c0002t0001g0196 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.94-422_94-421insTA others(17): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108787610 | |||||||
| chr2:108787611 | G | C | 1 | a0002c0002t0001g0196 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.94-421G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108787611 | |||||||
| chr2:108787651 | T | C | 1 | a0001c0001t0002g0004 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.94-381T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108787651 | |||||||
| chr2:108787757 | C | T | 1 | a0002c0002t0003g0195 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.94-275C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108787757 | |||||||
| chr2:108788018 | C | CT | 78 | a0002c0002t0001g0126 a0002c0002t0001g0127 a0002c0002t0001g0128 others(75): Show |
79 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(76): Show |
splice_acceptor_variant&intron_variant | HIGH | c.94-3dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | 108788018 | ||||||
| chr2:108788295 | C | A | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.151+206C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 2/14 | chr2 | 108788295 | |||||||
| chr2:108788443 | G | A | 5 | a0004c0007t0002g0121 a0004c0007t0002g0122 a0004c0007t0002g0123 others(2): Show |
5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+354G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 2/14 | chr2 | 108788443 | |||||||
| chr2:108788447 | G | A | 1 | a0001c0001t0002g0005 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.151+358G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 2/14 | chr2 | 108788447 | |||||||
| chr2:108788461 | G | A | 11 | a0001c0005t0001g0207 a0001c0005t0001g0208 a0001c0005t0001g0209 others(8): Show |
11 | HG01175.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+372G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 2/14 | chr2 | 108788461 | |||||||
| chr2:108788578 | G | C | 7 | a0002c0002t0001g0126 a0002c0002t0001g0127 a0002c0002t0001g0128 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.152-274G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 2/14 | chr2 | 108788578 | |||||||
| chr2:108788719 | CAAAGAAA others(3): Show |
C | 5 | a0004c0007t0002g0121 a0004c0007t0002g0122 a0004c0007t0002g0123 others(2): Show |
5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-119_152-110del others(10): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr2 | 108788719 | ||||||
| chr2:108789026 | G | A | 1 | a0002c0002t0001g0133 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.266+60G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108789026 | |||||||
| chr2:108789083 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.266+117T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108789083 | |||||||
| chr2:108789248 | C | G | 5 | a0004c0007t0002g0121 a0004c0007t0002g0122 a0004c0007t0002g0123 others(2): Show |
5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.266+282C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108789248 | |||||||
| chr2:108789330 | C | T | 79 | a0002c0002t0001g0126 a0002c0002t0001g0127 a0002c0002t0001g0128 others(76): Show |
80 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.266+364C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108789330 | |||||||
| chr2:108789408 | C | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.266+442C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108789408 | |||||||
| chr2:108789585 | T | G | 2 | a0001c0001t0002g0007 a0001c0001t0002g0008 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.266+619T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108789585 | |||||||
| chr2:108789630 | A | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.266+664A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108789630 | |||||||
| chr2:108790021 | C | T | 1 | a0002c0002t0001g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.266+1055C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108790021 | |||||||
| chr2:108790022 | A | G | 1 | a0008c0015t0001g0193 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.266+1056A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108790022 | |||||||
| chr2:108790097 | A | G | 2 | a0001c0005t0001g0207 a0001c0005t0001g0208 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.266+1131A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108790097 | |||||||
| chr2:108790109 | C | T | 20 | a0001c0005t0001g0111 a0001c0005t0001g0112 a0001c0005t0001g0113 others(17): Show |
20 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.266+1143C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108790109 | |||||||
| chr2:108790575 | GC | G | 5 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.267-1098delC | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr2 | 108790575 | ||||||
| chr2:108790595 | G | A | 1 | a0001c0001t0002g0009 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.267-1080G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108790595 | |||||||
| chr2:108790627 | G | A | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.267-1048G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108790627 | |||||||
| chr2:108790913 | A | G | 129 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(126): Show |
130 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(127): Show |
intron_variant | MODIFIER | c.267-762A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108790913 | |||||||
| chr2:108791042 | G | A | 209 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(206): Show |
212 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.267-633G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108791042 | |||||||
| chr2:108791054 | G | A | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.267-621G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108791054 | |||||||
| chr2:108791113 | ATATAT | A | 3 | a0001c0005t0001g0111 a0001c0005t0001g0209 a0001c0005t0001g0210 |
3 | HG02145.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.267-554_267-550del others(5): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr2 | 108791113 | ||||||
| chr2:108791198 | T | C | 6 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0004t0001g0102 others(3): Show |
6 | HG01081.hp2 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.267-477T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108791198 | |||||||
| chr2:108791438 | A | G | 8 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0002g0082 others(5): Show |
8 | HG00741.hp2 HG01515.hp2 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.267-237A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108791438 | |||||||
| chr2:108791865 | C | T | 1 | a0001c0005t0001g0111 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.394+63C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108791865 | |||||||
| chr2:108792078 | A | T | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.394+276A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108792078 | |||||||
| chr2:108792233 | A | C | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394+431A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108792233 | |||||||
| chr2:108792282 | C | T | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394+480C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108792282 | |||||||
| chr2:108792312 | C | G | 1 | a0001c0001t0002g0079 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.394+510C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108792312 | |||||||
| chr2:108792320 | T | C | 122 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(119): Show |
123 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(120): Show |
intron_variant | MODIFIER | c.394+518T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108792320 | |||||||
| chr2:108792502 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0078 |
2 | HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.394+700C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108792502 | |||||||
| chr2:108792503 | T | A | 1 | a0003c0003t0001g0134 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.394+701T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108792503 | |||||||
| chr2:108792538 | G | A | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.394+736G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108792538 | |||||||
| chr2:108792995 | C | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.394+1193C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108792995 | |||||||
| chr2:108793017 | CTG | C | 5 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.394+1218_394+1219d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 108793017 | ||||||
| chr2:108793061 | C | CAAAAAAA others(5): Show |
1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.394+1269_394+1270i others(14): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 108793061 | ||||||
| chr2:108793175 | G | A | 1 | a0002c0002t0001g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.395-1365G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108793175 | |||||||
| chr2:108793193 | TA | T | 79 | a0002c0002t0001g0126 a0002c0002t0001g0127 a0002c0002t0001g0128 others(76): Show |
80 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.395-1336delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 108793193 | ||||||
| chr2:108793576 | C | T | 7 | a0002c0002t0001g0126 a0002c0002t0001g0127 a0002c0002t0001g0128 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.395-964C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108793576 | |||||||
| chr2:108793589 | T | G | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.395-951T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108793589 | |||||||
| chr2:108793621 | G | A | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.395-919G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108793621 | |||||||
| chr2:108793631 | C | G | 1 | a0001c0005t0001g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.395-909C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108793631 | |||||||
| chr2:108793777 | T | C | 20 | a0001c0005t0001g0111 a0001c0005t0001g0112 a0001c0005t0001g0113 others(17): Show |
20 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.395-763T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108793777 | |||||||
| chr2:108793796 | A | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.395-744A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108793796 | |||||||
| chr2:108793854 | G | A | 22 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0005t0001g0111 others(19): Show |
22 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.395-686G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108793854 | |||||||
| chr2:108794092 | CATATAAA | C | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.395-439_395-433del others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 108794092 | ||||||
| chr2:108794175 | A | G | 5 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.395-365A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108794175 | |||||||
| chr2:108794182 | C | T | 80 | a0001c0004t0001g0197 a0002c0002t0001g0126 a0002c0002t0001g0127 others(77): Show |
81 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.395-358C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108794182 | |||||||
| chr2:108794361 | CT | C | 27 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0004t0001g0106 others(24): Show |
27 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.395-177delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 108794361 | ||||||
| chr2:108794393 | C | T | 10 | a0002c0002t0001g0191 a0002c0002t0002g0184 a0002c0002t0002g0185 others(7): Show |
10 | HG01099.hp1 HG01175.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.395-147C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108794393 | |||||||
| chr2:108794403 | A | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.395-137A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108794403 | |||||||
| chr2:108794458 | A | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.395-82A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108794458 | |||||||
| chr2:108794471 | G | A | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.395-69G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108794471 | |||||||
| chr2:108794724 | A | G | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.576+3A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108794724 | |||||||
| chr2:108794792 | GAATAT | G | 135 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(132): Show |
137 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(134): Show |
intron_variant | MODIFIER | c.576+78_576+82delAT others(3): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 108794792 | ||||||
| chr2:108795051 | G | A | 1 | a0008c0015t0001g0193 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.576+330G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108795051 | |||||||
| chr2:108795057 | A | AT | 90 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(87): Show |
92 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(89): Show |
intron_variant | MODIFIER | c.576+337dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 108795057 | ||||||
| chr2:108795061 | A | G | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+340A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108795061 | |||||||
| chr2:108795150 | A | AT | 38 | a0001c0001t0002g0018 a0001c0001t0002g0205 a0001c0004t0001g0010 others(35): Show |
38 | HG00741.hp1 HG01175.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.576+451dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 108795150 | ||||||
| chr2:108795150 | A | ATT | 91 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(88): Show |
93 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(90): Show |
intron_variant | MODIFIER | c.576+450_576+451dup others(2): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 108795150 | ||||||
| chr2:108795150 | A | ATTT | 16 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 others(13): Show |
16 | HG01109.hp1 HG01261.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.576+449_576+451dup others(3): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 108795150 | ||||||
| chr2:108795174 | C | T | 20 | a0001c0005t0001g0111 a0001c0005t0001g0112 a0001c0005t0001g0113 others(17): Show |
20 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.576+453C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108795174 | |||||||
| chr2:108795792 | G | A | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.576+1071G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108795792 | |||||||
| chr2:108795876 | A | G | 4 | a0001c0004t0001g0102 a0001c0004t0001g0103 a0001c0004t0001g0104 others(1): Show |
4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+1155A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108795876 | |||||||
| chr2:108795934 | G | T | 5 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.576+1213G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108795934 | |||||||
| chr2:108796090 | C | T | 2 | a0001c0005t0001g0209 a0001c0005t0001g0210 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.576+1369C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796090 | |||||||
| chr2:108796173 | C | G | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.576+1452C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796173 | |||||||
| chr2:108796203 | C | T | 1 | a0001c0001t0002g0069 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.576+1482C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796203 | |||||||
| chr2:108796209 | C | T | 4 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 others(1): Show |
4 | HG00741.hp2 HG01515.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+1488C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796209 | |||||||
| chr2:108796277 | A | C | 1 | a0003c0003t0001g0183 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.576+1556A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796277 | |||||||
| chr2:108796388 | T | C | 1 | a0005c0014t0001g0135 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.576+1667T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796388 | |||||||
| chr2:108796503 | G | A | 136 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(133): Show |
138 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(135): Show |
intron_variant | MODIFIER | c.576+1782G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796503 | |||||||
| chr2:108796674 | A | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.577-1754A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796674 | |||||||
| chr2:108796874 | TTAGA | T | 3 | a0001c0005t0001g0117 a0001c0005t0001g0118 a0001c0005t0001g0119 |
3 | HG02615.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.577-1550_577-1547d others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 108796874 | ||||||
| chr2:108796956 | C | G | 5 | a0004c0007t0002g0121 a0004c0007t0002g0122 a0004c0007t0002g0123 others(2): Show |
5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-1472C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796956 | |||||||
| chr2:108796970 | T | C | 1 | a0002c0002t0002g0184 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.577-1458T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796970 | |||||||
| chr2:108797136 | A | G | 1 | a0003c0003t0001g0179 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.577-1292A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108797136 | |||||||
| chr2:108797354 | G | A | 44 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(41): Show |
45 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.577-1074G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108797354 | |||||||
| chr2:108797390 | A | G | 7 | a0001c0001t0002g0068 a0001c0001t0002g0090 a0001c0001t0002g0091 others(4): Show |
7 | HG02622.hp1 HG02818.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.577-1038A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108797390 | |||||||
| chr2:108797402 | G | A | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.577-1026G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108797402 | |||||||
| chr2:108797647 | T | C | 90 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(87): Show |
92 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(89): Show |
intron_variant | MODIFIER | c.577-781T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108797647 | |||||||
| chr2:108797825 | G | A | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.577-603G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108797825 | |||||||
| chr2:108797933 | C | T | 172 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(169): Show |
175 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.577-495C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108797933 | |||||||
| chr2:108797962 | AT | A | 174 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(171): Show |
177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.577-450delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 108797962 | ||||||
| chr2:108797974 | T | A | 4 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0070 others(1): Show |
4 | HG01074.hp1 HG01358.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-454T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108797974 | |||||||
| chr2:108798010 | C | T | 1 | a0003c0003t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.577-418C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108798010 | |||||||
| chr2:108798099 | A | G | 37 | a0002c0002t0001g0194 a0003c0003t0001g0003 a0003c0003t0001g0120 others(34): Show |
38 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.577-329A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108798099 | |||||||
| chr2:108798168 | T | C | 35 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0004t0001g0102 others(32): Show |
35 | HG01081.hp2 HG01175.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.577-260T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108798168 | |||||||
| chr2:108798266 | G | A | 1 | a0007c0009t0001g0164 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.577-162G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108798266 | |||||||
| chr2:108798610 | A | C | 1 | a0001c0004t0002g0099 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.735+24A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108798610 | |||||||
| chr2:108798643 | C | G | 1 | a0001c0010t0002g0067 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.735+57C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108798643 | |||||||
| chr2:108798708 | T | TAC | 21 | a0001c0004t0001g0103 a0001c0004t0001g0104 a0001c0004t0001g0105 others(18): Show |
21 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.735+153_735+154dup others(2): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798708 | ||||||
| chr2:108798708 | T | TACAC | 11 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0004t0001g0102 others(8): Show |
11 | HG02895.hp2 HG02897.hp1 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.735+151_735+154dup others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798708 | ||||||
| chr2:108798708 | TAC | T | 53 | a0001c0001t0001g0030 a0001c0001t0002g0001 a0001c0001t0002g0005 others(50): Show |
54 | HG00408.hp1 HG01081.hp1 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.735+153_735+154del others(2): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798708 | ||||||
| chr2:108798708 | TACAC | T | 44 | a0001c0001t0001g0056 a0001c0001t0001g0078 a0001c0001t0002g0002 others(41): Show |
45 | HG00099.hp1 HG00741.hp2 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.735+151_735+154del others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798708 | ||||||
| chr2:108798708 | TACACACA others(3): Show |
T | 37 | a0002c0002t0001g0194 a0003c0003t0001g0003 a0003c0003t0001g0120 others(34): Show |
38 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.735+145_735+154del others(10): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798708 | ||||||
| chr2:108798740 | C | T | 1 | a0001c0001t0002g0021 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.735+154C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108798740 | |||||||
| chr2:108798816 | T | TAC | 33 | a0001c0001t0002g0066 a0001c0001t0002g0069 a0001c0001t0002g0071 others(30): Show |
33 | HG00099.hp1 HG00408.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.735+266_735+267dup others(2): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798816 | ||||||
| chr2:108798816 | T | TACAC | 31 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0001t0002g0002 others(28): Show |
32 | HG01074.hp1 HG01074.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.735+264_735+267dup others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798816 | ||||||
| chr2:108798816 | T | TACACAC | 46 | a0001c0001t0001g0030 a0001c0001t0002g0001 a0001c0001t0002g0004 others(43): Show |
47 | HG00408.hp1 HG01167.hp1 HG01168.hp1 others(44): Show |
intron_variant | MODIFIER | c.735+262_735+267dup others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798816 | ||||||
| chr2:108798816 | T | TACACACA others(1): Show |
16 | a0001c0001t0001g0056 a0001c0001t0002g0022 a0001c0001t0002g0023 others(13): Show |
16 | HG01081.hp1 HG01109.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.735+260_735+267dup others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798816 | ||||||
| chr2:108798816 | T | TACACACA others(5): Show |
1 | a0001c0001t0002g0079 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.735+256_735+267dup others(12): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798816 | ||||||
| chr2:108798816 | TAC | T | 2 | a0001c0006t0001g0203 a0005c0014t0001g0135 |
2 | HG01891.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.735+266_735+267del others(2): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798816 | ||||||
| chr2:108798816 | TACAC | T | 9 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0004t0001g0197 others(6): Show |
9 | HG01175.hp2 HG01257.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+264_735+267del others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798816 | ||||||
| chr2:108798816 | TACACACA others(1): Show |
T | 20 | a0001c0005t0001g0111 a0001c0005t0001g0112 a0001c0005t0001g0113 others(17): Show |
20 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.735+260_735+267del others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798816 | ||||||
| chr2:108798816 | TACACACA others(3): Show |
T | 5 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.735+258_735+267del others(10): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798816 | ||||||
| chr2:108798891 | A | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.735+305A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108798891 | |||||||
| chr2:108799084 | G | T | 5 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.735+498G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108799084 | |||||||
| chr2:108799264 | T | C | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.735+678T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108799264 | |||||||
| chr2:108799293 | T | C | 173 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.735+707T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108799293 | |||||||
| chr2:108799300 | T | C | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.735+714T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108799300 | |||||||
| chr2:108799303 | T | A | 173 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.735+717T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108799303 | |||||||
| chr2:108799779 | A | C | 173 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.735+1193A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108799779 | |||||||
| chr2:108799879 | C | T | 2 | a0001c0005t0001g0207 a0001c0005t0001g0208 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.735+1293C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108799879 | |||||||
| chr2:108799964 | ATTT | A | 5 | a0004c0007t0002g0121 a0004c0007t0002g0122 a0004c0007t0002g0123 others(2): Show |
5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.735+1381_735+1383d others(5): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108799964 | ||||||
| chr2:108800161 | A | C | 7 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0174 others(4): Show |
7 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+1575A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800161 | |||||||
| chr2:108800222 | G | C | 7 | a0001c0005t0001g0209 a0001c0005t0001g0210 a0001c0005t0001g0212 others(4): Show |
7 | HG01175.hp1 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.735+1636G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800222 | |||||||
