Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84318 |
| ensemblid | ENSG00000120647.10 |
| hgncid | 28203 |
| symbol | CCDC77 |
| name | coiled-coil domain containing 77 |
| refseq_nuc | NM_032358.4 |
| refseq_prot | NP_115734.1 |
| ensembl_nuc | ENST00000239830.9 |
| ensembl_prot | ENSP00000239830.4 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 401644 |
| end | 442642 |
| strand | + |
| ver | v1.2 |
| region | chr12:401644-442642 |
| region5000 | chr12:396644-447642 |
| regionname0 | CCDC77_chr12_401644_442642 |
| regionname5000 | CCDC77_chr12_396644_447642 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 488 | 205 | 30 | 47 | 93 | 7 | 27 | 69 | CCDC77_chr12_396644_447642 | CCDC77 | MNFTP others(483): Show |
chr12 | 396644 | 447642 |
| a0002 | 0/0 | 488 | 103 | 20 | 21 | 45 | 2 | 15 | 37 | CCDC77_chr12_396644_447642 | CCDC77 | MNFTP others(483): Show |
chr12 | 396644 | 447642 |
| a0003 | 0/0 | 488 | 78 | 20 | 4 | 51 | 0 | 3 | 48 | CCDC77_chr12_396644_447642 | CCDC77 | MNFTP others(483): Show |
chr12 | 396644 | 447642 |
| a0004 | 0/1 | 488 | 28 | 8 | 5 | 8 | 3 | 3 | 7 | CCDC77_chr12_396644_447642 | CCDC77 | MNFTP others(483): Show |
chr12 | 396644 | 447642 |
| a0005 | 0/0 | 488 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | MNFTP others(483): Show |
chr12 | 396644 | 447642 |
| a0006 | 0/0 | 456 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | MADSL others(451): Show |
chr12 | 396644 | 447642 |
| a0007 | 0/0 | 488 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | MNFTP others(483): Show |
chr12 | 396644 | 447642 |
| a0008 | 0/0 | 13 | 2 | 0 | 1 | 1 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | MNFTP others(8): Show |
chr12 | 396644 | 447642 |
| a0009 | 0/0 | 488 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | MNFTP others(483): Show |
chr12 | 396644 | 447642 |
| a0010 | 0/0 | 488 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | MNFTP others(483): Show |
chr12 | 396644 | 447642 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1464 | 205 | 30 | 47 | 93 | 7 | 27 | CCDC77_chr12_396644_447642 | CCDC77 | ATGAA others(1459): Show |
chr12 | 396644 | 447642 | ||
| a0002c0002 | 0/0 | 1464 | 102 | 19 | 21 | 45 | 2 | 15 | CCDC77_chr12_396644_447642 | CCDC77 | ATGAA others(1459): Show |
chr12 | 396644 | 447642 | ||
| a0002c0009 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | ATGAA others(1459): Show |
chr12 | 396644 | 447642 | ||
| a0003c0003 | 0/0 | 1464 | 78 | 20 | 4 | 51 | 0 | 3 | CCDC77_chr12_396644_447642 | CCDC77 | ATGAA others(1459): Show |
chr12 | 396644 | 447642 | ||
| a0004c0004 | 0/1 | 1464 | 27 | 7 | 5 | 8 | 3 | 3 | CCDC77_chr12_396644_447642 | CCDC77 | ATGAA others(1459): Show |
chr12 | 396644 | 447642 | ||
| a0004c0012 | 0/0 | 1464 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | ATGAA others(1459): Show |
chr12 | 396644 | 447642 | ||
| a0005c0005 | 0/0 | 1464 | 7 | 7 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | ATGAA others(1459): Show |
chr12 | 396644 | 447642 | ||
| a0006c0006 | 0/0 | 1426 | 4 | 4 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GCGAA others(1421): Show |
chr12 | 396644 | 447642 | ||
| a0007c0007 | 0/0 | 1464 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | ATGAA others(1459): Show |
chr12 | 396644 | 447642 | ||
| a0008c0011 | 0/0 | 1464 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | ATGAA others(1459): Show |
chr12 | 396644 | 447642 | ||
| a0008c0013 | 0/0 | 1464 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | ATGAA others(1459): Show |
chr12 | 396644 | 447642 | ||
| a0009c0008 | 0/0 | 1464 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | ATGAA others(1459): Show |
chr12 | 396644 | 447642 | ||
| a0010c0010 | 0/0 | 1464 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | ATGAA others(1459): Show |
chr12 | 396644 | 447642 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2300 | 69 | 8 | 22 | 17 | 3 | 19 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0001c0001t0002 | 0/0 | 2300 | 46 | 6 | 12 | 21 | 4 | 3 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0001c0001t0003 | 0/0 | 2300 | 45 | 0 | 5 | 36 | 0 | 4 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0001c0001t0004 | 0/0 | 2300 | 28 | 13 | 6 | 9 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0001c0001t0006 | 0/0 | 2300 | 8 | 0 | 1 | 7 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0001c0001t0007 | 1/0 | 2300 | 3 | 0 | 0 | 2 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0001c0001t0008 | 0/0 | 2300 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTGTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0001c0001t0009 | 0/0 | 2300 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTGTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0001c0001t0010 | 0/0 | 2300 | 2 | 0 | 1 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0001c0001t0016 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0002c0002t0001 | 0/0 | 2300 | 92 | 18 | 21 | 36 | 2 | 15 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0002c0002t0002 | 0/0 | 2300 | 8 | 0 | 0 | 8 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0002c0002t0013 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0002c0002t0014 | 0/0 | 2300 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0002c0009t0001 | 0/0 | 2300 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0003c0003t0001 | 0/0 | 2300 | 19 | 8 | 2 | 9 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0003c0003t0002 | 0/0 | 2300 | 47 | 5 | 0 | 39 | 0 | 3 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0003c0003t0003 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0003c0003t0004 | 0/0 | 2300 | 5 | 4 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0003c0003t0006 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0003c0003t0007 | 0/0 | 2300 | 2 | 1 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0003c0003t0008 | 0/0 | 2300 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTGTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0003c0003t0009 | 0/0 | 2300 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTGTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0003c0003t0015 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0004c0004t0001 | 0/1 | 2300 | 20 | 5 | 5 | 3 | 3 | 3 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0004c0004t0002 | 0/0 | 2300 | 6 | 1 | 0 | 5 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0004c0004t0005 | 0/0 | 2300 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0004c0012t0001 | 0/0 | 2300 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0005c0005t0005 | 0/0 | 2300 | 7 | 7 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0006c0006t0011 | 0/0 | 2246 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2241): Show |
chr12 | 396644 | 447642 |
| a0006c0006t0012 | 0/0 | 2246 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2241): Show |
chr12 | 396644 | 447642 |
| a0007c0007t0005 | 0/0 | 2300 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0008c0011t0002 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0008c0013t0004 | 0/0 | 2300 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0009c0008t0002 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| a0010c0010t0003 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | GTTTT others(2295): Show |
chr12 | 396644 | 447642 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0375 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0396 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0406 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0407 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0408 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0358 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0398 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0384 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0397 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0415 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0006g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0006g0388 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0006g0389 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0006g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0006g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0006g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0006g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0006g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0007g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0007g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0007g0344 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0009g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0010g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0010g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0016g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0385 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0401 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0013g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0014g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0009t0001g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0411 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0413 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0383 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0004g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0004g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0004g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0007g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0007g0412 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0008g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0009g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0015g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0283 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0005g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0012t0001g0414 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0005c0005t0005g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0005c0005t0005g0409 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0005c0005t0005g0410 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0005c0005t0005g0416 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0005c0005t0005g0418 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0005c0005t0005g0419 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0005c0005t0005g0420 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0006c0006t0011g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0006c0006t0011g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0006c0006t0012g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0006c0006t0012g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0007c0007t0005g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0007c0007t0005g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0007c0007t0005g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0008c0011t0002g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0008c0013t0004g0417 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0009c0008t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0010c0010t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | FIN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00280 | hp2 | a0004 | c0004 | t0001 | g0304 | EUR | FIN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0161 | EUR | FIN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | FIN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00408 | hp1 | a0004 | c0004 | t0002 | g0309 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00423 | hp2 | a0002 | c0002 | t0013 | g0361 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00544 | hp1 | a0003 | c0003 | t0002 | g0157 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0102 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0064 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0384 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0378 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0012 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0347 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0032 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0359 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0050 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0130 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0336 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01074 | hp2 | a0008 | c0013 | t0004 | g0417 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0328 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01106 | hp2 | a0003 | c0003 | t0001 | g0342 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01109 | hp1 | a0003 | c0003 | t0004 | g0363 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0314 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01167 | hp1 | a0004 | c0004 | t0001 | g0095 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01167 | hp2 | a0001 | c0001 | t0004 | g0160 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0406 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0159 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0298 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01243 | hp1 | a0003 | c0003 | t0007 | g0412 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0352 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01256 | hp1 | a0004 | c0004 | t0001 | g0142 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0141 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0183 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0408 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0116 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01346 | hp2 | a0003 | c0003 | t0001 | g0316 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01433 | hp1 | a0001 | c0001 | t0010 | g0278 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0276 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0244 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0232 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | IBS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0226 | EUR | IBS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0011 | EUR | IBS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0399 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01884 | hp2 | a0003 | c0003 | t0001 | g0250 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01891 | hp1 | a0006 | c0006 | t0011 | g0106 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01891 | hp2 | a0003 | c0003 | t0004 | g0175 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01928 | hp2 | a0004 | c0004 | t0001 | g0072 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0046 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0185 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0176 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0345 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0184 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01978 | hp1 | a0004 | c0004 | t0001 | g0073 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0371 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01981 | hp1 | a0004 | c0004 | t0001 | g0067 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0182 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0348 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0179 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0124 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0239 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0092 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0377 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02145 | hp1 | a0005 | c0005 | t0005 | g0332 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02145 | hp2 | a0006 | c0006 | t0011 | g0103 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02148 | hp1 | a0002 | c0002 | t0001 | g0181 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0353 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | CDX | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02155 | hp2 | a0001 | c0001 | t0006 | g0388 | EAS | CDX | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02165 | hp1 | a0003 | c0003 | t0002 | g0267 | EAS | CDX | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0113 | EAS | CDX | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0400 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0415 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02258 | hp2 | a0004 | c0004 | t0001 | g0171 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0227 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0290 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0402 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0282 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0180 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0358 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0188 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0405 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02451 | hp2 | a0002 | c0009 | t0001 | g0404 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0331 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02572 | hp2 | a0005 | c0005 | t0005 | g0420 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0407 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02615 | hp2 | a0004 | c0004 | t0002 | g0097 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02622 | hp1 | a0003 | c0003 | t0004 | g0369 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0324 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02630 | hp1 | a0003 | c0003 | t0002 | g0379 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0396 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02647 | hp1 | a0003 | c0003 | t0002 | g0372 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02647 | hp2 | a0004 | c0012 | t0001 | g0414 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0110 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0118 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02717 | hp1 | a0003 | c0003 | t0004 | g0329 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0251 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02735 | hp1 | a0004 | c0004 | t0001 | g0279 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0375 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0376 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02809 | hp1 | a0006 | c0006 | t0012 | g0105 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02809 | hp2 | a0007 | c0007 | t0005 | g0197 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0403 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0381 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02886 | hp2 | a0003 | c0003 | t0001 | g0341 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0317 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02895 | hp2 | a0005 | c0005 | t0005 | g0418 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02896 | hp1 | a0003 | c0003 | t0001 | g0413 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0234 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0233 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0318 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0174 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0093 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02970 | hp1 | a0005 | c0005 | t0005 | g0416 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02970 | hp2 | a0004 | c0004 | t0001 | g0373 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0397 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02976 | hp2 | a0005 | c0005 | t0005 | g0409 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03017 | hp2 | a0003 | c0003 | t0002 | g0280 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0094 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0246 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0333 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03098 | hp2 | a0003 | c0003 | t0002 | g0368 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0325 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0387 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03139 | hp2 | a0004 | c0004 | t0001 | g0315 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03195 | hp1 | a0002 | c0002 | t0014 | g0321 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03195 | hp2 | a0006 | c0006 | t0012 | g0104 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0319 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03209 | hp2 | a0007 | c0007 | t0005 | g0382 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0334 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03225 | hp2 | a0007 | c0007 | t0005 | g0326 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0364 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03453 | hp1 | a0003 | c0003 | t0001 | g0148 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0177 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03486 | hp1 | a0003 | c0003 | t0008 | g0247 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0323 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0154 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0225 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03516 | hp2 | a0003 | c0003 | t0001 | g0411 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0401 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0289 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0386 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03579 | hp2 | a0005 | c0005 | t0005 | g0419 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0169 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0112 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0051 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0230 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0362 | SAS | STU | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03688 | hp2 | a0004 | c0004 | t0001 | g0007 | SAS | STU | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0260 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03704 | hp2 | a0003 | c0003 | t0002 | g0269 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03710 | hp2 | a0004 | c0004 | t0001 | g0007 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0221 | SAS | BEB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | BEB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | BEB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0228 | SAS | BEB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0127 | SAS | BEB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0335 | SAS | BEB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0199 | SAS | BEB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0109 | SAS | BEB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG04115 | hp1 | a0003 | c0003 | t0002 | g0302 | SAS | STU | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0111 | SAS | STU | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0222 | SAS | BEB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0208 | SAS | BEB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0090 | SAS | STU | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | STU | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | STU | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0125 | SAS | STU | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG04228 | hp1 | a0002 | c0002 | t0001 | g0243 | SAS | STU | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | STU | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0252 | EAS | CHB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0091 | EAS | CHB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18747 | hp1 | a0001 | c0001 | t0007 | g0015 | EAS | CHB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | CHB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18906 | hp1 | a0003 | c0003 | t0001 | g0287 | AFR | YRI | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18906 | hp2 | a0003 | c0003 | t0007 | g0327 | AFR | YRI | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18941 | hp2 | a0001 | c0001 | t0006 | g0389 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18942 | hp2 | a0001 | c0001 | t0007 | g0016 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0291 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18945 | hp1 | a0003 | c0003 | t0002 | g0262 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18948 | hp1 | a0003 | c0003 | t0002 | g0081 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18949 | hp1 | a0001 | c0001 | t0006 | g0393 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0089 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18950 | hp2 | a0003 | c0003 | t0002 | g0213 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18951 | hp1 | a0003 | c0003 | t0002 | g0205 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18952 | hp1 | a0004 | c0004 | t0001 | g0139 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18952 | hp2 | a0003 | c0003 | t0002 | g0209 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0306 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18957 | hp2 | a0003 | c0003 | t0002 | g0266 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0066 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18960 | hp1 | a0003 | c0003 | t0002 | g0256 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18960 | hp2 | a0003 | c0003 | t0001 | g0019 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0365 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18961 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18962 | hp1 | a0003 | c0003 | t0002 | g0271 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18962 | hp2 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18963 | hp2 | a0004 | c0004 | t0002 | g0305 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18965 | hp1 | a0003 | c0003 | t0001 | g0140 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0350 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18971 | hp1 | a0003 | c0003 | t0002 | g0383 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18973 | hp1 | a0009 | c0008 | t0002 | g0101 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18973 | hp2 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18977 | hp1 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18977 | hp2 | a0003 | c0003 | t0002 | g0008 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18979 | hp2 | a0003 | c0003 | t0002 | g0300 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18980 | hp2 | a0003 | c0003 | t0002 | g0265 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18981 | hp1 | a0001 | c0001 | t0006 | g0391 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18982 | hp1 | a0004 | c0004 | t0002 | g0312 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18982 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18983 | hp1 | a0003 | c0003 | t0002 | g0258 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0351 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18984 | hp2 | a0003 | c0003 | t0002 | g0272 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18985 | hp1 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18985 | hp2 | a0003 | c0003 | t0002 | g0214 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18988 | hp1 | a0003 | c0003 | t0002 | g0270 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18990 | hp1 | a0010 | c0010 | t0003 | g0076 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18990 | hp2 | a0003 | c0003 | t0002 | g0263 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18991 | hp1 | a0003 | c0003 | t0002 | g0255 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18992 | hp1 | a0003 | c0003 | t0003 | g0065 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18992 | hp2 | a0003 | c0003 | t0002 | g0367 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18995 | hp1 | a0003 | c0003 | t0002 | g0313 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0296 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18998 | hp2 | a0001 | c0001 | t0006 | g0392 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19000 | hp1 | a0003 | c0003 | t0001 | g0070 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19000 | hp2 | a0003 | c0003 | t0001 | g0071 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19003 | hp2 | a0004 | c0004 | t0002 | g0311 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19004 | hp2 | a0001 | c0001 | t0006 | g0394 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19005 | hp1 | a0003 | c0003 | t0006 | g0084 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19006 | hp1 | a0003 | c0003 | t0002 | g0257 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19007 | hp1 | a0003 | c0003 | t0002 | g0001 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19007 | hp2 | a0003 | c0003 | t0002 | g0231 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19009 | hp1 | a0004 | c0004 | t0001 | g0273 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19009 | hp2 | a0003 | c0003 | t0002 | g0268 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19011 | hp1 | a0003 | c0003 | t0002 | g0008 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0162 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0398 | AFR | LWK | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19030 | hp2 | a0004 | c0004 | t0005 | g0340 | AFR | LWK | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0385 | AFR | LWK | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0320 | AFR | LWK | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0145 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0370 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19058 | hp2 | a0001 | c0001 | t0006 | g0390 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19065 | hp1 | a0008 | c0011 | t0002 | g0395 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19067 | hp1 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19067 | hp2 | a0003 | c0003 | t0015 | g0301 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19068 | hp2 | a0004 | c0004 | t0001 | g0069 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19074 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19074 | hp2 | a0003 | c0003 | t0002 | g0249 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19077 | hp2 | a0003 | c0003 | t0002 | g0261 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19078 | hp1 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19078 | hp2 | a0001 | c0001 | t0016 | g0077 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19079 | hp1 | a0003 | c0003 | t0002 | g0253 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19079 | hp2 | a0003 | c0003 | t0002 | g0215 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19080 | hp1 | a0003 | c0003 | t0001 | g0062 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19080 | hp2 | a0004 | c0004 | t0002 | g0310 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19081 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19081 | hp2 | a0003 | c0003 | t0002 | g0374 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19082 | hp2 | a0003 | c0003 | t0002 | g0366 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0096 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0349 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19087 | hp1 | a0003 | c0003 | t0002 | g0068 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19088 | hp2 | a0003 | c0003 | t0002 | g0264 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19090 | hp2 | a0003 | c0003 | t0001 | g0063 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19240 | hp1 | a0001 | c0001 | t0008 | g0170 | AFR | YRI | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0173 | AFR | YRI | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA20129 | hp1 | a0003 | c0003 | t0009 | g0168 | AFR | ASW | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | ASW | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA20752 | hp1 | a0004 | c0004 | t0001 | g0240 | EUR | TSI | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0360 | EUR | TSI | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0346 | EUR | TSI | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA20805 | hp2 | a0004 | c0004 | t0001 | g0356 | EUR | TSI | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA20905 | hp1 | a0001 | c0001 | t0010 | g0277 | SAS | GIH | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0194 | SAS | GIH | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0355 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0357 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02109 | hp2 | a0004 | c0004 | t0001 | g0085 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0172 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02559 | hp1 | a0003 | c0003 | t0004 | g0337 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0322 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03471 | hp1 | a0003 | c0003 | t0002 | g0380 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03471 | hp2 | a0003 | c0003 | t0002 | g0343 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA20300 | hp1 | a0005 | c0005 | t0005 | g0410 | AFR | USA | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0187 | AFR | USA | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA21309 | hp1 | a0004 | c0004 | t0001 | g0339 | AFR | LWK | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0330 | AFR | LWK | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| homoSapiens | chm13v2 | a0004 | c0004 | t0001 | g0283 | REF | REF | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0007 | g0344 | REF | REF | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:409154 | GAGATCAC others(786): Show |
G | 1 | a0006 | 4 | HG01891.hp1 HG02145.hp2 HG02809.hp1 others(1): Show |
exon_loss_variant&splice_region_variant | HIGH | c.-16-206_38+533del | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr12 | 409154 | ||||||
| chr12:411748 | C | T | 1 | a0008 | 1 | HG01074.hp2 | stop_gained&splice_region_variant | HIGH | c.40C>T | p.Arg14* | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/13 | 151/2300 | 40/1467 | 14/488 | chr12 | 411748 | |||
| chr12:411781 | A | C | 3 | a0003 a0004 a0005 |
112 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(109): Show |
missense_variant | MODERATE | c.73A>C | p.Ser25Arg | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/13 | 184/2300 | 73/1467 | 25/488 | chr12 | 411781 | |||
| chr12:411844 | G | A | 1 | a0008 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.136G>A | p.Glu46Lys | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/13 | 247/2300 | 136/1467 | 46/488 | chr12 | 411844 | |||
| chr12:418623 | C | T | 1 | a0008 | 1 | NA19065.hp1 | stop_gained | HIGH | c.400C>T | p.Arg134* | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/13 | 511/2300 | 400/1467 | 134/488 | chr12 | 418623 | |||
| chr12:438517 | T | C | 3 | a0002 a0004 a0009 |
131 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(128): Show |
missense_variant | MODERATE | c.1004T>C | p.Met335Thr | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/13 | 1115/2300 | 1004/1467 | 335/488 | chr12 | 438517 | |||
| chr12:440704 | A | G | 1 | a0010 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.1129A>G | p.Ile377Val | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 11/13 | 1240/2300 | 1129/1467 | 377/488 | chr12 | 440704 | |||
| chr12:440708 | G | A | 1 | a0009 | 1 | NA18973.hp1 | missense_variant | MODERATE | c.1133G>A | p.Arg378His | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 11/13 | 1244/2300 | 1133/1467 | 378/488 | chr12 | 440708 | |||
| chr12:440737 | T | G | 2 | a0005 a0007 |
10 | HG02145.hp1 HG02572.hp2 HG02809.hp2 others(7): Show |
missense_variant | MODERATE | c.1162T>G | p.Phe388Val | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 11/13 | 1273/2300 | 1162/1467 | 388/488 | chr12 | 440737 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:418626 | C | T | 1 | a0004c0012 | 1 | HG02647.hp2 | synonymous_variant | LOW | c.403C>T | p.Leu135Leu | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/13 | 514/2300 | 403/1467 | 135/488 | chr12 | 418626 | |||
| chr12:433236 | G | C | 2 | a0005c0005 a0007c0007 |
10 | HG02145.hp1 HG02572.hp2 HG02809.hp2 others(7): Show |
synonymous_variant | LOW | c.735G>C | p.Gly245Gly | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/13 | 846/2300 | 735/1467 | 245/488 | chr12 | 433236 | |||
| chr12:440712 | G | A | 1 | a0002c0009 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.1137G>A | p.Glu379Glu | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 11/13 | 1248/2300 | 1137/1467 | 379/488 | chr12 | 440712 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:401646 | T | G | 4 | a0001c0001t0008 a0001c0001t0009 a0003c0003t0008 others(1): Show |
5 | HG03453.hp2 HG03486.hp1 HG03540.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-109T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/13 | 7738 | chr12 | 401646 | ||||||
| chr12:405556 | T | A | 1 | a0002c0002t0013 | 1 | HG00423.hp2 | 5_prime_UTR_variant | MODIFIER | c.-25T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/13 | 3828 | chr12 | 405556 | ||||||
| chr12:442129 | C | T | 33 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(30): Show |
424 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(421): Show |
3_prime_UTR_variant | MODIFIER | c.*209C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 13/13 | 209 | chr12 | 442129 | ||||||
| chr12:442206 | G | T | 1 | a0001c0001t0016 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*286G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 13/13 | 286 | chr12 | 442206 | ||||||
| chr12:442221 | A | G | 1 | a0003c0003t0015 | 1 | NA19067.hp2 | 3_prime_UTR_variant | MODIFIER | c.*301A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 13/13 | 301 | chr12 | 442221 | ||||||
| chr12:442228 | A | C | 1 | a0001c0001t0010 | 2 | HG01433.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*308A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 13/13 | 308 | chr12 | 442228 | ||||||
| chr12:442294 | C | T | 3 | a0001c0001t0003 a0003c0003t0003 a0010c0010t0003 |
47 | HG00609.hp2 HG00738.hp1 HG01496.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*374C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 13/13 | 374 | chr12 | 442294 | ||||||
| chr12:442384 | G | A | 11 | a0001c0001t0002 a0001c0001t0016 a0002c0002t0002 others(8): Show |
115 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*464G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 13/13 | 464 | chr12 | 442384 | ||||||
| chr12:442476 | T | C | 2 | a0001c0001t0006 a0003c0003t0006 |
9 | HG00735.hp1 HG02155.hp2 NA18941.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*556T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 13/13 | 556 | chr12 | 442476 | ||||||
| chr12:442534 | G | C | 1 | a0002c0002t0014 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*614G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 13/13 | 614 | chr12 | 442534 | ||||||