| chr2:108800368 | G | A | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+1782G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800368 | |||||||
| chr2:108800421 | T | C | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.735+1835T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800421 | |||||||
| chr2:108800425 | C | T | 1 | a0002c0002t0001g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.735+1839C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800425 | |||||||
| chr2:108800466 | T | C | 4 | a0001c0004t0001g0102 a0001c0004t0001g0103 a0001c0004t0001g0104 others(1): Show |
4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.735+1880T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800466 | |||||||
| chr2:108800471 | G | C | 7 | a0002c0002t0001g0126 a0002c0002t0001g0127 a0002c0002t0001g0128 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+1885G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800471 | |||||||
| chr2:108800516 | C | T | 1 | a0001c0001t0002g0077 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.735+1930C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800516 | |||||||
| chr2:108800574 | C | T | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+1988C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800574 | |||||||
| chr2:108800592 | T | A | 3 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0203 |
3 | NA18941.hp1 NA18946.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.735+2006T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800592 | |||||||
| chr2:108800608 | CT | C | 99 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(96): Show |
101 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(98): Show |
intron_variant | MODIFIER | c.735+2052delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108800608 | ||||||
| chr2:108800608 | CTT | C | 19 | a0001c0001t0002g0022 a0001c0001t0002g0028 a0001c0001t0002g0050 others(16): Show |
19 | HG00738.hp2 HG00741.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.735+2051_735+2052d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108800608 | ||||||
| chr2:108800608 | CTTTTTTT others(10): Show |
C | 1 | a0001c0006t0001g0200 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.735+2036_735+2052d others(19): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108800608 | ||||||
| chr2:108800610 | T | C | 1 | a0007c0009t0001g0164 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.735+2024T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800610 | |||||||
| chr2:108800637 | T | A | 1 | a0001c0005t0001g0211 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.735+2051T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800637 | |||||||
| chr2:108800638 | T | A | 133 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(130): Show |
136 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.735+2052T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800638 | |||||||
| chr2:108800638 | T | TA | 20 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0004t0002g0098 others(17): Show |
20 | HG01243.hp2 HG01261.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.735+2054dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108800638 | ||||||
| chr2:108800638 | T | TTA | 14 | a0001c0004t0001g0102 a0001c0004t0001g0103 a0001c0004t0001g0104 others(11): Show |
14 | HG01081.hp2 HG01175.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.735+2052_735+2053i others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800638 | |||||||
| chr2:108800734 | A | G | 185 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(182): Show |
188 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.735+2148A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800734 | |||||||
| chr2:108800896 | C | G | 1 | a0001c0001t0002g0076 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.735+2310C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800896 | |||||||
| chr2:108800992 | A | G | 173 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.735+2406A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800992 | |||||||
| chr2:108801072 | A | G | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+2486A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801072 | |||||||
| chr2:108801077 | A | G | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+2491A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801077 | |||||||
| chr2:108801247 | G | T | 172 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(169): Show |
175 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.735+2661G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801247 | |||||||
| chr2:108801337 | G | A | 172 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(169): Show |
175 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.735+2751G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801337 | |||||||
| chr2:108801346 | A | T | 5 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.735+2760A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801346 | |||||||
| chr2:108801374 | G | A | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.735+2788G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801374 | |||||||
| chr2:108801402 | G | A | 1 | a0001c0001t0002g0029 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.735+2816G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801402 | |||||||
| chr2:108801405 | T | G | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+2819T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801405 | |||||||
| chr2:108801454 | C | T | 2 | a0001c0001t0002g0027 a0001c0001t0002g0047 |
2 | NA18985.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.735+2868C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801454 | |||||||
| chr2:108801668 | A | G | 1 | a0003c0003t0001g0140 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.735+3082A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801668 | |||||||
| chr2:108801705 | C | T | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+3119C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801705 | |||||||
| chr2:108801861 | T | C | 97 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(94): Show |
99 | HG00099.hp1 HG00408.hp1 HG00738.hp2 others(96): Show |
intron_variant | MODIFIER | c.736-3028T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801861 | |||||||
| chr2:108801944 | T | A | 2 | a0001c0001t0001g0030 a0001c0001t0002g0017 |
2 | NA18971.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.736-2945T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801944 | |||||||
| chr2:108801946 | C | T | 1 | a0005c0014t0001g0135 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.736-2943C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801946 | |||||||
| chr2:108802067 | G | C | 1 | a0006c0008t0001g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.736-2822G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802067 | |||||||
| chr2:108802105 | G | A | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.736-2784G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802105 | |||||||
| chr2:108802107 | T | C | 5 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.736-2782T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802107 | |||||||
| chr2:108802240 | A | G | 61 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(58): Show |
62 | HG00099.hp1 HG00408.hp1 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.736-2649A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802240 | |||||||
| chr2:108802358 | T | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.736-2531T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802358 | |||||||
| chr2:108802417 | G | T | 27 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0004t0001g0106 others(24): Show |
27 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.736-2472G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802417 | |||||||
| chr2:108802436 | T | C | 7 | a0002c0002t0001g0126 a0002c0002t0001g0127 a0002c0002t0001g0128 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.736-2453T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802436 | |||||||
| chr2:108802468 | T | C | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.736-2421T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802468 | |||||||
| chr2:108802526 | T | G | 1 | a0001c0005t0001g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.736-2363T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802526 | |||||||
| chr2:108802567 | G | A | 5 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.736-2322G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802567 | |||||||
| chr2:108802602 | C | T | 1 | a0001c0005t0001g0113 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.736-2287C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802602 | |||||||
| chr2:108802626 | TCTC | T | 2 | a0001c0004t0001g0100 a0001c0004t0001g0101 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.736-2260_736-2258d others(5): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108802626 | ||||||
| chr2:108802688 | A | G | 173 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.736-2201A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802688 | |||||||
| chr2:108802755 | C | T | 1 | a0001c0001t0002g0083 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.736-2134C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802755 | |||||||
| chr2:108802831 | C | G | 1 | a0003c0003t0001g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.736-2058C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802831 | |||||||
| chr2:108803061 | G | C | 1 | a0001c0005t0001g0111 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.736-1828G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108803061 | |||||||
| chr2:108803125 | G | T | 1 | a0001c0005t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.736-1764G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108803125 | |||||||
| chr2:108803144 | A | G | 178 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(175): Show |
181 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.736-1745A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108803144 | |||||||
| chr2:108803232 | C | T | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.736-1657C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108803232 | |||||||
| chr2:108803393 | AT | A | 173 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.736-1493delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108803393 | ||||||
| chr2:108803441 | A | T | 3 | a0002c0002t0003g0186 a0002c0002t0003g0192 a0002c0002t0004g0187 |
3 | HG01099.hp1 HG01993.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.736-1448A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108803441 | |||||||
| chr2:108803442 | T | A | 3 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0011t0002g0031 |
3 | HG02895.hp2 HG02897.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.736-1447T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108803442 | |||||||
| chr2:108803514 | C | T | 2 | a0004c0007t0002g0121 a0004c0007t0002g0122 |
2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.736-1375C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108803514 | |||||||
| chr2:108803518 | A | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.736-1371A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108803518 | |||||||
| chr2:108803624 | C | T | 6 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0092 others(3): Show |
6 | HG02622.hp1 HG02818.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.736-1265C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108803624 | |||||||
| chr2:108804169 | A | G | 1 | a0002c0002t0001g0171 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.736-720A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108804169 | |||||||
| chr2:108804567 | A | G | 1 | a0002c0002t0001g0206 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.736-322A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108804567 | |||||||
| chr2:108804777 | A | G | 1 | a0001c0004t0001g0107 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.736-112A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108804777 | |||||||
| chr2:108804841 | T | C | 1 | a0003c0003t0001g0183 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.736-48T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108804841 | |||||||
| chr2:108804878 | TCTC | T | 35 | a0002c0002t0001g0194 a0003c0003t0001g0003 a0003c0003t0001g0120 others(32): Show |
36 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(33): Show |
splice_region_variant&intron_variant | LOW | c.736-5_736-3delCCT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108804878 | ||||||
| chr2:108805074 | A | T | 1 | a0002c0002t0001g0181 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.855+66A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805074 | |||||||
| chr2:108805165 | G | A | 173 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.855+157G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805165 | |||||||
| chr2:108805376 | A | G | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.855+368A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805376 | |||||||
| chr2:108805396 | T | C | 1 | a0002c0002t0001g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.855+388T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805396 | |||||||
| chr2:108805454 | G | A | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.855+446G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805454 | |||||||
| chr2:108805463 | C | T | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.855+455C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805463 | |||||||
| chr2:108805496 | T | C | 92 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(89): Show |
94 | HG00099.hp1 HG00408.hp1 HG00738.hp2 others(91): Show |
intron_variant | MODIFIER | c.855+488T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805496 | |||||||
| chr2:108805569 | C | CA | 169 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(166): Show |
172 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.855+570dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108805569 | ||||||
| chr2:108805775 | A | G | 5 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.855+767A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805775 | |||||||
| chr2:108805809 | T | C | 5 | a0004c0007t0002g0121 a0004c0007t0002g0122 a0004c0007t0002g0123 others(2): Show |
5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.855+801T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805809 | |||||||
| chr2:108805968 | G | T | 1 | a0001c0001t0002g0080 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.855+960G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805968 | |||||||
| chr2:108806016 | AGT | A | 103 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(100): Show |
105 | HG00099.hp1 HG00408.hp1 HG00738.hp2 others(102): Show |
intron_variant | MODIFIER | c.855+1009_855+1010d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108806016 | |||||||
| chr2:108806077 | T | A | 1 | a0001c0006t0001g0200 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.855+1069T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108806077 | |||||||
| chr2:108806655 | G | A | 2 | a0001c0004t0001g0100 a0001c0004t0001g0101 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.855+1647G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108806655 | |||||||
| chr2:108806806 | A | G | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.855+1798A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108806806 | |||||||
| chr2:108807357 | C | A | 1 | a0001c0001t0002g0029 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.855+2349C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108807357 | |||||||
| chr2:108807659 | C | T | 172 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(169): Show |
175 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.855+2651C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108807659 | |||||||
| chr2:108807743 | G | A | 5 | a0004c0007t0002g0121 a0004c0007t0002g0122 a0004c0007t0002g0123 others(2): Show |
5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.855+2735G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108807743 | |||||||
| chr2:108808299 | C | T | 2 | a0002c0002t0002g0185 a0002c0002t0002g0189 |
2 | HG01175.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.855+3291C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108808299 | |||||||
| chr2:108808448 | G | A | 1 | a0002c0002t0001g0128 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.855+3440G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108808448 | |||||||
| chr2:108808496 | C | T | 1 | a0001c0004t0001g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.855+3488C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108808496 | |||||||
| chr2:108808619 | A | G | 1 | a0006c0008t0001g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.855+3611A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108808619 | |||||||
| chr2:108808925 | T | C | 1 | a0002c0002t0003g0190 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.856-3706T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108808925 | |||||||
| chr2:108809225 | A | G | 1 | a0002c0002t0001g0131 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.856-3406A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809225 | |||||||
| chr2:108809274 | G | A | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.856-3357G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809274 | |||||||
| chr2:108809350 | A | C | 1 | a0001c0001t0002g0058 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.856-3281A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809350 | |||||||
| chr2:108809410 | T | A | 7 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0174 others(4): Show |
7 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.856-3221T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809410 | |||||||
| chr2:108809448 | T | TTG | 12 | a0001c0001t0002g0027 a0002c0002t0001g0172 a0002c0002t0001g0173 others(9): Show |
12 | HG01175.hp2 HG01261.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.856-3144_856-3143d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809448 | ||||||
| chr2:108809448 | T | TTGTG | 3 | a0001c0004t0002g0098 a0002c0002t0001g0171 a0002c0002t0001g0178 |
3 | HG02040.hp2 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.856-3146_856-3143d others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809448 | ||||||
| chr2:108809448 | T | TTGTGTGT others(1): Show |
6 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0201 others(3): Show |
6 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.856-3150_856-3143d others(10): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809448 | ||||||
| chr2:108809448 | TTG | T | 114 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(111): Show |
117 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.856-3144_856-3143d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809448 | ||||||
| chr2:108809448 | TTGTG | T | 15 | a0001c0001t0002g0032 a0001c0001t0002g0061 a0001c0005t0001g0111 others(12): Show |
15 | HG02055.hp1 HG02257.hp1 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.856-3146_856-3143d others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809448 | ||||||
| chr2:108809448 | TTGTGTG | T | 11 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0005t0001g0112 others(8): Show |
11 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.856-3148_856-3143d others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809448 | ||||||
| chr2:108809448 | TTGTGTGT others(1): Show |
T | 9 | a0001c0004t0001g0197 a0001c0005t0001g0115 a0001c0005t0001g0116 others(6): Show |
9 | HG02615.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-3150_856-3143d others(10): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809448 | ||||||
| chr2:108809448 | TTGTGTGT others(3): Show |
T | 7 | a0002c0002t0001g0126 a0002c0002t0001g0127 a0002c0002t0001g0128 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.856-3152_856-3143d others(12): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809448 | ||||||
| chr2:108809448 | TTGTGTGT others(5): Show |
T | 1 | a0003c0003t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.856-3154_856-3143d others(14): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809448 | ||||||
| chr2:108809450 | G | T | 9 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(6): Show |
9 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.856-3181G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809450 | |||||||
| chr2:108809452 | G | T | 34 | a0002c0002t0001g0194 a0003c0003t0001g0003 a0003c0003t0001g0120 others(31): Show |
35 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.856-3179G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809452 | |||||||
| chr2:108809462 | G | T | 1 | a0003c0003t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.856-3169G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809462 | |||||||
| chr2:108809480 | G | T | 4 | a0001c0004t0001g0102 a0001c0004t0001g0103 a0001c0004t0001g0104 others(1): Show |
4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-3151G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809480 | |||||||
| chr2:108809487 | T | A | 1 | a0006c0008t0001g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.856-3144T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809487 | |||||||
| chr2:108809796 | T | TTTTG | 4 | a0001c0004t0001g0197 a0003c0003t0001g0159 a0003c0003t0001g0160 others(1): Show |
4 | HG02723.hp2 HG03098.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.856-2809_856-2806d others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809796 | ||||||
| chr2:108809796 | TTTTG | T | 113 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(110): Show |
115 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(112): Show |
intron_variant | MODIFIER | c.856-2809_856-2806d others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809796 | ||||||
| chr2:108809868 | C | T | 4 | a0001c0004t0001g0102 a0001c0004t0001g0103 a0001c0004t0001g0104 others(1): Show |
4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-2763C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809868 | |||||||
| chr2:108809881 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.856-2750C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809881 | |||||||
| chr2:108810195 | G | A | 5 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.856-2436G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108810195 | |||||||
| chr2:108810258 | A | G | 1 | a0002c0002t0001g0196 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.856-2373A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108810258 | |||||||
| chr2:108810263 | G | T | 1 | a0001c0001t0002g0086 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.856-2368G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108810263 | |||||||
| chr2:108810328 | A | T | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.856-2303A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108810328 | |||||||
| chr2:108810364 | G | T | 1 | a0002c0002t0002g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856-2267G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108810364 | |||||||
| chr2:108810474 | T | A | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.856-2157T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108810474 | |||||||
| chr2:108810771 | G | T | 173 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.856-1860G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108810771 | |||||||
| chr2:108810776 | A | T | 1 | a0003c0003t0001g0137 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.856-1855A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108810776 | |||||||
| chr2:108810815 | G | A | 2 | a0001c0010t0002g0067 a0003c0003t0001g0139 |
2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.856-1816G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108810815 | |||||||
| chr2:108811021 | G | C | 1 | a0002c0002t0002g0182 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856-1610G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108811021 | |||||||
| chr2:108811087 | CCTTTTTT others(17): Show |
C | 1 | a0001c0004t0001g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.856-1532_856-1509d others(26): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811087 | ||||||
| chr2:108811100 | C | CT | 10 | a0002c0002t0001g0133 a0002c0002t0001g0166 a0002c0002t0001g0167 others(7): Show |
10 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.856-1520dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811100 | ||||||
| chr2:108811100 | CTTTTTTT | C | 171 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(168): Show |
174 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.856-1526_856-1520d others(9): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811100 | ||||||
| chr2:108811241 | C | G | 11 | a0001c0005t0001g0207 a0001c0005t0001g0208 a0001c0005t0001g0209 others(8): Show |
11 | HG01175.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.856-1390C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108811241 | |||||||
| chr2:108811245 | C | CTTTT | 83 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(80): Show |
85 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.856-1385_856-1384i others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811245 | ||||||
| chr2:108811245 | C | CTTTTT | 10 | a0001c0001t0002g0009 a0001c0001t0002g0026 a0001c0001t0002g0046 others(7): Show |
10 | HG01361.hp1 HG01361.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.856-1385_856-1384i others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811245 | ||||||
| chr2:108811245 | C | CTTTTTT | 7 | a0001c0001t0002g0077 a0001c0004t0001g0100 a0001c0004t0001g0101 others(4): Show |
7 | HG01243.hp2 HG02738.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.856-1385_856-1384i others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811245 | ||||||
| chr2:108811245 | C | CTTTTTTT | 20 | a0001c0005t0001g0114 a0001c0005t0001g0115 a0001c0005t0001g0116 others(17): Show |
20 | HG01175.hp1 HG01261.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.856-1385_856-1384i others(9): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811245 | ||||||
| chr2:108811245 | C | CTTTTTTT others(2): Show |
8 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(5): Show |
8 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.856-1385_856-1384i others(11): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811245 | ||||||
| chr2:108811245 | C | CTTTTTTT others(3): Show |
1 | a0004c0007t0002g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.856-1385_856-1384i others(12): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811245 | ||||||
| chr2:108811247 | C | CTCTTTTT others(4): Show |
1 | a0003c0003t0001g0157 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.856-1383_856-1382i others(13): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | ||||||
| chr2:108811247 | C | CTCTTTTT others(9): Show |
3 | a0003c0003t0001g0136 a0003c0003t0001g0137 a0003c0003t0001g0155 |
3 | HG01109.hp2 NA19070.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.856-1383_856-1382i others(18): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | ||||||
| chr2:108811247 | C | CTCTTTTT others(15): Show |
2 | a0001c0004t0001g0014 a0001c0012t0001g0013 |
2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.856-1383_856-1382i others(24): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | ||||||
| chr2:108811247 | C | CTCTTTTT others(16): Show |
5 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(2): Show |
5 | HG02572.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.856-1383_856-1382i others(25): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | ||||||
| chr2:108811247 | C | CTCTTTTT others(18): Show |
1 | a0001c0004t0001g0015 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.856-1383_856-1382i others(27): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | ||||||
| chr2:108811247 | C | CTCTTTTT others(19): Show |
1 | a0003c0003t0001g0179 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.856-1383_856-1382i others(28): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | ||||||
| chr2:108811247 | C | CTCTTTTT others(20): Show |
1 | a0008c0015t0001g0193 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.856-1383_856-1382i others(29): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | ||||||
| chr2:108811247 | C | CTCTTTTT others(21): Show |
8 | a0003c0003t0001g0134 a0003c0003t0001g0138 a0003c0003t0001g0144 others(5): Show |
8 | HG00099.hp2 HG00408.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.856-1383_856-1382i others(30): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | ||||||
| chr2:108811247 | C | CTCTTTTT others(22): Show |
11 | a0002c0002t0001g0194 a0003c0003t0001g0139 a0003c0003t0001g0142 others(8): Show |
11 | HG00738.hp1 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.856-1383_856-1382i others(31): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | ||||||
| chr2:108811247 | C | CTCTTTTT others(23): Show |
3 | a0003c0003t0001g0003 a0003c0003t0001g0140 a0003c0003t0001g0158 |
4 | NA18977.hp2 NA18993.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-1383_856-1382i others(32): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | ||||||
| chr2:108811247 | C | CTCTTTTT others(24): Show |
2 | a0003c0003t0001g0161 a0003c0003t0001g0162 |
2 | NA18945.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.856-1383_856-1382i others(33): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | ||||||
| chr2:108811247 | C | CTCTTTTT others(27): Show |
1 | a0003c0003t0001g0120 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.856-1383_856-1382i others(36): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | ||||||
| chr2:108811247 | C | CTCTTTTT others(47): Show |
2 | a0003c0003t0001g0141 a0003c0003t0001g0180 |
2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.856-1383_856-1382i others(56): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | ||||||
| chr2:108811247 | C | CTTTTTTT others(5): Show |
1 | a0002c0002t0001g0130 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.856-1380_856-1369d others(14): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | ||||||
| chr2:108811247 | C | CTTTTTTT others(6): Show |
6 | a0002c0002t0001g0126 a0002c0002t0001g0127 a0002c0002t0001g0128 others(3): Show |
6 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.856-1381_856-1369d others(15): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | ||||||
| chr2:108811247 | C | T | 133 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(130): Show |
135 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(132): Show |
intron_variant | MODIFIER | c.856-1384C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108811247 | |||||||
| chr2:108811287 | T | C | 176 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(173): Show |
179 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.856-1344T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108811287 | |||||||
| chr2:108811320 | A | G | 1 | a0001c0001t0002g0043 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.856-1311A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108811320 | |||||||
| chr2:108811395 | C | T | 2 | a0001c0001t0002g0002 a0001c0005t0001g0111 |
3 | HG01074.hp2 HG01099.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.856-1236C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108811395 | |||||||
| chr2:108812045 | A | G | 1 | a0001c0005t0001g0116 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.856-586A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108812045 | |||||||
| chr2:108812085 | A | G | 1 | a0001c0004t0001g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.856-546A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108812085 | |||||||
| chr2:108812150 | T | C | 1 | a0001c0010t0002g0067 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.856-481T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108812150 | |||||||
| chr2:108812219 | T | C | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.856-412T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108812219 | |||||||
| chr2:108812387 | A | G | 27 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0004t0001g0106 others(24): Show |
27 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.856-244A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108812387 | |||||||
| chr2:108812472 | C | T | 7 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0004t0001g0106 others(4): Show |
7 | HG02258.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.856-159C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108812472 | |||||||
| chr2:108812806 | A | G | 31 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0004t0001g0102 others(28): Show |
31 | HG01081.hp2 HG01175.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.934-14A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 8/14 | chr2 | 108812806 | |||||||
| chr2:108812968 | G | A | 5 | a0004c0007t0002g0121 a0004c0007t0002g0122 a0004c0007t0002g0123 others(2): Show |
5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1041+41G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108812968 | |||||||
| chr2:108812983 | C | T | 1 | a0003c0003t0001g0158 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1041+56C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108812983 | |||||||
| chr2:108813076 | C | T | 5 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041+149C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813076 | |||||||
| chr2:108813121 | C | T | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041+194C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813121 | |||||||
| chr2:108813141 | C | T | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1041+214C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813141 | |||||||
| chr2:108813188 | G | A | 86 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(83): Show |
88 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.1041+261G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813188 | |||||||
| chr2:108813248 | C | CA | 12 | a0001c0004t0001g0197 a0001c0004t0002g0099 a0001c0005t0001g0116 others(9): Show |
12 | HG01099.hp1 HG01109.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1041+345dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108813248 | ||||||
| chr2:108813248 | C | CAA | 57 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(54): Show |
58 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1041+344_1041+345d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108813248 | ||||||
| chr2:108813248 | C | CAAA | 82 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(79): Show |
84 | HG00099.hp1 HG00408.hp1 HG00741.hp1 others(81): Show |
intron_variant | MODIFIER | c.1041+343_1041+345d others(5): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108813248 | ||||||
| chr2:108813248 | C | CAAAA | 16 | a0001c0001t0002g0005 a0001c0001t0002g0033 a0001c0001t0002g0034 others(13): Show |
16 | HG00741.hp2 HG01361.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.1041+342_1041+345d others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108813248 | ||||||
| chr2:108813269 | A | G | 2 | a0001c0004t0001g0100 a0001c0004t0001g0101 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1041+342A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813269 | |||||||
| chr2:108813365 | A | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1041+438A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813365 | |||||||
| chr2:108813484 | T | C | 7 | a0002c0002t0001g0126 a0002c0002t0001g0127 a0002c0002t0001g0128 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041+557T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813484 | |||||||
| chr2:108813760 | A | C | 2 | a0003c0003t0001g0141 a0003c0003t0001g0180 |
2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1041+833A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813760 | |||||||
| chr2:108813782 | C | T | 22 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0005t0001g0111 others(19): Show |
22 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1041+855C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813782 | |||||||
| chr2:108813848 | G | T | 1 | a0002c0002t0001g0130 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1041+921G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813848 | |||||||
| chr2:108813934 | A | G | 2 | a0002c0002t0002g0185 a0002c0002t0002g0189 |
2 | HG01175.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1041+1007A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813934 | |||||||
| chr2:108814249 | G | C | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041+1322G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108814249 | |||||||
| chr2:108814353 | A | G | 1 | a0003c0003t0001g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1041+1426A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108814353 | |||||||
| chr2:108814419 | C | T | 173 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1041+1492C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108814419 | |||||||
| chr2:108814450 | T | A | 1 | a0001c0001t0002g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1042-1491T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108814450 | |||||||
| chr2:108814549 | C | T | 1 | a0003c0003t0001g0157 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1042-1392C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108814549 | |||||||
| chr2:108814632 | AT | A | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-1302delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108814632 | ||||||
| chr2:108814761 | G | A | 5 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-1180G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108814761 | |||||||
| chr2:108814881 | C | G | 1 | a0001c0001t0002g0054 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1042-1060C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108814881 | |||||||
| chr2:108814947 | A | T | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1042-994A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108814947 | |||||||
| chr2:108815109 | CAG | C | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1042-829_1042-828d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108815109 | ||||||
| chr2:108815205 | G | A | 5 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-736G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815205 | |||||||
| chr2:108815284 | A | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1042-657A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815284 | |||||||
| chr2:108815369 | A | G | 2 | a0001c0004t0002g0098 a0001c0004t0002g0099 |
2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1042-572A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815369 | |||||||
| chr2:108815393 | T | C | 5 | a0004c0007t0002g0121 a0004c0007t0002g0122 a0004c0007t0002g0123 others(2): Show |
5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1042-548T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815393 | |||||||
| chr2:108815448 | G | A | 173 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1042-493G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815448 | |||||||
| chr2:108815461 | G | GT | 105 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(102): Show |
107 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1042-457dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108815461 | ||||||
| chr2:108815461 | G | GTT | 16 | a0001c0001t0001g0078 a0001c0001t0002g0042 a0001c0001t0002g0061 others(13): Show |
16 | HG01175.hp1 HG01516.hp2 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.1042-458_1042-457d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108815461 | ||||||
| chr2:108815461 | G | GTTT | 5 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0201 others(2): Show |
5 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.1042-459_1042-457d others(5): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108815461 | ||||||
| chr2:108815461 | GT | G | 13 | a0002c0002t0001g0128 a0002c0002t0001g0129 a0002c0002t0001g0130 others(10): Show |
13 | HG01167.hp2 HG01884.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1042-457delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108815461 | ||||||
| chr2:108815464 | T | TG | 2 | a0001c0004t0001g0100 a0001c0004t0001g0101 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1042-477_1042-476i others(3): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815464 | |||||||
| chr2:108815466 | T | G | 1 | a0002c0002t0001g0206 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1042-475T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815466 | |||||||
| chr2:108815473 | T | TTG | 9 | a0001c0004t0001g0102 a0001c0004t0001g0103 a0001c0004t0001g0104 others(6): Show |
9 | HG01081.hp2 HG02258.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1042-467_1042-466i others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108815473 | ||||||
| chr2:108815479 | T | G | 4 | a0001c0004t0001g0102 a0001c0004t0001g0103 a0001c0004t0001g0104 others(1): Show |
4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1042-462T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815479 | |||||||
| chr2:108815516 | G | C | 44 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(41): Show |
45 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1042-425G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815516 | |||||||
| chr2:108815530 | G | A | 5 | a0004c0007t0002g0121 a0004c0007t0002g0122 a0004c0007t0002g0123 others(2): Show |
5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1042-411G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815530 | |||||||
| chr2:108816366 | G | A | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+261G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108816366 | |||||||
| chr2:108816552 | T | TA | 178 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(175): Show |
181 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1206+447_1206+448i others(3): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108816552 | |||||||
| chr2:108816696 | T | A | 31 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0004t0001g0102 others(28): Show |
31 | HG01081.hp2 HG01175.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1206+591T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108816696 | |||||||
| chr2:108816814 | A | G | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+709A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108816814 | |||||||
| chr2:108816873 | T | A | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1206+768T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108816873 | |||||||
| chr2:108817079 | G | A | 1 | a0002c0002t0001g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1206+974G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108817079 | |||||||
| chr2:108817299 | C | CT | 5 | a0001c0001t0002g0026 a0001c0004t0001g0108 a0001c0004t0001g0109 others(2): Show |
5 | HG03195.hp1 HG03225.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1206+1206dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108817299 | ||||||
| chr2:108817316 | C | T | 2 | a0003c0003t0001g0159 a0003c0003t0001g0160 |
2 | HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1206+1211C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108817316 | |||||||
| chr2:108817481 | C | T | 1 | a0003c0003t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1206+1376C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108817481 | |||||||
| chr2:108817520 | C | T | 172 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(169): Show |
175 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1206+1415C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108817520 | |||||||
| chr2:108817542 | C | T | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+1437C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108817542 | |||||||
| chr2:108817641 | G | A | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+1536G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108817641 | |||||||
| chr2:108817859 | C | T | 185 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(182): Show |
188 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1206+1754C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108817859 | |||||||
| chr2:108818056 | T | C | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+1951T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108818056 | |||||||
| chr2:108818325 | G | A | 1 | a0001c0004t0002g0097 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1206+2220G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108818325 | |||||||
| chr2:108818820 | C | CT | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+2727dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108818820 | ||||||
| chr2:108818820 | CT | C | 36 | a0002c0002t0001g0194 a0003c0003t0001g0003 a0003c0003t0001g0120 others(33): Show |
37 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1206+2727delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108818820 | ||||||
| chr2:108819176 | T | C | 5 | a0001c0001t0002g0046 a0001c0004t0002g0096 a0001c0004t0002g0097 others(2): Show |
5 | HG01361.hp1 HG02486.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1206+3071T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108819176 | |||||||
| chr2:108819257 | T | C | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1206+3152T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108819257 | |||||||
| chr2:108819296 | G | A | 1 | a0002c0002t0001g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1206+3191G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108819296 | |||||||
| chr2:108819331 | C | G | 1 | a0001c0013t0002g0075 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1206+3226C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108819331 | |||||||
| chr2:108819447 | A | C | 1 | a0003c0003t0001g0140 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1206+3342A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108819447 | |||||||
| chr2:108819523 | G | A | 172 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(169): Show |
175 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1206+3418G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108819523 | |||||||
| chr2:108819547 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0078 |
2 | HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1206+3442A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108819547 | |||||||
| chr2:108819868 | GA | G | 93 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(90): Show |
95 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(92): Show |
intron_variant | MODIFIER | c.1206+3765delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108819868 | ||||||
| chr2:108820052 | A | G | 1 | a0001c0004t0001g0110 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1206+3947A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820052 | |||||||
| chr2:108820061 | AGCAGACT others(7): Show |
A | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1206+3962_1206+397 others(18): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108820061 | ||||||
| chr2:108820236 | C | T | 3 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0070 |
3 | HG01074.hp1 HG01358.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1206+4131C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820236 | |||||||
| chr2:108820273 | T | C | 1 | a0001c0001t0002g0079 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1206+4168T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820273 | |||||||
| chr2:108820329 | A | C | 2 | a0001c0004t0001g0100 a0001c0004t0001g0101 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1206+4224A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820329 | |||||||
| chr2:108820384 | G | T | 9 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0174 others(6): Show |
9 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1206+4279G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820384 | |||||||
| chr2:108820503 | G | A | 1 | a0002c0002t0003g0188 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1206+4398G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820503 | |||||||
| chr2:108820681 | G | T | 7 | a0002c0002t0001g0126 a0002c0002t0001g0127 a0002c0002t0001g0128 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+4576G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820681 | |||||||
| chr2:108820690 | T | G | 2 | a0003c0003t0001g0120 a0003c0003t0001g0148 |
2 | NA18974.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1206+4585T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820690 | |||||||
| chr2:108820712 | A | AAAAAC | 34 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0001t0002g0002 others(31): Show |
35 | HG00408.hp2 HG01074.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1206+4610_1206+461 others(9): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108820712 | ||||||
| chr2:108820712 | A | AAAC | 9 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0006t0001g0198 others(6): Show |
9 | HG01261.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1206+4609_1206+461 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108820712 | ||||||
| chr2:108820712 | A | C | 1 | a0001c0001t0002g0054 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1206+4607A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820712 | |||||||
| chr2:108820713 | A | T | 1 | a0001c0001t0002g0054 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1206+4608A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820713 | |||||||
| chr2:108820720 | C | A | 45 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0001t0002g0002 others(42): Show |
46 | HG00408.hp2 HG01074.hp2 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.1206+4615C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820720 | |||||||
| chr2:108820720 | C | CAAAA | 160 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(157): Show |
162 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1206+4617_1206+461 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108820720 | ||||||
| chr2:108820971 | G | A | 173 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1206+4866G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820971 | |||||||
| chr2:108821018 | T | TA | 169 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(166): Show |
172 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.1206+4921dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108821018 | ||||||
| chr2:108821100 | G | A | 1 | a0003c0003t0001g0149 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1206+4995G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108821100 | |||||||
| chr2:108821119 | AGGCTAAG others(6): Show |
A | 1 | a0003c0003t0001g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1206+5017_1206+502 others(17): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108821119 | ||||||
| chr2:108821129 | A | G | 1 | a0002c0002t0001g0176 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1206+5024A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108821129 | |||||||
| chr2:108821352 | C | T | 1 | a0001c0001t0002g0074 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1206+5247C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108821352 | |||||||
| chr2:108821357 | C | CA | 31 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0004t0001g0102 others(28): Show |
31 | HG01081.hp2 HG01175.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1206+5260dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108821357 | ||||||
| chr2:108821415 | A | G | 185 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(182): Show |
188 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1206+5310A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108821415 | |||||||
| chr2:108821622 | A | G | 1 | a0001c0001t0002g0054 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1206+5517A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108821622 | |||||||
| chr2:108821711 | G | GA | 2 | a0003c0003t0001g0136 a0003c0003t0001g0163 |
2 | HG01109.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1206+5607dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108821711 | ||||||
| chr2:108821826 | T | A | 1 | a0001c0001t0002g0004 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1206+5721T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108821826 | |||||||
| chr2:108821892 | C | T | 2 | a0001c0004t0001g0100 a0001c0004t0001g0101 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1206+5787C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108821892 | |||||||
| chr2:108821928 | C | CA | 123 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(120): Show |
125 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(122): Show |
intron_variant | MODIFIER | c.1206+5840dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108821928 | ||||||
| chr2:108821928 | C | CAA | 9 | a0001c0005t0001g0114 a0001c0005t0002g0214 a0001c0006t0001g0198 others(6): Show |
9 | HG01175.hp1 HG01261.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.1206+5839_1206+584 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108821928 | ||||||