| chr12:442557 | T | C | 3 | a0004c0004t0005 a0005c0005t0005 a0007c0007t0005 |
11 | HG02145.hp1 HG02572.hp2 HG02809.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*637T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 13/13 | 637 | chr12 | 442557 | ||||||
| chr12:442636 | C | T | 5 | a0001c0001t0004 a0001c0001t0008 a0003c0003t0004 others(2): Show |
37 | HG00597.hp1 HG00639.hp1 HG01074.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*716C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 13/13 | 716 | chr12 | 442636 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:401699 | T | A | 3 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0006g0012 |
3 | HG00735.hp1 HG01928.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.-71+15T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 401699 | |||||||
| chr12:401882 | G | A | 2 | a0001c0001t0007g0015 a0001c0001t0007g0016 |
2 | NA18747.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.-71+198G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 401882 | |||||||
| chr12:401973 | ACT | A | 96 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0002g0004 others(93): Show |
99 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.-71+292_-71+293del others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 401973 | ||||||
| chr12:402008 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-71+324T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 402008 | |||||||
| chr12:402078 | C | T | 3 | a0005c0005t0005g0418 a0005c0005t0005g0419 a0005c0005t0005g0420 |
3 | HG02572.hp2 HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-71+394C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 402078 | |||||||
| chr12:402092 | A | C | 30 | a0001c0001t0001g0396 a0001c0001t0001g0402 a0001c0001t0001g0405 others(27): Show |
30 | HG01074.hp2 HG01168.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.-71+408A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 402092 | |||||||
| chr12:402117 | T | A | 8 | a0001c0001t0006g0388 a0001c0001t0006g0389 a0001c0001t0006g0390 others(5): Show |
8 | HG02155.hp2 NA18941.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.-71+433T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 402117 | |||||||
| chr12:402208 | T | C | 22 | a0001c0001t0001g0108 a0001c0001t0002g0115 a0001c0001t0003g0125 others(19): Show |
22 | HG00597.hp2 HG00673.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.-71+524T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 402208 | |||||||
| chr12:402263 | C | T | 4 | a0001c0001t0002g0386 a0001c0001t0004g0384 a0002c0002t0001g0385 others(1): Show |
4 | HG00639.hp1 HG03139.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-71+579C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 402263 | |||||||
| chr12:402280 | A | T | 1 | a0002c0002t0001g0107 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-71+596A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 402280 | |||||||
| chr12:402291 | G | C | 92 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0002g0004 others(89): Show |
95 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.-71+607G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 402291 | |||||||
| chr12:402345 | A | G | 9 | a0001c0001t0004g0415 a0003c0003t0001g0411 a0003c0003t0001g0413 others(6): Show |
9 | HG01074.hp2 HG01243.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-71+661A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 402345 | |||||||
| chr12:402513 | G | T | 1 | a0002c0002t0001g0129 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-71+829G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 402513 | |||||||
| chr12:402572 | T | C | 2 | a0001c0001t0001g0131 a0002c0002t0001g0130 |
2 | HG00741.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-71+888T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 402572 | |||||||
| chr12:402815 | A | T | 1 | a0003c0003t0002g0383 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-71+1131A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 402815 | |||||||
| chr12:403171 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-71+1487G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 403171 | |||||||
| chr12:403402 | C | T | 2 | a0001c0001t0004g0381 a0007c0007t0005g0382 |
2 | HG02886.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-71+1718C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 403402 | |||||||
| chr12:403459 | A | G | 2 | a0003c0003t0002g0379 a0003c0003t0002g0380 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-71+1775A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 403459 | |||||||
| chr12:403554 | G | A | 3 | a0002c0002t0001g0109 a0002c0002t0001g0110 a0002c0002t0001g0111 |
3 | HG02683.hp1 HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-71+1870G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 403554 | |||||||
| chr12:403584 | C | T | 33 | a0001c0001t0001g0402 a0001c0001t0001g0405 a0001c0001t0001g0406 others(30): Show |
33 | HG01074.hp2 HG01168.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.-71+1900C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 403584 | |||||||
| chr12:403854 | G | C | 3 | a0002c0002t0001g0133 a0002c0002t0001g0134 a0002c0002t0001g0135 |
3 | NA18962.hp2 NA19054.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-70-1657G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 403854 | |||||||
| chr12:403865 | G | A | 93 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0396 others(90): Show |
96 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.-70-1646G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 403865 | |||||||
| chr12:403907 | A | T | 1 | a0001c0001t0002g0378 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-70-1604A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 403907 | |||||||
| chr12:403914 | G | T | 1 | a0001c0001t0001g0396 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-70-1597G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 403914 | |||||||
| chr12:403930 | T | G | 68 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0002g0004 others(65): Show |
71 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-70-1581T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 403930 | |||||||
| chr12:403999 | G | A | 1 | a0001c0001t0001g0396 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-70-1512G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 403999 | |||||||
| chr12:404014 | T | C | 3 | a0001c0001t0002g0136 a0001c0001t0002g0137 a0001c0001t0002g0138 |
3 | NA18942.hp1 NA18963.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.-70-1497T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 404014 | |||||||
| chr12:404115 | G | A | 2 | a0003c0003t0001g0140 a0004c0004t0001g0139 |
2 | NA18952.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.-70-1396G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 404115 | |||||||
| chr12:404447 | C | T | 3 | a0001c0001t0001g0406 a0001c0001t0001g0407 a0001c0001t0001g0408 |
3 | HG01168.hp1 HG01261.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-70-1064C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 404447 | |||||||
| chr12:404487 | G | T | 1 | a0001c0001t0001g0396 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-70-1024G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 404487 | |||||||
| chr12:404721 | C | CT | 72 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0375 others(69): Show |
75 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.-70-772dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 404721 | ||||||
| chr12:404721 | C | CTT | 6 | a0001c0001t0003g0080 a0002c0002t0001g0079 a0006c0006t0011g0103 others(3): Show |
6 | HG00621.hp2 HG01891.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-70-773_-70-772dup others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 404721 | ||||||
| chr12:404721 | CT | C | 7 | a0001c0001t0001g0143 a0001c0001t0002g0144 a0001c0001t0004g0397 others(4): Show |
7 | HG01256.hp1 HG01256.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-70-772delT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 404721 | ||||||
| chr12:404745 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-70-766G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 404745 | |||||||
| chr12:404811 | C | T | 1 | a0003c0003t0001g0017 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-70-700C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 404811 | |||||||
| chr12:404812 | T | C | 1 | a0003c0003t0001g0017 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-70-699T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 404812 | |||||||
| chr12:404902 | A | T | 1 | a0002c0002t0001g0371 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-70-609A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 404902 | |||||||
| chr12:405022 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-70-489G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 405022 | |||||||
| chr12:405201 | T | C | 1 | a0003c0003t0001g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-70-310T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 405201 | |||||||
| chr12:405317 | T | A | 1 | a0002c0002t0001g0149 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-70-194T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 405317 | |||||||
| chr12:405320 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-70-191T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 1/12 | chr12 | 405320 | |||||||
| chr12:405616 | A | C | 1 | a0002c0002t0001g0370 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-17+52A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 405616 | |||||||
| chr12:405620 | C | T | 1 | a0003c0003t0004g0369 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-17+56C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 405620 | |||||||
| chr12:405702 | T | C | 1 | a0002c0002t0001g0128 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-17+138T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 405702 | |||||||
| chr12:405703 | G | T | 1 | a0002c0002t0001g0128 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-17+139G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 405703 | |||||||
| chr12:405705 | C | G | 1 | a0002c0002t0001g0128 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-17+141C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 405705 | |||||||
| chr12:405904 | A | G | 8 | a0001c0001t0006g0388 a0001c0001t0006g0389 a0001c0001t0006g0390 others(5): Show |
8 | HG02155.hp2 NA18941.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17+340A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 405904 | |||||||
| chr12:405916 | CT | C | 282 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0132 others(279): Show |
292 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(289): Show |
intron_variant | MODIFIER | c.-17+372delT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 405916 | ||||||
| chr12:405916 | CTT | C | 13 | a0001c0001t0001g0146 a0001c0001t0001g0151 a0001c0001t0001g0152 others(10): Show |
13 | HG00544.hp1 HG01167.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.-17+371_-17+372del others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 405916 | ||||||
| chr12:406020 | C | T | 1 | a0001c0001t0001g0396 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-17+456C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 406020 | |||||||
| chr12:406024 | C | T | 1 | a0001c0001t0001g0376 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-17+460C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 406024 | |||||||
| chr12:406037 | C | T | 4 | a0001c0001t0002g0004 a0001c0001t0002g0074 a0001c0001t0002g0075 others(1): Show |
5 | NA18953.hp2 NA18990.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.-17+473C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 406037 | |||||||
| chr12:406190 | G | A | 8 | a0001c0001t0006g0388 a0001c0001t0006g0389 a0001c0001t0006g0390 others(5): Show |
8 | HG02155.hp2 NA18941.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.-17+626G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 406190 | |||||||
| chr12:406216 | G | GT | 24 | a0001c0001t0002g0325 a0001c0001t0004g0159 a0001c0001t0004g0160 others(21): Show |
24 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.-17+653dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 406216 | ||||||
| chr12:406286 | A | C | 1 | a0009c0008t0002g0101 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-17+722A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 406286 | |||||||
| chr12:406418 | A | G | 1 | a0002c0002t0001g0314 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-17+854A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 406418 | |||||||
| chr12:406447 | C | T | 2 | a0003c0003t0001g0148 a0003c0003t0002g0368 |
2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-17+883C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 406447 | |||||||
| chr12:406605 | C | T | 125 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0402 others(122): Show |
128 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.-17+1041C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 406605 | |||||||
| chr12:406720 | G | T | 14 | a0003c0003t0001g0017 a0003c0003t0001g0019 a0003c0003t0001g0062 others(11): Show |
14 | HG00609.hp1 HG01928.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.-17+1156G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 406720 | |||||||
| chr12:406804 | A | T | 1 | a0001c0001t0002g0138 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-17+1240A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 406804 | |||||||
| chr12:406909 | C | T | 1 | a0001c0001t0001g0405 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-17+1345C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 406909 | |||||||
| chr12:407055 | C | T | 22 | a0001c0001t0001g0108 a0001c0001t0002g0115 a0001c0001t0003g0125 others(19): Show |
22 | HG00597.hp2 HG00673.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.-17+1491C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407055 | |||||||
| chr12:407180 | A | G | 218 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0143 others(215): Show |
225 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.-17+1616A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407180 | |||||||
| chr12:407276 | A | C | 1 | a0003c0003t0002g0313 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-17+1712A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407276 | |||||||
| chr12:407283 | G | A | 14 | a0003c0003t0001g0017 a0003c0003t0001g0019 a0003c0003t0001g0062 others(11): Show |
14 | HG00609.hp1 HG01928.hp2 HG01978.hp1 others(11): Show |
intron_variant | MODIFIER | c.-17+1719G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407283 | |||||||
| chr12:407353 | G | A | 4 | a0001c0001t0001g0151 a0001c0001t0001g0365 a0002c0002t0001g0163 others(1): Show |
4 | HG02027.hp1 NA18961.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.-17+1789G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407353 | |||||||
| chr12:407356 | A | G | 1 | a0001c0001t0003g0061 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-17+1792A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407356 | |||||||
| chr12:407386 | T | C | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG00323.hp2 HG01106.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-17+1822T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407386 | |||||||
| chr12:407442 | C | T | 8 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0002c0002t0001g0306 others(5): Show |
8 | HG00408.hp1 NA18957.hp1 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.-17+1878C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407442 | |||||||
| chr12:407467 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-16-1901G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407467 | |||||||
| chr12:407527 | A | G | 1 | a0001c0001t0001g0364 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-16-1841A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407527 | |||||||
| chr12:407553 | C | G | 3 | a0003c0003t0001g0148 a0003c0003t0002g0368 a0003c0003t0004g0363 |
3 | HG01109.hp1 HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-16-1815C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407553 | |||||||
| chr12:407632 | G | T | 2 | a0001c0001t0007g0015 a0001c0001t0007g0016 |
2 | NA18747.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.-16-1736G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407632 | |||||||
| chr12:407659 | C | T | 1 | a0010c0010t0003g0076 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-16-1709C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407659 | |||||||
| chr12:407714 | A | G | 9 | a0001c0001t0004g0415 a0003c0003t0001g0411 a0003c0003t0001g0413 others(6): Show |
9 | HG01074.hp2 HG01243.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.-16-1654A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407714 | |||||||
| chr12:407729 | G | T | 3 | a0001c0001t0001g0405 a0001c0001t0002g0403 a0002c0009t0001g0404 |
3 | HG02451.hp1 HG02451.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-16-1639G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407729 | |||||||
| chr12:407755 | A | G | 1 | a0004c0004t0001g0304 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-16-1613A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407755 | |||||||
| chr12:407782 | A | AT | 73 | a0001c0001t0001g0108 a0001c0001t0001g0152 a0001c0001t0001g0153 others(70): Show |
73 | HG00423.hp2 HG00597.hp2 HG00639.hp1 others(70): Show |
intron_variant | MODIFIER | c.-16-1563dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 407782 | ||||||
| chr12:407782 | A | ATT | 241 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0131 others(238): Show |
249 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.-16-1564_-16-1563d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 407782 | ||||||
| chr12:407782 | A | ATTT | 48 | a0001c0001t0001g0147 a0001c0001t0001g0292 a0001c0001t0001g0375 others(45): Show |
50 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.-16-1565_-16-1563d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 407782 | ||||||
| chr12:407806 | G | A | 1 | a0003c0003t0002g0372 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-16-1562G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407806 | |||||||
| chr12:407824 | G | A | 1 | a0001c0001t0002g0335 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-16-1544G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407824 | |||||||
| chr12:407844 | A | G | 3 | a0001c0001t0002g0004 a0001c0001t0002g0074 a0001c0001t0002g0075 |
4 | NA18953.hp2 NA19004.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16-1524A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407844 | |||||||
| chr12:407893 | C | T | 344 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0131 others(341): Show |
354 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(351): Show |
intron_variant | MODIFIER | c.-16-1475C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407893 | |||||||
| chr12:407976 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-16-1392A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 407976 | |||||||
| chr12:408001 | A | C | 1 | a0004c0004t0002g0097 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-16-1367A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 408001 | |||||||
| chr12:408065 | G | A | 1 | a0001c0001t0002g0336 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-16-1303G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 408065 | |||||||
| chr12:408236 | C | G | 1 | a0001c0001t0001g0286 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-16-1132C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 408236 | |||||||
| chr12:408355 | G | C | 344 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0131 others(341): Show |
354 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(351): Show |
intron_variant | MODIFIER | c.-16-1013G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 408355 | |||||||
| chr12:408398 | TA | T | 68 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0002g0004 others(65): Show |
71 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.-16-969delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 408398 | |||||||
| chr12:408531 | C | T | 1 | a0002c0002t0013g0361 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-16-837C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 408531 | |||||||
| chr12:408648 | C | T | 1 | a0008c0013t0004g0417 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-16-720C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 408648 | |||||||
| chr12:408789 | T | A | 4 | a0003c0003t0004g0337 a0005c0005t0005g0418 a0005c0005t0005g0419 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16-579T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 408789 | |||||||
| chr12:408814 | T | A | 2 | a0001c0001t0007g0015 a0001c0001t0007g0016 |
2 | NA18747.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.-16-554T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 408814 | |||||||
| chr12:408817 | A | G | 2 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
2 | NA18971.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-16-551A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 408817 | |||||||
| chr12:409066 | G | A | 1 | a0003c0003t0001g0287 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-16-302G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 409066 | |||||||
| chr12:409137 | A | G | 312 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0131 others(309): Show |
322 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(319): Show |
intron_variant | MODIFIER | c.-16-231A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 409137 | |||||||
| chr12:409209 | T | C | 1 | a0002c0002t0001g0128 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-16-159T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 409209 | |||||||
| chr12:409210 | C | T | 1 | a0002c0002t0001g0128 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-16-158C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 409210 | |||||||
| chr12:409210 | CA | C | 119 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0402 others(116): Show |
121 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.-16-144delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 409210 | ||||||
| chr12:409211 | A | C | 1 | a0002c0002t0001g0128 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-16-157A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 409211 | |||||||
| chr12:409225 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-16-143G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 409225 | |||||||
| chr12:409226 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-16-142A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 409226 | |||||||
| chr12:409530 | T | G | 15 | a0001c0001t0003g0099 a0001c0001t0004g0086 a0001c0001t0004g0087 others(12): Show |
15 | HG00597.hp1 HG02080.hp1 NA18612.hp2 others(12): Show |
intron_variant | MODIFIER | c.38+109T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 409530 | |||||||
| chr12:409621 | A | G | 68 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0002g0004 others(65): Show |
71 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.38+200A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 409621 | |||||||
| chr12:409629 | A | G | 308 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0131 others(305): Show |
318 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(315): Show |
intron_variant | MODIFIER | c.38+208A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 409629 | |||||||
| chr12:409752 | T | C | 10 | a0003c0003t0002g0009 a0003c0003t0002g0157 a0003c0003t0002g0262 others(7): Show |
11 | HG00544.hp1 NA18945.hp1 NA18957.hp2 others(8): Show |
intron_variant | MODIFIER | c.38+331T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 409752 | |||||||
| chr12:409805 | C | T | 71 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0002g0004 others(68): Show |
74 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.38+384C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 409805 | |||||||
| chr12:409820 | T | C | 375 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(372): Show |
385 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(382): Show |
intron_variant | MODIFIER | c.38+399T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 409820 | |||||||
| chr12:409822 | C | T | 1 | a0003c0003t0003g0065 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.38+401C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 409822 | |||||||
| chr12:409831 | T | TA | 298 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0131 others(295): Show |
308 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(305): Show |
intron_variant | MODIFIER | c.38+427dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 409831 | ||||||
| chr12:409831 | T | TAA | 7 | a0001c0001t0001g0207 a0001c0001t0001g0224 a0001c0001t0001g0375 others(4): Show |
7 | HG02080.hp1 HG02738.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.38+426_38+427dupAA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 409831 | ||||||
| chr12:409831 | TA | T | 30 | a0001c0001t0002g0325 a0001c0001t0002g0386 a0001c0001t0004g0159 others(27): Show |
30 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.38+427delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 409831 | ||||||
| chr12:409883 | A | G | 1 | a0002c0002t0001g0334 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.38+462A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 409883 | |||||||
| chr12:409884 | G | A | 1 | a0004c0004t0001g0356 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.38+463G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 409884 | |||||||
| chr12:409925 | T | G | 414 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(411): Show |
426 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(423): Show |
intron_variant | MODIFIER | c.38+504T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 409925 | |||||||
| chr12:410037 | C | T | 1 | a0001c0001t0003g0054 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.38+616C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 410037 | |||||||
| chr12:410085 | G | C | 3 | a0001c0001t0004g0384 a0002c0002t0001g0385 a0003c0003t0004g0363 |
3 | HG00639.hp1 HG01109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.38+664G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 410085 | |||||||
| chr12:410139 | T | C | 2 | a0001c0001t0002g0386 a0002c0002t0001g0387 |
2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.38+718T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 410139 | |||||||
| chr12:410170 | A | G | 4 | a0003c0003t0004g0337 a0005c0005t0005g0418 a0005c0005t0005g0419 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.38+749A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 410170 | |||||||
| chr12:410267 | G | GT | 205 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0143 others(202): Show |
212 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(209): Show |
intron_variant | MODIFIER | c.38+856dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 410267 | ||||||
| chr12:410267 | G | GTT | 103 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0002g0004 others(100): Show |
106 | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.38+855_38+856dupTT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 410267 | ||||||
| chr12:410350 | G | T | 1 | a0003c0003t0002g0380 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.38+929G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 410350 | |||||||
| chr12:410392 | CGAGTAGC others(271): Show |
C | 1 | a0002c0002t0001g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.38+1012_39-1037del | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 410392 | ||||||
| chr12:410393 | G | A | 2 | a0001c0001t0002g0386 a0002c0002t0001g0387 |
2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.38+972G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 410393 | |||||||
| chr12:410428 | C | T | 3 | a0001c0001t0001g0178 a0001c0001t0010g0278 a0002c0002t0001g0276 |
3 | HG01433.hp1 HG01433.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.38+1007C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 410428 | |||||||
| chr12:410627 | A | G | 152 | a0001c0001t0001g0108 a0001c0001t0001g0131 a0001c0001t0001g0132 others(149): Show |
154 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.39-1120A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 410627 | |||||||
| chr12:410690 | C | T | 20 | a0001c0001t0002g0325 a0001c0001t0004g0159 a0001c0001t0004g0160 others(17): Show |
20 | HG01081.hp1 HG01167.hp2 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.39-1057C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 410690 | |||||||
| chr12:410699 | C | G | 1 | a0002c0002t0001g0282 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.39-1048C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 410699 | |||||||
| chr12:410748 | G | A | 3 | a0001c0001t0001g0402 a0001c0001t0002g0398 a0001c0001t0004g0399 |
3 | HG01884.hp1 HG02280.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.39-999G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 410748 | |||||||
| chr12:410782 | C | A | 19 | a0001c0001t0002g0325 a0001c0001t0004g0159 a0001c0001t0004g0160 others(16): Show |
19 | HG01081.hp1 HG01109.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.39-965C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 410782 | |||||||
| chr12:411081 | T | C | 21 | a0001c0001t0001g0402 a0001c0001t0002g0398 a0001c0001t0004g0357 others(18): Show |
21 | HG01074.hp2 HG01243.hp1 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.39-666T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 411081 | |||||||
| chr12:411098 | T | C | 4 | a0003c0003t0004g0337 a0005c0005t0005g0418 a0005c0005t0005g0419 others(1): Show |
4 | HG02559.hp1 HG02572.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.39-649T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 411098 | |||||||
| chr12:411177 | T | C | 3 | a0003c0003t0002g0379 a0003c0003t0002g0380 a0003c0003t0009g0168 |
3 | HG02630.hp1 HG03471.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.39-570T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 411177 | |||||||
| chr12:411180 | GT | G | 263 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0131 others(260): Show |
268 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.39-555delT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 411180 | ||||||
| chr12:411181 | T | G | 1 | a0001c0001t0002g0336 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.39-566T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 411181 | |||||||
| chr12:411206 | G | A | 7 | a0001c0001t0002g0144 a0001c0001t0006g0388 a0001c0001t0006g0389 others(4): Show |
7 | HG02155.hp2 NA18941.hp2 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.39-541G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 411206 | |||||||
| chr12:411369 | G | A | 2 | a0002c0002t0001g0053 a0002c0002t0001g0149 |
2 | NA18941.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.39-378G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 411369 | |||||||
| chr12:411471 | C | T | 8 | a0001c0001t0002g0144 a0001c0001t0006g0388 a0001c0001t0006g0389 others(5): Show |
8 | HG02155.hp2 NA18941.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.39-276C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 411471 | |||||||
| chr12:411569 | T | G | 2 | a0001c0001t0004g0317 a0001c0001t0004g0318 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.39-178T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 411569 | |||||||
| chr12:411625 | C | T | 1 | a0003c0003t0002g0249 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.39-122C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 411625 | |||||||
| chr12:411707 | C | T | 1 | a0004c0004t0002g0097 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.39-40C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 3/12 | chr12 | 411707 | |||||||
| chr12:412030 | A | T | 1 | a0001c0001t0004g0331 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.270+52A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 412030 | |||||||
| chr12:412044 | A | C | 1 | a0002c0002t0002g0100 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.270+66A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 412044 | |||||||
| chr12:412234 | T | C | 8 | a0001c0001t0001g0396 a0001c0001t0004g0176 a0001c0001t0008g0177 others(5): Show |
8 | HG01891.hp2 HG01952.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.270+256T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 412234 | |||||||
| chr12:412325 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.270+347C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 412325 | |||||||
| chr12:412444 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.270+466G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 412444 | |||||||
| chr12:412460 | G | A | 1 | a0001c0001t0004g0331 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.270+482G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 412460 | |||||||
| chr12:412478 | A | C | 1 | a0001c0001t0003g0052 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.270+500A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 412478 | |||||||
| chr12:412616 | C | T | 2 | a0001c0001t0001g0405 a0004c0004t0001g0095 |
2 | HG01167.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.270+638C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 412616 | |||||||
| chr12:412647 | G | A | 1 | a0001c0001t0002g0403 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.270+669G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 412647 | |||||||
| chr12:412760 | C | A | 1 | a0004c0004t0002g0305 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.270+782C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 412760 | |||||||
| chr12:412797 | C | CCTTCCAC others(1): Show |
8 | a0002c0002t0014g0321 a0003c0003t0001g0250 a0003c0003t0001g0251 others(5): Show |
8 | HG01106.hp2 HG01884.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.270+820_270+827dup others(8): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 412797 | ||||||
| chr12:412819 | C | T | 1 | a0001c0001t0003g0125 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.270+841C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 412819 | |||||||
| chr12:412845 | T | C | 1 | a0005c0005t0005g0409 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.270+867T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 412845 | |||||||
| chr12:412961 | C | T | 1 | a0001c0001t0001g0405 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.270+983C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 412961 | |||||||
| chr12:412970 | G | T | 23 | a0001c0001t0001g0281 a0001c0001t0002g0299 a0001c0001t0004g0246 others(20): Show |
23 | HG01081.hp1 HG01109.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.270+992G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 412970 | |||||||
| chr12:413013 | A | G | 270 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0131 others(267): Show |
276 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(273): Show |
intron_variant | MODIFIER | c.270+1035A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413013 | |||||||
| chr12:413032 | G | A | 8 | a0002c0002t0014g0321 a0003c0003t0001g0250 a0003c0003t0001g0251 others(5): Show |
8 | HG01106.hp2 HG01884.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.270+1054G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413032 | |||||||
| chr12:413132 | G | A | 34 | a0001c0001t0004g0159 a0001c0001t0004g0160 a0001c0001t0004g0317 others(31): Show |
35 | HG00673.hp1 HG01167.hp2 HG01169.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+1154G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413132 | |||||||
| chr12:413160 | A | G | 1 | a0003c0003t0002g0280 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.270+1182A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413160 | |||||||
| chr12:413261 | G | A | 15 | a0002c0002t0001g0005 a0002c0002t0001g0124 a0002c0002t0001g0141 others(12): Show |
16 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.270+1283G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413261 | |||||||
| chr12:413411 | G | A | 1 | a0002c0002t0001g0291 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.270+1433G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413411 | |||||||
| chr12:413465 | G | T | 1 | a0001c0001t0004g0397 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.270+1487G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413465 | |||||||
| chr12:413474 | C | T | 1 | a0001c0001t0004g0397 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.270+1496C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413474 | |||||||
| chr12:413519 | ATGAGCCA others(844): Show |
A | 2 | a0003c0003t0002g0372 a0003c0003t0004g0175 |
2 | HG01891.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.270+1548_270+2398d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 413519 | ||||||
| chr12:413526 | A | G | 19 | a0001c0001t0002g0004 a0001c0001t0002g0041 a0001c0001t0002g0074 others(16): Show |
20 | HG00621.hp2 HG02071.hp2 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.270+1548A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413526 | |||||||
| chr12:413534 | C | T | 196 | a0001c0001t0001g0024 a0001c0001t0001g0131 a0001c0001t0001g0132 others(193): Show |
199 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.270+1556C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413534 | |||||||
| chr12:413535 | G | A | 33 | a0001c0001t0004g0159 a0001c0001t0004g0160 a0001c0001t0004g0317 others(30): Show |
34 | HG00673.hp1 HG01167.hp2 HG01169.hp1 others(31): Show |
intron_variant | MODIFIER | c.270+1557G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413535 | |||||||
| chr12:413626 | A | AT | 35 | a0001c0001t0001g0131 a0001c0001t0001g0203 a0001c0001t0001g0204 others(32): Show |
35 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.270+1667dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 413626 | ||||||
| chr12:413657 | T | C | 6 | a0002c0002t0014g0321 a0003c0003t0001g0250 a0003c0003t0001g0251 others(3): Show |
6 | HG01106.hp2 HG01884.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+1679T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413657 | |||||||
| chr12:413666 | C | T | 11 | a0001c0001t0004g0159 a0001c0001t0004g0160 a0001c0001t0004g0317 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.270+1688C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413666 | |||||||
| chr12:413681 | G | A | 6 | a0001c0001t0004g0093 a0003c0003t0004g0337 a0005c0005t0005g0332 others(3): Show |
6 | HG02145.hp1 HG02559.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.270+1703G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413681 | |||||||