| chr2:108822248 | C | G | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+6143C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108822248 | |||||||
| chr2:108822268 | A | G | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+6163A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108822268 | |||||||
| chr2:108822449 | C | T | 1 | a0002c0002t0001g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1206+6344C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108822449 | |||||||
| chr2:108822644 | A | G | 2 | a0001c0001t0001g0056 a0001c0001t0002g0057 |
2 | HG04204.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1206+6539A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108822644 | |||||||
| chr2:108822699 | A | G | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+6594A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108822699 | |||||||
| chr2:108822837 | T | G | 31 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0004t0001g0102 others(28): Show |
31 | HG01081.hp2 HG01175.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1206+6732T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108822837 | |||||||
| chr2:108822996 | T | A | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1206+6891T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108822996 | |||||||
| chr2:108823358 | G | A | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+7253G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108823358 | |||||||
| chr2:108823485 | A | G | 31 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0004t0001g0102 others(28): Show |
31 | HG01081.hp2 HG01175.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1206+7380A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108823485 | |||||||
| chr2:108823586 | T | C | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1206+7481T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108823586 | |||||||
| chr2:108823777 | C | T | 86 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(83): Show |
88 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.1206+7672C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108823777 | |||||||
| chr2:108823945 | C | T | 141 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(138): Show |
144 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.1206+7840C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108823945 | |||||||
| chr2:108823996 | TG | T | 37 | a0002c0002t0001g0194 a0003c0003t0001g0003 a0003c0003t0001g0120 others(34): Show |
38 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1206+7897delG | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108823996 | ||||||
| chr2:108824170 | AT | A | 172 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(169): Show |
175 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1206+8071delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108824170 | ||||||
| chr2:108824504 | A | G | 1 | a0001c0001t0002g0032 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1206+8399A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108824504 | |||||||
| chr2:108824604 | T | A | 2 | a0001c0005t0001g0207 a0003c0003t0001g0147 |
2 | HG02647.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1206+8499T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108824604 | |||||||
| chr2:108824744 | A | G | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+8639A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108824744 | |||||||
| chr2:108824848 | G | T | 19 | a0001c0005t0001g0112 a0001c0005t0001g0113 a0001c0005t0001g0114 others(16): Show |
19 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1206+8743G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108824848 | |||||||
| chr2:108824994 | A | G | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+8889A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108824994 | |||||||
| chr2:108825044 | A | G | 4 | a0001c0004t0001g0102 a0001c0004t0001g0103 a0001c0004t0001g0104 others(1): Show |
4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1206+8939A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108825044 | |||||||
| chr2:108825058 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1206+8953A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108825058 | |||||||
| chr2:108825231 | A | G | 1 | a0002c0002t0001g0129 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1206+9126A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108825231 | |||||||
| chr2:108825274 | TTTTG | T | 97 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(94): Show |
99 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(96): Show |
intron_variant | MODIFIER | c.1206+9186_1206+918 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108825274 | ||||||
| chr2:108825394 | G | A | 2 | a0002c0002t0001g0175 a0002c0002t0001g0176 |
2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1206+9289G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108825394 | |||||||
| chr2:108825440 | A | C | 1 | a0001c0011t0002g0031 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1206+9335A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108825440 | |||||||
| chr2:108825558 | G | A | 185 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(182): Show |
188 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1206+9453G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108825558 | |||||||
| chr2:108825588 | A | G | 5 | a0004c0007t0002g0121 a0004c0007t0002g0122 a0004c0007t0002g0123 others(2): Show |
5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1206+9483A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108825588 | |||||||
| chr2:108825737 | T | C | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+9632T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108825737 | |||||||
| chr2:108825787 | A | G | 172 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(169): Show |
175 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1206+9682A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108825787 | |||||||
| chr2:108826128 | G | A | 1 | a0001c0001t0002g0037 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1206+10023G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108826128 | |||||||
| chr2:108826170 | C | A | 1 | a0004c0007t0002g0121 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1206+10065C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108826170 | |||||||
| chr2:108826203 | G | A | 1 | a0001c0001t0002g0080 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1206+10098G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108826203 | |||||||
| chr2:108826264 | A | G | 1 | a0001c0005t0001g0119 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1206+10159A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108826264 | |||||||
| chr2:108826296 | A | G | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | HG02735.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1206+10191A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108826296 | |||||||
| chr2:108826348 | T | G | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+10243T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108826348 | |||||||
| chr2:108826474 | A | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1206+10369A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108826474 | |||||||
| chr2:108826687 | A | G | 173 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1206+10582A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108826687 | |||||||
| chr2:108826691 | TC | T | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+10588delC | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108826691 | ||||||
| chr2:108826930 | C | T | 5 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1206+10825C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108826930 | |||||||
| chr2:108827051 | T | C | 5 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1206+10946T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827051 | |||||||
| chr2:108827334 | C | T | 20 | a0001c0005t0001g0111 a0001c0005t0001g0112 a0001c0005t0001g0113 others(17): Show |
20 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1206+11229C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827334 | |||||||
| chr2:108827473 | A | C | 22 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0005t0001g0111 others(19): Show |
22 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206+11368A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827473 | |||||||
| chr2:108827483 | A | G | 90 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(87): Show |
92 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(89): Show |
intron_variant | MODIFIER | c.1206+11378A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827483 | |||||||
| chr2:108827542 | C | T | 1 | a0002c0002t0001g0133 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1206+11437C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827542 | |||||||
| chr2:108827591 | C | CA | 37 | a0002c0002t0001g0194 a0003c0003t0001g0003 a0003c0003t0001g0120 others(34): Show |
38 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1206+11486_1206+11 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827591 | |||||||
| chr2:108827594 | ATC | A | 37 | a0002c0002t0001g0194 a0003c0003t0001g0003 a0003c0003t0001g0120 others(34): Show |
38 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1206+11490_1206+11 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827594 | |||||||
| chr2:108827611 | C | T | 1 | a0001c0006t0001g0204 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1206+11506C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827611 | |||||||
| chr2:108827612 | G | C | 1 | a0001c0006t0001g0204 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1206+11507G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827612 | |||||||
| chr2:108827614 | A | G | 1 | a0001c0006t0001g0204 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1206+11509A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827614 | |||||||
| chr2:108827617 | C | G | 1 | a0001c0006t0001g0204 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1206+11512C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827617 | |||||||
| chr2:108827618 | T | C | 1 | a0001c0006t0001g0204 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1206+11513T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827618 | |||||||
| chr2:108827673 | A | G | 1 | a0001c0013t0002g0075 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1207-11512A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827673 | |||||||
| chr2:108827676 | C | T | 44 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(41): Show |
45 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1207-11509C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827676 | |||||||
| chr2:108827748 | G | A | 2 | a0001c0004t0001g0106 a0001c0004t0001g0107 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1207-11437G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827748 | |||||||
| chr2:108827814 | T | TA | 11 | a0001c0004t0001g0011 a0001c0006t0001g0204 a0002c0002t0001g0171 others(8): Show |
11 | HG01109.hp2 HG01167.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.1207-11353dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108827814 | ||||||
| chr2:108827814 | TA | T | 111 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(108): Show |
113 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(110): Show |
intron_variant | MODIFIER | c.1207-11353delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108827814 | ||||||
| chr2:108827814 | TAA | T | 5 | a0001c0001t0002g0008 a0001c0004t0002g0096 a0001c0004t0002g0097 others(2): Show |
5 | HG01167.hp1 HG02486.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-11354_1207-11 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108827814 | ||||||
| chr2:108827817 | A | T | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207-11368A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827817 | |||||||
| chr2:108827902 | C | T | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1207-11283C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827902 | |||||||
| chr2:108828027 | A | G | 5 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(2): Show |
5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207-11158A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828027 | |||||||
| chr2:108828040 | A | G | 11 | a0001c0001t0001g0030 a0001c0001t0002g0001 a0001c0001t0002g0005 others(8): Show |
12 | HG00408.hp1 HG01978.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.1207-11145A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828040 | |||||||
| chr2:108828176 | A | G | 1 | a0001c0001t0002g0079 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1207-11009A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828176 | |||||||
| chr2:108828244 | G | A | 7 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0174 others(4): Show |
7 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-10941G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828244 | |||||||
| chr2:108828370 | A | G | 1 | a0001c0005t0001g0216 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1207-10815A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828370 | |||||||
| chr2:108828408 | T | C | 1 | a0001c0004t0001g0012 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1207-10777T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828408 | |||||||
| chr2:108828662 | G | A | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-10523G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828662 | |||||||
| chr2:108828760 | C | G | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207-10425C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828760 | |||||||
| chr2:108828864 | G | C | 2 | a0001c0004t0001g0100 a0001c0004t0001g0101 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1207-10321G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828864 | |||||||
| chr2:108828927 | G | A | 86 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(83): Show |
88 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.1207-10258G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828927 | |||||||
| chr2:108828958 | A | G | 7 | a0002c0002t0001g0126 a0002c0002t0001g0127 a0002c0002t0001g0128 others(4): Show |
7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-10227A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828958 | |||||||
| chr2:108829246 | T | C | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-9939T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829246 | |||||||
| chr2:108829348 | A | G | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-9837A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829348 | |||||||
| chr2:108829413 | A | G | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-9772A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829413 | |||||||
| chr2:108829469 | A | AACAGGGC others(3): Show |
1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1207-9713_1207-971 others(14): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108829469 | ||||||
| chr2:108829472 | A | G | 1 | a0001c0006t0001g0201 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1207-9713A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829472 | |||||||
| chr2:108829490 | A | G | 101 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(98): Show |
103 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(100): Show |
intron_variant | MODIFIER | c.1207-9695A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829490 | |||||||
| chr2:108829533 | G | A | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1207-9652G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829533 | |||||||
| chr2:108829555 | G | C | 1 | a0001c0001t0002g0004 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1207-9630G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829555 | |||||||
| chr2:108829565 | G | C | 1 | a0001c0001t0002g0038 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1207-9620G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829565 | |||||||
| chr2:108829626 | G | A | 22 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0005t0001g0111 others(19): Show |
22 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-9559G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829626 | |||||||
| chr2:108829657 | A | C | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1207-9528A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829657 | |||||||
| chr2:108830000 | AAAG | A | 27 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0004t0001g0106 others(24): Show |
27 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.1207-9181_1207-917 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108830000 | ||||||
| chr2:108830187 | G | A | 1 | a0003c0003t0001g0136 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1207-8998G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108830187 | |||||||
| chr2:108830498 | CT | C | 5 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-8684delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108830498 | ||||||
| chr2:108830585 | TC | T | 19 | a0001c0005t0001g0111 a0001c0005t0001g0112 a0001c0005t0001g0113 others(16): Show |
19 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1207-8599delC | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108830585 | |||||||
| chr2:108830607 | G | C | 1 | a0001c0004t0001g0103 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1207-8578G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108830607 | |||||||
| chr2:108830608 | T | A | 173 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(170): Show |
176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1207-8577T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108830608 | |||||||
| chr2:108830693 | A | T | 2 | a0001c0001t0002g0055 a0001c0001t0002g0073 |
2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1207-8492A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108830693 | |||||||
| chr2:108830722 | C | T | 99 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(96): Show |
100 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(97): Show |
intron_variant | MODIFIER | c.1207-8463C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108830722 | |||||||
| chr2:108830736 | A | C | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1207-8449A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108830736 | |||||||
| chr2:108830874 | A | C | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1207-8311A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108830874 | |||||||
| chr2:108830880 | G | A | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-8305G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108830880 | |||||||
| chr2:108831059 | C | T | 27 | a0001c0005t0001g0111 a0001c0005t0001g0112 a0001c0005t0001g0113 others(24): Show |
27 | HG01243.hp2 HG02055.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.1207-8126C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831059 | |||||||
| chr2:108831100 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1207-8085C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831100 | |||||||
| chr2:108831151 | C | G | 5 | a0004c0007t0002g0121 a0004c0007t0002g0122 a0004c0007t0002g0123 others(2): Show |
5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-8034C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831151 | |||||||
| chr2:108831178 | CA | C | 28 | a0001c0001t0001g0030 a0001c0001t0002g0082 a0001c0005t0001g0111 others(25): Show |
28 | HG01243.hp2 HG02055.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.1207-7998delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108831178 | ||||||
| chr2:108831210 | G | A | 184 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(181): Show |
187 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1207-7975G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831210 | |||||||
| chr2:108831331 | T | G | 17 | a0001c0001t0001g0078 a0001c0001t0002g0019 a0001c0001t0002g0074 others(14): Show |
17 | HG01074.hp1 HG01167.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1207-7854T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831331 | |||||||
| chr2:108831420 | A | G | 1 | a0002c0002t0003g0190 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1207-7765A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831420 | |||||||
| chr2:108831700 | T | TCTTC | 28 | a0001c0001t0002g0004 a0001c0001t0002g0020 a0001c0001t0002g0070 others(25): Show |
28 | HG01261.hp2 HG01358.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.1207-7451_1207-744 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108831700 | ||||||
| chr2:108831700 | T | TCTTCCTT others(1): Show |
28 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0078 others(25): Show |
28 | HG00099.hp1 HG00741.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1207-7455_1207-744 others(12): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108831700 | ||||||
| chr2:108831700 | T | TCTTCCTT others(5): Show |
64 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0005 others(61): Show |
66 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.1207-7459_1207-744 others(16): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108831700 | ||||||
| chr2:108831700 | T | TCTTCCTT others(9): Show |
35 | a0001c0001t0002g0017 a0001c0001t0002g0024 a0001c0001t0002g0028 others(32): Show |
36 | HG01081.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1207-7463_1207-744 others(20): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108831700 | ||||||
| chr2:108831700 | T | TCTTCCTT others(13): Show |
10 | a0001c0001t0001g0030 a0001c0001t0002g0009 a0001c0001t0002g0069 others(7): Show |
10 | HG01167.hp2 HG02451.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207-7467_1207-744 others(24): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108831700 | ||||||
| chr2:108831700 | T | TCTTCCTT others(17): Show |
26 | a0001c0004t0001g0011 a0001c0004t0001g0012 a0001c0004t0001g0015 others(23): Show |
26 | HG01243.hp1 HG01261.hp1 HG02523.hp1 others(23): Show |
intron_variant | MODIFIER | c.1207-7471_1207-744 others(28): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108831700 | ||||||
| chr2:108831700 | T | TCTTCCTT others(21): Show |
7 | a0001c0004t0001g0010 a0001c0004t0001g0014 a0001c0004t0001g0106 others(4): Show |
7 | HG02055.hp1 HG02258.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1207-7475_1207-744 others(32): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108831700 | ||||||
| chr2:108831700 | TCTTC | T | 4 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 others(1): Show |
4 | HG02818.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207-7451_1207-744 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108831700 | ||||||
| chr2:108831785 | C | T | 9 | a0001c0001t0001g0030 a0002c0002t0001g0133 a0002c0002t0001g0167 others(6): Show |
9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207-7400C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831785 | |||||||
| chr2:108831809 | T | G | 1 | a0003c0003t0001g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1207-7376T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831809 | |||||||
| chr2:108831857 | C | T | 4 | a0002c0002t0001g0166 a0003c0003t0001g0159 a0003c0003t0001g0160 others(1): Show |
4 | HG02622.hp2 HG02723.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207-7328C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831857 | |||||||
| chr2:108831985 | G | A | 7 | a0003c0003t0001g0143 a0003c0003t0001g0149 a0003c0003t0001g0151 others(4): Show |
7 | HG00099.hp2 HG00738.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-7200G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831985 | |||||||
| chr2:108831992 | C | T | 1 | a0003c0003t0001g0155 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1207-7193C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831992 | |||||||
| chr2:108832024 | C | T | 1 | a0002c0002t0001g0133 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1207-7161C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832024 | |||||||
| chr2:108832107 | T | G | 202 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1207-7078T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832107 | |||||||
| chr2:108832170 | C | T | 4 | a0002c0002t0001g0174 a0002c0002t0001g0175 a0002c0002t0001g0176 others(1): Show |
4 | HG02451.hp2 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207-7015C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832170 | |||||||
| chr2:108832173 | G | T | 4 | a0001c0004t0001g0102 a0001c0004t0001g0103 a0001c0004t0001g0104 others(1): Show |
4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207-7012G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832173 | |||||||
| chr2:108832216 | G | A | 2 | a0001c0004t0001g0010 a0001c0004t0001g0014 |
2 | HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1207-6969G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832216 | |||||||
| chr2:108832336 | ATTTC | A | 5 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-6841_1207-683 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108832336 | ||||||
| chr2:108832344 | C | CT | 12 | a0001c0001t0001g0030 a0001c0004t0001g0016 a0002c0002t0001g0133 others(9): Show |
12 | HG01099.hp1 HG01993.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1207-6821dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108832344 | ||||||
| chr2:108832344 | CT | C | 79 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0001t0002g0034 others(76): Show |
80 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.1207-6821delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108832344 | ||||||
| chr2:108832348 | T | C | 2 | a0001c0001t0002g0032 a0002c0002t0001g0181 |
2 | NA18988.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1207-6837T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832348 | |||||||
| chr2:108832349 | T | C | 14 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(11): Show |
14 | HG01261.hp1 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1207-6836T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832349 | |||||||
| chr2:108832425 | G | A | 9 | a0001c0001t0001g0030 a0002c0002t0001g0133 a0002c0002t0001g0167 others(6): Show |
9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207-6760G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832425 | |||||||
| chr2:108832479 | C | G | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-6706C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832479 | |||||||
| chr2:108832530 | A | G | 8 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(5): Show |
8 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1207-6655A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832530 | |||||||
| chr2:108832766 | A | C | 1 | a0001c0005t0001g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1207-6419A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832766 | |||||||
| chr2:108832796 | T | C | 9 | a0001c0001t0001g0030 a0002c0002t0001g0133 a0002c0002t0001g0167 others(6): Show |
9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207-6389T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832796 | |||||||
| chr2:108832814 | A | G | 1 | a0001c0001t0002g0058 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1207-6371A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832814 | |||||||
| chr2:108832935 | A | C | 5 | a0001c0004t0001g0108 a0001c0004t0001g0109 a0001c0004t0001g0110 others(2): Show |
5 | HG02055.hp2 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207-6250A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832935 | |||||||
| chr2:108832998 | C | A | 183 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(180): Show |
186 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1207-6187C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832998 | |||||||
| chr2:108833317 | G | A | 1 | a0003c0003t0001g0143 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1207-5868G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108833317 | |||||||
| chr2:108833418 | T | A | 7 | a0003c0003t0001g0143 a0003c0003t0001g0149 a0003c0003t0001g0151 others(4): Show |
7 | HG00099.hp2 HG00738.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-5767T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108833418 | |||||||
| chr2:108833546 | A | G | 1 | a0002c0002t0001g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1207-5639A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108833546 | |||||||
| chr2:108833726 | CT | C | 186 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0001t0002g0001 others(183): Show |
189 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.1207-5440delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108833726 | ||||||
| chr2:108833726 | CTT | C | 11 | a0001c0001t0002g0025 a0001c0001t0002g0072 a0001c0005t0001g0113 others(8): Show |
11 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1207-5441_1207-544 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108833726 | ||||||
| chr2:108833770 | C | G | 7 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1207-5415C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108833770 | |||||||
| chr2:108833889 | G | A | 9 | a0001c0001t0001g0030 a0002c0002t0001g0133 a0002c0002t0001g0167 others(6): Show |
9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207-5296G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108833889 | |||||||
| chr2:108833894 | A | AT | 132 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0002 others(129): Show |
135 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.1207-5267dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108833894 | ||||||
| chr2:108833894 | A | ATT | 36 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0078 others(33): Show |
36 | HG00741.hp2 HG01175.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.1207-5268_1207-526 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108833894 | ||||||
| chr2:108833894 | A | ATTT | 13 | a0001c0001t0002g0026 a0001c0001t0002g0059 a0001c0004t0001g0106 others(10): Show |
13 | HG01175.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1207-5269_1207-526 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108833894 | ||||||
| chr2:108833894 | A | ATTTT | 5 | a0001c0004t0001g0108 a0001c0004t0001g0109 a0001c0004t0001g0110 others(2): Show |
5 | HG02055.hp2 HG03195.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-5270_1207-526 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108833894 | ||||||
| chr2:108833894 | AT | A | 5 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-5267delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108833894 | ||||||
| chr2:108833894 | ATTTTTTT | A | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-5273_1207-526 others(11): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108833894 | ||||||
| chr2:108834048 | T | C | 102 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0002 others(99): Show |
104 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(101): Show |
intron_variant | MODIFIER | c.1207-5137T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108834048 | |||||||
| chr2:108834214 | A | AT | 43 | a0001c0001t0002g0071 a0001c0004t0001g0106 a0001c0004t0001g0107 others(40): Show |
44 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1207-4955dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108834214 | ||||||
| chr2:108834215 | T | A | 1 | a0002c0002t0001g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1207-4970T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108834215 | |||||||
| chr2:108834215 | T | TTTTTTTT others(5997): Show |
6 | a0001c0004t0001g0011 a0001c0004t0001g0012 a0001c0004t0001g0014 others(3): Show |
6 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207-4959_1207-495 others(6008): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108834215 | ||||||
| chr2:108834215 | T | TTTTTTTT others(5998): Show |
1 | a0001c0004t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1207-4959_1207-495 others(6009): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108834215 | ||||||
| chr2:108834274 | G | A | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-4911G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108834274 | |||||||
| chr2:108834460 | A | G | 202 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1207-4725A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108834460 | |||||||
| chr2:108834461 | C | T | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-4724C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108834461 | |||||||
| chr2:108834662 | A | G | 37 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0007 others(34): Show |
38 | HG00408.hp1 HG01081.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1207-4523A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108834662 | |||||||
| chr2:108834758 | C | T | 1 | a0002c0002t0001g0181 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1207-4427C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108834758 | |||||||
| chr2:108834801 | A | G | 51 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(48): Show |
52 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1207-4384A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108834801 | |||||||
| chr2:108834982 | T | C | 1 | a0001c0005t0001g0211 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1207-4203T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108834982 | |||||||
| chr2:108835089 | A | G | 51 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(48): Show |
52 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1207-4096A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108835089 | |||||||
| chr2:108835094 | G | T | 168 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0002 others(165): Show |
171 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.1207-4091G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108835094 | |||||||
| chr2:108835174 | CATT | C | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207-4009_1207-400 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108835174 | ||||||
| chr2:108835264 | T | G | 1 | a0001c0001t0002g0063 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1207-3921T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108835264 | |||||||
| chr2:108835301 | T | A | 6 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(3): Show |
6 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207-3884T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108835301 | |||||||
| chr2:108835651 | C | T | 1 | a0002c0002t0001g0181 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1207-3534C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108835651 | |||||||
| chr2:108835754 | A | G | 6 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(3): Show |
6 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207-3431A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108835754 | |||||||
| chr2:108835862 | T | C | 1 | a0002c0002t0001g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1207-3323T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108835862 | |||||||
| chr2:108835972 | G | A | 9 | a0001c0001t0001g0030 a0002c0002t0001g0133 a0002c0002t0001g0167 others(6): Show |
9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207-3213G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108835972 | |||||||
| chr2:108836045 | G | A | 1 | a0001c0005t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1207-3140G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836045 | |||||||
| chr2:108836082 | G | A | 1 | a0003c0003t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1207-3103G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836082 | |||||||
| chr2:108836110 | A | G | 102 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0002 others(99): Show |
104 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(101): Show |
intron_variant | MODIFIER | c.1207-3075A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836110 | |||||||
| chr2:108836357 | A | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1207-2828A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836357 | |||||||
| chr2:108836417 | G | C | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-2768G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836417 | |||||||
| chr2:108836481 | T | C | 1 | a0001c0004t0001g0016 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1207-2704T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836481 | |||||||
| chr2:108836487 | G | A | 1 | a0001c0006t0001g0204 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1207-2698G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836487 | |||||||
| chr2:108836629 | T | C | 17 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0005t0001g0111 others(14): Show |
17 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1207-2556T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836629 | |||||||
| chr2:108836936 | A | G | 1 | a0002c0002t0001g0170 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1207-2249A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836936 | |||||||
| chr2:108836978 | C | T | 1 | a0002c0002t0001g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1207-2207C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836978 | |||||||
| chr2:108836985 | T | A | 1 | a0001c0001t0002g0081 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1207-2200T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836985 | |||||||
| chr2:108837084 | G | A | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-2101G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837084 | |||||||
| chr2:108837099 | G | A | 2 | a0001c0004t0001g0100 a0001c0004t0001g0101 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1207-2086G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837099 | |||||||
| chr2:108837102 | T | C | 183 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(180): Show |
186 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1207-2083T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837102 | |||||||
| chr2:108837248 | G | C | 39 | a0002c0002t0001g0166 a0002c0002t0001g0172 a0002c0002t0001g0173 others(36): Show |
40 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1207-1937G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837248 | |||||||
| chr2:108837268 | C | T | 1 | a0001c0006t0001g0204 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1207-1917C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837268 | |||||||
| chr2:108837296 | G | A | 45 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(42): Show |
46 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.1207-1889G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837296 | |||||||
| chr2:108837419 | C | T | 1 | a0003c0003t0001g0137 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1207-1766C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837419 | |||||||
| chr2:108837922 | C | T | 8 | a0001c0001t0002g0061 a0001c0004t0001g0010 a0001c0004t0001g0011 others(5): Show |
8 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1207-1263C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837922 | |||||||
| chr2:108837924 | AT | A | 10 | a0001c0001t0002g0063 a0001c0004t0001g0106 a0001c0004t0001g0107 others(7): Show |
10 | HG01257.hp1 HG01257.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207-1247delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108837924 | ||||||
| chr2:108837978 | C | T | 1 | a0002c0002t0001g0206 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1207-1207C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837978 | |||||||
| chr2:108838219 | C | T | 3 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0177 |
3 | HG01891.hp2 HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1207-966C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108838219 | |||||||
| chr2:108838269 | C | G | 5 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-916C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108838269 | |||||||
| chr2:108838377 | C | T | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1207-808C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108838377 | |||||||
| chr2:108838583 | C | T | 9 | a0001c0001t0001g0030 a0002c0002t0001g0133 a0002c0002t0001g0167 others(6): Show |
9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207-602C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108838583 | |||||||
| chr2:108838705 | A | T | 1 | a0003c0003t0001g0183 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1207-480A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108838705 | |||||||
| chr2:108838900 | T | C | 1 | a0001c0001t0002g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1207-285T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108838900 | |||||||
| chr2:108839360 | T | A | 5 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1323+59T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108839360 | |||||||
| chr2:108839723 | A | T | 9 | a0001c0001t0001g0030 a0002c0002t0001g0133 a0002c0002t0001g0167 others(6): Show |
9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1323+422A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108839723 | |||||||
| chr2:108839907 | G | A | 9 | a0001c0001t0001g0030 a0002c0002t0001g0133 a0002c0002t0001g0167 others(6): Show |
9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1323+606G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108839907 | |||||||
| chr2:108840313 | CTT | C | 5 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1323+1014_1323+101 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108840313 | ||||||
| chr2:108840507 | GT | G | 2 | a0001c0001t0002g0047 a0001c0001t0002g0052 |
2 | NA18985.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1323+1208delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108840507 | ||||||
| chr2:108840540 | C | G | 134 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0002 others(131): Show |
136 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(133): Show |
intron_variant | MODIFIER | c.1323+1239C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108840540 | |||||||
| chr2:108840607 | G | A | 1 | a0003c0003t0001g0183 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1323+1306G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108840607 | |||||||
| chr2:108840693 | T | A | 5 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 others(2): Show |
5 | HG00741.hp2 HG01515.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1323+1392T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108840693 | |||||||
| chr2:108840782 | T | C | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1323+1481T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108840782 | |||||||
| chr2:108840784 | A | ATTTCTTT others(1): Show |
42 | a0001c0001t0002g0002 a0001c0001t0002g0009 a0001c0001t0002g0036 others(39): Show |
43 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1323+1509_1323+151 others(12): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108840784 | ||||||
| chr2:108840784 | ATTTCTTT others(1): Show |
A | 21 | a0001c0001t0002g0059 a0001c0004t0001g0106 a0001c0004t0001g0107 others(18): Show |
21 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1323+1509_1323+151 others(12): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108840784 | ||||||
| chr2:108840964 | A | G | 1 | a0002c0002t0001g0181 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1323+1663A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108840964 | |||||||
| chr2:108840993 | G | T | 15 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(12): Show |
15 | HG01261.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1323+1692G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108840993 | |||||||
| chr2:108841003 | T | G | 1 | a0001c0001t0002g0072 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1323+1702T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841003 | |||||||
| chr2:108841004 | T | TTTTG | 10 | a0001c0004t0002g0096 a0001c0004t0002g0098 a0001c0004t0002g0099 others(7): Show |
10 | HG01243.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1323+1731_1323+173 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108841004 | ||||||
| chr2:108841004 | TTTTGTTT others(1): Show |
T | 6 | a0001c0001t0002g0024 a0001c0005t0001g0115 a0001c0005t0001g0116 others(3): Show |
6 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323+1727_1323+173 others(12): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108841004 | ||||||
| chr2:108841108 | T | C | 1 | a0001c0005t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1323+1807T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841108 | |||||||
| chr2:108841237 | G | T | 1 | a0001c0005t0001g0115 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1323+1936G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841237 | |||||||
| chr2:108841306 | A | G | 5 | a0001c0004t0001g0108 a0001c0004t0001g0109 a0001c0004t0001g0110 others(2): Show |
5 | HG02055.hp2 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1323+2005A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841306 | |||||||
| chr2:108841318 | A | G | 39 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(36): Show |
40 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1323+2017A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841318 | |||||||
| chr2:108841376 | A | G | 17 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0005t0001g0111 others(14): Show |
17 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1323+2075A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841376 | |||||||
| chr2:108841513 | A | C | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1323+2212A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841513 | |||||||
| chr2:108841540 | T | C | 1 | a0001c0005t0001g0115 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1323+2239T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841540 | |||||||
| chr2:108841642 | T | A | 2 | a0001c0005t0001g0111 a0003c0003t0001g0139 |
2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1323+2341T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841642 | |||||||
| chr2:108841662 | C | T | 183 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(180): Show |
186 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1323+2361C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841662 | |||||||
| chr2:108841784 | C | T | 40 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(37): Show |
41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1323+2483C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841784 | |||||||
| chr2:108842016 | G | C | 8 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(5): Show |
8 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1323+2715G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842016 | |||||||
| chr2:108842072 | C | T | 2 | a0003c0003t0001g0141 a0003c0003t0001g0180 |
2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1323+2771C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842072 | |||||||
| chr2:108842075 | G | A | 34 | a0002c0002t0001g0166 a0003c0003t0001g0003 a0003c0003t0001g0120 others(31): Show |
35 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1323+2774G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842075 | |||||||
| chr2:108842117 | T | C | 9 | a0001c0001t0001g0030 a0002c0002t0001g0133 a0002c0002t0001g0167 others(6): Show |
9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1323+2816T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842117 | |||||||
| chr2:108842132 | A | G | 1 | a0001c0001t0002g0025 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1323+2831A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842132 | |||||||
| chr2:108842185 | A | G | 1 | a0002c0002t0001g0191 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1323+2884A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842185 | |||||||
| chr2:108842202 | GT | G | 132 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0002 others(129): Show |
134 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(131): Show |
intron_variant | MODIFIER | c.1323+2917delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108842202 | ||||||
| chr2:108842428 | A | G | 2 | a0003c0003t0001g0120 a0003c0003t0001g0148 |
2 | NA18974.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1323+3127A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842428 | |||||||
| chr2:108842525 | G | C | 4 | a0001c0004t0001g0102 a0001c0004t0001g0103 a0001c0004t0001g0104 others(1): Show |
4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1323+3224G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842525 | |||||||
| chr2:108842545 | A | T | 40 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(37): Show |
41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1323+3244A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842545 | |||||||
| chr2:108842901 | G | A | 4 | a0001c0004t0001g0102 a0001c0004t0001g0103 a0001c0004t0001g0104 others(1): Show |
4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1323+3600G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842901 | |||||||
| chr2:108842955 | AACC | A | 5 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0177 others(2): Show |
5 | HG01109.hp2 HG01167.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1323+3657_1323+365 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108842955 | ||||||
| chr2:108842992 | G | A | 202 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1323+3691G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842992 | |||||||
| chr2:108843118 | A | G | 40 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(37): Show |
41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1324-3620A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843118 | |||||||
| chr2:108843124 | T | TTAGAGGA others(6042): Show |
1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1324-3600_1324-359 others(6053): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843124 | ||||||
| chr2:108843186 | C | T | 5 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1324-3552C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843186 | |||||||
| chr2:108843408 | G | A | 1 | a0001c0010t0002g0067 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1324-3330G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843408 | |||||||
| chr2:108843542 | T | C | 202 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1324-3196T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843542 | |||||||
| chr2:108843564 | C | T | 8 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(5): Show |
8 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1324-3174C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843564 | |||||||
| chr2:108843777 | C | A | 4 | a0001c0001t0002g0032 a0001c0001t0002g0048 a0001c0001t0002g0071 others(1): Show |
4 | NA18954.hp1 NA18959.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324-2961C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843777 | |||||||
| chr2:108843844 | T | TTGTG | 16 | a0001c0001t0001g0006 a0001c0004t0001g0100 a0001c0004t0001g0101 others(13): Show |
16 | HG01243.hp2 HG01261.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.1324-2862_1324-285 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843844 | ||||||
| chr2:108843844 | T | TTGTGTGT others(3): Show |
2 | a0001c0005t0001g0207 a0001c0005t0001g0208 |
2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1324-2868_1324-285 others(14): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843844 | ||||||
| chr2:108843844 | T | TTGTGTGT others(9): Show |
1 | a0003c0003t0001g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1324-2874_1324-285 others(20): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843844 | ||||||
| chr2:108843844 | TTG | T | 15 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0026 others(12): Show |
16 | HG00099.hp1 HG01074.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1324-2860_1324-285 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843844 | ||||||
| chr2:108843844 | TTGTGTG | T | 124 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0004 others(121): Show |
126 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(123): Show |
intron_variant | MODIFIER | c.1324-2864_1324-285 others(10): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843844 | ||||||
| chr2:108843872 | G | T | 6 | a0001c0001t0002g0017 a0001c0001t0002g0026 a0001c0001t0002g0038 others(3): Show |
6 | HG01978.hp2 HG02615.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324-2866G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843872 | |||||||
| chr2:108843876 | G | GTGTGTGT others(13): Show |
2 | a0001c0004t0001g0106 a0001c0004t0001g0107 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1324-2859_1324-285 others(24): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843876 | ||||||
| chr2:108843876 | G | GTGTGTGT others(11): Show |
4 | a0001c0004t0001g0110 a0001c0006t0001g0200 a0002c0002t0001g0126 others(1): Show |
4 | HG02055.hp2 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324-2859_1324-285 others(22): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843876 | ||||||
| chr2:108843876 | G | GTGTGTGT others(9): Show |
8 | a0001c0004t0001g0108 a0001c0004t0001g0109 a0001c0006t0001g0198 others(5): Show |
8 | HG01261.hp1 HG03225.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.1324-2859_1324-285 others(20): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843876 | ||||||
| chr2:108843876 | G | GTGTGTGT others(7): Show |
2 | a0001c0004t0001g0104 a0002c0002t0001g0194 |