| chr12:413688 | C | T | 2 | a0001c0001t0007g0015 a0001c0001t0007g0016 |
2 | NA18747.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.270+1710C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413688 | |||||||
| chr12:413753 | G | A | 17 | a0001c0001t0001g0241 a0001c0001t0004g0086 a0001c0001t0004g0087 others(14): Show |
17 | HG00597.hp1 HG00639.hp1 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.270+1775G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413753 | |||||||
| chr12:413791 | C | A | 1 | a0001c0001t0002g0403 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.270+1813C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413791 | |||||||
| chr12:413809 | G | T | 52 | a0001c0001t0001g0108 a0001c0001t0001g0348 a0001c0001t0001g0406 others(49): Show |
57 | HG00323.hp1 HG00423.hp2 HG00673.hp2 others(54): Show |
intron_variant | MODIFIER | c.270+1831G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413809 | |||||||
| chr12:413914 | C | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0014 |
2 | HG01928.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.270+1936C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413914 | |||||||
| chr12:413916 | C | G | 15 | a0001c0001t0001g0241 a0001c0001t0004g0086 a0001c0001t0004g0087 others(12): Show |
15 | HG00597.hp1 HG00639.hp1 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.270+1938C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413916 | |||||||
| chr12:413968 | T | C | 146 | a0001c0001t0001g0143 a0001c0001t0001g0178 a0001c0001t0001g0241 others(143): Show |
147 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.270+1990T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413968 | |||||||
| chr12:413981 | G | A | 1 | a0004c0004t0001g0171 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.270+2003G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413981 | |||||||
| chr12:413985 | C | T | 19 | a0002c0002t0001g0053 a0002c0002t0001g0109 a0002c0002t0001g0110 others(16): Show |
20 | HG00673.hp1 HG01346.hp1 HG02683.hp1 others(17): Show |
intron_variant | MODIFIER | c.270+2007C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413985 | |||||||
| chr12:414004 | C | T | 1 | a0001c0001t0004g0397 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.270+2026C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 414004 | |||||||
| chr12:414065 | T | C | 1 | a0002c0002t0001g0291 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.270+2087T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 414065 | |||||||
| chr12:414095 | C | CT | 20 | a0001c0001t0001g0241 a0001c0001t0003g0002 a0001c0001t0004g0086 others(17): Show |
20 | HG00597.hp1 HG01106.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.270+2131dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 414095 | ||||||
| chr12:414156 | A | G | 1 | a0001c0001t0010g0277 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.270+2178A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 414156 | |||||||
| chr12:414161 | G | A | 1 | a0004c0004t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.270+2183G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 414161 | |||||||
| chr12:414184 | C | T | 49 | a0001c0001t0001g0348 a0001c0001t0001g0406 a0001c0001t0001g0407 others(46): Show |
54 | HG00323.hp1 HG00423.hp2 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.270+2206C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 414184 | |||||||
| chr12:414369 | C | T | 1 | a0001c0001t0003g0002 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.270+2391C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 414369 | |||||||
| chr12:414373 | A | G | 3 | a0001c0001t0001g0178 a0001c0001t0009g0289 a0003c0003t0001g0287 |
3 | HG02717.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.270+2395A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 414373 | |||||||
| chr12:414511 | A | G | 14 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0001c0001t0008g0177 others(11): Show |
14 | HG01106.hp2 HG01884.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.270+2533A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 414511 | |||||||
| chr12:414516 | T | C | 1 | a0001c0001t0001g0292 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.270+2538T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 414516 | |||||||
| chr12:414566 | T | C | 1 | a0004c0004t0002g0305 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.270+2588T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 414566 | |||||||
| chr12:414611 | C | G | 1 | a0003c0003t0009g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.270+2633C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 414611 | |||||||
| chr12:414784 | TA | T | 9 | a0001c0001t0008g0170 a0002c0009t0001g0404 a0003c0003t0001g0094 others(6): Show |
9 | HG01346.hp2 HG02451.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.270+2807delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 414784 | |||||||
| chr12:414785 | ATTAC | A | 4 | a0001c0001t0001g0402 a0001c0001t0004g0357 a0003c0003t0002g0380 others(1): Show |
4 | HG02109.hp1 HG02280.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.270+2811_270+2814d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 414785 | ||||||
| chr12:414863 | A | G | 12 | a0001c0001t0001g0245 a0001c0001t0002g0299 a0001c0001t0004g0244 others(9): Show |
12 | HG01074.hp2 HG01358.hp2 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.270+2885A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 414863 | |||||||
| chr12:414865 | G | A | 7 | a0001c0001t0003g0125 a0001c0001t0006g0388 a0001c0001t0006g0389 others(4): Show |
7 | HG02155.hp2 HG04204.hp2 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.270+2887G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 414865 | |||||||
| chr12:414895 | C | T | 40 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0242 others(37): Show |
42 | HG00738.hp2 HG01123.hp2 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.270+2917C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 414895 | |||||||
| chr12:414913 | G | T | 1 | a0002c0002t0001g0109 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.270+2935G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 414913 | |||||||
| chr12:415018 | A | G | 92 | a0001c0001t0001g0108 a0001c0001t0001g0178 a0001c0001t0001g0236 others(89): Show |
93 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.270+3040A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415018 | |||||||
| chr12:415054 | T | G | 1 | a0003c0003t0009g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.270+3076T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415054 | |||||||
| chr12:415158 | CTAAT | C | 3 | a0001c0001t0004g0357 a0003c0003t0002g0368 a0003c0003t0002g0379 |
3 | HG02109.hp1 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.270+3182_270+3185d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415158 | ||||||
| chr12:415185 | A | G | 2 | a0001c0001t0003g0042 a0001c0001t0003g0043 |
2 | NA18965.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.270+3207A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415185 | |||||||
| chr12:415255 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.271-3239T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415255 | |||||||
| chr12:415271 | T | TATTAACA others(18): Show |
2 | a0001c0001t0001g0407 a0001c0001t0001g0408 |
2 | HG01261.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.271-3220_271-3196d others(27): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415271 | ||||||
| chr12:415271 | T | TATTAACA others(43): Show |
1 | a0001c0001t0001g0406 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.271-3196_271-3195i others(52): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415271 | ||||||
| chr12:415274 | T | TAACATAA others(18): Show |
14 | a0001c0001t0002g0403 a0001c0001t0004g0176 a0001c0001t0006g0012 others(11): Show |
14 | HG00735.hp1 HG01891.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.271-3109_271-3085d others(27): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415274 | ||||||
| chr12:415274 | T | TAACATAA others(43): Show |
2 | a0001c0001t0001g0405 a0001c0001t0006g0394 |
2 | HG02451.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.271-3134_271-3085d others(52): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415274 | ||||||
| chr12:415274 | TAACATAA others(18): Show |
T | 4 | a0003c0003t0001g0250 a0003c0003t0001g0251 a0003c0003t0001g0341 others(1): Show |
4 | HG01106.hp2 HG01884.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-3109_271-3085d others(27): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415274 | ||||||
| chr12:415274 | TAACATAA others(43): Show |
T | 1 | a0002c0002t0001g0387 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.271-3134_271-3085d others(52): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415274 | ||||||
| chr12:415280 | A | AATATTAT others(15): Show |
1 | a0003c0003t0004g0337 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.271-3210_271-3189d others(24): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415280 | ||||||
| chr12:415288 | G | A | 1 | a0001c0001t0004g0384 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.271-3206G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415288 | |||||||
| chr12:415288 | G | GTTAATTA others(19): Show |
1 | a0001c0001t0002g0041 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.271-3201_271-3200i others(28): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415288 | ||||||
| chr12:415292 | A | AT | 3 | a0001c0001t0004g0091 a0001c0001t0004g0092 a0001c0001t0004g0102 |
3 | HG00597.hp1 HG02080.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.271-3201dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415292 | ||||||
| chr12:415296 | A | T | 1 | a0001c0001t0002g0041 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.271-3198A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415296 | |||||||
| chr12:415299 | C | CAACATAT others(37): Show |
1 | a0002c0002t0001g0282 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.271-3189_271-3188i others(46): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415299 | ||||||
| chr12:415299 | C | CAACATAT others(15): Show |
4 | a0001c0001t0004g0159 a0001c0001t0004g0160 a0001c0001t0004g0317 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-3189_271-3188i others(24): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415299 | ||||||
| chr12:415299 | C | T | 222 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(219): Show |
227 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.271-3195C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415299 | |||||||
| chr12:415302 | CATA | C | 61 | a0001c0001t0001g0178 a0001c0001t0001g0402 a0001c0001t0002g0259 others(58): Show |
62 | HG00438.hp2 HG00621.hp2 HG01243.hp1 others(59): Show |
intron_variant | MODIFIER | c.271-3188_271-3186d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415302 | ||||||
| chr12:415302 | CATAATAT others(46): Show |
C | 1 | a0001c0001t0004g0415 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.271-3188_271-3136d others(55): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415302 | ||||||
| chr12:415308 | ATTATGTT others(96): Show |
A | 1 | a0001c0001t0004g0384 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.271-3184_271-3082d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415308 | ||||||
| chr12:415309 | T | TGTTAATA others(103): Show |
1 | a0004c0004t0001g0315 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.271-3185_271-3184i others(112): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415309 | |||||||
| chr12:415309 | T | TTATGTTA others(15): Show |
1 | a0001c0001t0002g0051 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.271-3181_271-3160d others(24): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415309 | ||||||
| chr12:415313 | G | A | 55 | a0001c0001t0001g0245 a0001c0001t0002g0004 a0001c0001t0002g0074 others(52): Show |
58 | HG00609.hp2 HG00738.hp1 HG01496.hp2 others(55): Show |
intron_variant | MODIFIER | c.271-3181G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415313 | |||||||
| chr12:415321 | A | T | 118 | a0001c0001t0001g0396 a0001c0001t0002g0004 a0001c0001t0002g0049 others(115): Show |
123 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.271-3173A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415321 | |||||||
| chr12:415324 | C | T | 228 | a0001c0001t0001g0024 a0001c0001t0001g0108 a0001c0001t0001g0131 others(225): Show |
233 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(230): Show |
intron_variant | MODIFIER | c.271-3170C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415324 | |||||||
| chr12:415327 | CATA | C | 12 | a0002c0002t0002g0082 a0002c0002t0002g0113 a0002c0002t0002g0145 others(9): Show |
12 | HG00423.hp2 HG01167.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-3163_271-3161d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415327 | ||||||
| chr12:415327 | CATAATAT others(21): Show |
C | 12 | a0001c0001t0002g0299 a0002c0002t0001g0173 a0002c0002t0002g0100 others(9): Show |
12 | HG00408.hp1 HG01074.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-3163_271-3136d others(30): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415327 | ||||||
| chr12:415328 | A | G | 2 | a0001c0001t0001g0164 a0003c0003t0002g0379 |
2 | HG02630.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.271-3166A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415328 | |||||||
| chr12:415328 | ATAATATT others(24): Show |
A | 1 | a0001c0001t0002g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.271-3163_271-3133d others(33): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415328 | ||||||
| chr12:415330 | A | AATATTAT others(15): Show |
25 | a0001c0001t0002g0044 a0001c0001t0002g0055 a0001c0001t0002g0059 others(22): Show |
26 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(23): Show |
intron_variant | MODIFIER | c.271-3160_271-3139d others(24): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415330 | ||||||
| chr12:415330 | A | AATATTAT others(40): Show |
1 | a0001c0001t0004g0328 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.271-3160_271-3114d others(49): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415330 | ||||||
| chr12:415333 | ATTATGTT others(71): Show |
A | 7 | a0001c0001t0001g0245 a0002c0002t0001g0114 a0002c0002t0001g0129 others(4): Show |
7 | HG02486.hp1 HG02723.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.271-3159_271-3082d others(80): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415333 | ||||||
| chr12:415338 | G | A | 1 | a0001c0001t0002g0041 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.271-3156G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415338 | |||||||
| chr12:415346 | A | T | 2 | a0001c0001t0002g0041 a0002c0002t0001g0111 |
2 | HG04115.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.271-3148A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415346 | |||||||
| chr12:415349 | C | T | 149 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0241 others(146): Show |
154 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(151): Show |
intron_variant | MODIFIER | c.271-3145C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415349 | |||||||
| chr12:415352 | CATA | C | 41 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0051 others(38): Show |
44 | HG00673.hp2 HG00738.hp2 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.271-3138_271-3136d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415352 | ||||||
| chr12:415352 | CATAATAT others(48): Show |
C | 11 | a0001c0001t0001g0147 a0001c0001t0001g0281 a0002c0002t0001g0174 others(8): Show |
11 | HG01192.hp1 HG01346.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.271-3139_271-3085d others(57): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415352 | ||||||
| chr12:415353 | ATAATAT | A | 5 | a0001c0001t0002g0011 a0001c0001t0002g0161 a0001c0001t0002g0346 others(2): Show |
6 | HG00323.hp1 HG00735.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.271-3138_271-3133d others(8): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415353 | ||||||
| chr12:415355 | A | G | 1 | a0005c0005t0005g0409 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.271-3139A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415355 | |||||||
| chr12:415358 | ATTATGTT others(46): Show |
A | 5 | a0001c0001t0001g0164 a0001c0001t0001g0167 a0001c0001t0001g0191 others(2): Show |
5 | HG01071.hp1 HG02683.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-3134_271-3082d others(55): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415358 | ||||||
| chr12:415360 | T | G | 2 | a0003c0003t0007g0327 a0003c0003t0007g0412 |
2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.271-3134T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415360 | |||||||
| chr12:415361 | A | T | 2 | a0003c0003t0007g0327 a0003c0003t0007g0412 |
2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.271-3133A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415361 | |||||||
| chr12:415363 | G | A | 110 | a0001c0001t0001g0396 a0001c0001t0002g0004 a0001c0001t0002g0049 others(107): Show |
115 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.271-3131G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415363 | |||||||
| chr12:415368 | T | C | 3 | a0003c0003t0007g0327 a0003c0003t0007g0412 a0005c0005t0005g0409 |
3 | HG01243.hp1 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.271-3126T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415368 | |||||||
| chr12:415374 | C | T | 95 | a0001c0001t0001g0024 a0001c0001t0001g0132 a0001c0001t0001g0151 others(92): Show |
95 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.271-3120C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415374 | |||||||
| chr12:415378 | A | ATAATATT others(18): Show |
2 | a0001c0001t0001g0146 a0001c0001t0001g0153 |
2 | HG03490.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.271-3096_271-3095i others(27): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415378 | ||||||
| chr12:415378 | A | G | 71 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(68): Show |
71 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.271-3116A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415378 | |||||||
| chr12:415381 | ATAT | A | 46 | a0001c0001t0002g0136 a0001c0001t0002g0259 a0001c0001t0004g0399 others(43): Show |
47 | HG00438.hp2 HG00621.hp2 HG01257.hp1 others(44): Show |
intron_variant | MODIFIER | c.271-3109_271-3107d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415381 | ||||||
| chr12:415381 | ATATTATG others(23): Show |
A | 1 | a0001c0001t0003g0056 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.271-3111_271-3082d others(32): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415381 | ||||||
| chr12:415383 | ATTATGTT others(21): Show |
A | 110 | a0001c0001t0001g0396 a0001c0001t0002g0004 a0001c0001t0002g0049 others(107): Show |
115 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.271-3109_271-3082d others(30): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415383 | ||||||
| chr12:415384 | T | A | 1 | a0005c0005t0005g0409 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.271-3110T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415384 | |||||||
| chr12:415385 | T | G | 2 | a0003c0003t0007g0327 a0003c0003t0007g0412 |
2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.271-3109T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415385 | |||||||
| chr12:415388 | G | A | 21 | a0001c0001t0002g0041 a0001c0001t0002g0299 a0001c0001t0004g0089 others(18): Show |
21 | HG00408.hp1 HG01074.hp2 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.271-3106G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415388 | |||||||
| chr12:415391 | A | G | 45 | a0001c0001t0002g0259 a0001c0001t0004g0399 a0001c0001t0010g0277 others(42): Show |
46 | HG00438.hp2 HG00621.hp2 HG01257.hp1 others(43): Show |
intron_variant | MODIFIER | c.271-3103A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415391 | |||||||
| chr12:415393 | T | C | 4 | a0001c0001t0004g0089 a0001c0001t0004g0096 a0003c0003t0007g0327 others(1): Show |
4 | HG01243.hp1 NA18906.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-3101T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415393 | |||||||
| chr12:415393 | T | TATTAACA others(70): Show |
1 | a0005c0005t0005g0409 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.271-3099_271-3098i others(79): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415393 | ||||||
| chr12:415396 | A | T | 46 | a0001c0001t0002g0259 a0001c0001t0004g0399 a0001c0001t0010g0277 others(43): Show |
47 | HG00438.hp2 HG00621.hp2 HG01257.hp1 others(44): Show |
intron_variant | MODIFIER | c.271-3098A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415396 | |||||||
| chr12:415399 | C | T | 79 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(76): Show |
80 | HG00438.hp2 HG00597.hp1 HG00621.hp2 others(77): Show |
intron_variant | MODIFIER | c.271-3095C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415399 | |||||||
| chr12:415401 | A | T | 2 | a0003c0003t0007g0327 a0003c0003t0007g0412 |
2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.271-3093A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415401 | |||||||
| chr12:415402 | C | A | 2 | a0003c0003t0007g0327 a0003c0003t0007g0412 |
2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.271-3092C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415402 | |||||||
| chr12:415402 | C | CATAATTA others(39): Show |
44 | a0001c0001t0002g0259 a0001c0001t0004g0399 a0001c0001t0010g0277 others(41): Show |
45 | HG00438.hp2 HG00621.hp2 HG01257.hp1 others(42): Show |
intron_variant | MODIFIER | c.271-3087_271-3086i others(48): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415402 | ||||||
| chr12:415402 | C | CATAATTA others(76): Show |
1 | a0002c0002t0001g0295 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.271-3087_271-3086i others(85): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415402 | ||||||
| chr12:415406 | A | ATAT | 8 | a0001c0001t0002g0083 a0001c0001t0007g0015 a0001c0001t0007g0016 others(5): Show |
8 | HG01109.hp1 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-3087_271-3085d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415406 | ||||||
| chr12:415409 | T | A | 2 | a0001c0001t0004g0089 a0001c0001t0004g0096 |
2 | NA18949.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.271-3085T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415409 | |||||||
| chr12:415410 | G | T | 2 | a0001c0001t0004g0089 a0001c0001t0004g0096 |
2 | NA18949.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.271-3084G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415410 | |||||||
| chr12:415411 | T | A | 2 | a0001c0001t0004g0089 a0001c0001t0004g0096 |
2 | NA18949.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.271-3083T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415411 | |||||||
| chr12:415411 | T | TTAATATA others(12): Show |
1 | a0001c0001t0002g0083 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.271-3082_271-3081i others(21): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415411 | ||||||
| chr12:415411 | T | TTAATATA others(15): Show |
2 | a0001c0001t0007g0015 a0001c0001t0007g0016 |
2 | NA18747.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.271-3082_271-3081i others(24): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415411 | ||||||
| chr12:415411 | T | TTAATATA others(37): Show |
1 | a0003c0003t0002g0231 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.271-3082_271-3081i others(46): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415411 | ||||||
| chr12:415411 | TTGA | T | 117 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(114): Show |
117 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.271-3081_271-3079d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415411 | ||||||
| chr12:415413 | G | A | 4 | a0001c0001t0008g0170 a0003c0003t0004g0363 a0006c0006t0011g0103 others(1): Show |
4 | HG01109.hp1 HG01891.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-3081G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415413 | |||||||
| chr12:415414 | A | T | 130 | a0001c0001t0001g0164 a0001c0001t0001g0167 a0001c0001t0001g0191 others(127): Show |
135 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.271-3080A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415414 | |||||||
| chr12:415414 | ATAT | A | 3 | a0001c0001t0004g0246 a0001c0001t0004g0328 a0003c0003t0004g0329 |
3 | HG01081.hp1 HG02717.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.271-3074_271-3072d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415414 | ||||||
| chr12:415417 | T | A | 3 | a0001c0001t0001g0198 a0001c0001t0004g0089 a0001c0001t0004g0096 |
3 | HG01517.hp1 NA18949.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.271-3077T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415417 | |||||||
| chr12:415417 | T | TAATCAAC others(12): Show |
1 | a0001c0001t0008g0170 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.271-3077_271-3076i others(21): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415417 | |||||||
| chr12:415417 | T | TAATCAAC others(37): Show |
3 | a0003c0003t0004g0363 a0006c0006t0011g0103 a0006c0006t0011g0106 |
3 | HG01109.hp1 HG01891.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.271-3077_271-3076i others(46): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415417 | |||||||
| chr12:415427 | A | AATT | 50 | a0001c0001t0002g0259 a0001c0001t0004g0089 a0001c0001t0004g0096 others(47): Show |
51 | HG00438.hp2 HG00621.hp2 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.271-3065_271-3063d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415427 | ||||||
| chr12:415427 | A | AATTATTA others(64): Show |
2 | a0002c0002t0001g0291 a0005c0005t0005g0416 |
2 | HG02970.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.271-3063_271-3062i others(73): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415427 | ||||||
| chr12:415432 | A | T | 1 | a0001c0001t0004g0384 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.271-3062A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415432 | |||||||
| chr12:415433 | C | T | 1 | a0001c0001t0004g0384 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.271-3061C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415433 | |||||||
| chr12:415433 | CATA | C | 33 | a0001c0001t0002g0011 a0001c0001t0002g0049 a0002c0002t0001g0050 others(30): Show |
35 | HG00673.hp1 HG00741.hp1 HG01346.hp1 others(32): Show |
intron_variant | MODIFIER | c.271-3054_271-3052d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415433 | ||||||
| chr12:415436 | AATAATAT others(61): Show |
A | 1 | a0003c0003t0001g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.271-2996_271-2929d others(70): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415436 | ||||||
| chr12:415437 | A | C | 17 | a0001c0001t0004g0093 a0001c0001t0004g0159 a0001c0001t0004g0160 others(14): Show |
17 | HG01167.hp2 HG01169.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.271-3057A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415437 | |||||||
| chr12:415445 | T | TTGA | 52 | a0001c0001t0002g0259 a0001c0001t0004g0089 a0001c0001t0004g0096 others(49): Show |
53 | HG00438.hp2 HG00621.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.271-3048_271-3047i others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415445 | ||||||
| chr12:415447 | A | G | 1 | a0001c0001t0002g0083 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.271-3047A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415447 | |||||||
| chr12:415448 | A | T | 52 | a0001c0001t0002g0259 a0001c0001t0004g0089 a0001c0001t0004g0096 others(49): Show |
53 | HG00438.hp2 HG00621.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.271-3046A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415448 | |||||||
| chr12:415455 | CAT | C | 9 | a0002c0002t0001g0154 a0002c0002t0001g0199 a0002c0002t0001g0225 others(6): Show |
9 | HG01109.hp2 HG01175.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.271-3037_271-3036d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415455 | ||||||
| chr12:415458 | AATT | A | 4 | a0001c0001t0003g0026 a0001c0001t0003g0056 a0001c0001t0003g0228 others(1): Show |
4 | HG02129.hp2 HG03834.hp2 NA18747.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-3031_271-3029d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415458 | ||||||
| chr12:415470 | A | AATAATAT others(27): Show |
7 | a0001c0001t0004g0086 a0001c0001t0004g0087 a0001c0001t0004g0088 others(4): Show |
7 | HG00597.hp1 HG02080.hp1 NA18612.hp2 others(4): Show |
intron_variant | MODIFIER | c.271-3013_271-2980d others(36): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415470 | ||||||
| chr12:415485 | T | TTATTAAC others(24): Show |
2 | a0003c0003t0002g0271 a0003c0003t0002g0272 |
2 | NA18962.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.271-2983_271-2953d others(33): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415485 | ||||||
| chr12:415487 | A | G | 1 | a0002c0002t0001g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.271-3007A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415487 | |||||||
| chr12:415495 | A | G | 1 | a0001c0001t0003g0040 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.271-2999A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415495 | |||||||
| chr12:415504 | CATAATAT others(27): Show |
C | 7 | a0003c0003t0001g0017 a0003c0003t0001g0062 a0003c0003t0001g0063 others(4): Show |
7 | HG00609.hp1 NA18959.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-2979_271-2946d others(36): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415504 | ||||||
| chr12:415515 | A | G | 332 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(329): Show |
338 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(335): Show |
intron_variant | MODIFIER | c.271-2979A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415515 | |||||||
| chr12:415535 | CATA | C | 10 | a0001c0001t0001g0147 a0001c0001t0001g0281 a0002c0002t0001g0322 others(7): Show |
10 | HG01192.hp1 HG01346.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-2952_271-2950d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415535 | ||||||
| chr12:415629 | GGTTTTTT | G | 7 | a0003c0003t0001g0017 a0003c0003t0001g0062 a0003c0003t0001g0063 others(4): Show |
7 | HG00609.hp1 NA18959.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-2849_271-2843d others(9): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415629 | ||||||
| chr12:415741 | G | T | 171 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0281 others(168): Show |
178 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.271-2753G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415741 | |||||||
| chr12:415808 | T | TTTTTATT others(3): Show |
171 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0245 others(168): Show |
178 | HG00323.hp1 HG00423.hp1 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.271-2681_271-2672d others(12): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 415808 | ||||||
| chr12:415951 | G | A | 6 | a0001c0001t0002g0299 a0001c0001t0002g0386 a0001c0001t0002g0398 others(3): Show |
6 | HG01358.hp2 HG02809.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.271-2543G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415951 | |||||||
| chr12:415966 | C | T | 2 | a0002c0002t0001g0163 a0002c0002t0001g0370 |
2 | HG02027.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.271-2528C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415966 | |||||||
| chr12:416030 | G | A | 342 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(339): Show |
348 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(345): Show |
intron_variant | MODIFIER | c.271-2464G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416030 | |||||||
| chr12:416046 | C | T | 1 | a0007c0007t0005g0326 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.271-2448C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416046 | |||||||
| chr12:416057 | C | T | 7 | a0001c0001t0004g0246 a0001c0001t0004g0328 a0001c0001t0008g0170 others(4): Show |
7 | HG01081.hp1 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-2437C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416057 | |||||||
| chr12:416190 | T | C | 282 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(279): Show |
288 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.271-2304T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416190 | |||||||
| chr12:416216 | C | T | 1 | a0004c0004t0001g0139 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.271-2278C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416216 | |||||||
| chr12:416307 | A | ATG | 149 | a0001c0001t0001g0396 a0001c0001t0002g0004 a0001c0001t0002g0041 others(146): Show |
155 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.271-2170_271-2169d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416307 | ||||||
| chr12:416323 | GTGAGTC | G | 18 | a0001c0001t0002g0075 a0002c0002t0001g0050 a0002c0002t0001g0119 others(15): Show |
18 | HG00741.hp1 HG01256.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.271-2168_271-2163d others(8): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416323 | ||||||
| chr12:416324 | TGAGTCTG others(13): Show |
T | 1 | a0001c0001t0003g0230 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.271-2168_271-2149d others(22): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416324 | ||||||
| chr12:416329 | CTGTGGGT others(1): Show |
C | 8 | a0001c0001t0002g0083 a0001c0001t0004g0159 a0001c0001t0004g0160 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-2158_271-2151d others(10): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416329 | ||||||
| chr12:416332 | TGGGTGTG others(3): Show |
T | 1 | a0001c0001t0004g0244 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.271-2152_271-2143d others(12): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416332 | ||||||
| chr12:416334 | G | A | 18 | a0001c0001t0002g0075 a0002c0002t0001g0050 a0002c0002t0001g0119 others(15): Show |
18 | HG00741.hp1 HG01256.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.271-2160G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416334 | |||||||
| chr12:416334 | GGTGTGTG others(5): Show |
G | 16 | a0001c0001t0004g0093 a0001c0001t0004g0096 a0001c0001t0004g0098 others(13): Show |
16 | HG00609.hp1 HG02258.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.271-2152_271-2141d others(14): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416334 | ||||||
| chr12:416334 | GGTGTGTG others(7): Show |
G | 11 | a0001c0001t0001g0151 a0001c0001t0001g0365 a0001c0001t0002g0115 others(8): Show |
11 | HG00597.hp2 NA18612.hp2 NA18961.hp1 others(8): Show |
intron_variant | MODIFIER | c.271-2152_271-2139d others(16): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416334 | ||||||
| chr12:416334 | GGTGTGTG others(9): Show |
G | 12 | a0001c0001t0001g0024 a0001c0001t0001g0143 a0001c0001t0001g0210 others(9): Show |
12 | HG00438.hp1 HG00597.hp1 HG01256.hp2 others(9): Show |
intron_variant | MODIFIER | c.271-2152_271-2137d others(18): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416334 | ||||||
| chr12:416334 | GGTGTGTG others(11): Show |
G | 48 | a0001c0001t0001g0025 a0001c0001t0001g0108 a0001c0001t0001g0131 others(45): Show |
48 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.271-2152_271-2135d others(20): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416334 | ||||||
| chr12:416334 | GGTGTGTG others(13): Show |
G | 3 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0003c0003t0002g0368 |
3 | HG01081.hp2 HG03098.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.271-2152_271-2133d others(22): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416334 | ||||||
| chr12:416334 | GGTGTGTG others(15): Show |
G | 3 | a0001c0001t0003g0042 a0001c0001t0003g0043 a0001c0001t0003g0125 |
3 | HG04204.hp2 NA18965.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.271-2152_271-2131d others(24): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416334 | ||||||
| chr12:416334 | GGTGTGTG others(17): Show |
G | 43 | a0001c0001t0002g0004 a0001c0001t0002g0041 a0001c0001t0002g0074 others(40): Show |
46 | HG00609.hp2 HG00738.hp1 HG01496.hp2 others(43): Show |
intron_variant | MODIFIER | c.271-2152_271-2129d others(26): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416334 | ||||||
| chr12:416334 | GGTGTGTG others(19): Show |
G | 1 | a0001c0001t0003g0039 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.271-2152_271-2127d others(28): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416334 | ||||||
| chr12:416336 | T | G | 1 | a0001c0001t0004g0089 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.271-2158T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416336 | |||||||
| chr12:416337 | G | C | 18 | a0001c0001t0002g0075 a0002c0002t0001g0050 a0002c0002t0001g0119 others(15): Show |
18 | HG00741.hp1 HG01256.hp1 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.271-2157G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416337 | |||||||
| chr12:416338 | TGTGGGG | T | 4 | a0001c0001t0002g0049 a0002c0002t0001g0172 a0002c0002t0001g0235 others(1): Show |
4 | HG01981.hp1 HG02486.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-2152_271-2147d others(8): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416338 | ||||||
| chr12:416340 | TGGGG | T | 30 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(27): Show |
30 | HG00673.hp1 HG01074.hp2 HG01346.hp1 others(27): Show |
intron_variant | MODIFIER | c.271-2152_271-2149d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416340 | ||||||
| chr12:416342 | G | T | 81 | a0001c0001t0001g0396 a0001c0001t0004g0089 a0001c0001t0004g0384 others(78): Show |
84 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.271-2152G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416342 | |||||||
| chr12:416342 | GGGGT | G | 7 | a0002c0002t0001g0119 a0002c0002t0001g0120 a0002c0002t0001g0121 others(4): Show |
7 | HG01346.hp2 NA18906.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.271-2150_271-2147d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416342 | ||||||
| chr12:416342 | GGGGTGTG others(3): Show |
G | 1 | a0004c0004t0001g0142 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.271-2150_271-2141d others(12): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416342 | ||||||
| chr12:416342 | GGGGTGTG others(5): Show |
G | 2 | a0001c0001t0002g0075 a0002c0002t0001g0174 |
2 | HG02965.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.271-2150_271-2139d others(14): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416342 | ||||||
| chr12:416344 | G | T | 114 | a0001c0001t0001g0396 a0001c0001t0002g0044 a0001c0001t0002g0059 others(111): Show |
117 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.271-2150G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416344 | |||||||
| chr12:416344 | GGT | G | 5 | a0001c0001t0002g0013 a0001c0001t0002g0137 a0003c0003t0002g0268 others(2): Show |