2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1324-2859_1324-285 others(18): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843876 | ||||||
| chr2:108843876 | G | GTGTGTGT others(5): Show |
11 | a0001c0001t0001g0030 a0001c0004t0001g0102 a0001c0004t0001g0103 others(8): Show |
11 | HG01081.hp2 HG02523.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.1324-2859_1324-285 others(16): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843876 | ||||||
| chr2:108843876 | G | GTGTGTGT others(1): Show |
10 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0130 others(7): Show |
10 | HG01109.hp2 HG01167.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1324-2859_1324-285 others(12): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843876 | ||||||
| chr2:108843876 | G | T | 144 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0002 others(141): Show |
147 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.1324-2862G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843876 | |||||||
| chr2:108843878 | G | C | 7 | a0001c0001t0002g0017 a0001c0001t0002g0026 a0001c0001t0002g0038 others(4): Show |
7 | HG00099.hp1 HG01978.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324-2860G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843878 | |||||||
| chr2:108843880 | T | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1324-2858T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843880 | |||||||
| chr2:108843882 | C | G | 8 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(5): Show |
8 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1324-2856C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843882 | |||||||
| chr2:108843884 | T | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1324-2854T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843884 | |||||||
| chr2:108843884 | TTC | T | 5 | a0001c0001t0002g0017 a0001c0001t0002g0026 a0001c0001t0002g0066 others(2): Show |
5 | HG00099.hp1 HG02615.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1324-2852_1324-285 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843884 | ||||||
| chr2:108843886 | C | CT | 56 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0004 others(53): Show |
56 | HG00741.hp2 HG01081.hp2 HG01109.hp1 others(53): Show |
intron_variant | MODIFIER | c.1324-2830dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843886 | ||||||
| chr2:108843886 | C | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1324-2852C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843886 | |||||||
| chr2:108843886 | CTT | C | 38 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(35): Show |
39 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1324-2831_1324-283 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843886 | ||||||
| chr2:108843893 | T | C | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1324-2845T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843893 | |||||||
| chr2:108843915 | G | A | 11 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(8): Show |
11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1324-2823G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843915 | |||||||
| chr2:108843959 | C | T | 1 | a0003c0003t0001g0183 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1324-2779C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843959 | |||||||
| chr2:108843990 | A | T | 1 | a0002c0002t0001g0130 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1324-2748A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843990 | |||||||
| chr2:108844062 | A | C | 97 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0002 others(94): Show |
99 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(96): Show |
intron_variant | MODIFIER | c.1324-2676A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108844062 | |||||||
| chr2:108844132 | A | T | 5 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1324-2606A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108844132 | |||||||
| chr2:108844167 | A | G | 2 | a0001c0004t0001g0106 a0001c0004t0001g0107 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1324-2571A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108844167 | |||||||
| chr2:108844177 | C | T | 1 | a0001c0004t0001g0107 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1324-2561C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108844177 | |||||||
| chr2:108844419 | TG | T | 67 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0004 others(64): Show |
68 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.1324-2317delG | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108844419 | ||||||
| chr2:108844433 | G | A | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324-2305G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108844433 | |||||||
| chr2:108844748 | A | AT | 6 | a0001c0001t0002g0017 a0001c0001t0002g0033 a0001c0001t0002g0042 others(3): Show |
6 | HG01978.hp1 HG01978.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324-1973dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108844748 | ||||||
| chr2:108844748 | A | ATT | 10 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(7): Show |
10 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1324-1974_1324-197 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108844748 | ||||||
| chr2:108844748 | AT | A | 46 | a0001c0001t0002g0002 a0001c0001t0002g0050 a0001c0001t0002g0051 others(43): Show |
48 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1324-1973delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108844748 | ||||||
| chr2:108844772 | G | C | 3 | a0003c0003t0001g0141 a0003c0003t0001g0180 a0003c0003t0001g0183 |
3 | HG00738.hp2 HG00741.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1324-1966G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108844772 | |||||||
| chr2:108844971 | A | C | 183 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(180): Show |
186 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1324-1767A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108844971 | |||||||
| chr2:108844975 | T | C | 1 | a0001c0001t0002g0021 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1324-1763T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108844975 | |||||||
| chr2:108845158 | T | C | 1 | a0003c0003t0001g0120 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1324-1580T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108845158 | |||||||
| chr2:108845218 | T | A | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324-1520T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108845218 | |||||||
| chr2:108845367 | C | T | 1 | a0001c0005t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1324-1371C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108845367 | |||||||
| chr2:108845571 | AT | A | 180 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0078 others(177): Show |
183 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.1324-1149delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108845571 | ||||||
| chr2:108845664 | C | T | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324-1074C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108845664 | |||||||
| chr2:108845665 | G | A | 1 | a0006c0008t0001g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1324-1073G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108845665 | |||||||
| chr2:108845712 | T | C | 183 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(180): Show |
186 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1324-1026T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108845712 | |||||||
| chr2:108845817 | T | C | 202 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1324-921T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108845817 | |||||||
| chr2:108846060 | A | T | 202 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1324-678A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108846060 | |||||||
| chr2:108846195 | T | C | 1 | a0002c0002t0001g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1324-543T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108846195 | |||||||
| chr2:108846205 | A | G | 2 | a0001c0001t0002g0055 a0001c0001t0002g0073 |
2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1324-533A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108846205 | |||||||
| chr2:108846221 | A | C | 101 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0002 others(98): Show |
103 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(100): Show |
intron_variant | MODIFIER | c.1324-517A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108846221 | |||||||
| chr2:108846281 | TTTAAGTT others(44): Show |
T | 1 | a0003c0003t0001g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1324-453_1324-403d others(53): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108846281 | ||||||
| chr2:108846336 | G | A | 1 | a0002c0002t0003g0192 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1324-402G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108846336 | |||||||
| chr2:108846339 | A | G | 1 | a0007c0009t0001g0164 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1324-399A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108846339 | |||||||
| chr2:108846442 | G | T | 1 | a0008c0015t0001g0193 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1324-296G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108846442 | |||||||
| chr2:108846516 | G | GA | 10 | a0001c0001t0002g0066 a0001c0001t0002g0077 a0001c0004t0002g0096 others(7): Show |
10 | HG00099.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1324-208dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108846516 | ||||||
| chr2:108846521 | A | T | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324-217A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108846521 | |||||||
| chr2:108846633 | C | T | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324-105C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108846633 | |||||||
| chr2:108847148 | G | A | 3 | a0003c0003t0001g0141 a0003c0003t0001g0180 a0003c0003t0001g0183 |
3 | HG00738.hp2 HG00741.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1516+218G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108847148 | |||||||
| chr2:108847160 | A | G | 15 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(12): Show |
15 | HG01261.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1516+230A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108847160 | |||||||
| chr2:108847318 | A | T | 116 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0002 others(113): Show |
118 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(115): Show |
intron_variant | MODIFIER | c.1516+388A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108847318 | |||||||
| chr2:108847351 | T | C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0005t0001g0209 others(7): Show |
10 | HG02145.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1516+421T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108847351 | |||||||
| chr2:108847419 | G | A | 40 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(37): Show |
41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1516+489G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108847419 | |||||||
| chr2:108847484 | A | C | 6 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0044 others(3): Show |
6 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1516+554A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108847484 | |||||||
| chr2:108848058 | A | G | 7 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1516+1128A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108848058 | |||||||
| chr2:108848096 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1516+1166C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108848096 | |||||||
| chr2:108848247 | A | G | 1 | a0002c0002t0001g0181 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1516+1317A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108848247 | |||||||
| chr2:108848488 | A | T | 8 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(5): Show |
8 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1516+1558A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108848488 | |||||||
| chr2:108848553 | C | T | 2 | a0002c0002t0001g0171 a0002c0002t0001g0191 |
2 | HG01261.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.1516+1623C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108848553 | |||||||
| chr2:108848615 | A | C | 11 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(8): Show |
11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1516+1685A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108848615 | |||||||
| chr2:108848678 | C | T | 5 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0177 others(2): Show |
5 | HG01109.hp2 HG01167.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1516+1748C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108848678 | |||||||
| chr2:108848747 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1516+1817A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108848747 | |||||||
| chr2:108848782 | T | C | 57 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0004 others(54): Show |
58 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.1516+1852T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108848782 | |||||||
| chr2:108849152 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0078 |
2 | HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1516+2222A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108849152 | |||||||
| chr2:108849544 | G | A | 18 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(15): Show |
18 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1516+2614G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108849544 | |||||||
| chr2:108849564 | T | C | 1 | a0001c0001t0002g0054 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1516+2634T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108849564 | |||||||
| chr2:108849625 | C | A | 11 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(8): Show |
11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1516+2695C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108849625 | |||||||
| chr2:108849715 | G | C | 34 | a0002c0002t0001g0166 a0003c0003t0001g0003 a0003c0003t0001g0120 others(31): Show |
35 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1516+2785G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108849715 | |||||||
| chr2:108849735 | C | G | 1 | a0001c0005t0001g0211 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1516+2805C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108849735 | |||||||
| chr2:108849744 | C | T | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1516+2814C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108849744 | |||||||
| chr2:108849985 | G | A | 17 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0005t0001g0111 others(14): Show |
17 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1516+3055G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108849985 | |||||||
| chr2:108850030 | C | T | 1 | a0001c0006t0001g0203 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1516+3100C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108850030 | |||||||
| chr2:108850589 | T | C | 17 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0005t0001g0111 others(14): Show |
17 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1516+3659T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108850589 | |||||||
| chr2:108850672 | C | T | 2 | a0001c0001t0002g0055 a0001c0001t0002g0073 |
2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1516+3742C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108850672 | |||||||
| chr2:108850742 | C | T | 1 | a0003c0003t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1516+3812C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108850742 | |||||||
| chr2:108850841 | CAGA | C | 5 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1516+3918_1516+392 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108850841 | ||||||
| chr2:108850893 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1516+3963G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108850893 | |||||||
| chr2:108850955 | C | G | 1 | a0001c0004t0001g0105 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1516+4025C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108850955 | |||||||
| chr2:108851595 | G | GC | 11 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(8): Show |
11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1516+4668dupC | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108851595 | ||||||
| chr2:108851598 | C | T | 1 | a0001c0004t0001g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1516+4668C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108851598 | |||||||
| chr2:108851600 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1516+4670G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108851600 | |||||||
| chr2:108851611 | G | T | 3 | a0004c0007t0002g0123 a0004c0007t0002g0124 a0004c0007t0002g0125 |
3 | HG03579.hp2 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1516+4681G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108851611 | |||||||
| chr2:108851612 | G | C | 3 | a0004c0007t0002g0123 a0004c0007t0002g0124 a0004c0007t0002g0125 |
3 | HG03579.hp2 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1516+4682G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108851612 | |||||||
| chr2:108851680 | G | A | 1 | a0002c0002t0003g0186 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1516+4750G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108851680 | |||||||
| chr2:108851994 | C | T | 1 | a0001c0010t0002g0067 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1517-4800C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108851994 | |||||||
| chr2:108852171 | A | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1517-4623A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108852171 | |||||||
| chr2:108852314 | T | A | 6 | a0003c0003t0001g0003 a0003c0003t0001g0140 a0003c0003t0001g0146 others(3): Show |
7 | NA18968.hp2 NA18977.hp2 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.1517-4480T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108852314 | |||||||
| chr2:108852384 | A | G | 1 | a0002c0002t0001g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1517-4410A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108852384 | |||||||
| chr2:108852386 | A | G | 39 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(36): Show |
40 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1517-4408A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108852386 | |||||||
| chr2:108852550 | A | G | 1 | a0002c0002t0001g0181 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1517-4244A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108852550 | |||||||
| chr2:108852807 | C | G | 100 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(97): Show |
102 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(99): Show |
intron_variant | MODIFIER | c.1517-3987C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108852807 | |||||||
| chr2:108852877 | G | T | 197 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(194): Show |
200 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1517-3917G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108852877 | |||||||
| chr2:108852939 | A | T | 1 | a0002c0002t0001g0171 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1517-3855A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108852939 | |||||||
| chr2:108853019 | C | T | 3 | a0004c0007t0002g0123 a0004c0007t0002g0124 a0004c0007t0002g0125 |
3 | HG03579.hp2 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1517-3775C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853019 | |||||||
| chr2:108853093 | G | A | 1 | a0001c0001t0002g0005 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1517-3701G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853093 | |||||||
| chr2:108853176 | A | G | 1 | a0003c0003t0001g0138 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1517-3618A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853176 | |||||||
| chr2:108853295 | G | A | 5 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1517-3499G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853295 | |||||||
| chr2:108853528 | C | CT | 22 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0059 others(19): Show |
22 | HG01081.hp2 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1517-3252dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853528 | ||||||
| chr2:108853528 | CT | C | 11 | a0001c0001t0002g0018 a0001c0001t0002g0034 a0001c0001t0002g0044 others(8): Show |
11 | HG01168.hp1 HG01261.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.1517-3252delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853528 | ||||||
| chr2:108853563 | A | G | 1 | a0001c0005t0001g0115 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1517-3231A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853563 | |||||||
| chr2:108853592 | G | C | 2 | a0003c0003t0001g0120 a0003c0003t0001g0148 |
2 | NA18974.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1517-3202G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853592 | |||||||
| chr2:108853641 | C | T | 14 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0004t0001g0102 others(11): Show |
14 | HG01081.hp2 HG02055.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.1517-3153C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853641 | |||||||
| chr2:108853643 | C | G | 96 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(93): Show |
98 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(95): Show |
intron_variant | MODIFIER | c.1517-3151C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853643 | |||||||
| chr2:108853730 | T | C | 8 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(5): Show |
8 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1517-3064T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853730 | |||||||
| chr2:108853879 | A | G | 1 | a0001c0005t0001g0215 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1517-2915A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853879 | |||||||
| chr2:108853882 | T | G | 1 | a0002c0002t0001g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1517-2912T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853882 | |||||||
| chr2:108853891 | G | A | 1 | a0002c0002t0001g0196 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1517-2903G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853891 | |||||||
| chr2:108853893 | ATATATAT | A | 6 | a0001c0005t0001g0209 a0001c0005t0001g0210 a0001c0005t0001g0212 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1517-2887_1517-288 others(11): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853893 | ||||||
| chr2:108853901 | T | A | 1 | a0002c0002t0001g0196 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1517-2893T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853901 | |||||||
| chr2:108853908 | T | C | 11 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0050 others(8): Show |
11 | HG01074.hp1 HG01358.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.1517-2886T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853908 | |||||||
| chr2:108853914 | G | A | 1 | a0006c0008t0001g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2880G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853914 | |||||||
| chr2:108853923 | TTA | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0005t0001g0111 others(14): Show |
17 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1517-2864_1517-286 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853923 | ||||||
| chr2:108853924 | T | A | 1 | a0006c0008t0001g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2870T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853924 | |||||||
| chr2:108853932 | A | T | 1 | a0006c0008t0001g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2862A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853932 | |||||||
| chr2:108853933 | T | A | 1 | a0006c0008t0001g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2861T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853933 | |||||||
| chr2:108853935 | T | A | 1 | a0006c0008t0001g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2859T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853935 | |||||||
| chr2:108853948 | C | T | 1 | a0006c0008t0001g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2846C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853948 | |||||||
| chr2:108853956 | A | T | 1 | a0006c0008t0001g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2838A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853956 | |||||||
| chr2:108853965 | A | ATATAATA others(6): Show |
1 | a0006c0008t0001g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2829_1517-282 others(17): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853965 | |||||||
| chr2:108853966 | AAATATAT others(19): Show |
A | 1 | a0001c0001t0002g0048 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1517-2825_1517-280 others(30): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853966 | ||||||
| chr2:108853970 | A | ATATATAA others(20): Show |
1 | a0002c0002t0001g0133 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1517-2818_1517-279 others(31): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853970 | ||||||
| chr2:108853970 | A | T | 1 | a0006c0008t0001g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2824A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853970 | |||||||
| chr2:108853976 | A | AATATATA others(47): Show |
8 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0002c0002t0001g0167 others(5): Show |
8 | HG02523.hp1 HG03654.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.1517-2792_1517-279 others(58): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853976 | ||||||
| chr2:108853976 | A | AATATATA others(20): Show |
3 | a0001c0005t0001g0114 a0002c0002t0001g0171 a0003c0003t0001g0139 |
3 | HG02040.hp2 NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1517-2756_1517-273 others(31): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853976 | ||||||
| chr2:108853976 | A | AATATATA others(47): Show |
2 | a0001c0004t0001g0100 a0001c0004t0001g0101 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1517-2783_1517-273 others(58): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853976 | ||||||
| chr2:108853976 | A | T | 1 | a0006c0008t0001g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2818A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853976 | |||||||
| chr2:108853976 | AATATATA others(20): Show |
A | 121 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(118): Show |
123 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(120): Show |
intron_variant | MODIFIER | c.1517-2756_1517-273 others(31): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853976 | ||||||
| chr2:108853976 | AATATATA others(47): Show |
A | 1 | a0001c0004t0001g0107 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1517-2783_1517-273 others(58): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853976 | ||||||
| chr2:108853981 | ATAATATA others(21): Show |
A | 39 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(36): Show |
40 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1517-2812_1517-278 others(32): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853981 | |||||||
| chr2:108853997 | T | A | 1 | a0001c0001t0002g0048 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1517-2797T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853997 | |||||||
| chr2:108854003 | T | A | 1 | a0001c0001t0002g0048 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1517-2791T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108854003 | |||||||
| chr2:108854003 | T | TATATATA others(27): Show |
1 | a0001c0005t0001g0111 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1517-2780_1517-274 others(38): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108854003 | ||||||
| chr2:108854029 | TTATATAT others(22): Show |
T | 12 | a0001c0004t0001g0109 a0002c0002t0001g0127 a0002c0002t0001g0128 others(9): Show |
12 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1517-2757_1517-272 others(33): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108854029 | ||||||
| chr2:108854066 | T | A | 2 | a0001c0005t0001g0209 a0001c0005t0001g0210 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1517-2728T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108854066 | |||||||
| chr2:108854074 | TA | T | 5 | a0001c0004t0001g0108 a0001c0004t0001g0109 a0001c0004t0001g0110 others(2): Show |
5 | HG02055.hp2 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1517-2718delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108854074 | ||||||
| chr2:108854106 | AATAT | A | 3 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0177 |
3 | HG01891.hp2 HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1517-2682_1517-267 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108854106 | ||||||
| chr2:108854111 | A | G | 5 | a0002c0002t0001g0166 a0003c0003t0001g0159 a0003c0003t0001g0160 others(2): Show |
5 | HG01891.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1517-2683A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108854111 | |||||||
| chr2:108854292 | G | A | 4 | a0001c0004t0002g0096 a0001c0004t0002g0097 a0001c0004t0002g0098 others(1): Show |
4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1517-2502G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108854292 | |||||||
| chr2:108854392 | TTTTG | T | 39 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(36): Show |
40 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1517-2390_1517-238 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108854392 | ||||||
| chr2:108854652 | CAATTCTT others(3): Show |
C | 1 | a0001c0001t0002g0048 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1517-2141_1517-213 others(14): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108854652 | |||||||
| chr2:108854682 | C | G | 40 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(37): Show |
41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1517-2112C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108854682 | |||||||
| chr2:108854861 | G | A | 9 | a0001c0001t0001g0030 a0002c0002t0001g0133 a0002c0002t0001g0167 others(6): Show |
9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1517-1933G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108854861 | |||||||
| chr2:108854962 | A | G | 1 | a0001c0005t0001g0112 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1517-1832A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108854962 | |||||||
| chr2:108855338 | A | G | 1 | a0002c0002t0001g0175 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1517-1456A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108855338 | |||||||
| chr2:108855487 | T | TA | 16 | a0001c0001t0001g0030 a0001c0001t0002g0076 a0001c0001t0002g0091 others(13): Show |
16 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1517-1294dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108855487 | ||||||
| chr2:108855645 | A | G | 97 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0002 others(94): Show |
99 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(96): Show |
intron_variant | MODIFIER | c.1517-1149A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108855645 | |||||||
| chr2:108855774 | A | G | 13 | a0001c0001t0001g0030 a0001c0004t0001g0102 a0001c0004t0001g0103 others(10): Show |
13 | HG01081.hp2 HG02055.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1517-1020A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108855774 | |||||||
| chr2:108855782 | T | C | 2 | a0001c0005t0001g0209 a0001c0005t0001g0210 |
2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1517-1012T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108855782 | |||||||
| chr2:108855944 | C | T | 40 | a0001c0004t0001g0197 a0001c0005t0001g0115 a0001c0005t0001g0116 others(37): Show |
41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1517-850C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108855944 | |||||||
| chr2:108855946 | G | GT | 4 | a0001c0001t0002g0026 a0001c0001t0002g0034 a0001c0001t0002g0076 others(1): Show |
4 | HG03516.hp2 HG03927.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1517-840dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108855946 | ||||||
| chr2:108856026 | A | T | 3 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0177 |
3 | HG01891.hp2 HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1517-768A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108856026 | |||||||
| chr2:108856132 | A | G | 1 | a0001c0006t0001g0202 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1517-662A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108856132 | |||||||
| chr2:108856163 | T | TG | 5 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(2): Show |
5 | HG01884.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1517-628dupG | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108856163 | ||||||
| chr2:108856215 | A | G | 200 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(197): Show |
203 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1517-579A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108856215 | |||||||
| chr2:108856221 | C | T | 8 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(5): Show |
8 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1517-573C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108856221 | |||||||
| chr2:108856306 | C | CTT | 202 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1517-487_1517-486d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108856306 | ||||||
| chr2:108856700 | T | G | 1 | a0003c0003t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1517-94T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108856700 | |||||||
| chr2:108856765 | G | A | 1 | a0001c0004t0002g0097 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1517-29G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108856765 | |||||||
| chr2:108856983 | G | A | 6 | a0001c0005t0001g0209 a0001c0005t0001g0210 a0001c0005t0001g0212 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1693+13G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108856983 | |||||||
| chr2:108857066 | C | CT | 17 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0004t0001g0010 others(14): Show |
17 | HG01109.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1693+127dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108857066 | ||||||
| chr2:108857066 | C | CTT | 6 | a0001c0001t0001g0078 a0001c0001t0002g0051 a0001c0005t0001g0210 others(3): Show |
6 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1693+126_1693+127d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108857066 | ||||||
| chr2:108857066 | CT | C | 64 | a0001c0001t0001g0030 a0001c0001t0002g0021 a0001c0001t0002g0036 others(61): Show |
65 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.1693+127delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108857066 | ||||||
| chr2:108857066 | CTT | C | 86 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(83): Show |
88 | HG00099.hp1 HG00408.hp1 HG01074.hp1 others(85): Show |
intron_variant | MODIFIER | c.1693+126_1693+127d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108857066 | ||||||
| chr2:108857066 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0061 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1693+116_1693+127d others(14): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108857066 | ||||||
| chr2:108857066 | CTTTTTTT others(7): Show |
C | 1 | a0001c0004t0001g0105 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1693+114_1693+127d others(16): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108857066 | ||||||
| chr2:108857204 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1693+234G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108857204 | |||||||
| chr2:108857349 | G | A | 4 | a0001c0004t0001g0102 a0001c0004t0001g0103 a0001c0004t0001g0104 others(1): Show |
4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1693+379G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108857349 | |||||||
| chr2:108857365 | G | A | 97 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(94): Show |
99 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(96): Show |
intron_variant | MODIFIER | c.1693+395G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108857365 | |||||||
| chr2:108857506 | C | T | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693+536C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108857506 | |||||||
| chr2:108857699 | A | G | 3 | a0001c0004t0002g0096 a0001c0004t0002g0098 a0001c0004t0002g0099 |
3 | HG02486.hp1 HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1693+729A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108857699 | |||||||
| chr2:108857756 | G | C | 96 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(93): Show |
98 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(95): Show |
intron_variant | MODIFIER | c.1693+786G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108857756 | |||||||
| chr2:108857894 | T | C | 2 | a0002c0002t0002g0185 a0002c0002t0002g0189 |
2 | HG01175.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1693+924T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108857894 | |||||||
| chr2:108857962 | A | T | 7 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1693+992A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108857962 | |||||||
| chr2:108858058 | A | G | 1 | a0001c0001t0002g0021 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1693+1088A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108858058 | |||||||
| chr2:108858061 | C | T | 11 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(8): Show |
11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1693+1091C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108858061 | |||||||
| chr2:108858114 | C | T | 7 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1693+1144C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108858114 | |||||||
| chr2:108858361 | C | CA | 6 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(3): Show |
6 | HG01243.hp1 HG02572.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1693+1399dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108858361 | ||||||
| chr2:108858621 | C | T | 96 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(93): Show |
98 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(95): Show |
intron_variant | MODIFIER | c.1693+1651C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108858621 | |||||||
| chr2:108858695 | T | C | 11 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(8): Show |
11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1693+1725T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108858695 | |||||||
| chr2:108858710 | T | A | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693+1740T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108858710 | |||||||
| chr2:108858746 | T | C | 101 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0002 others(98): Show |
103 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(100): Show |
intron_variant | MODIFIER | c.1693+1776T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108858746 | |||||||
| chr2:108858912 | A | C | 134 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0002 others(131): Show |
136 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(133): Show |
intron_variant | MODIFIER | c.1693+1942A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108858912 | |||||||
| chr2:108859053 | T | C | 1 | a0003c0003t0001g0163 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1693+2083T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108859053 | |||||||
| chr2:108859058 | C | T | 57 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0005t0001g0111 others(54): Show |
58 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1693+2088C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108859058 | |||||||
| chr2:108859059 | G | A | 2 | a0001c0004t0001g0106 a0001c0004t0001g0107 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1693+2089G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108859059 | |||||||
| chr2:108859244 | G | A | 1 | a0003c0003t0001g0147 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1693+2274G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108859244 | |||||||
| chr2:108859812 | AT | A | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693+2854delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108859812 | ||||||
| chr2:108860011 | A | G | 13 | a0001c0001t0001g0030 a0001c0004t0001g0102 a0001c0004t0001g0103 others(10): Show |
13 | HG01081.hp2 HG02055.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1693+3041A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108860011 | |||||||
| chr2:108860049 | G | T | 1 | a0002c0002t0001g0181 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1693+3079G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108860049 | |||||||
| chr2:108860513 | G | GT | 6 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(3): Show |
6 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.1693+3556dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860513 | ||||||
| chr2:108860513 | GT | G | 7 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(4): Show |
7 | HG01516.hp1 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693+3556delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860513 | ||||||
| chr2:108860607 | C | G | 5 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 others(2): Show |
5 | HG00741.hp2 HG01515.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1693+3637C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108860607 | |||||||
| chr2:108860823 | G | A | 5 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(2): Show |
5 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1693+3853G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108860823 | |||||||
| chr2:108860867 | A | G | 13 | a0001c0001t0001g0030 a0001c0004t0001g0102 a0001c0004t0001g0103 others(10): Show |
13 | HG01081.hp2 HG02055.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1693+3897A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108860867 | |||||||
| chr2:108860904 | G | A | 1 | a0002c0002t0001g0132 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1693+3934G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108860904 | |||||||
| chr2:108860935 | C | CT | 64 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0078 others(61): Show |
65 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.1693+3988dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860935 | ||||||
| chr2:108860935 | C | CTT | 15 | a0001c0005t0001g0112 a0001c0005t0001g0113 a0002c0002t0001g0127 others(12): Show |
15 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1693+3987_1693+398 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860935 | ||||||
| chr2:108860935 | C | CTTT | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01243.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1693+3986_1693+398 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860935 | ||||||
| chr2:108860935 | C | CTTTTTTT | 5 | a0001c0001t0002g0023 a0001c0001t0002g0028 a0001c0001t0002g0032 others(2): Show |
5 | HG01515.hp2 NA18942.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.1693+3982_1693+398 others(11): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860935 | ||||||
| chr2:108860935 | C | CTTTTTTT others(1): Show |
62 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(59): Show |
64 | HG00408.hp1 HG00741.hp2 HG01074.hp2 others(61): Show |
intron_variant | MODIFIER | c.1693+3981_1693+398 others(12): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860935 | ||||||
| chr2:108860935 | C | CTTTTTTT others(2): Show |
21 | a0001c0001t0001g0056 a0001c0001t0002g0007 a0001c0001t0002g0019 others(18): Show |
21 | HG00099.hp1 HG01074.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.1693+3980_1693+398 others(13): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860935 | ||||||
| chr2:108860935 | C | CTTTTTTT others(3): Show |
4 | a0001c0001t0002g0020 a0001c0001t0002g0065 a0001c0001t0002g0070 others(1): Show |
4 | HG01358.hp2 HG01361.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1693+3979_1693+398 others(14): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860935 | ||||||
| chr2:108860935 | C | CTTTTTTT others(4): Show |
2 | a0004c0007t0002g0123 a0004c0007t0002g0124 |
2 | NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1693+3978_1693+398 others(15): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860935 | ||||||
| chr2:108860935 | C | CTTTTTTT others(5): Show |
1 | a0004c0007t0002g0125 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1693+3977_1693+398 others(16): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860935 | ||||||
| chr2:108861144 | T | A | 15 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(12): Show |
15 | HG01261.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1693+4174T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108861144 | |||||||
| chr2:108861472 | C | CT | 54 | a0001c0004t0001g0100 a0001c0004t0001g0101 a0001c0004t0001g0106 others(51): Show |
55 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1693+4528dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | ||||||
| chr2:108861472 | C | CTT | 23 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0004t0001g0011 others(20): Show |
23 | HG00741.hp1 HG01243.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.1693+4527_1693+452 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | ||||||
| chr2:108861472 | C | CTTT | 10 | a0001c0004t0001g0010 a0001c0004t0001g0015 a0001c0004t0001g0016 others(7): Show |
10 | HG01243.hp2 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1693+4526_1693+452 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | ||||||
| chr2:108861472 | C | CTTTTTTT others(3): Show |
2 | a0002c0002t0001g0168 a0002c0002t0001g0169 |
2 | NA18955.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1693+4519_1693+452 others(14): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | ||||||
| chr2:108861472 | C | CTTTTTTT others(4): Show |
3 | a0002c0002t0001g0167 a0002c0002t0001g0170 a0007c0009t0001g0164 |
3 | HG02523.hp1 HG03654.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1693+4518_1693+452 others(15): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | ||||||
| chr2:108861472 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0056 a0006c0008t0001g0165 |
2 | HG02055.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1693+4517_1693+452 others(16): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | ||||||
| chr2:108861472 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0030 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1693+4516_1693+452 others(17): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | ||||||
| chr2:108861472 | CT | C | 6 | a0002c0002t0001g0174 a0002c0002t0001g0175 a0002c0002t0001g0176 others(3): Show |
6 | HG01099.hp1 HG02451.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.1693+4528delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | ||||||
| chr2:108861472 | CTTTTTTT others(5): Show |
C | 1 | a0002c0002t0001g0194 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1693+4517_1693+452 others(16): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | ||||||
| chr2:108861472 | CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0002g0028 a0001c0001t0002g0036 a0001c0001t0002g0064 |
3 | NA18942.hp1 NA18969.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1693+4516_1693+452 others(17): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | ||||||
| chr2:108861472 | CTTTTTTT others(7): Show |
C | 96 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(93): Show |
98 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(95): Show |
intron_variant | MODIFIER | c.1693+4515_1693+452 others(18): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | ||||||
| chr2:108861472 | CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0002g0044 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1693+4514_1693+452 others(19): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | ||||||
| chr2:108861724 | G | A | 8 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(5): Show |
8 | HG01243.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1693+4754G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108861724 | |||||||
| chr2:108861771 | G | A | 1 | a0002c0002t0001g0171 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1693+4801G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108861771 | |||||||
| chr2:108861886 | T | C | 1 | a0002c0002t0001g0196 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1693+4916T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108861886 | |||||||
| chr2:108862077 | G | GT | 183 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(180): Show |
186 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1693+5121dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108862077 | ||||||
| chr2:108862139 | C | A | 6 | a0001c0001t0002g0050 a0001c0001t0002g0091 a0001c0001t0002g0092 others(3): Show |
6 | HG02622.hp1 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1693+5169C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108862139 | |||||||
| chr2:108862195 | T | TA | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693+5235dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108862195 | ||||||
| chr2:108862367 | A | G | 183 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(180): Show |
186 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1693+5397A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108862367 | |||||||
| chr2:108862398 | A | G | 202 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1693+5428A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108862398 | |||||||
| chr2:108862540 | G | A | 1 | a0002c0002t0001g0206 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1693+5570G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108862540 | |||||||
| chr2:108862782 | T | C | 2 | a0001c0001t0002g0051 a0001c0001t0002g0090 |
2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1693+5812T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108862782 | |||||||
| chr2:108862808 | C | T | 3 | a0002c0002t0003g0186 a0002c0002t0003g0192 a0002c0002t0004g0187 |
3 | HG01099.hp1 HG01993.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1693+5838C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108862808 | |||||||
| chr2:108862848 | G | A | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1693+5878G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108862848 | |||||||
| chr2:108862936 | T | C | 101 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0002 others(98): Show |
103 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(100): Show |
intron_variant | MODIFIER | c.1693+5966T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108862936 | |||||||
| chr2:108862948 | TA | T | 202 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1693+5985delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108862948 | ||||||
| chr2:108863187 | G | A | 2 | a0001c0001t0002g0007 a0001c0001t0002g0008 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1693+6217G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108863187 | |||||||
| chr2:108863295 | A | G | 34 | a0002c0002t0001g0166 a0003c0003t0001g0003 a0003c0003t0001g0120 others(31): Show |
35 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1693+6325A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108863295 | |||||||
| chr2:108863350 | A | G | 40 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(37): Show |
41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1693+6380A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108863350 | |||||||
| chr2:108863477 | G | A | 11 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(8): Show |
11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1693+6507G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108863477 | |||||||
| chr2:108863582 | C | T | 4 | a0002c0002t0001g0174 a0002c0002t0001g0175 a0002c0002t0001g0176 others(1): Show |
4 | HG02451.hp2 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1693+6612C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108863582 | |||||||
| chr2:108863594 | A | G | 1 | a0001c0001t0002g0004 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1693+6624A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108863594 | |||||||
| chr2:108863882 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1693+6912C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108863882 | |||||||
| chr2:108864036 | CAT | C | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693+7067_1693+706 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864036 | |||||||
| chr2:108864123 | TTA | T | 2 | a0001c0004t0001g0100 a0001c0004t0001g0101 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1693+7158_1693+715 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108864123 | ||||||
| chr2:108864272 | C | T | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1693+7302C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864272 | |||||||
| chr2:108864405 | G | A | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693+7435G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864405 | |||||||