5 | HG01952.hp2 HG03195.hp2 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.271-2117_271-2116d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416344 | ||||||
| chr12:416346 | T | G | 3 | a0001c0001t0004g0244 a0003c0003t0009g0168 a0004c0004t0001g0085 |
3 | HG01496.hp1 HG02109.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.271-2148T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416346 | |||||||
| chr12:416348 | T | G | 12 | a0001c0001t0004g0093 a0001c0001t0004g0096 a0001c0001t0004g0098 others(9): Show |
12 | HG02258.hp1 HG02572.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.271-2146T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416348 | |||||||
| chr12:416350 | T | A | 1 | a0001c0001t0003g0230 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.271-2144T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416350 | |||||||
| chr12:416350 | T | G | 6 | a0001c0001t0001g0151 a0001c0001t0001g0365 a0001c0001t0004g0086 others(3): Show |
6 | NA18612.hp2 NA18961.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.271-2144T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416350 | |||||||
| chr12:416351 | G | GTATATAT others(9): Show |
1 | a0004c0004t0002g0305 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.271-2142_271-2141i others(18): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416351 | ||||||
| chr12:416351 | G | GTATATAT others(15): Show |
1 | a0004c0004t0002g0309 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.271-2142_271-2141i others(24): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416351 | ||||||
| chr12:416352 | T | G | 3 | a0001c0001t0001g0241 a0001c0001t0004g0092 a0001c0001t0004g0102 |
3 | HG00597.hp1 HG02080.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.271-2142T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416352 | |||||||
| chr12:416353 | G | A | 11 | a0001c0001t0004g0384 a0002c0002t0001g0370 a0002c0002t0002g0100 others(8): Show |
11 | HG00423.hp2 HG00639.hp1 HG02165.hp2 others(8): Show |
intron_variant | MODIFIER | c.271-2141G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416353 | |||||||
| chr12:416353 | G | C | 1 | a0001c0001t0003g0230 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.271-2141G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416353 | |||||||
| chr12:416353 | G | GTA | 3 | a0002c0002t0001g0022 a0002c0002t0001g0079 a0002c0002t0001g0107 |
3 | HG00621.hp2 NA18950.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.271-2140_271-2139i others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416353 | ||||||
| chr12:416353 | G | GTATA | 12 | a0002c0002t0001g0005 a0002c0002t0001g0006 a0002c0002t0001g0111 others(9): Show |
14 | HG01109.hp2 HG01433.hp2 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.271-2140_271-2139i others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416353 | ||||||
| chr12:416353 | G | GTATATA | 24 | a0001c0001t0001g0396 a0002c0002t0001g0124 a0002c0002t0001g0133 others(21): Show |
24 | HG01175.hp2 HG01257.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.271-2140_271-2139i others(8): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416353 | ||||||
| chr12:416353 | G | GTATATAT others(1): Show |
4 | a0002c0002t0001g0023 a0002c0002t0001g0130 a0002c0002t0001g0195 others(1): Show |
4 | HG00438.hp2 HG00741.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-2140_271-2139i others(10): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416353 | ||||||
| chr12:416353 | G | GTATATAT others(3): Show |
4 | a0002c0002t0001g0134 a0002c0002t0001g0135 a0002c0002t0001g0330 others(1): Show |
4 | NA19054.hp2 NA19063.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-2140_271-2139i others(12): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416353 | ||||||
| chr12:416353 | G | GTATATAT others(5): Show |
1 | a0002c0002t0001g0090 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.271-2140_271-2139i others(14): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416353 | ||||||
| chr12:416353 | G | GTATATAT others(7): Show |
2 | a0002c0002t0001g0233 a0002c0002t0001g0295 |
2 | HG02897.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.271-2140_271-2139i others(16): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416353 | ||||||
| chr12:416353 | G | GTATATAT others(9): Show |
1 | a0004c0004t0002g0312 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.271-2140_271-2139i others(18): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416353 | ||||||
| chr12:416353 | G | GTATATAT others(41): Show |
1 | a0004c0004t0001g0304 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.271-2140_271-2139i others(50): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416353 | ||||||
| chr12:416353 | G | GTATATAT others(23): Show |
1 | a0002c0002t0001g0319 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.271-2140_271-2139i others(32): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416353 | ||||||
| chr12:416355 | G | A | 74 | a0001c0001t0001g0396 a0001c0001t0004g0384 a0002c0002t0001g0005 others(71): Show |
77 | HG00280.hp2 HG00423.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.271-2139G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416355 | |||||||
| chr12:416355 | G | GTATATAT others(3): Show |
1 | a0004c0004t0001g0356 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.271-2138_271-2137i others(12): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416355 | ||||||
| chr12:416355 | G | GTATATAT others(5): Show |
1 | a0002c0009t0001g0404 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.271-2138_271-2137i others(14): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416355 | ||||||
| chr12:416357 | G | A | 87 | a0001c0001t0001g0396 a0001c0001t0004g0384 a0002c0002t0001g0005 others(84): Show |
90 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.271-2137G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416357 | |||||||
| chr12:416357 | G | GTATATAT others(3): Show |
1 | a0002c0002t0001g0355 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.271-2136_271-2135i others(12): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416357 | ||||||
| chr12:416358 | T | G | 1 | a0001c0001t0003g0230 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.271-2136T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416358 | |||||||
| chr12:416359 | G | A | 98 | a0001c0001t0001g0396 a0001c0001t0004g0384 a0002c0002t0001g0005 others(95): Show |
101 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.271-2135G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416359 | |||||||
| chr12:416361 | G | A | 104 | a0001c0001t0001g0396 a0001c0001t0002g0049 a0001c0001t0004g0089 others(101): Show |
107 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.271-2133G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416361 | |||||||
| chr12:416361 | GTGTGTGT others(15): Show |
G | 1 | a0001c0001t0001g0292 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.271-2131_271-2110d others(24): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416361 | ||||||
| chr12:416363 | G | A | 113 | a0001c0001t0001g0396 a0001c0001t0002g0049 a0001c0001t0004g0089 others(110): Show |
116 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.271-2131G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416363 | |||||||
| chr12:416363 | GTGTGTGT others(15): Show |
G | 19 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(16): Show |
19 | HG01433.hp1 HG01884.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.271-2129_271-2108d others(24): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416363 | ||||||
| chr12:416363 | GTGTGTGT others(23): Show |
G | 1 | a0003c0003t0002g0379 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.271-2129_271-2100d others(32): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416363 | ||||||
| chr12:416363 | GTGTGTGT others(35): Show |
G | 1 | a0003c0003t0001g0019 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.271-2129_271-2088d others(44): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416363 | ||||||
| chr12:416365 | G | A | 110 | a0001c0001t0001g0396 a0001c0001t0002g0049 a0001c0001t0004g0089 others(107): Show |
113 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.271-2129G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416365 | |||||||
| chr12:416367 | G | A | 118 | a0001c0001t0001g0396 a0001c0001t0002g0049 a0001c0001t0004g0089 others(115): Show |
121 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.271-2127G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416367 | |||||||
| chr12:416367 | GTGTGTGT others(7): Show |
G | 4 | a0001c0001t0004g0176 a0003c0003t0002g0372 a0003c0003t0004g0175 others(1): Show |
4 | HG01891.hp2 HG01952.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-2125_271-2112d others(16): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416367 | ||||||
| chr12:416367 | GTGTGTGT others(13): Show |
G | 1 | a0004c0004t0001g0315 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.271-2125_271-2106d others(22): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416367 | ||||||
| chr12:416367 | GTGTGTGT others(31): Show |
G | 1 | a0002c0002t0001g0400 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.271-2125_271-2088d others(40): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416367 | ||||||
| chr12:416369 | G | A | 113 | a0001c0001t0001g0396 a0001c0001t0002g0049 a0001c0001t0004g0089 others(110): Show |
116 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(113): Show |
intron_variant | MODIFIER | c.271-2125G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416369 | |||||||
| chr12:416369 | G | GTATATAT others(17): Show |
1 | a0002c0002t0001g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.271-2124_271-2123i others(26): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416369 | ||||||
| chr12:416369 | GTGTGTGT others(15): Show |
G | 4 | a0003c0003t0001g0250 a0003c0003t0001g0251 a0003c0003t0001g0341 others(1): Show |
4 | HG01106.hp2 HG01884.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-2123_271-2102d others(24): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416369 | ||||||
| chr12:416369 | GTGTGTGT others(19): Show |
G | 1 | a0006c0006t0011g0103 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.271-2123_271-2098d others(28): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416369 | ||||||
| chr12:416369 | GTGTGTGT others(29): Show |
G | 1 | a0001c0001t0004g0357 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.271-2123_271-2088d others(38): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416369 | ||||||
| chr12:416369 | GTGTGTGT others(31): Show |
G | 1 | a0004c0004t0001g0095 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.271-2123_271-2086d others(40): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416369 | ||||||
| chr12:416371 | G | A | 112 | a0001c0001t0001g0396 a0001c0001t0002g0049 a0001c0001t0004g0089 others(109): Show |
114 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.271-2123G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416371 | |||||||
| chr12:416371 | G | GTA | 3 | a0001c0001t0002g0044 a0001c0001t0002g0055 a0003c0003t0002g0249 |
3 | HG00544.hp2 HG02027.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.271-2122_271-2121i others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416371 | ||||||
| chr12:416371 | GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0002g0294 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.271-2121_271-2112d others(12): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416371 | ||||||
| chr12:416371 | GTGTGTGT others(11): Show |
G | 2 | a0001c0001t0002g0083 a0003c0003t0002g0380 |
2 | HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.271-2121_271-2104d others(20): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416371 | ||||||
| chr12:416371 | GTGTGTGT others(15): Show |
G | 1 | a0002c0002t0001g0387 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.271-2121_271-2100d others(24): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416371 | ||||||
| chr12:416373 | G | A | 105 | a0001c0001t0002g0044 a0001c0001t0002g0049 a0001c0001t0002g0055 others(102): Show |
107 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.271-2121G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416373 | |||||||
| chr12:416373 | G | GTATATAT others(3): Show |
2 | a0003c0003t0002g0009 a0003c0003t0002g0266 |
3 | NA18957.hp2 NA18977.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.271-2120_271-2119i others(12): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416373 | ||||||
| chr12:416373 | G | GTATATAT others(5): Show |
3 | a0003c0003t0002g0265 a0003c0003t0002g0367 a0003c0003t0015g0301 |
3 | NA18980.hp2 NA18992.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.271-2120_271-2119i others(14): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416373 | ||||||
| chr12:416373 | G | GTATATAT others(7): Show |
1 | a0003c0003t0002g0264 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.271-2120_271-2119i others(16): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416373 | ||||||
| chr12:416373 | G | GTATATAT others(9): Show |
2 | a0003c0003t0002g0262 a0003c0003t0002g0263 |
2 | NA18945.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.271-2120_271-2119i others(18): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416373 | ||||||
| chr12:416373 | GTGTGTAT others(9): Show |
G | 2 | a0001c0001t0001g0281 a0004c0004t0001g0085 |
2 | HG02109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.271-2119_271-2104d others(18): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416373 | ||||||
| chr12:416373 | GTGTGTAT others(11): Show |
G | 8 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0002c0002t0001g0322 others(5): Show |
8 | HG01192.hp1 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.271-2119_271-2102d others(20): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416373 | ||||||
| chr12:416373 | GTGTGTAT others(25): Show |
G | 5 | a0001c0001t0001g0178 a0001c0001t0001g0406 a0001c0001t0001g0407 others(2): Show |
5 | HG01168.hp1 HG01261.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.271-2119_271-2088d others(34): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416373 | ||||||
| chr12:416375 | G | A | 147 | a0001c0001t0001g0151 a0001c0001t0001g0365 a0001c0001t0001g0396 others(144): Show |
151 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.271-2119G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416375 | |||||||
| chr12:416375 | G | GTA | 11 | a0001c0001t0002g0254 a0001c0001t0002g0260 a0001c0001t0002g0346 others(8): Show |
14 | HG00423.hp1 HG03704.hp1 NA18961.hp2 others(11): Show |
intron_variant | MODIFIER | c.271-2118_271-2117i others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416375 | ||||||
| chr12:416375 | G | GTATA | 4 | a0001c0001t0002g0136 a0001c0001t0002g0288 a0001c0001t0002g0352 others(1): Show |
4 | HG01243.hp2 HG02071.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.271-2118_271-2117i others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416375 | ||||||
| chr12:416375 | G | GTATATAT others(5): Show |
1 | a0003c0003t0002g0157 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.271-2118_271-2117i others(14): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416375 | ||||||
| chr12:416375 | G | GTATATAT others(19): Show |
1 | a0001c0001t0002g0144 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.271-2118_271-2117i others(28): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416375 | ||||||
| chr12:416375 | GTGTA | G | 3 | a0001c0001t0002g0014 a0001c0001t0002g0259 a0006c0006t0012g0105 |
3 | HG01928.hp1 HG02083.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.271-2117_271-2114d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416375 | ||||||
| chr12:416375 | GTGTATAT others(11): Show |
G | 8 | a0001c0001t0006g0012 a0001c0001t0006g0388 a0001c0001t0006g0389 others(5): Show |
8 | HG00735.hp1 HG02155.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-2117_271-2100d others(20): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416375 | ||||||
| chr12:416375 | GTGTATAT others(13): Show |
G | 1 | a0001c0001t0002g0051 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.271-2117_271-2098d others(22): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416375 | ||||||
| chr12:416375 | GTGTATAT others(15): Show |
G | 6 | a0001c0001t0004g0246 a0001c0001t0008g0170 a0003c0003t0004g0329 others(3): Show |
6 | HG01243.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-2117_271-2096d others(24): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416375 | ||||||
| chr12:416377 | G | A | 222 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(219): Show |
233 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.271-2117G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416377 | |||||||
| chr12:416377 | G | GTATATAT others(3): Show |
1 | a0001c0001t0002g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.271-2087_271-2078d others(12): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416377 | ||||||
| chr12:416377 | G | GTATATAT others(11): Show |
1 | a0003c0003t0002g0270 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.271-2095_271-2078d others(20): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416377 | ||||||
| chr12:416377 | GTATA | G | 16 | a0001c0001t0001g0131 a0001c0001t0001g0167 a0001c0001t0001g0191 others(13): Show |
16 | HG00642.hp2 HG01071.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.271-2081_271-2078d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416377 | ||||||
| chr12:416377 | GTATATA | G | 43 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(40): Show |
43 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(40): Show |
intron_variant | MODIFIER | c.271-2083_271-2078d others(8): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416377 | ||||||
| chr12:416377 | GTATATAT others(1): Show |
G | 8 | a0001c0001t0001g0143 a0001c0001t0001g0236 a0001c0001t0001g0242 others(5): Show |
8 | HG00609.hp1 HG01256.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-2085_271-2078d others(10): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416377 | ||||||
| chr12:416377 | GTATATAT others(9): Show |
G | 1 | a0003c0003t0006g0084 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.271-2093_271-2078d others(18): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416377 | ||||||
| chr12:416377 | GTATATAT others(13): Show |
G | 1 | a0003c0003t0004g0363 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.271-2097_271-2078d others(22): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416377 | ||||||
| chr12:416377 | GTATATAT others(15): Show |
G | 1 | a0001c0001t0004g0328 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.271-2099_271-2078d others(24): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416377 | ||||||
| chr12:416379 | A | G | 7 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0002g0335 others(4): Show |
7 | HG01081.hp2 HG03098.hp2 HG03927.hp2 others(4): Show |
intron_variant | MODIFIER | c.271-2115A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416379 | |||||||
| chr12:416381 | A | G | 8 | a0002c0002t0001g0119 a0002c0002t0001g0120 a0002c0002t0001g0121 others(5): Show |
8 | HG04228.hp1 NA18946.hp2 NA18986.hp2 others(5): Show |
intron_variant | MODIFIER | c.271-2113A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416381 | |||||||
| chr12:416383 | A | G | 2 | a0003c0003t0009g0168 a0004c0004t0001g0279 |
2 | HG02735.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.271-2111A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416383 | |||||||
| chr12:416385 | A | G | 2 | a0002c0002t0001g0169 a0002c0002t0001g0172 |
2 | HG02486.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.271-2109A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416385 | |||||||
| chr12:416387 | A | G | 2 | a0001c0001t0002g0358 a0003c0003t0001g0148 |
2 | HG02293.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.271-2107A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416387 | |||||||
| chr12:416389 | A | G | 1 | a0002c0002t0001g0186 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.271-2105A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416389 | |||||||
| chr12:416394 | T | C | 2 | a0002c0002t0001g0154 a0002c0002t0001g0225 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.271-2100T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416394 | |||||||
| chr12:416396 | T | C | 12 | a0001c0001t0004g0399 a0001c0001t0010g0277 a0001c0001t0010g0278 others(9): Show |
12 | HG01433.hp1 HG01884.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.271-2098T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416396 | |||||||
| chr12:416397 | A | G | 1 | a0002c0002t0001g0174 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.271-2097A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416397 | |||||||
| chr12:416399 | A | G | 1 | a0004c0004t0001g0356 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.271-2095A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416399 | |||||||
| chr12:416401 | A | G | 49 | a0001c0001t0002g0004 a0001c0001t0002g0041 a0001c0001t0002g0074 others(46): Show |
52 | HG00609.hp2 HG00738.hp1 HG01496.hp2 others(49): Show |
intron_variant | MODIFIER | c.271-2093A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416401 | |||||||
| chr12:416403 | ATATATAT others(7): Show |
A | 2 | a0003c0003t0001g0287 a0003c0003t0001g0316 |
2 | HG01346.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.271-2089_271-2076d others(16): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416403 | ||||||
| chr12:416405 | A | G | 62 | a0001c0001t0002g0004 a0001c0001t0002g0041 a0001c0001t0002g0074 others(59): Show |
65 | HG00609.hp2 HG00738.hp1 HG01433.hp1 others(62): Show |
intron_variant | MODIFIER | c.271-2089A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416405 | |||||||
| chr12:416416 | T | TATATATA others(6): Show |
1 | a0002c0002t0001g0234 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.271-2078_271-2077i others(15): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416416 | |||||||
| chr12:416417 | T | A | 93 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(90): Show |
96 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.271-2077T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416417 | |||||||
| chr12:416418 | T | A | 1 | a0002c0002t0001g0234 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.271-2076T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416418 | |||||||
| chr12:416419 | C | A | 2 | a0001c0001t0004g0384 a0004c0004t0002g0097 |
2 | HG00639.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.271-2075C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416419 | |||||||
| chr12:416419 | C | CT | 27 | a0001c0001t0002g0044 a0001c0001t0002g0055 a0001c0001t0002g0059 others(24): Show |
28 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.271-2061dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416419 | ||||||
| chr12:416419 | C | T | 83 | a0001c0001t0001g0396 a0001c0001t0004g0089 a0001c0001t0004g0324 others(80): Show |
86 | HG00423.hp2 HG00438.hp2 HG00741.hp2 others(83): Show |
intron_variant | MODIFIER | c.271-2075C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416419 | |||||||
| chr12:416419 | CTT | C | 197 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(194): Show |
200 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.271-2062_271-2061d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416419 | ||||||
| chr12:416421 | T | C | 82 | a0001c0001t0001g0396 a0001c0001t0004g0089 a0001c0001t0004g0324 others(79): Show |
85 | HG00423.hp2 HG00438.hp2 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.271-2073T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416421 | |||||||
| chr12:416422 | T | C | 1 | a0002c0002t0001g0234 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.271-2072T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416422 | |||||||
| chr12:416668 | C | T | 1 | a0007c0007t0005g0326 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.271-1826C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416668 | |||||||
| chr12:416872 | CCGAGGCC others(25): Show |
C | 171 | a0001c0001t0001g0396 a0001c0001t0002g0004 a0001c0001t0002g0041 others(168): Show |
177 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(174): Show |
intron_variant | MODIFIER | c.271-1585_271-1554d others(34): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 416872 | ||||||
| chr12:416911 | C | T | 7 | a0001c0001t0004g0246 a0001c0001t0004g0328 a0001c0001t0008g0170 others(4): Show |
7 | HG01081.hp1 HG01109.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-1583C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416911 | |||||||
| chr12:416938 | G | A | 9 | a0001c0001t0006g0012 a0001c0001t0006g0388 a0001c0001t0006g0389 others(6): Show |
9 | HG00735.hp1 HG02155.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.271-1556G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416938 | |||||||
| chr12:417033 | G | T | 1 | a0005c0005t0005g0416 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.271-1461G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 417033 | |||||||
| chr12:417054 | G | A | 282 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(279): Show |
288 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(285): Show |
intron_variant | MODIFIER | c.271-1440G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 417054 | |||||||
| chr12:417132 | C | CA | 327 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(324): Show |
338 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(335): Show |
intron_variant | MODIFIER | c.271-1346dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 417132 | ||||||
| chr12:417132 | C | CAA | 29 | a0001c0001t0001g0146 a0001c0001t0001g0375 a0001c0001t0001g0376 others(26): Show |
29 | HG00408.hp1 HG00423.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.271-1347_271-1346d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 417132 | ||||||
| chr12:417132 | C | CAAAA | 10 | a0001c0001t0001g0245 a0001c0001t0001g0281 a0002c0002t0001g0322 others(7): Show |
10 | HG01346.hp2 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.271-1349_271-1346d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 417132 | ||||||
| chr12:417316 | A | G | 343 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(340): Show |
349 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(346): Show |
intron_variant | MODIFIER | c.271-1178A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 417316 | |||||||
| chr12:417373 | A | G | 1 | a0001c0001t0002g0403 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.271-1121A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 417373 | |||||||
| chr12:417403 | C | T | 2 | a0001c0001t0010g0277 a0001c0001t0010g0278 |
2 | HG01433.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.271-1091C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 417403 | |||||||
| chr12:417433 | G | A | 1 | a0002c0002t0001g0133 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.271-1061G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 417433 | |||||||
| chr12:417652 | C | T | 1 | a0001c0001t0001g0348 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.271-842C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 417652 | |||||||
| chr12:417666 | G | A | 1 | a0001c0001t0004g0331 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.271-828G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 417666 | |||||||
| chr12:417875 | C | T | 9 | a0001c0001t0006g0012 a0001c0001t0006g0388 a0001c0001t0006g0389 others(6): Show |
9 | HG00735.hp1 HG02155.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.271-619C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 417875 | |||||||
| chr12:417952 | C | T | 2 | a0001c0001t0003g0042 a0001c0001t0003g0043 |
2 | NA18965.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.271-542C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 417952 | |||||||
| chr12:418050 | G | A | 4 | a0003c0003t0001g0250 a0003c0003t0001g0251 a0003c0003t0001g0341 others(1): Show |
4 | HG01106.hp2 HG01884.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-444G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 418050 | |||||||
| chr12:418055 | G | A | 6 | a0002c0002t0002g0113 a0004c0004t0002g0305 a0004c0004t0002g0309 others(3): Show |
6 | HG00408.hp1 HG02165.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.271-439G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 418055 | |||||||
| chr12:418154 | A | G | 15 | a0001c0001t0004g0399 a0001c0001t0010g0277 a0001c0001t0010g0278 others(12): Show |
15 | HG01243.hp1 HG01433.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.271-340A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 418154 | |||||||
| chr12:418182 | G | A | 1 | a0001c0001t0003g0127 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.271-312G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 418182 | |||||||
| chr12:418323 | AAAAC | A | 9 | a0001c0001t0006g0012 a0001c0001t0006g0388 a0001c0001t0006g0389 others(6): Show |
9 | HG00735.hp1 HG02155.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.271-162_271-159del others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 418323 | ||||||
| chr12:418394 | T | G | 1 | a0001c0001t0001g0348 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.271-100T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 418394 | |||||||
| chr12:418681 | A | ACATT | 31 | a0001c0001t0004g0093 a0001c0001t0004g0159 a0001c0001t0004g0160 others(28): Show |
31 | HG00408.hp1 HG01106.hp2 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.413+74_413+77dupCA others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 418681 | ||||||
| chr12:418681 | A | ACATTCAT others(1): Show |
9 | a0001c0001t0006g0012 a0001c0001t0006g0388 a0001c0001t0006g0389 others(6): Show |
9 | HG00735.hp1 HG02155.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+70_413+77dupCA others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 418681 | ||||||
| chr12:418719 | A | C | 1 | a0001c0001t0001g0242 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.413+83A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 418719 | |||||||
| chr12:418758 | G | A | 47 | a0001c0001t0002g0004 a0001c0001t0002g0041 a0001c0001t0002g0074 others(44): Show |
50 | HG00609.hp2 HG00738.hp1 HG01496.hp2 others(47): Show |
intron_variant | MODIFIER | c.413+122G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 418758 | |||||||
| chr12:418776 | T | C | 12 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(9): Show |
12 | HG00597.hp1 HG02080.hp1 NA18612.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+140T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 418776 | |||||||
| chr12:419094 | C | G | 64 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0245 others(61): Show |
64 | HG00735.hp1 HG01081.hp1 HG01106.hp2 others(61): Show |
intron_variant | MODIFIER | c.413+458C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419094 | |||||||
| chr12:419263 | T | C | 4 | a0001c0001t0001g0406 a0001c0001t0001g0407 a0001c0001t0001g0408 others(1): Show |
4 | HG01168.hp1 HG01261.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+627T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419263 | |||||||
| chr12:419286 | A | T | 51 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(48): Show |
51 | HG00735.hp1 HG01081.hp1 HG01106.hp2 others(48): Show |
intron_variant | MODIFIER | c.413+650A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419286 | |||||||
| chr12:419335 | A | G | 9 | a0001c0001t0006g0012 a0001c0001t0006g0388 a0001c0001t0006g0389 others(6): Show |
9 | HG00735.hp1 HG02155.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+699A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419335 | |||||||
| chr12:419376 | T | C | 1 | a0002c0002t0001g0355 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.413+740T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419376 | |||||||
| chr12:419385 | G | A | 9 | a0001c0001t0006g0012 a0001c0001t0006g0388 a0001c0001t0006g0389 others(6): Show |
9 | HG00735.hp1 HG02155.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+749G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419385 | |||||||
| chr12:419407 | A | C | 1 | a0002c0002t0001g0050 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.413+771A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419407 | |||||||
| chr12:419407 | ACATGTTC others(510): Show |
A | 1 | a0001c0001t0004g0399 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.413+790_413+1306de others(1): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419407 | ||||||
| chr12:419412 | T | TTCCATTA others(291): Show |
3 | a0002c0002t0001g0322 a0002c0002t0001g0385 a0004c0004t0001g0085 |
3 | HG02109.hp2 HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.413+789_413+790ins others(298): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419412 | ||||||
| chr12:419412 | T | TTCCATTA others(365): Show |
1 | a0003c0003t0004g0363 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.413+789_413+790ins others(372): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419412 | ||||||
| chr12:419412 | T | TTCCATTA others(66): Show |
1 | a0001c0001t0002g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.413+825_413+826ins others(73): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419412 | ||||||
| chr12:419412 | TTCCATTA others(140): Show |
T | 3 | a0001c0001t0010g0277 a0001c0001t0010g0278 a0005c0005t0005g0409 |
3 | HG01433.hp1 HG02976.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.413+827_413+973del | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419412 | ||||||
| chr12:419426 | T | G | 46 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0245 others(43): Show |
46 | HG00735.hp1 HG01081.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.413+790T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419426 | |||||||
| chr12:419452 | A | AGAGGGTA others(61): Show |
1 | a0001c0001t0006g0390 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.413+826_413+827ins others(68): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419452 | ||||||
| chr12:419452 | A | AGAGGGTA others(209): Show |
5 | a0001c0001t0001g0178 a0001c0001t0001g0406 a0001c0001t0001g0407 others(2): Show |
5 | HG01168.hp1 HG01261.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.413+826_413+827ins others(216): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419452 | ||||||
| chr12:419452 | A | AGAGGGTA others(61): Show |
3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 |
3 | HG00323.hp2 HG01106.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.413+831_413+832ins others(68): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419452 | ||||||
| chr12:419459 | A | AAAACACA others(364): Show |
8 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(5): Show |
8 | HG01192.hp1 HG01346.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+826_413+827ins others(371): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419459 | ||||||
| chr12:419459 | AAAATACA others(66): Show |
A | 7 | a0005c0005t0005g0332 a0005c0005t0005g0410 a0005c0005t0005g0418 others(4): Show |
7 | HG02145.hp1 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+827_413+899del others(73): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419459 | ||||||
| chr12:419463 | T | C | 37 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(34): Show |
37 | HG00735.hp1 HG01081.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.413+827T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419463 | |||||||
| chr12:419478 | A | C | 30 | a0001c0001t0002g0010 a0001c0001t0004g0176 a0001c0001t0004g0246 others(27): Show |
31 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.413+842A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419478 | |||||||
| chr12:419486 | T | C | 18 | a0001c0001t0001g0147 a0001c0001t0001g0164 a0001c0001t0001g0165 others(15): Show |
19 | HG00323.hp2 HG01069.hp2 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.413+850T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419486 | |||||||
| chr12:419486 | T | TTCCATTA others(61): Show |
69 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(66): Show |
69 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.413+863_413+864ins others(68): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419486 | ||||||
| chr12:419486 | T | TTCCATTA others(864): Show |
1 | a0001c0001t0001g0192 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.413+863_413+864ins others(871): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419486 | ||||||
| chr12:419486 | T | TTCCATTA others(207): Show |
1 | a0002c0002t0001g0387 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.413+863_413+864ins others(214): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419486 | ||||||
| chr12:419486 | TTCCATTA others(66): Show |
T | 2 | a0002c0002t0001g0290 a0003c0003t0001g0148 |
2 | HG02273.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.413+864_413+936del others(73): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419486 | ||||||
| chr12:419486 | TTCCATTA others(140): Show |
T | 2 | a0001c0001t0004g0323 a0002c0002t0001g0186 |
2 | HG01943.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.413+864_413+1010de others(1): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419486 | ||||||
| chr12:419500 | A | T | 311 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(308): Show |
318 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(315): Show |
intron_variant | MODIFIER | c.413+864A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419500 | |||||||
| chr12:419502 | T | TTCTGTGT others(278): Show |
1 | a0001c0001t0001g0191 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.413+876_413+877ins others(285): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419502 | ||||||
| chr12:419504 | CTGTG | C | 24 | a0001c0001t0004g0093 a0001c0001t0004g0244 a0001c0001t0004g0397 others(21): Show |
24 | HG00408.hp1 HG00423.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.413+877_413+880del others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419504 | ||||||
| chr12:419504 | CTGTGTGT others(70): Show |
C | 17 | a0001c0001t0001g0207 a0001c0001t0001g0224 a0001c0001t0001g0274 others(14): Show |
17 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.413+877_413+953del others(77): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419504 | ||||||
| chr12:419504 | CTGTGTGT others(144): Show |
C | 1 | a0002c0002t0002g0351 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.413+877_413+1027de others(1): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419504 | ||||||
| chr12:419504 | CTGTGTGT others(440): Show |
C | 147 | a0001c0001t0001g0396 a0001c0001t0002g0004 a0001c0001t0002g0041 others(144): Show |
153 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(150): Show |
intron_variant | MODIFIER | c.413+877_413+1323de others(1): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419504 | ||||||