| chr2:108864522 | G | A | 1 | a0002c0002t0003g0188 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1693+7552G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864522 | |||||||
| chr2:108864526 | G | A | 5 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0177 others(2): Show |
5 | HG01109.hp2 HG01167.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1693+7556G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864526 | |||||||
| chr2:108864568 | C | T | 26 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(23): Show |
26 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1693+7598C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864568 | |||||||
| chr2:108864598 | G | A | 6 | a0001c0005t0001g0209 a0001c0005t0001g0210 a0001c0005t0001g0212 others(3): Show |
6 | HG02145.hp1 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1693+7628G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864598 | |||||||
| chr2:108864598 | G | C | 197 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(194): Show |
200 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.1693+7628G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864598 | |||||||
| chr2:108864639 | A | T | 201 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(198): Show |
204 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.1693+7669A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864639 | |||||||
| chr2:108864649 | C | A | 5 | a0001c0004t0001g0108 a0001c0004t0001g0109 a0001c0004t0001g0110 others(2): Show |
5 | HG02055.hp2 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1693+7679C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864649 | |||||||
| chr2:108864666 | C | T | 40 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(37): Show |
41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1693+7696C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864666 | |||||||
| chr2:108864676 | C | T | 40 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(37): Show |
41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1693+7706C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864676 | |||||||
| chr2:108864734 | C | T | 8 | a0001c0004t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(5): Show |
8 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1693+7764C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864734 | |||||||
| chr2:108864791 | C | G | 8 | a0001c0004t0001g0197 a0001c0006t0001g0198 a0001c0006t0001g0199 others(5): Show |
8 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1693+7821C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864791 | |||||||
| chr2:108864793 | C | CA | 110 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0078 others(107): Show |
112 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(109): Show |
intron_variant | MODIFIER | c.1693+7841dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108864793 | ||||||
| chr2:108864793 | CA | C | 44 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(41): Show |
45 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1693+7841delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108864793 | ||||||
| chr2:108864828 | G | T | 101 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0002 others(98): Show |
103 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(100): Show |
intron_variant | MODIFIER | c.1693+7858G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864828 | |||||||
| chr2:108865005 | A | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1693+8035A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108865005 | |||||||
| chr2:108865027 | G | A | 101 | a0001c0001t0001g0056 a0001c0001t0002g0001 a0001c0001t0002g0002 others(98): Show |
103 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(100): Show |
intron_variant | MODIFIER | c.1693+8057G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108865027 | |||||||
| chr2:108865201 | A | T | 39 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(36): Show |
40 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1693+8231A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108865201 | |||||||
| chr2:108865441 | A | G | 2 | a0001c0004t0001g0106 a0001c0004t0001g0107 |
2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1694-8010A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108865441 | |||||||
| chr2:108865442 | T | C | 11 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0050 others(8): Show |
11 | HG01074.hp1 HG01358.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.1694-8009T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108865442 | |||||||
| chr2:108865915 | C | G | 1 | a0002c0002t0001g0169 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1694-7536C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108865915 | |||||||
| chr2:108866233 | A | T | 10 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0002c0002t0001g0133 others(7): Show |
10 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.1694-7218A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108866233 | |||||||
| chr2:108866839 | C | T | 37 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0007 others(34): Show |
38 | HG00408.hp1 HG01081.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1694-6612C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108866839 | |||||||
| chr2:108866840 | G | A | 2 | a0002c0002t0001g0171 a0002c0002t0001g0191 |
2 | HG01261.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.1694-6611G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108866840 | |||||||
| chr2:108866844 | C | T | 1 | a0006c0008t0001g0165 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1694-6607C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108866844 | |||||||
| chr2:108866880 | GA | G | 11 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(8): Show |
11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1694-6560delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108866880 | ||||||
| chr2:108866944 | G | A | 4 | a0001c0005t0001g0116 a0001c0005t0001g0117 a0001c0005t0001g0118 others(1): Show |
4 | HG02615.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1694-6507G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108866944 | |||||||
| chr2:108867003 | A | G | 3 | a0001c0004t0001g0102 a0001c0004t0001g0103 a0001c0004t0001g0104 |
3 | HG02886.hp1 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1694-6448A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867003 | |||||||
| chr2:108867177 | T | C | 1 | a0003c0003t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1694-6274T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867177 | |||||||
| chr2:108867211 | A | G | 39 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(36): Show |
40 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1694-6240A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867211 | |||||||
| chr2:108867234 | TAGA | T | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1694-6207_1694-620 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108867234 | ||||||
| chr2:108867273 | C | T | 7 | a0001c0006t0001g0198 a0001c0006t0001g0199 a0001c0006t0001g0200 others(4): Show |
7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1694-6178C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867273 | |||||||
| chr2:108867320 | T | C | 7 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1694-6131T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867320 | |||||||
| chr2:108867591 | A | G | 1 | a0001c0001t0002g0028 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1694-5860A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867591 | |||||||
| chr2:108867627 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1694-5824G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867627 | |||||||
| chr2:108867712 | T | G | 1 | a0001c0010t0002g0067 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1694-5739T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867712 | |||||||
| chr2:108867800 | G | A | 1 | a0001c0001t0002g0025 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1694-5651G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867800 | |||||||
| chr2:108867979 | G | T | 1 | a0001c0005t0001g0115 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1694-5472G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867979 | |||||||
| chr2:108868222 | AC | A | 9 | a0001c0001t0001g0030 a0002c0002t0001g0133 a0002c0002t0001g0167 others(6): Show |
9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1694-5228delC | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108868222 | |||||||
| chr2:108868225 | C | T | 1 | a0003c0003t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1694-5226C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108868225 | |||||||
| chr2:108868268 | G | T | 1 | a0001c0005t0001g0111 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1694-5183G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108868268 | |||||||
| chr2:108868649 | T | A | 5 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 others(2): Show |
5 | HG00741.hp2 HG01515.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1694-4802T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108868649 | |||||||
| chr2:108868786 | A | G | 1 | a0001c0005t0001g0114 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1694-4665A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108868786 | |||||||
| chr2:108868805 | A | T | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1694-4646A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108868805 | |||||||
| chr2:108869179 | A | G | 1 | a0001c0004t0001g0108 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1694-4272A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108869179 | |||||||
| chr2:108869311 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1694-4140A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108869311 | |||||||
| chr2:108869710 | A | G | 1 | a0001c0001t0002g0024 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1694-3741A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108869710 | |||||||
| chr2:108869776 | C | T | 8 | a0001c0001t0002g0042 a0001c0006t0001g0198 a0001c0006t0001g0199 others(5): Show |
8 | HG01261.hp1 HG01978.hp1 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.1694-3675C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108869776 | |||||||
| chr2:108869813 | C | T | 200 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(197): Show |
203 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1694-3638C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108869813 | |||||||
| chr2:108869818 | C | G | 2 | a0003c0003t0001g0141 a0003c0003t0001g0180 |
2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1694-3633C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108869818 | |||||||
| chr2:108870048 | C | G | 40 | a0001c0005t0001g0115 a0001c0005t0001g0116 a0001c0005t0001g0117 others(37): Show |
41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1694-3403C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108870048 | |||||||
| chr2:108870461 | A | T | 1 | a0001c0001t0002g0048 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1694-2990A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108870461 | |||||||
| chr2:108870540 | C | T | 2 | a0003c0003t0001g0120 a0003c0003t0001g0148 |
2 | NA18974.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1694-2911C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108870540 | |||||||
| chr2:108870570 | CAAAAGT | C | 6 | a0001c0001t0002g0050 a0001c0001t0002g0091 a0001c0001t0002g0092 others(3): Show |
6 | HG02622.hp1 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1694-2875_1694-287 others(10): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108870570 | ||||||
| chr2:108870801 | A | G | 2 | a0003c0003t0001g0141 a0003c0003t0001g0180 |
2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1694-2650A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108870801 | |||||||
| chr2:108870910 | ATTTAC | A | 5 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0177 others(2): Show |
5 | HG01109.hp2 HG01167.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1694-2538_1694-253 others(9): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108870910 | ||||||
| chr2:108871035 | C | T | 11 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(8): Show |
11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1694-2416C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108871035 | |||||||
| chr2:108871095 | A | G | 13 | a0001c0001t0001g0030 a0001c0004t0001g0102 a0001c0004t0001g0103 others(10): Show |
13 | HG01081.hp2 HG02055.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1694-2356A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108871095 | |||||||
| chr2:108871314 | C | G | 5 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0177 others(2): Show |
5 | HG01109.hp2 HG01167.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1694-2137C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108871314 | |||||||
| chr2:108871365 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0078 |
2 | HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1694-2086T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108871365 | |||||||
| chr2:108871368 | A | AC | 2 | a0001c0004t0001g0197 a0001c0005t0001g0210 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1694-2083_1694-208 others(5): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108871368 | |||||||
| chr2:108871369 | T | C | 200 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0056 others(197): Show |
203 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.1694-2082T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108871369 | |||||||
| chr2:108871370 | T | A | 2 | a0001c0004t0001g0197 a0001c0005t0001g0210 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1694-2081T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108871370 | |||||||
| chr2:108871370 | TA | T | 109 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0078 others(106): Show |
111 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(108): Show |
intron_variant | MODIFIER | c.1694-2056delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108871370 | ||||||
| chr2:108871370 | TAA | T | 55 | a0001c0001t0001g0030 a0001c0001t0002g0007 a0001c0001t0002g0022 others(52): Show |
55 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1694-2057_1694-205 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108871370 | ||||||
| chr2:108871370 | TAAA | T | 30 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(27): Show |
31 | HG01243.hp1 HG01261.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.1694-2058_1694-205 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108871370 | ||||||
| chr2:108871659 | T | C | 1 | a0003c0003t0001g0161 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1694-1792T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108871659 | |||||||
| chr2:108871834 | C | A | 11 | a0002c0002t0001g0127 a0002c0002t0001g0128 a0002c0002t0001g0129 others(8): Show |
11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1694-1617C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108871834 | |||||||
| chr2:108872262 | T | C | 183 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(180): Show |
186 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1694-1189T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872262 | |||||||
| chr2:108872538 | C | T | 4 | a0001c0004t0001g0102 a0001c0004t0001g0103 a0001c0004t0001g0104 others(1): Show |
4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1694-913C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872538 | |||||||
| chr2:108872539 | T | G | 110 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(107): Show |
112 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(109): Show |
intron_variant | MODIFIER | c.1694-912T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872539 | |||||||
| chr2:108872562 | C | T | 110 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(107): Show |
112 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(109): Show |
intron_variant | MODIFIER | c.1694-889C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872562 | |||||||
| chr2:108872610 | T | C | 110 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(107): Show |
112 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(109): Show |
intron_variant | MODIFIER | c.1694-841T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872610 | |||||||
| chr2:108872653 | G | A | 110 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(107): Show |
112 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(109): Show |
intron_variant | MODIFIER | c.1694-798G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872653 | |||||||
| chr2:108872737 | C | T | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1694-714C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872737 | |||||||
| chr2:108872789 | G | C | 17 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0005t0001g0111 others(14): Show |
17 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1694-662G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872789 | |||||||
| chr2:108872864 | T | G | 1 | a0003c0003t0001g0179 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1694-587T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872864 | |||||||
| chr2:108872909 | A | G | 110 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(107): Show |
112 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(109): Show |
intron_variant | MODIFIER | c.1694-542A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872909 | |||||||
| chr2:108872946 | G | C | 110 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(107): Show |
112 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(109): Show |
intron_variant | MODIFIER | c.1694-505G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872946 | |||||||
| chr2:108872973 | C | T | 73 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(70): Show |
74 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.1694-478C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872973 | |||||||
| chr2:108873160 | A | C | 47 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(44): Show |
48 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1694-291A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108873160 | |||||||
| chr2:108873297 | AATG | A | 96 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(93): Show |
98 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(95): Show |
intron_variant | MODIFIER | c.1694-148_1694-146d others(5): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108873297 | ||||||
| chr2:108873338 | T | A | 1 | a0001c0001t0002g0053 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1694-113T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108873338 | |||||||
| chr2:108873370 | A | G | 1 | a0001c0004t0001g0197 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1694-81A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108873370 | |||||||
| chr2:108873635 | C | T | 1 | a0001c0005t0001g0111 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1832+46C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108873635 | |||||||
| chr2:108873690 | A | G | 100 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0004 others(97): Show |
102 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(99): Show |
intron_variant | MODIFIER | c.1832+101A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108873690 | |||||||
| chr2:108873700 | A | G | 3 | a0003c0003t0001g0141 a0003c0003t0001g0180 a0003c0003t0001g0183 |
3 | HG00738.hp2 HG00741.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1832+111A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108873700 | |||||||
| chr2:108873737 | C | T | 17 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0004t0001g0106 others(14): Show |
17 | HG02055.hp1 HG02055.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1832+148C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108873737 | |||||||
| chr2:108873880 | C | T | 1 | a0001c0001t0002g0047 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1832+291C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108873880 | |||||||
| chr2:108873920 | A | T | 12 | a0003c0003t0001g0003 a0003c0003t0001g0140 a0003c0003t0001g0142 others(9): Show |
13 | NA18968.hp2 NA18970.hp2 NA18977.hp2 others(10): Show |
intron_variant | MODIFIER | c.1832+331A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108873920 | |||||||
| chr2:108874564 | A | G | 47 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(44): Show |
48 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1832+975A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108874564 | |||||||
| chr2:108874834 | G | A | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1832+1245G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108874834 | |||||||
| chr2:108874922 | A | AT | 108 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(105): Show |
110 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(107): Show |
intron_variant | MODIFIER | c.1833-1154dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 108874922 | ||||||
| chr2:108874988 | A | G | 183 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0002g0001 others(180): Show |
186 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1833-1100A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108874988 | |||||||
| chr2:108875026 | TA | T | 9 | a0001c0001t0001g0030 a0002c0002t0001g0133 a0002c0002t0001g0167 others(6): Show |
9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1833-1055delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 108875026 | ||||||
| chr2:108875146 | T | C | 6 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0044 others(3): Show |
6 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1833-942T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875146 | |||||||
| chr2:108875159 | A | G | 7 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(4): Show |
7 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1833-929A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875159 | |||||||
| chr2:108875316 | TAA | T | 5 | a0002c0002t0001g0172 a0002c0002t0001g0173 a0002c0002t0001g0177 others(2): Show |
5 | HG01109.hp2 HG01167.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1833-771_1833-770d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875316 | |||||||
| chr2:108875317 | AAT | A | 25 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0004t0001g0010 others(22): Show |
25 | HG01243.hp1 HG01243.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.1833-769_1833-768d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 108875317 | ||||||
| chr2:108875318 | AT | A | 60 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(57): Show |
61 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.1833-769delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875318 | |||||||
| chr2:108875319 | TA | T | 5 | a0001c0001t0002g0057 a0001c0004t0001g0101 a0002c0002t0001g0171 others(2): Show |
5 | HG01261.hp2 HG02040.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1833-752delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 108875319 | ||||||
| chr2:108875319 | TAAA | T | 59 | a0001c0001t0001g0056 a0001c0001t0002g0004 a0001c0001t0002g0009 others(56): Show |
59 | HG00099.hp1 HG00741.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.1833-754_1833-752d others(5): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 108875319 | ||||||
| chr2:108875328 | AAAAAAAA others(2): Show |
A | 37 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0007 others(34): Show |
38 | HG00408.hp1 HG01081.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1833-756_1833-748d others(11): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 108875328 | ||||||
| chr2:108875332 | AAAAAG | A | 7 | a0002c0002t0001g0133 a0002c0002t0001g0167 a0002c0002t0001g0168 others(4): Show |
7 | HG02055.hp1 HG02602.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.1833-752_1833-748d others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 108875332 | ||||||
| chr2:108875335 | A | C | 1 | a0001c0001t0002g0059 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1833-753A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875335 | |||||||
| chr2:108875337 | G | C | 64 | a0001c0001t0001g0056 a0001c0001t0002g0002 a0001c0001t0002g0004 others(61): Show |
65 | HG00099.hp1 HG00741.hp2 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.1833-751G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875337 | |||||||
| chr2:108875352 | T | C | 34 | a0002c0002t0001g0166 a0003c0003t0001g0003 a0003c0003t0001g0120 others(31): Show |
35 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1833-736T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875352 | |||||||
| chr2:108875587 | G | A | 1 | a0002c0002t0001g0181 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1833-501G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875587 | |||||||
| chr2:108875690 | T | C | 34 | a0002c0002t0001g0166 a0003c0003t0001g0003 a0003c0003t0001g0120 others(31): Show |
35 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1833-398T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875690 | |||||||
| chr2:108875765 | G | A | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1833-323G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875765 | |||||||
| chr2:108875783 | G | A | 7 | a0001c0004t0001g0010 a0001c0004t0001g0011 a0001c0004t0001g0012 others(4): Show |
7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1833-305G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875783 | |||||||
| chr2:108875797 | T | A | 1 | a0002c0002t0001g0167 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1833-291T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875797 | |||||||
| chr2:108875820 | C | T | 10 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0002c0002t0001g0133 others(7): Show |
10 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.1833-268C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875820 | |||||||
| chr2:108875989 | G | A | 8 | a0001c0004t0001g0106 a0001c0004t0001g0107 a0001c0004t0001g0108 others(5): Show |
8 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1833-99G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875989 | |||||||
| chr2:108875999 | C | G | 16 | a0001c0001t0001g0006 a0001c0001t0001g0078 a0001c0005t0001g0111 others(13): Show |
16 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1833-89C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875999 | |||||||
| chr2:108876075 | A | T | 1 | a0003c0003t0001g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1833-13A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108876075 |