| chr12:419504 | CTGTGTGT others(810): Show |
C | 17 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(14): Show |
17 | HG00597.hp1 HG02080.hp1 HG03139.hp2 others(14): Show |
intron_variant | MODIFIER | c.413+877_413+1693de others(1): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419504 | ||||||
| chr12:419504 | CTGTGTGT others(1473): Show |
C | 1 | a0002c0002t0002g0082 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.413+877_413+2356de others(1): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419504 | ||||||
| chr12:419527 | GA | G | 24 | a0001c0001t0004g0093 a0001c0001t0004g0244 a0001c0001t0004g0397 others(21): Show |
24 | HG00408.hp1 HG00423.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.413+892delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419527 | |||||||
| chr12:419531 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.413+895G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419531 | |||||||
| chr12:419531 | G | T | 24 | a0001c0001t0004g0093 a0001c0001t0004g0244 a0001c0001t0004g0397 others(21): Show |
24 | HG00408.hp1 HG00423.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.413+895G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419531 | |||||||
| chr12:419532 | T | A | 24 | a0001c0001t0004g0093 a0001c0001t0004g0244 a0001c0001t0004g0397 others(21): Show |
24 | HG00408.hp1 HG00423.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.413+896T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419532 | |||||||
| chr12:419532 | T | TA | 27 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0004g0176 others(24): Show |
27 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.413+899dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419532 | ||||||
| chr12:419532 | TAAACACA others(67): Show |
T | 57 | a0001c0001t0002g0044 a0001c0001t0002g0051 a0001c0001t0002g0055 others(54): Show |
61 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.413+974_413+1047de others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419532 | ||||||
| chr12:419536 | C | T | 25 | a0001c0001t0001g0192 a0001c0001t0004g0093 a0001c0001t0004g0244 others(22): Show |
25 | HG00408.hp1 HG00423.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.413+900C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419536 | |||||||
| chr12:419551 | C | A | 32 | a0001c0001t0001g0167 a0001c0001t0001g0191 a0001c0001t0002g0010 others(29): Show |
33 | HG00408.hp1 HG00423.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.413+915C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419551 | |||||||
| chr12:419559 | C | T | 9 | a0001c0001t0001g0167 a0001c0001t0002g0010 a0005c0005t0005g0332 others(6): Show |
10 | HG01069.hp2 HG01071.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+923C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419559 | |||||||
| chr12:419573 | T | A | 115 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(112): Show |
115 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.413+937T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419573 | |||||||
| chr12:419573 | T | G | 3 | a0001c0001t0010g0277 a0001c0001t0010g0278 a0005c0005t0005g0409 |
3 | HG01433.hp1 HG02976.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.413+937T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419573 | |||||||
| chr12:419597 | TGA | T | 18 | a0001c0001t0001g0207 a0001c0001t0001g0224 a0001c0001t0001g0274 others(15): Show |
18 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.413+965_413+966del others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419597 | ||||||
| chr12:419605 | TA | T | 31 | a0001c0001t0002g0136 a0001c0001t0004g0093 a0001c0001t0004g0244 others(28): Show |
31 | HG00408.hp1 HG00423.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.413+973delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419605 | ||||||
| chr12:419605 | TAAAACAC others(68): Show |
T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0014 |
2 | HG01928.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.413+973_413+1047de others(76): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419605 | ||||||
| chr12:419606 | A | AAAATACA others(363): Show |
4 | a0003c0003t0001g0250 a0003c0003t0001g0251 a0003c0003t0001g0341 others(1): Show |
4 | HG01106.hp2 HG01884.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+973_413+974ins others(370): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419606 | ||||||
| chr12:419606 | A | AAAATACA others(363): Show |
3 | a0003c0003t0007g0327 a0006c0006t0011g0103 a0006c0006t0011g0106 |
3 | HG01891.hp1 HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.413+973_413+974ins others(370): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419606 | ||||||
| chr12:419606 | A | AAACACAC others(801): Show |
1 | a0001c0001t0004g0328 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.413+972_413+973ins others(808): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419606 | ||||||
| chr12:419608 | A | AAT | 8 | a0001c0001t0004g0176 a0001c0001t0004g0246 a0001c0001t0008g0170 others(5): Show |
8 | HG01243.hp1 HG01891.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+973_413+974ins others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419608 | ||||||
| chr12:419610 | C | T | 36 | a0001c0001t0001g0192 a0001c0001t0001g0207 a0001c0001t0001g0224 others(33): Show |
38 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.413+974C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419610 | |||||||
| chr12:419625 | C | A | 38 | a0001c0001t0001g0207 a0001c0001t0001g0224 a0001c0001t0001g0274 others(35): Show |
40 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.413+989C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419625 | |||||||
| chr12:419633 | C | T | 30 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(27): Show |
32 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.413+997C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419633 | |||||||
| chr12:419633 | CTCCATTA others(67): Show |
C | 3 | a0001c0001t0004g0093 a0001c0001t0004g0397 a0007c0007t0005g0326 |
3 | HG02965.hp2 HG02976.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.413+1011_413+1084d others(76): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419633 | ||||||
| chr12:419647 | T | A | 68 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0192 others(65): Show |
70 | HG00408.hp1 HG00423.hp2 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.413+1011T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419647 | |||||||
| chr12:419651 | CTGTG | C | 3 | a0001c0001t0001g0167 a0002c0002t0001g0186 a0002c0002t0001g0290 |
3 | HG01943.hp2 HG02273.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.413+1024_413+1027d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419651 | ||||||
| chr12:419671 | TGA | T | 3 | a0002c0002t0001g0186 a0002c0002t0001g0290 a0002c0002t0002g0351 |
3 | HG01943.hp2 HG02273.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.413+1039_413+1040d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419671 | ||||||
| chr12:419679 | TA | T | 26 | a0001c0001t0001g0147 a0001c0001t0001g0191 a0001c0001t0001g0207 others(23): Show |
26 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.413+1047delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419679 | ||||||
| chr12:419682 | AATACACA others(510): Show |
A | 1 | a0005c0005t0005g0416 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.413+1048_413+1564d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419682 | ||||||
| chr12:419684 | T | C | 80 | a0001c0001t0001g0147 a0001c0001t0001g0191 a0001c0001t0001g0207 others(77): Show |
80 | HG00408.hp1 HG00423.hp2 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.413+1048T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419684 | |||||||
| chr12:419684 | T | TACACATA others(434): Show |
2 | a0001c0001t0008g0170 a0003c0003t0004g0329 |
2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.413+1062_413+1063i others(443): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419684 | ||||||
| chr12:419699 | A | C | 75 | a0001c0001t0001g0192 a0001c0001t0001g0207 a0001c0001t0001g0224 others(72): Show |
75 | HG00408.hp1 HG00423.hp2 HG00735.hp1 others(72): Show |
intron_variant | MODIFIER | c.413+1063A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419699 | |||||||
| chr12:419707 | T | C | 68 | a0001c0001t0001g0147 a0001c0001t0001g0191 a0001c0001t0001g0192 others(65): Show |
68 | HG00408.hp1 HG00423.hp2 HG01071.hp1 others(65): Show |
intron_variant | MODIFIER | c.413+1071T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419707 | |||||||
| chr12:419707 | T | TTCCATTA others(1317): Show |
1 | a0003c0003t0007g0412 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.413+1136_413+1137i others(1326): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419707 | ||||||
| chr12:419707 | T | TTCCATTA others(140): Show |
1 | a0001c0001t0001g0204 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.413+1084_413+1085i others(149): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419707 | ||||||
| chr12:419721 | A | T | 98 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(95): Show |
98 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.413+1085A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419721 | |||||||
| chr12:419725 | C | G | 1 | a0003c0003t0001g0287 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.413+1089C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419725 | |||||||
| chr12:419752 | G | A | 2 | a0001c0001t0001g0166 a0003c0003t0001g0019 |
2 | HG01106.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.413+1116G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419752 | |||||||
| chr12:419753 | TA | T | 26 | a0001c0001t0001g0147 a0001c0001t0001g0166 a0001c0001t0001g0191 others(23): Show |
26 | HG01106.hp1 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.413+1121delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419753 | ||||||
| chr12:419758 | T | C | 59 | a0001c0001t0001g0147 a0001c0001t0001g0166 a0001c0001t0001g0167 others(56): Show |
59 | HG01074.hp2 HG01106.hp1 HG01106.hp2 others(56): Show |
intron_variant | MODIFIER | c.413+1122T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419758 | |||||||
| chr12:419758 | T | TAC | 8 | a0001c0001t0006g0012 a0001c0001t0006g0388 a0001c0001t0006g0389 others(5): Show |
8 | HG00735.hp1 HG02155.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+1126_413+1127d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419758 | ||||||
| chr12:419758 | T | TACACATA others(66): Show |
2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG00323.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.413+1158_413+1159i others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419758 | ||||||
| chr12:419773 | A | C | 48 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0204 others(45): Show |
48 | HG00642.hp2 HG01071.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.413+1137A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419773 | |||||||
| chr12:419781 | T | C | 66 | a0001c0001t0001g0147 a0001c0001t0001g0167 a0001c0001t0001g0192 others(63): Show |
66 | HG00642.hp2 HG00735.hp1 HG01071.hp1 others(63): Show |
intron_variant | MODIFIER | c.413+1145T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419781 | |||||||
| chr12:419781 | T | TTCCATTA others(210): Show |
1 | a0003c0003t0002g0209 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.413+1158_413+1159i others(219): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419781 | ||||||
| chr12:419781 | T | TTCCATTA others(722): Show |
1 | a0001c0001t0001g0203 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.413+1158_413+1159i others(731): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419781 | ||||||
| chr12:419781 | T | TTCCATTA others(870): Show |
1 | a0001c0001t0001g0146 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.413+1158_413+1159i others(879): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419781 | ||||||
| chr12:419781 | T | TTCCATTA others(944): Show |
1 | a0003c0003t0001g0070 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.413+1158_413+1159i others(953): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419781 | ||||||
| chr12:419795 | A | ACTTCTGT others(213): Show |
1 | a0002c0002t0001g0385 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.413+1194_413+1195i others(222): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419795 | ||||||
| chr12:419795 | A | T | 129 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(126): Show |
129 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.413+1159A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419795 | |||||||
| chr12:419801 | G | C | 1 | a0002c0002t0014g0321 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.413+1165G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419801 | |||||||
| chr12:419803 | G | GTGTGTGT others(1465): Show |
1 | a0003c0003t0004g0337 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.413+1189_413+1190i others(1474): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419803 | ||||||
| chr12:419826 | G | A | 59 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(56): Show |
59 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.413+1190G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419826 | |||||||
| chr12:419827 | TA | T | 71 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(68): Show |
71 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.413+1195delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419827 | ||||||
| chr12:419828 | A | AAAACACA others(140): Show |
1 | a0002c0002t0014g0321 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.413+1195_413+1196i others(149): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419828 | ||||||
| chr12:419828 | AAAATACA others(880): Show |
A | 3 | a0001c0001t0004g0176 a0003c0003t0002g0372 a0003c0003t0004g0175 |
3 | HG01891.hp2 HG01952.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.413+1196_413+2082d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419828 | ||||||
| chr12:419832 | T | C | 87 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(84): Show |
87 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.413+1196T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419832 | |||||||
| chr12:419832 | T | TAC | 8 | a0003c0003t0001g0148 a0005c0005t0005g0332 a0005c0005t0005g0410 others(5): Show |
8 | HG02145.hp1 HG02572.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+1200_413+1201d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419832 | ||||||
| chr12:419832 | T | TACACATA others(360): Show |
1 | a0002c0002t0001g0387 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.413+1210_413+1211i others(369): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419832 | ||||||
| chr12:419835 | A | G | 1 | a0002c0002t0001g0400 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.413+1199A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419835 | |||||||
| chr12:419844 | C | T | 5 | a0001c0001t0001g0178 a0001c0001t0001g0406 a0001c0001t0001g0407 others(2): Show |
5 | HG01168.hp1 HG01261.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.413+1208C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419844 | |||||||
| chr12:419847 | A | ACTCCATG others(214): Show |
2 | a0002c0002t0001g0322 a0004c0004t0001g0085 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.413+1218_413+1219i others(223): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419847 | ||||||
| chr12:419847 | A | C | 38 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0167 others(35): Show |
38 | HG00642.hp2 HG00735.hp1 HG01071.hp1 others(35): Show |
intron_variant | MODIFIER | c.413+1211A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419847 | |||||||
| chr12:419850 | C | A | 5 | a0001c0001t0001g0178 a0001c0001t0001g0406 a0001c0001t0001g0407 others(2): Show |
5 | HG01168.hp1 HG01261.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.413+1214C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419850 | |||||||
| chr12:419855 | T | C | 31 | a0001c0001t0001g0146 a0001c0001t0001g0167 a0001c0001t0001g0192 others(28): Show |
31 | HG00642.hp2 HG01071.hp1 HG01106.hp2 others(28): Show |
intron_variant | MODIFIER | c.413+1219T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419855 | |||||||
| chr12:419855 | TTCCATTA others(214): Show |
T | 1 | a0002c0002t0001g0291 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.413+1269_413+1489d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419855 | ||||||
| chr12:419855 | TTCCATTA others(1100): Show |
T | 1 | a0003c0003t0002g0267 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.413+1293_413+2399d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419855 | ||||||
| chr12:419869 | A | T | 68 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0166 others(65): Show |
68 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.413+1233A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419869 | |||||||
| chr12:419877 | G | GTGTGTGT others(430): Show |
1 | a0003c0003t0001g0019 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.413+1263_413+1264i others(439): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419877 | ||||||
| chr12:419877 | G | GTGTGTGT others(63): Show |
44 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(41): Show |
44 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.413+1269_413+1270i others(72): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419877 | ||||||
| chr12:419877 | G | GTGTGTGT others(427): Show |
2 | a0001c0001t0001g0206 a0001c0001t0001g0402 |
2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.413+1269_413+1270i others(436): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419877 | ||||||
| chr12:419877 | G | GTGTGTGT others(282): Show |
1 | a0002c0002t0001g0208 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.413+1269_413+1270i others(291): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419877 | ||||||
| chr12:419877 | G | GTGTGTGT others(63): Show |
2 | a0001c0001t0001g0362 a0001c0001t0001g0364 |
2 | HG03239.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.413+1269_413+1270i others(72): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419877 | ||||||
| chr12:419877 | G | GTGTGTGT others(210): Show |
1 | a0001c0001t0001g0164 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.413+1306_413+1307i others(219): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419877 | ||||||
| chr12:419877 | G | GTGTGTGT others(135): Show |
1 | a0001c0001t0001g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.413+1268_413+1269i others(144): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419877 | ||||||
| chr12:419901 | TA | T | 31 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(28): Show |
31 | HG00408.hp1 HG00423.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.413+1269delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419901 | ||||||
| chr12:419902 | A | AAACACAC others(65): Show |
2 | a0001c0001t0008g0170 a0003c0003t0004g0329 |
2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.413+1268_413+1269i others(74): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419902 | ||||||
| chr12:419906 | T | C | 44 | a0001c0001t0001g0132 a0001c0001t0001g0147 a0001c0001t0001g0211 others(41): Show |
44 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.413+1270T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419906 | |||||||
| chr12:419906 | T | TAC | 5 | a0001c0001t0006g0390 a0001c0001t0010g0277 a0001c0001t0010g0278 others(2): Show |
5 | HG01433.hp1 HG02559.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.413+1274_413+1275d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419906 | ||||||
| chr12:419919 | A | C | 1 | a0002c0002t0001g0208 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.413+1283A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419919 | |||||||
| chr12:419921 | A | C | 52 | a0001c0001t0001g0132 a0001c0001t0001g0146 a0001c0001t0001g0167 others(49): Show |
52 | HG00408.hp2 HG00639.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.413+1285A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419921 | |||||||
| chr12:419929 | T | C | 43 | a0001c0001t0001g0132 a0001c0001t0001g0146 a0001c0001t0001g0147 others(40): Show |
43 | HG00408.hp2 HG00639.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.413+1293T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419929 | |||||||
| chr12:419929 | T | TTCCATTA others(652): Show |
1 | a0001c0001t0001g0166 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.413+1306_413+1307i others(661): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419929 | ||||||
| chr12:419943 | A | G | 1 | a0001c0001t0004g0399 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.413+1307A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419943 | |||||||
| chr12:419943 | A | T | 110 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(107): Show |
110 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.413+1307A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419943 | |||||||
| chr12:419947 | CTGTG | C | 7 | a0001c0001t0001g0178 a0001c0001t0001g0406 a0001c0001t0001g0407 others(4): Show |
7 | HG01167.hp1 HG01168.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+1320_413+1323d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419947 | ||||||
| chr12:419951 | G | GTGTGCTG others(353): Show |
10 | a0001c0001t0001g0132 a0001c0001t0001g0211 a0001c0001t0001g0212 others(7): Show |
10 | HG00408.hp2 HG00639.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.413+1319_413+1320i others(362): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419951 | ||||||
| chr12:419967 | TGA | T | 152 | a0001c0001t0001g0178 a0001c0001t0001g0396 a0001c0001t0001g0406 others(149): Show |
158 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(155): Show |
intron_variant | MODIFIER | c.413+1335_413+1336d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419967 | ||||||
| chr12:419974 | G | A | 5 | a0001c0001t0001g0165 a0001c0001t0001g0207 a0001c0001t0001g0224 others(2): Show |
5 | HG00323.hp2 HG02738.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+1338G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419974 | |||||||
| chr12:419975 | TA | T | 27 | a0001c0001t0001g0165 a0001c0001t0001g0207 a0001c0001t0001g0224 others(24): Show |
27 | HG00323.hp2 HG01074.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.413+1343delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419975 | ||||||
| chr12:419976 | A | AAAACACA others(140): Show |
1 | a0003c0003t0002g0205 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.413+1343_413+1344i others(149): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419976 | ||||||
| chr12:419976 | A | AAACACAC others(212): Show |
7 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(4): Show |
7 | HG01192.hp1 HG01346.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+1342_413+1343i others(221): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419976 | ||||||
| chr12:419976 | AAAATACA others(66): Show |
A | 14 | a0002c0002t0002g0100 a0002c0002t0002g0113 a0002c0002t0013g0361 others(11): Show |
14 | HG00408.hp1 HG00423.hp2 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.413+1344_413+1416d others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419976 | ||||||
| chr12:419977 | AAATACAC others(215): Show |
A | 12 | a0001c0001t0004g0159 a0001c0001t0004g0160 a0001c0001t0004g0317 others(9): Show |
12 | HG01167.hp2 HG01169.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.413+1343_413+1564d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419977 | ||||||
| chr12:419980 | T | C | 104 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(101): Show |
104 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.413+1344T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419980 | |||||||
| chr12:419980 | T | TACACATA others(513): Show |
1 | a0001c0001t0004g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.413+1358_413+1359i others(522): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 419980 | ||||||
| chr12:419995 | A | C | 48 | a0001c0001t0001g0132 a0001c0001t0001g0146 a0001c0001t0001g0166 others(45): Show |
48 | HG00408.hp2 HG00639.hp2 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.413+1359A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419995 | |||||||
| chr12:420003 | T | C | 253 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(250): Show |
259 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(256): Show |
intron_variant | MODIFIER | c.413+1367T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420003 | |||||||
| chr12:420003 | T | CTCCATTA others(438): Show |
1 | a0003c0003t0002g0209 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.413+1366_413+1367i others(447): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420003 | |||||||
| chr12:420003 | TTCCATTA others(66): Show |
T | 1 | a0002c0002t0001g0196 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.413+1440_413+1512d others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420003 | ||||||
| chr12:420003 | TTCCATTA others(732): Show |
T | 3 | a0001c0001t0002g0403 a0003c0003t0002g0368 a0003c0003t0002g0379 |
3 | HG02630.hp1 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.413+1527_413+2265d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420003 | ||||||
| chr12:420017 | A | ACTTCTGT others(67): Show |
5 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0237 others(2): Show |
5 | HG01192.hp2 HG02698.hp2 HG03239.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+1416_413+1417i others(76): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420017 | ||||||
| chr12:420017 | A | T | 19 | a0001c0001t0001g0166 a0001c0001t0001g0178 a0001c0001t0001g0406 others(16): Show |
19 | HG01106.hp1 HG01167.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.413+1381A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420017 | |||||||
| chr12:420021 | CTGTG | C | 6 | a0002c0002t0001g0400 a0002c0002t0002g0145 a0002c0002t0002g0162 others(3): Show |
6 | HG01167.hp1 HG02257.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+1394_413+1397d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420021 | ||||||
| chr12:420048 | G | T | 1 | a0004c0004t0001g0095 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.413+1412G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420048 | |||||||
| chr12:420049 | T | A | 1 | a0004c0004t0001g0095 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.413+1413T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420049 | |||||||
| chr12:420049 | T | TA | 94 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(91): Show |
94 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.413+1416dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420049 | ||||||
| chr12:420049 | T | TAAACACA others(214): Show |
1 | a0003c0003t0001g0287 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.413+1431_413+1432i others(223): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420049 | ||||||
| chr12:420050 | AAACACAC others(65): Show |
A | 56 | a0001c0001t0002g0044 a0001c0001t0002g0051 a0001c0001t0002g0055 others(53): Show |
60 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.413+1417_413+1488d others(74): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420050 | ||||||
| chr12:420053 | C | T | 26 | a0001c0001t0001g0132 a0001c0001t0001g0167 a0001c0001t0001g0191 others(23): Show |
26 | HG00408.hp2 HG00639.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.413+1417C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420053 | |||||||
| chr12:420068 | C | A | 46 | a0001c0001t0001g0147 a0001c0001t0001g0166 a0001c0001t0001g0216 others(43): Show |
46 | HG00735.hp1 HG01106.hp1 HG01106.hp2 others(43): Show |
intron_variant | MODIFIER | c.413+1432C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420068 | |||||||
| chr12:420071 | C | A | 1 | a0001c0001t0004g0399 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.413+1435C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420071 | |||||||
| chr12:420076 | C | CTCCATTA others(67): Show |
1 | a0002c0002t0014g0321 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.413+1453_413+1454i others(76): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420076 | ||||||
| chr12:420076 | C | T | 12 | a0001c0001t0002g0136 a0001c0001t0004g0244 a0001c0001t0004g0323 others(9): Show |
12 | HG01496.hp1 HG02257.hp2 HG02273.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+1440C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420076 | |||||||
| chr12:420090 | A | ACTTCTGT others(67): Show |
1 | a0004c0004t0002g0097 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.413+1489_413+1490i others(76): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420090 | ||||||
| chr12:420090 | A | ACTTCTGT others(66): Show |
2 | a0001c0001t0004g0328 a0003c0003t0007g0412 |
2 | HG01081.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.413+1526_413+1527i others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420090 | ||||||
| chr12:420090 | A | G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0203 a0003c0003t0001g0070 |
3 | HG01261.hp1 HG03710.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.413+1454A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420090 | |||||||
| chr12:420090 | A | T | 92 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(89): Show |
92 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.413+1454A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420090 | |||||||
| chr12:420094 | CTGTG | C | 20 | a0001c0001t0001g0207 a0001c0001t0001g0224 a0001c0001t0001g0274 others(17): Show |
20 | HG00408.hp1 HG00423.hp2 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.413+1467_413+1470d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420094 | ||||||
| chr12:420094 | CTGTGTGT others(220): Show |
C | 2 | a0001c0001t0004g0093 a0001c0001t0004g0397 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.413+1467_413+1693d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420094 | ||||||
| chr12:420094 | CTGTGTGT others(368): Show |
C | 1 | a0002c0002t0001g0186 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.413+1467_413+1841d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420094 | ||||||
| chr12:420094 | CTGTGTGT others(1254): Show |
C | 1 | a0001c0001t0004g0323 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.413+1467_413+2727d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420094 | ||||||
| chr12:420098 | G | GTGTGCTG others(353): Show |
1 | a0001c0001t0001g0165 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.413+1466_413+1467i others(362): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420098 | ||||||
| chr12:420121 | G | T | 1 | a0002c0002t0001g0400 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.413+1485G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420121 | |||||||
| chr12:420122 | T | A | 1 | a0002c0002t0001g0400 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.413+1486T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420122 | |||||||
| chr12:420122 | T | TA | 223 | a0001c0001t0001g0132 a0001c0001t0001g0147 a0001c0001t0001g0165 others(220): Show |
229 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(226): Show |
intron_variant | MODIFIER | c.413+1489dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420122 | ||||||
| chr12:420124 | A | AAT | 3 | a0001c0001t0001g0146 a0001c0001t0001g0203 a0003c0003t0001g0070 |
3 | HG01261.hp1 HG03710.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.413+1489_413+1490i others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420124 | ||||||
| chr12:420124 | AACACACA others(143): Show |
A | 2 | a0001c0001t0002g0013 a0001c0001t0002g0014 |
2 | HG01928.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.413+1527_413+1676d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420124 | ||||||
| chr12:420125 | ACACACAT others(67): Show |
A | 1 | a0002c0002t0001g0290 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.413+1490_413+1563d others(76): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420125 | |||||||
| chr12:420126 | C | CACACATA others(136): Show |
12 | a0001c0001t0001g0156 a0001c0001t0001g0189 a0001c0001t0001g0198 others(9): Show |
12 | HG00597.hp2 HG00609.hp1 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.413+1504_413+1505i others(145): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420126 | ||||||
| chr12:420126 | C | T | 117 | a0001c0001t0001g0132 a0001c0001t0001g0147 a0001c0001t0001g0165 others(114): Show |
121 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.413+1490C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420126 | |||||||
| chr12:420141 | C | A | 128 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(125): Show |
132 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.413+1505C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420141 | |||||||
| chr12:420141 | C | CCTCCATG others(67): Show |
1 | a0001c0001t0001g0408 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.413+1512_413+1513i others(76): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420141 | ||||||
| chr12:420141 | CCTCCATG others(291): Show |
C | 2 | a0001c0001t0010g0277 a0001c0001t0010g0278 |
2 | HG01433.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.413+1513_413+1810d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420141 | ||||||
| chr12:420149 | T | C | 226 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(223): Show |
232 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(229): Show |
intron_variant | MODIFIER | c.413+1513T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420149 | |||||||
| chr12:420163 | A | ACTTCTGT others(140): Show |
1 | a0001c0001t0001g0402 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.413+1562_413+1563i others(149): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420163 | ||||||
| chr12:420163 | A | G | 1 | a0003c0003t0004g0337 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.413+1527A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420163 | |||||||
| chr12:420163 | A | T | 202 | a0001c0001t0001g0166 a0001c0001t0001g0178 a0001c0001t0001g0207 others(199): Show |
210 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.413+1527A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420163 | |||||||
| chr12:420167 | CTGTG | C | 3 | a0001c0001t0001g0166 a0001c0001t0001g0364 a0002c0002t0002g0351 |
3 | HG01106.hp1 HG03239.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.413+1540_413+1543d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420167 | ||||||
| chr12:420171 | G | GTGTGTGT others(62): Show |
22 | a0001c0001t0001g0025 a0001c0001t0001g0108 a0001c0001t0001g0131 others(19): Show |
22 | HG00642.hp1 HG01168.hp2 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.413+1562_413+1563i others(71): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420171 | ||||||
| chr12:420196 | A | AAACACAC others(65): Show |
2 | a0001c0001t0008g0170 a0003c0003t0004g0329 |
2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.413+1562_413+1563i others(74): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420196 | ||||||
| chr12:420197 | AAT | A | 98 | a0001c0001t0001g0024 a0001c0001t0001g0147 a0001c0001t0001g0150 others(95): Show |
102 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.413+1563_413+1564d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420197 | ||||||
| chr12:420197 | AATACACA others(70): Show |
A | 1 | a0001c0001t0002g0136 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.413+1563_413+1639d others(79): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420197 | ||||||
| chr12:420198 | AT | A | 257 | a0001c0001t0001g0025 a0001c0001t0001g0108 a0001c0001t0001g0131 others(254): Show |
265 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.413+1563delT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420198 | |||||||
| chr12:420198 | ATACACAC others(69): Show |
A | 6 | a0001c0001t0001g0207 a0001c0001t0001g0224 a0001c0001t0001g0274 others(3): Show |
6 | HG02738.hp2 HG03017.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+1563_413+1638d others(78): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420198 | |||||||
| chr12:420199 | T | A | 2 | a0001c0001t0008g0170 a0003c0003t0004g0329 |
2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.413+1563T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420199 | |||||||
| chr12:420199 | T | C | 2 | a0001c0001t0001g0223 a0001c0001t0001g0338 |
2 | HG01074.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.413+1563T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420199 | |||||||
| chr12:420201 | C | CACATAGC others(61): Show |
1 | a0001c0001t0001g0223 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.413+1568_413+1569i others(70): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420201 | ||||||
| chr12:420201 | C | CACATAGC others(283): Show |
1 | a0001c0001t0001g0338 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.413+1568_413+1569i others(292): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420201 | ||||||
| chr12:420201 | C | T | 207 | a0001c0001t0001g0025 a0001c0001t0001g0108 a0001c0001t0001g0131 others(204): Show |
213 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.413+1565C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420201 | |||||||
| chr12:420216 | C | A | 200 | a0001c0001t0001g0178 a0001c0001t0001g0396 a0001c0001t0001g0402 others(197): Show |
206 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.413+1580C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420216 | |||||||
| chr12:420216 | CCTCCATG others(216): Show |
C | 7 | a0005c0005t0005g0332 a0005c0005t0005g0410 a0005c0005t0005g0418 others(4): Show |
7 | HG02145.hp1 HG02572.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+1588_413+1810d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420216 | ||||||
| chr12:420224 | T | C | 151 | a0001c0001t0001g0025 a0001c0001t0001g0132 a0001c0001t0001g0143 others(148): Show |
157 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.413+1588T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420224 | |||||||
| chr12:420224 | T | TTCCATTA others(66): Show |
4 | a0003c0003t0001g0250 a0003c0003t0001g0251 a0003c0003t0001g0341 others(1): Show |
4 | HG01106.hp2 HG01884.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+1601_413+1602i others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420224 | ||||||
| chr12:420224 | T | TTCCATTA others(141): Show |
3 | a0003c0003t0007g0327 a0006c0006t0011g0103 a0006c0006t0011g0106 |
3 | HG01891.hp1 HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.413+1601_413+1602i others(150): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420224 | ||||||
| chr12:420238 | A | T | 170 | a0001c0001t0001g0024 a0001c0001t0001g0150 a0001c0001t0001g0164 others(167): Show |
176 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(173): Show |
intron_variant | MODIFIER | c.413+1602A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420238 | |||||||
| chr12:420242 | CTGTG | C | 8 | a0001c0001t0001g0024 a0001c0001t0001g0150 a0001c0001t0001g0164 others(5): Show |
8 | HG00280.hp1 HG00438.hp1 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+1615_413+1618d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420242 | ||||||
| chr12:420242 | CTGTGTGT others(220): Show |
C | 1 | a0002c0002t0001g0196 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.413+1615_413+1841d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420242 | ||||||
| chr12:420270 | T | TA | 6 | a0001c0001t0001g0242 a0001c0001t0001g0375 a0001c0001t0002g0260 others(3): Show |
6 | HG01257.hp2 HG01884.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+1637dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420270 | ||||||
| chr12:420270 | TAAATACA others(69): Show |
T | 1 | a0007c0007t0005g0326 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.413+1638_413+1713d others(78): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420270 | ||||||
| chr12:420272 | AAT | A | 71 | a0001c0001t0001g0338 a0001c0001t0001g0408 a0001c0001t0002g0044 others(68): Show |
75 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.413+1638_413+1639d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420272 | ||||||
| chr12:420273 | AT | A | 282 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(279): Show |
290 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(287): Show |
intron_variant | MODIFIER | c.413+1638delT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420273 | |||||||
| chr12:420274 | T | C | 1 | a0002c0002t0001g0385 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.413+1638T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420274 | |||||||
| chr12:420274 | T | TACACACA others(213): Show |
1 | a0001c0001t0001g0146 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.413+1662_413+1663i others(222): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420274 | ||||||
| chr12:420274 | T | TACACATA others(137): Show |
1 | a0001c0001t0002g0386 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.413+1643_413+1644i others(146): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420274 | ||||||
| chr12:420276 | C | CACACATA others(67): Show |
1 | a0001c0001t0001g0242 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.413+1654_413+1655i others(76): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420276 | ||||||
| chr12:420276 | C | CACACATA others(434): Show |
1 | a0003c0003t0001g0070 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.413+1662_413+1663i others(443): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420276 | ||||||
| chr12:420276 | C | CACATAGC others(65): Show |
2 | a0001c0001t0002g0260 a0003c0003t0009g0168 |
2 | HG03704.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.413+1643_413+1644i others(74): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420276 | ||||||
| chr12:420276 | C | CACATAGC others(506): Show |
1 | a0002c0002t0001g0385 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.413+1643_413+1644i others(515): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420276 | ||||||
| chr12:420276 | C | CACATAGC others(65): Show |
1 | a0001c0001t0001g0375 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.413+1643_413+1644i others(74): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420276 | ||||||
| chr12:420276 | C | T | 228 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(225): Show |
236 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.413+1640C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420276 | |||||||
| chr12:420290 | C | T | 1 | a0001c0001t0003g0230 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.413+1654C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420290 | |||||||
| chr12:420291 | C | A | 183 | a0001c0001t0001g0178 a0001c0001t0001g0207 a0001c0001t0001g0224 others(180): Show |
191 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(188): Show |
intron_variant | MODIFIER | c.413+1655C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420291 | |||||||
| chr12:420299 | T | C | 120 | a0001c0001t0001g0025 a0001c0001t0001g0108 a0001c0001t0001g0131 others(117): Show |
122 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.413+1663T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420299 | |||||||
| chr12:420305 | T | C | 1 | a0002c0002t0001g0306 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.413+1669T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420305 | |||||||
| chr12:420313 | T | A | 105 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(102): Show |
107 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.413+1677T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420313 | |||||||
| chr12:420313 | T | G | 1 | a0001c0001t0001g0242 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.413+1677T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420313 | |||||||
| chr12:420313 | T | TCTTCTGT others(137): Show |
1 | a0002c0002t0001g0208 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.413+1689_413+1690i others(146): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420313 | ||||||
| chr12:420317 | CTGTG | C | 14 | a0001c0001t0004g0159 a0001c0001t0004g0160 a0001c0001t0004g0244 others(11): Show |
14 | HG01167.hp2 HG01169.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.413+1690_413+1693d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420317 | ||||||
| chr12:420337 | TGA | T | 17 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(14): Show |
17 | HG00597.hp1 HG02080.hp1 HG03139.hp2 others(14): Show |
intron_variant | MODIFIER | c.413+1705_413+1706d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420337 | ||||||
| chr12:420345 | TA | T | 176 | a0001c0001t0001g0146 a0001c0001t0001g0178 a0001c0001t0001g0203 others(173): Show |
182 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(179): Show |
intron_variant | MODIFIER | c.413+1713delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420345 | ||||||
| chr12:420346 | A | AAAATACA others(66): Show |
7 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(4): Show |
7 | HG01192.hp1 HG01346.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+1713_413+1714i others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420346 | ||||||
| chr12:420346 | A | AAACACAC others(213): Show |
1 | a0001c0001t0001g0204 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.413+1712_413+1713i others(222): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420346 | ||||||
| chr12:420346 | A | AAACACAC others(508): Show |
1 | a0001c0001t0001g0192 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.413+1712_413+1713i others(517): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420346 | ||||||
| chr12:420346 | A | AAACACAC others(209): Show |
1 | a0001c0001t0001g0406 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.413+1712_413+1713i others(218): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420346 | ||||||
| chr12:420348 | A | ACACACAT others(141): Show |
1 | a0001c0001t0001g0402 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.413+1712_413+1713i others(150): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420348 | |||||||
| chr12:420350 | C | T | 138 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(135): Show |
140 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.413+1714C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420350 | |||||||
| chr12:420365 | C | A | 213 | a0001c0001t0001g0146 a0001c0001t0001g0151 a0001c0001t0001g0178 others(210): Show |
219 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(216): Show |
intron_variant | MODIFIER | c.413+1729C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420365 | |||||||
| chr12:420373 | C | T | 208 | a0001c0001t0001g0178 a0001c0001t0001g0192 a0001c0001t0001g0203 others(205): Show |
214 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(211): Show |
intron_variant | MODIFIER | c.413+1737C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420373 | |||||||
| chr12:420387 | A | G | 1 | a0001c0001t0001g0375 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.413+1751A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420387 | |||||||
| chr12:420387 | A | T | 76 | a0001c0001t0001g0146 a0001c0001t0001g0151 a0001c0001t0001g0207 others(73): Show |
78 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.413+1751A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420387 | |||||||
| chr12:420419 | TA | T | 69 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0203 others(66): Show |
69 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.413+1787delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420419 | ||||||
| chr12:420420 | A | AAACACAC others(65): Show |
1 | a0001c0001t0004g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.413+1786_413+1787i others(74): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420420 | ||||||
| chr12:420420 | A | AAACACAC others(214): Show |
1 | a0001c0001t0004g0328 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.413+1786_413+1787i others(223): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420420 | ||||||
| chr12:420420 | A | AAACACAC others(1095): Show |
1 | a0003c0003t0007g0412 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.413+1786_413+1787i others(1104): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420420 | ||||||
| chr12:420424 | T | C | 254 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0151 others(251): Show |
260 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(257): Show |
intron_variant | MODIFIER | c.413+1788T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420424 | |||||||
| chr12:420424 | T | TACACATA others(212): Show |
2 | a0002c0002t0001g0322 a0004c0004t0001g0085 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.413+1802_413+1803i others(221): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420424 | ||||||
| chr12:420424 | T | TACACATA others(66): Show |
1 | a0002c0002t0001g0401 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.413+1802_413+1803i others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420424 | ||||||
| chr12:420426 | CACATAGC others(139): Show |
C | 1 | a0003c0003t0001g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.413+1794_413+1939d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420426 | ||||||
| chr12:420439 | A | C | 270 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(267): Show |
276 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(273): Show |
intron_variant | MODIFIER | c.413+1803A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420439 | |||||||
| chr12:420439 | A | G | 1 | a0002c0002t0001g0195 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.413+1803A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420439 | |||||||
| chr12:420447 | C | T | 49 | a0001c0001t0001g0146 a0001c0001t0001g0203 a0001c0001t0001g0204 others(46): Show |
51 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.413+1811C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420447 | |||||||
| chr12:420447 | CTCCATTA others(215): Show |
C | 1 | a0002c0002t0001g0290 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.413+1861_413+2082d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420447 | ||||||
| chr12:420461 | A | G | 3 | a0001c0001t0001g0204 a0003c0003t0001g0070 a0003c0003t0004g0337 |
3 | HG00642.hp2 HG02559.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.413+1825A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420461 | |||||||
| chr12:420461 | A | T | 169 | a0001c0001t0001g0178 a0001c0001t0001g0396 a0001c0001t0001g0406 others(166): Show |
175 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(172): Show |
intron_variant | MODIFIER | c.413+1825A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420461 | |||||||
| chr12:420465 | CTGTG | C | 150 | a0001c0001t0001g0178 a0001c0001t0001g0396 a0001c0001t0001g0407 others(147): Show |
156 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(153): Show |
intron_variant | MODIFIER | c.413+1838_413+1841d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420465 | ||||||
| chr12:420493 | TA | T | 44 | a0001c0001t0001g0147 a0001c0001t0001g0192 a0001c0001t0001g0207 others(41): Show |
44 | HG00735.hp1 HG01071.hp1 HG01167.hp2 others(41): Show |
intron_variant | MODIFIER | c.413+1861delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420493 | ||||||
| chr12:420494 | A | AAAACACA others(287): Show |
2 | a0002c0002t0001g0322 a0004c0004t0001g0085 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.413+1861_413+1862i others(296): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420494 | ||||||
| chr12:420494 | A | AAACACAC others(139): Show |
1 | a0001c0001t0001g0408 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.413+1860_413+1861i others(148): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420494 | ||||||
| chr12:420494 | A | AAACACAC others(139): Show |
1 | a0002c0002t0014g0321 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.413+1860_413+1861i others(148): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420494 | ||||||
| chr12:420498 | T | C | 157 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0192 others(154): Show |
160 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(157): Show |
intron_variant | MODIFIER | c.413+1862T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420498 | |||||||
| chr12:420498 | T | TACACACA others(219): Show |
1 | a0001c0001t0001g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.413+1867_413+1868i others(228): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420498 | ||||||
| chr12:420498 | T | TACACATA others(139): Show |
1 | a0001c0001t0002g0325 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.413+1876_413+1877i others(148): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420498 | ||||||
| chr12:420513 | C | A | 173 | a0001c0001t0001g0178 a0001c0001t0001g0396 a0001c0001t0001g0407 others(170): Show |
181 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(178): Show |
intron_variant | MODIFIER | c.413+1877C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420513 | |||||||
| chr12:420513 | C | CCTCCATG others(430): Show |
1 | a0002c0002t0001g0387 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.413+1884_413+1885i others(439): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420513 | ||||||
| chr12:420520 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.413+1884G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420520 | |||||||
| chr12:420521 | C | T | 190 | a0001c0001t0001g0146 a0001c0001t0001g0178 a0001c0001t0001g0192 others(187): Show |
198 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(195): Show |
intron_variant | MODIFIER | c.413+1885C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420521 | |||||||
| chr12:420535 | T | A | 97 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(94): Show |
99 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.413+1899T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420535 | |||||||
| chr12:420535 | T | G | 1 | a0001c0001t0001g0402 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.413+1899T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420535 | |||||||
| chr12:420535 | T | TCTTCTGT others(358): Show |
1 | a0004c0004t0002g0097 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.413+1972_413+1973i others(367): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420535 | ||||||
| chr12:420535 | T | TCTTCTGT others(214): Show |
2 | a0001c0001t0008g0170 a0003c0003t0004g0329 |
2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.413+1950_413+1951i others(223): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420535 | ||||||
| chr12:420539 | CTGTG | C | 34 | a0001c0001t0001g0207 a0001c0001t0001g0224 a0001c0001t0001g0274 others(31): Show |
34 | HG00408.hp1 HG00423.hp2 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.413+1912_413+1915d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420539 | ||||||
| chr12:420539 | CTGTGTGT others(71): Show |
C | 4 | a0002c0002t0002g0145 a0002c0002t0002g0162 a0002c0002t0002g0349 others(1): Show |
4 | NA18967.hp2 NA19012.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+1912_413+1989d others(80): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420539 | ||||||
| chr12:420552 | C | G | 1 | a0001c0001t0002g0293 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.413+1916C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420552 | |||||||
| chr12:420567 | TA | T | 18 | a0001c0001t0001g0146 a0001c0001t0001g0150 a0001c0001t0001g0203 others(15): Show |
20 | HG00280.hp1 HG00735.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.413+1935delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420567 | ||||||
| chr12:420568 | A | AAAACACA others(66): Show |
6 | a0001c0001t0001g0281 a0002c0002t0001g0385 a0003c0003t0001g0094 others(3): Show |
6 | HG01346.hp2 HG02486.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+1935_413+1936i others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420568 | ||||||
| chr12:420568 | A | AAACACAC others(65): Show |
1 | a0001c0001t0004g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.413+1934_413+1935i others(74): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420568 | ||||||
| chr12:420568 | A | AAACACAC others(287): Show |
2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG00639.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.413+1934_413+1935i others(296): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420568 | ||||||
| chr12:420568 | A | AAACACAC others(284): Show |
1 | a0001c0001t0004g0328 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.413+1934_413+1935i others(293): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420568 | ||||||
| chr12:420568 | A | AAATACAC others(141): Show |
1 | a0003c0003t0001g0413 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.413+1934_413+1935i others(150): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420568 | ||||||
| chr12:420572 | T | C | 200 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0150 others(197): Show |
208 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.413+1936T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420572 | |||||||
| chr12:420572 | T | TACACATA others(141): Show |
2 | a0001c0001t0001g0156 a0001c0001t0001g0292 |
2 | NA19056.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.413+1950_413+1951i others(150): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420572 | ||||||
| chr12:420572 | T | TACACATA others(68): Show |
1 | a0001c0001t0001g0242 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.413+1950_413+1951i others(77): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420572 | ||||||
| chr12:420572 | TACACATA others(140): Show |
T | 2 | a0001c0001t0004g0399 a0005c0005t0005g0416 |
2 | HG01884.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.413+1951_413+2097d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420572 | ||||||
| chr12:420587 | A | C | 122 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(119): Show |
124 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.413+1951A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420587 | |||||||
| chr12:420595 | T | C | 243 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(240): Show |
251 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.413+1959T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420595 | |||||||
| chr12:420595 | T | TTCCATTA others(800): Show |
1 | a0003c0003t0004g0363 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.413+2009_413+2010i others(809): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420595 | ||||||
| chr12:420609 | A | ACTTCTGT others(140): Show |
1 | a0003c0003t0007g0412 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.413+2008_413+2009i others(149): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420609 | ||||||
| chr12:420609 | A | G | 3 | a0001c0001t0001g0192 a0001c0001t0001g0211 a0001c0001t0001g0212 |
3 | HG00639.hp2 HG01071.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.413+1973A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420609 | |||||||
| chr12:420609 | A | T | 51 | a0001c0001t0001g0151 a0001c0001t0001g0203 a0001c0001t0001g0241 others(48): Show |
51 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.413+1973A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420609 | |||||||
| chr12:420613 | CTGTG | C | 3 | a0001c0001t0001g0406 a0001c0001t0001g0408 a0002c0002t0001g0400 |
3 | HG01168.hp1 HG01261.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.413+1986_413+1989d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420613 | ||||||
| chr12:420641 | TA | T | 10 | a0001c0001t0001g0146 a0001c0001t0001g0204 a0001c0001t0001g0206 others(7): Show |
11 | HG00642.hp2 HG00735.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.413+2009delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420641 | ||||||
| chr12:420642 | A | AAACACAC others(65): Show |
1 | a0001c0001t0002g0260 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.413+2008_413+2009i others(74): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420642 | ||||||
| chr12:420642 | A | AAACACAC others(288): Show |
1 | a0003c0003t0004g0337 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.413+2008_413+2009i others(297): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420642 | ||||||
| chr12:420642 | AAAATACA others(66): Show |
A | 13 | a0002c0002t0002g0100 a0002c0002t0002g0113 a0002c0002t0013g0361 others(10): Show |
13 | HG00408.hp1 HG00423.hp2 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.413+2010_413+2082d others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420642 | ||||||
| chr12:420644 | A | ACACACAT others(67): Show |
7 | a0001c0001t0001g0132 a0001c0001t0001g0307 a0003c0003t0002g0213 others(4): Show |
7 | HG00408.hp2 NA18950.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+2008_413+2009i others(76): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420644 | |||||||
| chr12:420644 | A | AT | 8 | a0001c0001t0001g0156 a0001c0001t0001g0167 a0001c0001t0001g0191 others(5): Show |
8 | HG00639.hp2 HG01071.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+2008_413+2009i others(3): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420644 | |||||||
| chr12:420646 | T | C | 184 | a0001c0001t0001g0132 a0001c0001t0001g0146 a0001c0001t0001g0156 others(181): Show |
191 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(188): Show |
intron_variant | MODIFIER | c.413+2010T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420646 | |||||||
| chr12:420646 | TACACATA others(68): Show |
T | 1 | a0008c0013t0004g0417 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.413+2014_413+2088d others(77): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420646 | ||||||
| chr12:420646 | TACACATA others(139): Show |
T | 1 | a0001c0001t0001g0224 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.413+2025_413+2170d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420646 | ||||||
| chr12:420646 | TACACATA others(286): Show |
T | 1 | a0001c0001t0001g0376 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.413+2025_413+2317d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420646 | ||||||
| chr12:420646 | TACACATA others(876): Show |
T | 15 | a0001c0001t0004g0093 a0001c0001t0004g0159 a0001c0001t0004g0160 others(12): Show |
15 | HG01167.hp2 HG01169.hp1 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.413+2016_413+2898d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420646 | ||||||
| chr12:420652 | TAGC | T | 49 | a0001c0001t0002g0004 a0001c0001t0002g0041 a0001c0001t0002g0074 others(46): Show |
52 | HG00609.hp2 HG00738.hp1 HG01496.hp2 others(49): Show |
intron_variant | MODIFIER | c.413+2021_413+2023d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420652 | ||||||
| chr12:420661 | A | C | 246 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(243): Show |
253 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.413+2025A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420661 | |||||||
| chr12:420669 | T | C | 219 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(216): Show |
226 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.413+2033T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420669 | |||||||
| chr12:420669 | TTCCATTA others(66): Show |
T | 62 | a0001c0001t0002g0044 a0001c0001t0002g0051 a0001c0001t0002g0055 others(59): Show |
66 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.413+2179_413+2251d others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420669 | ||||||
| chr12:420669 | TTCCATTA others(139): Show |
T | 1 | a0001c0001t0002g0336 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.413+2106_413+2251d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420669 | ||||||
| chr12:420683 | A | G | 2 | a0001c0001t0001g0146 a0003c0003t0002g0209 |
2 | HG03710.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.413+2047A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420683 | |||||||
| chr12:420683 | A | T | 190 | a0001c0001t0001g0151 a0001c0001t0001g0178 a0001c0001t0001g0204 others(187): Show |
197 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(194): Show |
intron_variant | MODIFIER | c.413+2047A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420683 | |||||||
| chr12:420701 | T | C | 8 | a0001c0001t0006g0012 a0001c0001t0006g0388 a0001c0001t0006g0389 others(5): Show |
8 | HG00735.hp1 HG02155.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+2065T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420701 | |||||||
| chr12:420715 | T | TA | 68 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(65): Show |
68 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(65): Show |
intron_variant | MODIFIER | c.413+2082dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420715 | ||||||
| chr12:420715 | T | TAAAATAC others(68): Show |
1 | a0001c0001t0001g0223 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.413+2082_413+2083i others(77): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420715 | ||||||
| chr12:420717 | A | AAT | 14 | a0001c0001t0001g0132 a0001c0001t0001g0156 a0001c0001t0001g0167 others(11): Show |
14 | HG00408.hp2 HG00639.hp2 HG01943.hp1 others(11): Show |
intron_variant | MODIFIER | c.413+2082_413+2083i others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420717 | ||||||
| chr12:420717 | A | AATACACA others(512): Show |
1 | a0001c0001t0001g0192 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.413+2082_413+2083i others(521): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420717 | ||||||
| chr12:420719 | C | T | 59 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(56): Show |
59 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.413+2083C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420719 | |||||||
| chr12:420734 | C | A | 37 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0178 others(34): Show |
37 | HG00597.hp1 HG01106.hp2 HG01192.hp1 others(34): Show |
intron_variant | MODIFIER | c.413+2098C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420734 | |||||||
| chr12:420734 | C | CCTCCATG others(67): Show |
5 | a0001c0001t0008g0170 a0003c0003t0004g0329 a0003c0003t0007g0327 others(2): Show |
5 | HG01891.hp1 HG02145.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+2105_413+2106i others(76): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420734 | ||||||
| chr12:420742 | C | CTCCATTA others(67): Show |
1 | a0003c0003t0002g0209 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.413+2155_413+2156i others(76): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420742 | ||||||
| chr12:420742 | C | CTCCATTA others(732): Show |
1 | a0003c0003t0009g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.413+2119_413+2120i others(741): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420742 | ||||||
| chr12:420742 | C | CTCCATTA others(67): Show |
1 | a0001c0001t0006g0390 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.413+2119_413+2120i others(76): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420742 | ||||||
| chr12:420742 | C | T | 58 | a0001c0001t0001g0132 a0001c0001t0001g0151 a0001c0001t0001g0203 others(55): Show |
59 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.413+2106C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420742 | |||||||
| chr12:420756 | A | G | 2 | a0001c0001t0001g0338 a0003c0003t0004g0337 |
2 | HG01074.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.413+2120A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420756 | |||||||
| chr12:420756 | A | T | 13 | a0001c0001t0001g0178 a0001c0001t0001g0203 a0001c0001t0002g0010 others(10): Show |
15 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.413+2120A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420756 | |||||||
| chr12:420756 | ACTTCTGT others(658): Show |
A | 6 | a0005c0005t0005g0332 a0005c0005t0005g0410 a0005c0005t0005g0418 others(3): Show |
6 | HG02145.hp1 HG02572.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+2179_413+2843d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420756 | ||||||
| chr12:420774 | T | C | 1 | a0001c0001t0006g0390 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.413+2138T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420774 | |||||||
| chr12:420788 | T | TA | 234 | a0001c0001t0001g0131 a0001c0001t0001g0146 a0001c0001t0001g0150 others(231): Show |
242 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.413+2155dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420788 | ||||||
| chr12:420788 | T | TAAAACAC others(64): Show |
1 | a0001c0001t0001g0407 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.413+2155_413+2156i others(73): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420788 | ||||||
| chr12:420788 | T | TAAAACAC others(141): Show |
1 | a0001c0001t0001g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.413+2155_413+2156i others(150): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420788 | ||||||
| chr12:420788 | T | TAAAATAC others(143): Show |
1 | a0002c0002t0001g0401 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.413+2155_413+2156i others(152): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420788 | ||||||
| chr12:420789 | AAACACAC others(65): Show |
A | 2 | a0001c0001t0010g0277 a0001c0001t0010g0278 |
2 | HG01433.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.413+2156_413+2227d others(74): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420789 | ||||||
| chr12:420790 | A | AAAT | 3 | a0001c0001t0001g0406 a0001c0001t0001g0408 a0003c0003t0004g0337 |
3 | HG01168.hp1 HG01261.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.413+2155_413+2156i others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420790 | ||||||
| chr12:420790 | A | AAT | 11 | a0001c0001t0001g0132 a0001c0001t0001g0211 a0001c0001t0001g0212 others(8): Show |
11 | HG00408.hp2 HG00639.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.413+2155_413+2156i others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420790 | ||||||
| chr12:420792 | C | CACACATA others(67): Show |
1 | a0003c0003t0001g0019 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.413+2228_413+2229i others(76): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420792 | ||||||
| chr12:420792 | C | T | 205 | a0001c0001t0001g0131 a0001c0001t0001g0146 a0001c0001t0001g0150 others(202): Show |
212 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.413+2156C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420792 | |||||||
| chr12:420807 | C | A | 20 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(17): Show |
21 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.413+2171C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420807 | |||||||
| chr12:420815 | C | CTCCATTA others(68): Show |
1 | a0001c0001t0001g0164 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.413+2192_413+2193i others(77): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420815 | ||||||
| chr12:420815 | C | CTCCATTA others(732): Show |
1 | a0003c0003t0001g0062 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.413+2192_413+2193i others(741): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420815 | ||||||
| chr12:420815 | C | CTCCATTA others(732): Show |
7 | a0001c0001t0001g0024 a0001c0001t0001g0108 a0001c0001t0001g0155 others(4): Show |
7 | HG00438.hp1 HG00609.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+2192_413+2193i others(741): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420815 | ||||||
| chr12:420815 | C | CTCCATTA others(732): Show |
1 | a0001c0001t0001g0025 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.413+2192_413+2193i others(741): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420815 | ||||||
| chr12:420815 | C | T | 19 | a0001c0001t0001g0146 a0001c0001t0001g0156 a0001c0001t0001g0167 others(16): Show |
19 | HG00642.hp2 HG01074.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.413+2179C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420815 | |||||||
| chr12:420829 | A | ACTTCTGT others(137): Show |
2 | a0001c0001t0001g0178 a0001c0001t0009g0289 |
2 | HG02717.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.413+2228_413+2229i others(146): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420829 | ||||||
| chr12:420829 | A | ACTTCTGT others(66): Show |
1 | a0003c0003t0007g0412 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.413+2229_413+2301d others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420829 | ||||||
| chr12:420829 | A | G | 13 | a0001c0001t0001g0143 a0001c0001t0001g0165 a0001c0001t0001g0198 others(10): Show |
13 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.413+2193A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420829 | |||||||
| chr12:420829 | A | T | 31 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(28): Show |
32 | HG00597.hp1 HG01069.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.413+2193A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420829 | |||||||
| chr12:420829 | ACTTCTGT others(66): Show |
A | 1 | a0001c0001t0001g0274 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.413+2229_413+2301d others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420829 | ||||||
| chr12:420833 | CTGTG | C | 19 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(16): Show |
19 | HG00597.hp1 HG02080.hp1 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.413+2206_413+2209d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420833 | ||||||
| chr12:420861 | T | TA | 206 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0202 others(203): Show |
213 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.413+2228dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420861 | ||||||
| chr12:420861 | T | TAAAATAC others(572): Show |
2 | a0001c0001t0001g0406 a0001c0001t0001g0408 |
2 | HG01168.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.413+2228_413+2229i others(581): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420861 | ||||||
| chr12:420861 | T | TAAAATAC others(68): Show |
1 | a0001c0001t0001g0375 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.413+2228_413+2229i others(77): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420861 | ||||||
| chr12:420861 | TAAACACA others(67): Show |
T | 1 | a0002c0002t0001g0291 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.413+2252_413+2325d others(76): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420861 | ||||||
| chr12:420863 | A | AAATACAC others(217): Show |
1 | a0003c0003t0002g0205 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.413+2228_413+2229i others(226): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420863 | ||||||
| chr12:420863 | A | AAATACAC others(1325): Show |
1 | a0001c0001t0001g0204 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.413+2228_413+2229i others(1334): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420863 | ||||||
| chr12:420863 | A | AACACACA others(142): Show |
1 | a0001c0001t0004g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.413+2243_413+2244i others(151): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420863 | ||||||
| chr12:420863 | A | AAT | 9 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0001g0198 others(6): Show |
10 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.413+2228_413+2229i others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420863 | ||||||
| chr12:420863 | A | AATACACA others(70): Show |
8 | a0001c0001t0001g0165 a0001c0001t0001g0210 a0001c0001t0001g0236 others(5): Show |
8 | HG00323.hp2 HG00597.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.413+2228_413+2229i others(79): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420863 | ||||||
| chr12:420863 | A | AATACACA others(70): Show |
1 | a0001c0001t0002g0325 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.413+2228_413+2229i others(79): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420863 | ||||||
| chr12:420865 | C | CACACATA others(732): Show |
1 | a0001c0001t0001g0402 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.413+2243_413+2244i others(741): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420865 | ||||||
| chr12:420865 | C | CACACATA others(3099): Show |
1 | a0001c0001t0001g0219 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.413+2251_413+2252i others(3108): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420865 | ||||||
| chr12:420865 | C | T | 203 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0202 others(200): Show |
210 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.413+2229C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420865 | |||||||
| chr12:420880 | C | A | 46 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(43): Show |
48 | HG00438.hp1 HG00597.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.413+2244C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420880 | |||||||
| chr12:420888 | T | C | 66 | a0001c0001t0001g0131 a0001c0001t0001g0146 a0001c0001t0001g0147 others(63): Show |
67 | HG00280.hp1 HG00735.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.413+2252T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420888 | |||||||
| chr12:420888 | T | TTCCATTA others(2420): Show |
1 | a0003c0003t0007g0327 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.413+2301_413+2302i others(2429): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420888 | ||||||
| chr12:420902 | T | A | 62 | a0001c0001t0001g0132 a0001c0001t0001g0143 a0001c0001t0001g0146 others(59): Show |
63 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.413+2266T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420902 | |||||||
| chr12:420902 | T | G | 28 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(25): Show |
29 | HG00438.hp1 HG00609.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.413+2266T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420902 | |||||||
| chr12:420902 | T | TCTTCTGT others(2419): Show |
1 | a0006c0006t0011g0103 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.413+2301_413+2302i others(2428): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420902 | ||||||
| chr12:420934 | TA | T | 20 | a0001c0001t0001g0132 a0001c0001t0001g0192 a0001c0001t0001g0202 others(17): Show |
21 | HG00408.hp2 HG00639.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.413+2302delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420934 | ||||||
| chr12:420935 | A | AAAATACA others(650): Show |
2 | a0003c0003t0001g0250 a0003c0003t0001g0342 |
2 | HG01106.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.413+2302_413+2303i others(659): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420935 | ||||||
| chr12:420935 | A | AAAATACA others(797): Show |
2 | a0003c0003t0001g0251 a0003c0003t0001g0341 |
2 | HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.413+2302_413+2303i others(806): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420935 | ||||||
| chr12:420937 | A | AAT | 16 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(13): Show |
16 | HG00438.hp1 HG00609.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.413+2302_413+2303i others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420937 | ||||||
| chr12:420937 | A | ACACACAT others(955): Show |
1 | a0001c0001t0001g0216 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.413+2301_413+2302i others(964): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420937 | |||||||
| chr12:420937 | A | ACACACAT others(1248): Show |
1 | a0001c0001t0001g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.413+2301_413+2302i others(1257): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420937 | |||||||
| chr12:420937 | A | ACACACAT others(732): Show |
1 | a0003c0003t0002g0209 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.413+2301_413+2302i others(741): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420937 | |||||||
| chr12:420937 | A | AT | 17 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0001g0165 others(14): Show |
18 | HG00323.hp2 HG00597.hp2 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.413+2301_413+2302i others(3): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420937 | |||||||
| chr12:420937 | A | ATACACAC others(69): Show |
2 | a0001c0001t0001g0200 a0003c0003t0001g0140 |
2 | NA18965.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.413+2301_413+2302i others(78): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420937 | |||||||
| chr12:420937 | A | ATACACAC others(732): Show |
3 | a0001c0001t0001g0201 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | NA18971.hp2 NA19060.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.413+2301_413+2302i others(741): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420937 | |||||||
| chr12:420937 | A | ATACACAC others(807): Show |
7 | a0001c0001t0001g0152 a0001c0001t0001g0217 a0001c0001t0001g0218 others(4): Show |
7 | HG01168.hp2 HG01169.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.413+2301_413+2302i others(816): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420937 | |||||||
| chr12:420937 | A | ATACACAC others(1768): Show |
1 | a0001c0001t0001g0131 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.413+2301_413+2302i others(1777): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420937 | |||||||
| chr12:420937 | A | ATACACAC others(1916): Show |
1 | a0001c0001t0001g0238 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.413+2301_413+2302i others(1925): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420937 | |||||||
| chr12:420937 | A | ATACACAC others(807): Show |
1 | a0001c0001t0001g0153 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.413+2301_413+2302i others(816): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420937 | |||||||
| chr12:420937 | A | ATACACAC others(883): Show |
1 | a0001c0001t0001g0146 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.413+2301_413+2302i others(892): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420937 | |||||||
| chr12:420937 | AAC | A | 169 | a0001c0001t0001g0396 a0001c0001t0002g0004 a0001c0001t0002g0041 others(166): Show |
175 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.413+2307_413+2308d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420937 | ||||||
| chr12:420939 | C | CACACATA others(655): Show |
1 | a0001c0001t0001g0156 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.413+2325_413+2326i others(664): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420939 | ||||||
| chr12:420939 | C | T | 28 | a0001c0001t0001g0150 a0001c0001t0001g0204 a0001c0001t0001g0207 others(25): Show |
28 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.413+2303C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420939 | |||||||
| chr12:420941 | C | T | 169 | a0001c0001t0001g0396 a0001c0001t0002g0004 a0001c0001t0002g0041 others(166): Show |
175 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.413+2305C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420941 | |||||||
| chr12:420954 | C | A | 26 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(23): Show |
27 | HG00597.hp1 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.413+2318C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420954 | |||||||
| chr12:420954 | C | CCTCCATG others(66): Show |
2 | a0001c0001t0001g0245 a0002c0002t0001g0385 |
2 | HG02723.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.413+2325_413+2326i others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420954 | ||||||
| chr12:420954 | C | CCTCCATG others(3013): Show |
1 | a0003c0003t0004g0329 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.413+2325_413+2326i others(3022): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420954 | ||||||
| chr12:420954 | C | CCTCCATG others(61): Show |
1 | a0001c0001t0001g0292 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.413+2325_413+2326i others(70): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420954 | ||||||
| chr12:420961 | G | A | 1 | a0003c0003t0001g0019 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.413+2325G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420961 | |||||||
| chr12:420962 | C | T | 48 | a0001c0001t0001g0132 a0001c0001t0001g0143 a0001c0001t0001g0147 others(45): Show |
49 | HG00408.hp2 HG00639.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.413+2326C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420962 | |||||||
| chr12:420976 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.413+2340A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420976 | |||||||
| chr12:420976 | A | T | 11 | a0001c0001t0001g0167 a0001c0001t0001g0191 a0001c0001t0001g0204 others(8): Show |
12 | HG00323.hp1 HG00642.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+2340A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420976 | |||||||
| chr12:420976 | ACTTCTGT others(438): Show |
A | 17 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(14): Show |
17 | HG00597.hp1 HG02080.hp1 HG03139.hp2 others(14): Show |
intron_variant | MODIFIER | c.413+2376_413+2820d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 420976 | ||||||
| chr12:421008 | TA | T | 36 | a0001c0001t0001g0131 a0001c0001t0001g0143 a0001c0001t0001g0146 others(33): Show |
36 | HG00597.hp2 HG01071.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.413+2376delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421008 | ||||||
| chr12:421009 | A | AAACACAC others(65): Show |
6 | a0001c0001t0001g0281 a0003c0003t0001g0094 a0003c0003t0001g0287 others(3): Show |
6 | HG01346.hp2 HG02486.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+2375_413+2376i others(74): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421009 | ||||||
| chr12:421009 | A | AAACACAC others(139): Show |
2 | a0002c0002t0001g0322 a0004c0004t0001g0085 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.413+2375_413+2376i others(148): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421009 | ||||||
| chr12:421009 | A | AAACACAC others(139): Show |
2 | a0001c0001t0008g0170 a0006c0006t0011g0106 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.413+2375_413+2376i others(148): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421009 | ||||||
| chr12:421009 | A | AAATACAC others(1837): Show |
1 | a0001c0001t0001g0198 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.413+2375_413+2376i others(1846): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421009 | ||||||
| chr12:421009 | AAAATACA others(66): Show |
A | 8 | a0001c0001t0006g0012 a0001c0001t0006g0388 a0001c0001t0006g0389 others(5): Show |
8 | HG00735.hp1 HG02155.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+2377_413+2449d others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421009 | ||||||
| chr12:421011 | A | AT | 4 | a0001c0001t0001g0220 a0001c0001t0001g0405 a0003c0003t0001g0019 others(1): Show |
4 | HG00642.hp1 HG02451.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+2375_413+2376i others(3): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421011 | |||||||
| chr12:421013 | T | C | 65 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0143 others(62): Show |
65 | HG00408.hp2 HG00597.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.413+2377T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421013 | |||||||
| chr12:421013 | T | TACACATA others(69): Show |
1 | a0001c0001t0001g0165 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.413+2399_413+2400i others(78): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421013 | ||||||
| chr12:421013 | T | TACACATA others(660): Show |
1 | a0003c0003t0001g0070 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.413+2391_413+2392i others(669): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421013 | ||||||
| chr12:421013 | TACACATA others(437): Show |
T | 1 | a0001c0001t0003g0042 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.413+2392_413+2835d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421013 | ||||||
| chr12:421028 | A | ACTCCATG others(288): Show |
1 | a0003c0003t0009g0168 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.413+2449_413+2450i others(297): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421028 | ||||||
| chr12:421028 | A | C | 265 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(262): Show |
271 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.413+2392A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421028 | |||||||
| chr12:421036 | C | CTCCATTA others(950): Show |
1 | a0003c0003t0001g0140 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.413+2422_413+2423i others(959): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421036 | ||||||
| chr12:421036 | C | T | 62 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(59): Show |
63 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.413+2400C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421036 | |||||||
| chr12:421050 | A | G | 3 | a0001c0001t0001g0192 a0001c0001t0001g0407 a0003c0003t0001g0063 |
3 | HG01071.hp1 HG02602.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.413+2414A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421050 | |||||||
| chr12:421050 | A | T | 198 | a0001c0001t0001g0132 a0001c0001t0001g0165 a0001c0001t0001g0167 others(195): Show |
206 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.413+2414A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421050 | |||||||
| chr12:421082 | T | TA | 27 | a0001c0001t0001g0156 a0001c0001t0001g0204 a0001c0001t0001g0219 others(24): Show |
27 | HG00642.hp2 HG01243.hp1 HG01928.hp1 others(24): Show |
intron_variant | MODIFIER | c.413+2449dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421082 | ||||||
| chr12:421083 | AAACACAC others(363): Show |
A | 47 | a0001c0001t0002g0004 a0001c0001t0002g0041 a0001c0001t0002g0074 others(44): Show |
50 | HG00609.hp2 HG00738.hp1 HG01496.hp2 others(47): Show |
intron_variant | MODIFIER | c.413+2450_413+2819d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421083 | ||||||
| chr12:421084 | A | AACACACA others(573): Show |
2 | a0001c0001t0001g0178 a0001c0001t0009g0289 |
2 | HG02717.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.413+2486_413+2487i others(582): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421084 | ||||||
| chr12:421084 | A | AAT | 4 | a0001c0001t0002g0011 a0001c0001t0002g0325 a0001c0001t0002g0347 others(1): Show |
5 | HG00735.hp2 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.413+2449_413+2450i others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421084 | ||||||
| chr12:421084 | A | AATACACA others(574): Show |
1 | a0001c0001t0001g0407 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.413+2449_413+2450i others(583): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421084 | ||||||
| chr12:421085 | ACACACAT others(216): Show |
A | 118 | a0001c0001t0001g0207 a0001c0001t0001g0396 a0001c0001t0002g0049 others(115): Show |
121 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.413+2450_413+2672d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421085 | |||||||
| chr12:421086 | C | CACACATA others(67): Show |
1 | a0001c0001t0004g0328 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.413+2472_413+2473i others(76): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421086 | ||||||
| chr12:421086 | C | T | 22 | a0001c0001t0001g0156 a0001c0001t0001g0192 a0001c0001t0001g0204 others(19): Show |
22 | HG00642.hp2 HG01071.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.413+2450C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421086 | |||||||
| chr12:421088 | C | CACATAGC others(65): Show |
1 | a0004c0004t0002g0097 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.413+2472_413+2473i others(74): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421088 | ||||||
| chr12:421101 | C | A | 24 | a0001c0001t0001g0132 a0001c0001t0001g0147 a0001c0001t0001g0192 others(21): Show |
25 | HG00408.hp2 HG00639.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.413+2465C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421101 | |||||||
| chr12:421109 | C | T | 61 | a0001c0001t0001g0131 a0001c0001t0001g0143 a0001c0001t0001g0146 others(58): Show |
62 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.413+2473C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421109 | |||||||
| chr12:421109 | CTCCATTA others(217): Show |
C | 2 | a0003c0003t0001g0148 a0005c0005t0005g0416 |
2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.413+2487_413+2710d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421109 | ||||||
| chr12:421109 | CTCCATTA others(291): Show |
C | 3 | a0001c0001t0004g0399 a0001c0001t0010g0277 a0001c0001t0010g0278 |
3 | HG01433.hp1 HG01884.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.413+2523_413+2820d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421109 | ||||||
| chr12:421123 | T | A | 82 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(79): Show |
83 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.413+2487T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421123 | |||||||
| chr12:421123 | T | G | 8 | a0001c0001t0001g0150 a0001c0001t0001g0192 a0001c0001t0001g0202 others(5): Show |
9 | HG00280.hp1 HG00735.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.413+2487T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421123 | |||||||
| chr12:421123 | TCTTCTGT others(142): Show |
T | 3 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0039 |
3 | NA18953.hp1 NA18995.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.413+2523_413+2671d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421123 | ||||||
| chr12:421155 | TA | T | 17 | a0001c0001t0001g0156 a0001c0001t0001g0223 a0001c0001t0001g0245 others(14): Show |
18 | HG01069.hp2 HG01071.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.413+2523delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421155 | ||||||
| chr12:421156 | A | AAACACAC others(289): Show |
1 | a0001c0001t0001g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.413+2522_413+2523i others(298): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421156 | ||||||
| chr12:421156 | A | AAACACAC others(1543): Show |
1 | a0001c0001t0001g0191 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.413+2522_413+2523i others(1552): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421156 | ||||||
| chr12:421158 | A | AAC | 3 | a0001c0001t0008g0170 a0003c0003t0007g0412 a0006c0006t0011g0106 |
3 | HG01243.hp1 HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.413+2523_413+2524i others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421158 | ||||||
| chr12:421158 | A | AT | 32 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(29): Show |
33 | HG00280.hp1 HG00438.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.413+2522_413+2523i others(3): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421158 | |||||||
| chr12:421160 | T | C | 90 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(87): Show |
92 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.413+2524T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421160 | |||||||
| chr12:421160 | T | TACACATA others(140): Show |
1 | a0001c0001t0004g0328 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.413+2538_413+2539i others(149): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421160 | ||||||
| chr12:421160 | TACACATA others(68): Show |
T | 1 | a0001c0001t0001g0224 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.413+2547_413+2621d others(77): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421160 | ||||||
| chr12:421160 | TACACATA others(143): Show |
T | 1 | a0005c0005t0005g0409 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.413+2547_413+2696d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421160 | ||||||
| chr12:421160 | TACACATA others(290): Show |
T | 1 | a0007c0007t0005g0197 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.413+2539_413+2835d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421160 | ||||||
| chr12:421175 | A | C | 97 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(94): Show |
98 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.413+2539A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421175 | |||||||
| chr12:421182 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.413+2546G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421182 | |||||||
| chr12:421183 | C | T | 76 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(73): Show |
78 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.413+2547C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421183 | |||||||
| chr12:421197 | T | A | 56 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0146 others(53): Show |
57 | HG00280.hp1 HG00408.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.413+2561T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421197 | |||||||
| chr12:421197 | T | G | 6 | a0001c0001t0001g0156 a0001c0001t0001g0223 a0001c0001t0001g0406 others(3): Show |
6 | HG01081.hp2 HG01168.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+2561T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421197 | |||||||
| chr12:421201 | C | G | 9 | a0001c0001t0006g0012 a0001c0001t0006g0388 a0001c0001t0006g0389 others(6): Show |
9 | HG00735.hp1 HG02155.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+2565C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421201 | |||||||
| chr12:421211 | G | T | 2 | a0001c0001t0002g0013 a0001c0001t0002g0014 |
2 | HG01928.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.413+2575G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421211 | |||||||
| chr12:421229 | T | TA | 10 | a0001c0001t0001g0132 a0001c0001t0001g0211 a0001c0001t0001g0212 others(7): Show |
10 | HG00408.hp2 HG00639.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+2596dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421229 | ||||||
| chr12:421229 | T | TAAAACAC others(1475): Show |
1 | a0001c0001t0001g0364 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.413+2596_413+2597i others(1484): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421229 | ||||||
| chr12:421230 | A | AAAACACA others(434): Show |
1 | a0002c0002t0014g0321 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.413+2596_413+2597i others(443): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421230 | ||||||
| chr12:421230 | A | AAAACACA others(730): Show |
1 | a0001c0001t0001g0362 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.413+2596_413+2597i others(739): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421230 | ||||||
| chr12:421230 | AAATACAC others(216): Show |
A | 1 | a0002c0002t0001g0291 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.413+2597_413+2819d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421230 | ||||||
| chr12:421231 | A | AACACACA others(649): Show |
1 | a0001c0001t0001g0147 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.413+2596_413+2597i others(658): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421231 | ||||||
| chr12:421231 | A | AACACACA others(3672): Show |
1 | a0001c0001t0004g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.413+2596_413+2597i others(3681): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421231 | ||||||
| chr12:421231 | A | AACACACA others(579): Show |
1 | a0003c0003t0004g0363 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.413+2596_413+2597i others(588): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421231 | ||||||
| chr12:421231 | A | AACACACA others(64): Show |
1 | a0001c0001t0001g0220 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.413+2596_413+2597i others(73): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421231 | ||||||
| chr12:421231 | A | AACACACA others(137): Show |
1 | a0006c0006t0011g0106 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.413+2596_413+2597i others(146): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421231 | ||||||
| chr12:421231 | AAT | A | 48 | a0001c0001t0001g0131 a0001c0001t0001g0143 a0001c0001t0001g0146 others(45): Show |
49 | HG00323.hp2 HG00597.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.413+2597_413+2598d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421231 | ||||||
| chr12:421231 | AATACACA others(587): Show |
A | 3 | a0001c0001t0004g0176 a0003c0003t0002g0372 a0003c0003t0004g0175 |
3 | HG01891.hp2 HG01952.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.413+2597_413+3190d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421231 | ||||||
| chr12:421232 | AT | A | 19 | a0001c0001t0001g0167 a0001c0001t0001g0204 a0001c0001t0001g0219 others(16): Show |
20 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.413+2597delT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421232 | |||||||
| chr12:421232 | ATACACAC others(69): Show |
A | 2 | a0001c0001t0001g0274 a0002c0002t0002g0082 |
2 | HG03017.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.413+2597_413+2672d others(78): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421232 | |||||||
| chr12:421232 | ATACACAC others(661): Show |
A | 1 | a0002c0002t0002g0100 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.413+2597_413+3264d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421232 | |||||||
| chr12:421233 | T | A | 7 | a0001c0001t0001g0147 a0001c0001t0001g0220 a0001c0001t0001g0362 others(4): Show |
7 | HG00642.hp1 HG01109.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+2597T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421233 | |||||||
| chr12:421233 | T | C | 23 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(20): Show |
23 | HG00438.hp1 HG00609.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.413+2597T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421233 | |||||||
| chr12:421235 | C | CACATAGC others(65): Show |
1 | a0001c0001t0008g0170 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.413+2602_413+2603i others(74): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421235 | ||||||
| chr12:421235 | C | CACATAGC others(1098): Show |
1 | a0001c0001t0004g0328 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.413+2602_413+2603i others(1107): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421235 | ||||||
| chr12:421235 | C | CACATAGC others(138): Show |
22 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(19): Show |
22 | HG00438.hp1 HG00609.hp1 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.413+2602_413+2603i others(147): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421235 | ||||||
| chr12:421235 | C | CACATAGC others(655): Show |
9 | a0001c0001t0001g0132 a0001c0001t0001g0211 a0001c0001t0001g0212 others(6): Show |
9 | HG00408.hp2 HG00639.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.413+2602_413+2603i others(664): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421235 | ||||||
| chr12:421235 | C | T | 16 | a0001c0001t0001g0167 a0001c0001t0001g0204 a0001c0001t0001g0219 others(13): Show |
17 | HG00642.hp2 HG00735.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.413+2599C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421235 | |||||||
| chr12:421250 | A | ACTCCATG others(68): Show |
1 | a0001c0001t0002g0325 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.413+2688_413+2689i others(77): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421250 | ||||||
| chr12:421250 | A | C | 92 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(89): Show |
94 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.413+2614A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421250 | |||||||
| chr12:421258 | T | C | 47 | a0001c0001t0001g0131 a0001c0001t0001g0143 a0001c0001t0001g0146 others(44): Show |
47 | HG00597.hp2 HG00642.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.413+2622T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421258 | |||||||
| chr12:421272 | G | A | 31 | a0001c0001t0001g0147 a0001c0001t0001g0150 a0001c0001t0001g0156 others(28): Show |
31 | HG00280.hp1 HG00323.hp2 HG01081.hp1 others(28): Show |
intron_variant | MODIFIER | c.413+2636G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421272 | |||||||
| chr12:421272 | G | GCTTCTGT others(732): Show |
1 | a0001c0001t0001g0192 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.413+2677_413+2678i others(741): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421272 | ||||||
| chr12:421272 | G | T | 47 | a0001c0001t0001g0143 a0001c0001t0001g0164 a0001c0001t0001g0200 others(44): Show |
49 | HG00597.hp2 HG00642.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.413+2636G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421272 | |||||||
| chr12:421286 | G | T | 32 | a0001c0001t0002g0051 a0001c0001t0002g0136 a0001c0001t0002g0137 others(29): Show |
35 | HG00323.hp1 HG00673.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.413+2650G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421286 | |||||||
| chr12:421304 | T | TA | 5 | a0001c0001t0001g0375 a0001c0001t0001g0402 a0002c0002t0001g0400 others(2): Show |
5 | HG02145.hp2 HG02257.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+2671dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421304 | ||||||
| chr12:421304 | T | TAAAATAC others(363): Show |
1 | a0003c0003t0004g0329 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.413+2671_413+2672i others(372): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421304 | ||||||
| chr12:421304 | T | TAAAATAC others(141): Show |
1 | a0004c0004t0002g0097 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.413+2671_413+2672i others(150): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421304 | ||||||
| chr12:421306 | A | AACACACA others(285): Show |
1 | a0003c0003t0007g0412 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.413+2671_413+2672i others(294): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421306 | ||||||
| chr12:421306 | AAT | A | 21 | a0001c0001t0001g0165 a0001c0001t0001g0245 a0001c0001t0001g0281 others(18): Show |
22 | HG00323.hp2 HG00735.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.413+2672_413+2673d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421306 | ||||||
| chr12:421307 | AT | A | 41 | a0001c0001t0001g0143 a0001c0001t0001g0147 a0001c0001t0001g0164 others(38): Show |
42 | HG00597.hp2 HG00642.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.413+2672delT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421307 | |||||||
| chr12:421308 | T | A | 1 | a0003c0003t0007g0412 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.413+2672T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421308 | |||||||
| chr12:421308 | T | C | 4 | a0001c0001t0001g0206 a0003c0003t0004g0329 a0003c0003t0007g0327 others(1): Show |
4 | HG02145.hp2 HG02257.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+2672T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421308 | |||||||
| chr12:421308 | T | TACACACA others(360): Show |
1 | a0001c0001t0001g0150 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.413+2688_413+2689i others(369): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421308 | ||||||
| chr12:421310 | C | CACACATA others(1469): Show |
1 | a0003c0003t0001g0140 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.413+2688_413+2689i others(1478): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421310 | ||||||
| chr12:421310 | C | CACATAGC others(434): Show |
1 | a0001c0001t0001g0375 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.413+2677_413+2678i others(443): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421310 | ||||||
| chr12:421310 | C | CACATAGC others(1025): Show |
1 | a0001c0001t0001g0206 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.413+2677_413+2678i others(1034): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421310 | ||||||
| chr12:421310 | C | CACATAGC others(65): Show |
1 | a0001c0001t0001g0402 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.413+2677_413+2678i others(74): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421310 | ||||||
| chr12:421310 | C | T | 142 | a0001c0001t0001g0204 a0001c0001t0001g0207 a0001c0001t0001g0219 others(139): Show |
145 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.413+2674C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421310 | |||||||
| chr12:421325 | A | C | 179 | a0001c0001t0001g0143 a0001c0001t0001g0147 a0001c0001t0001g0150 others(176): Show |
184 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.413+2689A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421325 | |||||||
| chr12:421333 | T | C | 41 | a0001c0001t0001g0147 a0001c0001t0001g0202 a0001c0001t0001g0224 others(38): Show |
43 | HG00735.hp1 HG00735.hp2 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.413+2697T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421333 | |||||||
| chr12:421347 | A | ACTTCTGT others(67): Show |
1 | a0001c0001t0001g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.413+2747_413+2748i others(76): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421347 | ||||||
| chr12:421347 | A | ACTTCTGT others(432): Show |
2 | a0002c0002t0001g0322 a0004c0004t0001g0085 |
2 | HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.413+2746_413+2747i others(441): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421347 | ||||||
| chr12:421347 | A | T | 16 | a0001c0001t0001g0147 a0001c0001t0001g0219 a0001c0001t0001g0224 others(13): Show |
16 | HG01167.hp1 HG01168.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.413+2711A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421347 | |||||||
| chr12:421379 | TA | T | 20 | a0001c0001t0001g0202 a0001c0001t0001g0219 a0001c0001t0001g0224 others(17): Show |
21 | HG00735.hp2 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.413+2747delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421379 | ||||||
| chr12:421380 | A | AAATACAC others(215): Show |
1 | a0002c0002t0001g0208 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.413+2746_413+2747i others(224): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421380 | ||||||
| chr12:421382 | A | AT | 46 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(43): Show |
46 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.413+2746_413+2747i others(3): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421382 | |||||||
| chr12:421382 | A | ATACACAC others(1322): Show |
1 | a0001c0001t0001g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.413+2746_413+2747i others(1331): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421382 | |||||||
| chr12:421384 | T | C | 79 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(76): Show |
80 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.413+2748T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421384 | |||||||
| chr12:421384 | T | TACACATA others(139): Show |
1 | a0001c0001t0002g0352 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.413+2843_413+2844i others(148): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421384 | ||||||
| chr12:421399 | C | A | 5 | a0001c0001t0001g0408 a0001c0001t0002g0010 a0002c0002t0002g0082 others(2): Show |
6 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+2763C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421399 | |||||||
| chr12:421406 | G | A | 3 | a0001c0001t0001g0219 a0001c0001t0001g0224 a0004c0004t0002g0097 |
3 | HG02615.hp2 HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.413+2770G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421406 | |||||||
| chr12:421407 | T | C | 23 | a0001c0001t0001g0156 a0001c0001t0001g0219 a0001c0001t0001g0223 others(20): Show |
24 | HG01069.hp2 HG01071.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.413+2771T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421407 | |||||||
| chr12:421421 | T | A | 30 | a0001c0001t0001g0147 a0001c0001t0001g0150 a0001c0001t0001g0156 others(27): Show |
31 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.413+2785T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421421 | |||||||
| chr12:421421 | T | G | 2 | a0001c0001t0001g0364 a0001c0001t0001g0408 |
2 | HG01261.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.413+2785T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421421 | |||||||
| chr12:421452 | G | A | 3 | a0001c0001t0001g0167 a0001c0001t0001g0191 a0001c0001t0001g0192 |
3 | HG01071.hp1 HG03239.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.413+2816G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421452 | |||||||
| chr12:421453 | T | TA | 16 | a0001c0001t0001g0219 a0001c0001t0001g0224 a0001c0001t0001g0375 others(13): Show |
16 | HG01106.hp2 HG01884.hp2 HG01928.hp1 others(13): Show |
intron_variant | MODIFIER | c.413+2820dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421453 | ||||||
| chr12:421453 | T | TAAAATAC others(363): Show |
6 | a0001c0001t0001g0245 a0002c0002t0001g0385 a0003c0003t0001g0094 others(3): Show |
6 | HG01346.hp2 HG02723.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+2820_413+2821i others(372): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421453 | ||||||
| chr12:421453 | T | TAAAATAC others(363): Show |
1 | a0003c0003t0001g0287 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.413+2820_413+2821i others(372): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421453 | ||||||
| chr12:421455 | A | AAAT | 4 | a0001c0001t0001g0408 a0001c0001t0004g0323 a0004c0004t0001g0095 others(1): Show |
4 | HG01167.hp1 HG01261.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+2820_413+2821i others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421455 | ||||||
| chr12:421457 | C | CACACATA others(1100): Show |
1 | a0001c0001t0001g0108 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.413+2857_413+2858i others(1109): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421457 | ||||||
| chr12:421457 | C | CACACATA others(215): Show |
1 | a0001c0001t0001g0198 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.413+2857_413+2858i others(224): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421457 | ||||||
| chr12:421457 | C | CACACATA others(215): Show |
5 | a0001c0001t0001g0131 a0001c0001t0001g0146 a0001c0001t0001g0238 others(2): Show |
5 | HG01175.hp1 HG02602.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+2857_413+2858i others(224): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421457 | ||||||
| chr12:421457 | C | T | 64 | a0001c0001t0001g0245 a0001c0001t0001g0364 a0001c0001t0001g0375 others(61): Show |
67 | HG00609.hp2 HG00738.hp1 HG01346.hp2 others(64): Show |
intron_variant | MODIFIER | c.413+2821C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421457 | |||||||
| chr12:421472 | C | A | 13 | a0001c0001t0001g0165 a0001c0001t0001g0245 a0001c0001t0001g0364 others(10): Show |
13 | HG00323.hp2 HG01168.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.413+2836C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421472 | |||||||
| chr12:421479 | G | A | 126 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0207 others(123): Show |
129 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.413+2843G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421479 | |||||||
| chr12:421480 | T | C | 204 | a0001c0001t0001g0147 a0001c0001t0001g0165 a0001c0001t0001g0204 others(201): Show |
211 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.413+2844T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421480 | |||||||
| chr12:421480 | T | TTCCATTA others(4045): Show |
1 | a0001c0001t0008g0170 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.413+2857_413+2858i others(4054): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421480 | ||||||
| chr12:421494 | T | A | 87 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0132 others(84): Show |
87 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.413+2858T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421494 | |||||||
| chr12:421494 | T | G | 11 | a0001c0001t0001g0167 a0001c0001t0001g0191 a0001c0001t0001g0192 others(8): Show |
11 | HG01071.hp1 HG01168.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.413+2858T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421494 | |||||||
| chr12:421494 | TCTTCTGT others(363): Show |
T | 101 | a0001c0001t0001g0396 a0001c0001t0002g0049 a0001c0001t0003g0028 others(98): Show |
103 | HG00280.hp2 HG00438.hp2 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.413+2894_413+3263d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421494 | ||||||
| chr12:421498 | CTGTG | C | 16 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(13): Show |
16 | HG00597.hp1 HG02080.hp1 HG03471.hp1 others(13): Show |
intron_variant | MODIFIER | c.413+2871_413+2874d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421498 | ||||||
| chr12:421526 | TA | T | 16 | a0001c0001t0001g0156 a0001c0001t0001g0178 a0001c0001t0001g0220 others(13): Show |
16 | HG00642.hp1 HG01081.hp1 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.413+2894delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421526 | ||||||
| chr12:421527 | A | AAAATACA others(364): Show |
1 | a0002c0002t0001g0401 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.413+2894_413+2895i others(373): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421527 | ||||||
| chr12:421527 | A | AAACACAC others(436): Show |
1 | a0003c0003t0001g0062 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.413+2893_413+2894i others(445): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421527 | ||||||
| chr12:421529 | A | AAT | 3 | a0001c0001t0001g0364 a0001c0001t0001g0406 a0004c0004t0001g0315 |
3 | HG01168.hp1 HG03139.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.413+2894_413+2895i others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421529 | ||||||
| chr12:421529 | A | ACACACAT others(1174): Show |
1 | a0001c0001t0002g0115 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.413+2893_413+2894i others(1183): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421529 | |||||||
| chr12:421529 | A | ACACACAT others(1251): Show |
1 | a0001c0001t0001g0248 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.413+2893_413+2894i others(1260): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421529 | |||||||
| chr12:421529 | A | ACACACAT others(1177): Show |
5 | a0001c0001t0001g0164 a0001c0001t0001g0210 a0001c0001t0001g0308 others(2): Show |
5 | HG02683.hp2 NA18959.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.413+2893_413+2894i others(1186): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421529 | |||||||
| chr12:421529 | A | ACACACAT others(1101): Show |
1 | a0001c0001t0001g0200 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.413+2893_413+2894i others(1110): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421529 | |||||||
| chr12:421529 | A | ACACACAT others(1104): Show |
1 | a0003c0003t0002g0205 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.413+2893_413+2894i others(1113): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421529 | |||||||
| chr12:421529 | A | ACACACAT others(141): Show |
1 | a0001c0001t0001g0286 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.413+2893_413+2894i others(150): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421529 | |||||||
| chr12:421529 | A | ACACACAT others(363): Show |
21 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0132 others(18): Show |
21 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.413+2893_413+2894i others(372): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421529 | |||||||
| chr12:421529 | A | ACACACAT others(287): Show |
3 | a0001c0001t0001g0201 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | NA18971.hp2 NA19060.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.413+2893_413+2894i others(296): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421529 | |||||||
| chr12:421529 | A | ACACACAT others(1175): Show |
1 | a0001c0001t0001g0236 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.413+2893_413+2894i others(1184): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421529 | |||||||
| chr12:421529 | A | ACACACAT others(68): Show |
2 | a0001c0001t0001g0143 a0001c0001t0001g0275 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.413+2893_413+2894i others(77): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421529 | |||||||
| chr12:421529 | A | ACACACAT others(1250): Show |
1 | a0002c0002t0001g0208 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.413+2893_413+2894i others(1259): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421529 | |||||||
| chr12:421529 | A | AT | 19 | a0001c0001t0001g0402 a0001c0001t0001g0405 a0002c0002t0001g0111 others(16): Show |
20 | HG00408.hp1 HG00423.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.413+2893_413+2894i others(3): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421529 | |||||||
| chr12:421529 | A | ATACACAT others(290): Show |
5 | a0003c0003t0002g0213 a0003c0003t0002g0214 a0003c0003t0002g0215 others(2): Show |
5 | NA18950.hp2 NA18971.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.413+2893_413+2894i others(299): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421529 | |||||||
| chr12:421529 | AACACACA others(289): Show |
A | 1 | a0003c0003t0002g0249 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.413+2910_413+3205d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421529 | ||||||
| chr12:421531 | C | T | 52 | a0001c0001t0001g0108 a0001c0001t0001g0131 a0001c0001t0001g0146 others(49): Show |
53 | HG00597.hp1 HG01069.hp2 HG01071.hp1 others(50): Show |
intron_variant | MODIFIER | c.413+2895C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421531 | |||||||
| chr12:421533 | C | T | 1 | a0004c0004t0002g0097 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.413+2897C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421533 | |||||||
| chr12:421546 | C | A | 25 | a0001c0001t0001g0178 a0001c0001t0001g0375 a0001c0001t0001g0405 others(22): Show |
27 | HG00408.hp1 HG00423.hp2 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.413+2910C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421546 | |||||||
| chr12:421554 | C | CTCCATTA others(67): Show |
2 | a0003c0003t0007g0327 a0003c0003t0007g0412 |
2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.413+2991_413+2992i others(76): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421554 | ||||||
| chr12:421554 | C | CTCCATTA others(878): Show |
1 | a0001c0001t0004g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.413+2931_413+2932i others(887): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421554 | ||||||
| chr12:421554 | C | T | 48 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0156 others(45): Show |
48 | HG00280.hp1 HG00323.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.413+2918C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421554 | |||||||
| chr12:421568 | A | G | 5 | a0001c0001t0001g0178 a0001c0001t0001g0375 a0001c0001t0001g0407 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.413+2932A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421568 | |||||||
| chr12:421568 | A | T | 52 | a0001c0001t0001g0147 a0001c0001t0001g0202 a0001c0001t0001g0204 others(49): Show |
54 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.413+2932A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421568 | |||||||
| chr12:421572 | CTGTG | C | 18 | a0002c0002t0001g0111 a0002c0002t0001g0196 a0002c0002t0002g0082 others(15): Show |
19 | HG00408.hp1 HG00423.hp2 HG02165.hp2 others(16): Show |
intron_variant | MODIFIER | c.413+2945_413+2948d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421572 | ||||||
| chr12:421594 | A | AGAGGGTA others(61): Show |
1 | a0001c0001t0001g0156 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.413+2968_413+2969i others(70): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421594 | ||||||
| chr12:421600 | TA | T | 49 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0132 others(46): Show |
49 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.413+2968delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421600 | ||||||
| chr12:421605 | T | C | 59 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0132 others(56): Show |
59 | HG00408.hp2 HG00438.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.413+2969T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421605 | |||||||
| chr12:421605 | T | TAC | 19 | a0001c0001t0001g0151 a0001c0001t0001g0178 a0001c0001t0001g0241 others(16): Show |
19 | HG00597.hp1 HG02080.hp1 HG02602.hp2 others(16): Show |
intron_variant | MODIFIER | c.413+2973_413+2974d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421605 | ||||||
| chr12:421605 | T | TACACATA others(66): Show |
2 | a0003c0003t0004g0363 a0006c0006t0011g0106 |
2 | HG01109.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.413+2983_413+2984i others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421605 | ||||||
| chr12:421605 | T | TACACATA others(510): Show |
1 | a0001c0001t0001g0165 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.413+2983_413+2984i others(519): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421605 | ||||||
| chr12:421605 | TACACATA others(66): Show |
T | 1 | a0001c0001t0003g0027 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.413+2984_413+3056d others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421605 | ||||||
| chr12:421620 | A | ACTCCATG others(141): Show |
1 | a0001c0001t0001g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.413+2991_413+2992i others(150): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421620 | ||||||
| chr12:421620 | A | ACTCCATG others(215): Show |
3 | a0001c0001t0001g0147 a0002c0002t0001g0322 a0004c0004t0001g0085 |
3 | HG01192.hp1 HG02109.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.413+2991_413+2992i others(224): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421620 | ||||||
| chr12:421620 | A | C | 218 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(215): Show |
223 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.413+2984A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421620 | |||||||
| chr12:421628 | C | T | 106 | a0001c0001t0001g0143 a0001c0001t0001g0150 a0001c0001t0001g0204 others(103): Show |
111 | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.413+2992C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421628 | |||||||
| chr12:421642 | A | T | 78 | a0001c0001t0001g0202 a0001c0001t0001g0219 a0001c0001t0001g0223 others(75): Show |
82 | HG00609.hp2 HG00621.hp2 HG00738.hp1 others(79): Show |
intron_variant | MODIFIER | c.413+3006A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421642 | |||||||
| chr12:421674 | T | TA | 99 | a0001c0001t0001g0108 a0001c0001t0001g0131 a0001c0001t0001g0146 others(96): Show |
100 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(97): Show |
intron_variant | MODIFIER | c.413+3041dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421674 | ||||||
| chr12:421674 | T | TAAAATAC others(68): Show |
1 | a0001c0001t0001g0406 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.413+3041_413+3042i others(77): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421674 | ||||||
| chr12:421676 | A | AACACACA others(1027): Show |
1 | a0003c0003t0004g0329 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.413+3078_413+3079i others(1036): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421676 | ||||||
| chr12:421677 | ACACACAT others(361): Show |
A | 1 | a0001c0001t0001g0224 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.413+3042_413+3409d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421677 | |||||||
| chr12:421678 | C | T | 87 | a0001c0001t0001g0108 a0001c0001t0001g0131 a0001c0001t0001g0146 others(84): Show |
88 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.413+3042C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421678 | |||||||
| chr12:421680 | CACATAGC others(436): Show |
C | 1 | a0002c0002t0001g0196 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.413+3048_413+3490d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421680 | ||||||
| chr12:421684 | TAGC | T | 15 | a0001c0001t0006g0012 a0001c0001t0006g0388 a0001c0001t0006g0389 others(12): Show |
15 | HG00735.hp1 HG02145.hp1 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.413+3053_413+3055d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421684 | ||||||
| chr12:421693 | C | A | 24 | a0001c0001t0001g0204 a0001c0001t0001g0206 a0001c0001t0001g0207 others(21): Show |
24 | HG00642.hp2 HG00735.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.413+3057C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421693 | |||||||
| chr12:421693 | CCTCCATG others(67): Show |
C | 1 | a0001c0001t0004g0323 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.413+3115_413+3188d others(76): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421693 | ||||||
| chr12:421700 | G | A | 52 | a0001c0001t0002g0004 a0001c0001t0002g0041 a0001c0001t0002g0074 others(49): Show |
55 | HG00609.hp2 HG00621.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.413+3064G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421700 | |||||||
| chr12:421701 | C | T | 75 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0132 others(72): Show |
75 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.413+3065C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421701 | |||||||
| chr12:421715 | T | A | 131 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(128): Show |
131 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.413+3079T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421715 | |||||||
| chr12:421715 | T | G | 2 | a0003c0003t0001g0062 a0004c0004t0001g0095 |
2 | HG01167.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.413+3079T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421715 | |||||||
| chr12:421715 | T | TCTTCTGT others(66): Show |
4 | a0001c0001t0001g0147 a0001c0001t0001g0281 a0002c0002t0001g0322 others(1): Show |
4 | HG01192.hp1 HG02109.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+3114_413+3115i others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421715 | ||||||
| chr12:421715 | T | TCTTCTGT others(582): Show |
1 | a0002c0002t0014g0321 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.413+3114_413+3115i others(591): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421715 | ||||||
| chr12:421715 | TCTTCTGT others(217): Show |
T | 1 | a0002c0002t0002g0082 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.413+3131_413+3354d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421715 | ||||||
| chr12:421719 | CTG | C | 2 | a0002c0002t0001g0111 a0004c0004t0001g0007 |
3 | HG03688.hp2 HG03710.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.413+3094_413+3095d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421719 | ||||||
| chr12:421747 | TA | T | 31 | a0001c0001t0001g0156 a0001c0001t0001g0220 a0001c0001t0001g0375 others(28): Show |
31 | HG00642.hp1 HG00735.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.413+3115delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421747 | ||||||
| chr12:421749 | AAATACAC others(289): Show |
A | 1 | a0005c0005t0005g0409 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.413+3116_413+3411d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421749 | ||||||
| chr12:421750 | A | AT | 57 | a0001c0001t0001g0143 a0001c0001t0001g0150 a0001c0001t0001g0275 others(54): Show |
60 | HG00280.hp1 HG00609.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.413+3114_413+3115i others(3): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421750 | |||||||
| chr12:421752 | T | C | 106 | a0001c0001t0001g0143 a0001c0001t0001g0147 a0001c0001t0001g0150 others(103): Show |
109 | HG00280.hp1 HG00609.hp2 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.413+3116T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421752 | |||||||
| chr12:421752 | TACACATA others(143): Show |
T | 3 | a0001c0001t0004g0399 a0001c0001t0010g0277 a0001c0001t0010g0278 |
3 | HG01433.hp1 HG01884.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.413+3139_413+3288d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421752 | ||||||
| chr12:421752 | TACACATA others(288): Show |
T | 3 | a0001c0001t0001g0207 a0001c0001t0001g0274 a0001c0001t0001g0376 |
3 | HG02738.hp2 HG03017.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.413+3122_413+3416d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421752 | ||||||
| chr12:421752 | TACACATA others(290): Show |
T | 1 | a0003c0003t0001g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.413+3131_413+3427d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421752 | ||||||
| chr12:421767 | A | C | 158 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(155): Show |
159 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.413+3131A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421767 | |||||||
| chr12:421767 | ACTCCATG others(217): Show |
A | 1 | a0005c0005t0005g0416 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.413+3139_413+3362d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421767 | ||||||
| chr12:421774 | G | A | 1 | a0003c0003t0001g0063 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.413+3138G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421774 | |||||||
| chr12:421774 | G | GTTCCATT others(140): Show |
4 | a0001c0001t0001g0146 a0001c0001t0001g0167 a0001c0001t0001g0191 others(1): Show |
4 | HG01071.hp1 HG03239.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+3138_413+3139i others(149): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421774 | |||||||
| chr12:421775 | C | T | 68 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0132 others(65): Show |
68 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.413+3139C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421775 | |||||||
| chr12:421789 | T | A | 81 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0132 others(78): Show |
81 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.413+3153T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421789 | |||||||
| chr12:421789 | T | G | 23 | a0001c0001t0001g0156 a0001c0001t0001g0204 a0001c0001t0001g0206 others(20): Show |
23 | HG00642.hp2 HG01167.hp2 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.413+3153T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421789 | |||||||
| chr12:421789 | TCTTCTGT others(143): Show |
T | 13 | a0002c0002t0002g0113 a0002c0002t0002g0145 a0002c0002t0002g0162 others(10): Show |
13 | HG00423.hp2 HG02165.hp2 HG02735.hp1 others(10): Show |
intron_variant | MODIFIER | c.413+3189_413+3338d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421789 | ||||||
| chr12:421793 | CTGTGTGT others(147): Show |
C | 51 | a0001c0001t0002g0004 a0001c0001t0002g0041 a0001c0001t0002g0074 others(48): Show |
54 | HG00609.hp2 HG00621.hp2 HG00738.hp1 others(51): Show |
intron_variant | MODIFIER | c.413+3166_413+3319d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421793 | ||||||
| chr12:421821 | T | TA | 3 | a0001c0001t0001g0223 a0002c0002t0001g0400 a0003c0003t0007g0412 |
3 | HG01081.hp2 HG01243.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.413+3188dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421821 | ||||||
| chr12:421822 | A | AAAACACA others(805): Show |
1 | a0003c0003t0001g0140 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.413+3188_413+3189i others(814): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421822 | ||||||
| chr12:421822 | A | AAAATACA others(213): Show |
6 | a0001c0001t0001g0108 a0001c0001t0001g0131 a0001c0001t0001g0198 others(3): Show |
6 | HG01175.hp1 HG01517.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.413+3188_413+3189i others(222): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421822 | ||||||
| chr12:421822 | AAATACAC others(216): Show |
A | 2 | a0002c0002t0001g0111 a0004c0004t0001g0007 |
3 | HG03688.hp2 HG03710.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.413+3189_413+3411d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421822 | ||||||
| chr12:421823 | A | AAACACAC others(508): Show |
3 | a0003c0003t0001g0250 a0003c0003t0001g0251 a0003c0003t0001g0341 |
3 | HG01884.hp2 HG02723.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.413+3188_413+3189i others(517): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421823 | ||||||
| chr12:421823 | A | AAACACAC others(1690): Show |
1 | a0001c0001t0001g0220 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.413+3188_413+3189i others(1699): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421823 | ||||||
| chr12:421823 | A | AAACACAC others(727): Show |
1 | a0002c0002t0001g0387 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.413+3188_413+3189i others(736): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421823 | ||||||
| chr12:421823 | A | AAATACAC others(139): Show |
1 | a0003c0003t0001g0342 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.413+3188_413+3189i others(148): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421823 | ||||||
| chr12:421823 | AAT | A | 73 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0132 others(70): Show |
73 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.413+3189_413+3190d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421823 | ||||||
| chr12:421824 | AT | A | 26 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0167 others(23): Show |
26 | HG00408.hp1 HG01071.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.413+3189delT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421824 | |||||||
| chr12:421824 | ATACACAC others(69): Show |
A | 6 | a0005c0005t0005g0332 a0005c0005t0005g0410 a0005c0005t0005g0418 others(3): Show |
6 | HG02145.hp1 HG02572.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+3189_413+3264d others(78): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421824 | |||||||
| chr12:421825 | T | A | 13 | a0001c0001t0001g0108 a0001c0001t0001g0131 a0001c0001t0001g0198 others(10): Show |
13 | HG00642.hp1 HG01106.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.413+3189T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421825 | |||||||
| chr12:421825 | T | C | 8 | a0001c0001t0001g0143 a0001c0001t0001g0202 a0001c0001t0001g0275 others(5): Show |
8 | HG01074.hp1 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.413+3189T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421825 | |||||||
| chr12:421825 | T | TACACATA others(64): Show |
1 | a0004c0004t0001g0095 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.413+3194_413+3195i others(73): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421825 | ||||||
| chr12:421827 | C | CACACATA others(366): Show |
2 | a0001c0001t0001g0204 a0001c0001t0001g0206 |
2 | HG00642.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.413+3213_413+3214i others(375): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421827 | ||||||
| chr12:421827 | C | CACATAGC others(1466): Show |
1 | a0006c0006t0011g0103 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.413+3194_413+3195i others(1475): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421827 | ||||||
| chr12:421827 | C | CACATAGC others(1245): Show |
1 | a0003c0003t0007g0412 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.413+3194_413+3195i others(1254): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421827 | ||||||
| chr12:421827 | C | CACATAGC others(582): Show |
4 | a0001c0001t0001g0202 a0001c0001t0001g0292 a0001c0001t0001g0338 others(1): Show |
4 | HG01074.hp1 NA18960.hp2 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+3194_413+3195i others(591): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421827 | ||||||
| chr12:421827 | C | CACATAGC others(1687): Show |
1 | a0003c0003t0007g0327 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.413+3194_413+3195i others(1696): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421827 | ||||||
| chr12:421827 | C | CACATAGC others(138): Show |
2 | a0001c0001t0001g0143 a0001c0001t0001g0275 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.413+3194_413+3195i others(147): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421827 | ||||||
| chr12:421827 | C | CACATAGC others(655): Show |
1 | a0001c0001t0001g0223 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.413+3194_413+3195i others(664): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421827 | ||||||
| chr12:421827 | C | T | 22 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0245 others(19): Show |
22 | HG00408.hp1 HG01081.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.413+3191C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421827 | |||||||
| chr12:421842 | A | C | 122 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(119): Show |
122 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.413+3206A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421842 | |||||||
| chr12:421842 | ACTCCATG others(142): Show |
A | 1 | a0007c0007t0005g0197 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.413+3228_413+3376d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421842 | ||||||
| chr12:421849 | G | A | 3 | a0001c0001t0003g0027 a0004c0004t0002g0097 a0006c0006t0012g0105 |
3 | HG02615.hp2 HG02809.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.413+3213G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421849 | |||||||
| chr12:421850 | T | C | 86 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0132 others(83): Show |
86 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.413+3214T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421850 | |||||||
| chr12:421864 | G | A | 48 | a0001c0001t0001g0147 a0001c0001t0001g0150 a0001c0001t0001g0156 others(45): Show |
48 | HG00280.hp1 HG01081.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.413+3228G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421864 | |||||||
| chr12:421864 | G | ACTTCTGT others(4049): Show |
1 | a0003c0003t0004g0363 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.413+3228delGinsACT others(4054): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421864 | |||||||
| chr12:421864 | G | ACTTCTGT others(3236): Show |
1 | a0006c0006t0011g0106 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.413+3228delGinsACT others(3241): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421864 | |||||||
| chr12:421864 | G | T | 38 | a0001c0001t0001g0108 a0001c0001t0001g0131 a0001c0001t0001g0146 others(35): Show |
38 | HG00408.hp1 HG00642.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.413+3228G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421864 | |||||||
| chr12:421896 | T | TA | 3 | a0001c0001t0001g0150 a0001c0001t0001g0405 a0004c0004t0001g0095 |
3 | HG00280.hp1 HG01167.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.413+3263dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421896 | ||||||
| chr12:421898 | AAT | A | 5 | a0001c0001t0001g0219 a0001c0001t0004g0176 a0003c0003t0002g0372 others(2): Show |
5 | HG00408.hp1 HG01891.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+3264_413+3265d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421898 | ||||||
| chr12:421899 | AT | A | 44 | a0001c0001t0001g0108 a0001c0001t0001g0131 a0001c0001t0001g0146 others(41): Show |
44 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.413+3264delT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421899 | |||||||
| chr12:421900 | T | C | 1 | a0003c0003t0001g0062 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.413+3264T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421900 | |||||||
| chr12:421900 | T | TACACACA others(1470): Show |
1 | a0001c0001t0001g0402 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.413+3280_413+3281i others(1479): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421900 | ||||||
| chr12:421900 | TAC | T | 16 | a0001c0001t0004g0093 a0001c0001t0004g0159 a0001c0001t0004g0160 others(13): Show |
16 | HG01167.hp2 HG01169.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.413+3270_413+3271d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421900 | ||||||
| chr12:421900 | TACACACA others(140): Show |
T | 1 | a0004c0004t0001g0315 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413+3281_413+3427d others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421900 | ||||||
| chr12:421902 | C | CACATAGC others(878): Show |
1 | a0003c0003t0001g0062 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.413+3269_413+3270i others(887): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421902 | ||||||
| chr12:421902 | C | CACATAGC others(138): Show |
1 | a0001c0001t0001g0405 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.413+3269_413+3270i others(147): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421902 | ||||||
| chr12:421902 | C | T | 39 | a0001c0001t0001g0108 a0001c0001t0001g0131 a0001c0001t0001g0146 others(36): Show |
39 | HG00735.hp1 HG01071.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.413+3266C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421902 | |||||||
| chr12:421917 | A | C | 72 | a0001c0001t0001g0108 a0001c0001t0001g0131 a0001c0001t0001g0146 others(69): Show |
72 | HG00280.hp1 HG00408.hp1 HG00735.hp1 others(69): Show |
intron_variant | MODIFIER | c.413+3281A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421917 | |||||||
| chr12:421925 | T | C | 149 | a0001c0001t0001g0150 a0001c0001t0001g0178 a0001c0001t0001g0219 others(146): Show |
151 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.413+3289T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421925 | |||||||
| chr12:421939 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.413+3303A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421939 | |||||||
| chr12:421939 | A | T | 122 | a0001c0001t0001g0178 a0001c0001t0001g0396 a0001c0001t0001g0405 others(119): Show |
124 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.413+3303A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421939 | |||||||
| chr12:421943 | CTGTG | C | 103 | a0001c0001t0001g0396 a0001c0001t0002g0049 a0001c0001t0003g0027 others(100): Show |
105 | HG00280.hp2 HG00438.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.413+3316_413+3319d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421943 | ||||||
| chr12:421971 | TA | T | 25 | a0001c0001t0004g0093 a0001c0001t0004g0159 a0001c0001t0004g0160 others(22): Show |
25 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.413+3339delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421971 | ||||||
| chr12:421972 | A | AAACACAC others(65): Show |
11 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(8): Show |
11 | HG01192.hp1 HG01346.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.413+3338_413+3339i others(74): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421972 | ||||||
| chr12:421973 | AAATACAC others(65): Show |
A | 16 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(13): Show |
16 | HG00597.hp1 HG02080.hp1 HG03471.hp1 others(13): Show |
intron_variant | MODIFIER | c.413+3340_413+3411d others(74): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421973 | ||||||
| chr12:421974 | A | AT | 55 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0132 others(52): Show |
55 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.413+3338_413+3339i others(3): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421974 | |||||||
| chr12:421976 | T | C | 85 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0132 others(82): Show |
85 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.413+3340T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421976 | |||||||
| chr12:421991 | C | A | 29 | a0001c0001t0001g0108 a0001c0001t0001g0131 a0001c0001t0001g0146 others(26): Show |
29 | HG00642.hp2 HG01071.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.413+3355C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421991 | |||||||
| chr12:421991 | C | CCTCCATG others(215): Show |
1 | a0002c0002t0001g0401 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.413+3363_413+3584d others(224): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 421991 | ||||||
| chr12:421999 | T | C | 53 | a0001c0001t0001g0108 a0001c0001t0001g0131 a0001c0001t0001g0146 others(50): Show |
53 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.413+3363T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421999 | |||||||
| chr12:422013 | T | A | 201 | a0001c0001t0001g0147 a0001c0001t0001g0150 a0001c0001t0001g0156 others(198): Show |
206 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.413+3377T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422013 | |||||||
| chr12:422045 | T | TA | 162 | a0001c0001t0001g0178 a0001c0001t0001g0396 a0001c0001t0001g0407 others(159): Show |
167 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.413+3412dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422045 | ||||||
| chr12:422047 | A | AAAT | 15 | a0001c0001t0001g0108 a0001c0001t0001g0131 a0001c0001t0001g0146 others(12): Show |
15 | HG00642.hp2 HG01071.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.413+3412_413+3413i others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422047 | ||||||
| chr12:422047 | A | AAATACAC others(1322): Show |
1 | a0001c0001t0004g0328 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.413+3412_413+3413i others(1331): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422047 | ||||||
| chr12:422047 | A | AAT | 24 | a0001c0001t0001g0219 a0001c0001t0004g0093 a0001c0001t0004g0159 others(21): Show |
24 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.413+3412_413+3413i others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422047 | ||||||
| chr12:422047 | A | T | 18 | a0001c0001t0001g0151 a0001c0001t0001g0224 a0001c0001t0001g0241 others(15): Show |
18 | HG00597.hp1 HG02080.hp1 HG02976.hp2 others(15): Show |
intron_variant | MODIFIER | c.413+3411A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422047 | |||||||
| chr12:422049 | C | CACACATA others(141): Show |
1 | a0001c0001t0001g0406 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.413+3434_413+3435i others(150): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422049 | ||||||
| chr12:422049 | C | T | 164 | a0001c0001t0001g0178 a0001c0001t0001g0396 a0001c0001t0001g0407 others(161): Show |
170 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.413+3413C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422049 | |||||||
| chr12:422064 | C | A | 30 | a0001c0001t0001g0108 a0001c0001t0001g0131 a0001c0001t0001g0146 others(27): Show |
30 | HG00642.hp2 HG00735.hp1 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.413+3428C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422064 | |||||||
| chr12:422064 | C | CCTCCATG others(2582): Show |
1 | a0001c0001t0001g0150 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.413+3449_413+3450i others(2591): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422064 | ||||||
| chr12:422064 | C | CCTCCATG others(1990): Show |
2 | a0001c0001t0001g0143 a0001c0001t0001g0275 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.413+3435_413+3436i others(1999): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422064 | ||||||
| chr12:422064 | C | CCTCCATG others(2212): Show |
1 | a0001c0001t0001g0338 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.413+3435_413+3436i others(2221): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422064 | ||||||
| chr12:422064 | C | CCTCCATG others(1916): Show |
1 | a0003c0003t0001g0019 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.413+3435_413+3436i others(1925): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422064 | ||||||
| chr12:422064 | C | CCTCCATG others(2287): Show |
1 | a0001c0001t0001g0223 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.413+3435_413+3436i others(2296): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422064 | ||||||
| chr12:422064 | C | CCTCCATG others(1768): Show |
2 | a0001c0001t0001g0202 a0001c0001t0001g0292 |
2 | NA18964.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.413+3435_413+3436i others(1777): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422064 | ||||||
| chr12:422064 | C | CCTCCATG others(3245): Show |
1 | a0001c0001t0001g0375 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.413+3435_413+3436i others(3254): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422064 | ||||||
| chr12:422064 | C | CCTCCATG others(3023): Show |
1 | a0001c0001t0001g0156 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.413+3435_413+3436i others(3032): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422064 | ||||||
| chr12:422064 | C | CCTCCATG others(1030): Show |
1 | a0001c0001t0002g0115 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.413+3435_413+3436i others(1039): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422064 | ||||||
| chr12:422064 | C | CCTCCATG others(1472): Show |
3 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0220 |
3 | HG00639.hp2 HG00642.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.413+3435_413+3436i others(1481): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422064 | ||||||
| chr12:422064 | C | CCTCCATG others(1178): Show |
1 | a0001c0001t0001g0308 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.413+3435_413+3436i others(1187): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422064 | ||||||
| chr12:422064 | C | CCTCCATG others(1030): Show |
25 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0132 others(22): Show |
25 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.413+3435_413+3436i others(1039): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422064 | ||||||
| chr12:422064 | C | CCTCCATG others(1028): Show |
1 | a0001c0001t0001g0248 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.413+3435_413+3436i others(1037): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422064 | ||||||
| chr12:422064 | C | CCTCCATG others(1178): Show |
1 | a0001c0001t0001g0242 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.413+3435_413+3436i others(1187): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422064 | ||||||
| chr12:422064 | C | CCTCCATG others(1176): Show |
3 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0237 |
3 | HG01192.hp2 HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.413+3435_413+3436i others(1185): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422064 | ||||||
| chr12:422064 | C | CCTCCATG others(956): Show |
1 | a0003c0003t0001g0017 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.413+3435_413+3436i others(965): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422064 | ||||||
| chr12:422064 | C | CCTCCATG others(956): Show |
2 | a0001c0001t0001g0155 a0001c0001t0001g0189 |
2 | HG01358.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.413+3435_413+3436i others(965): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422064 | ||||||
| chr12:422064 | C | CCTCCATG others(882): Show |
6 | a0001c0001t0001g0165 a0001c0001t0001g0166 a0001c0001t0001g0200 others(3): Show |
6 | HG00323.hp2 HG01106.hp1 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.413+3435_413+3436i others(891): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422064 | ||||||
| chr12:422072 | C | T | 27 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0245 others(24): Show |
27 | HG01106.hp2 HG01167.hp1 HG01192.hp1 others(24): Show |
intron_variant | MODIFIER | c.413+3436C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422072 | |||||||
| chr12:422086 | T | A | 44 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(41): Show |
44 | HG00597.hp1 HG00735.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.413+3450T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422086 | |||||||
| chr12:422086 | T | G | 1 | a0001c0001t0001g0402 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.413+3450T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422086 | |||||||
| chr12:422118 | TA | T | 5 | a0001c0001t0001g0178 a0001c0001t0001g0407 a0001c0001t0009g0289 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.413+3486delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422118 | ||||||
| chr12:422123 | T | C | 80 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(77): Show |
80 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.413+3487T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422123 | |||||||
| chr12:422138 | A | C | 301 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(298): Show |
307 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(304): Show |
intron_variant | MODIFIER | c.413+3502A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422138 | |||||||
| chr12:422145 | G | A | 5 | a0001c0001t0001g0178 a0001c0001t0001g0407 a0001c0001t0009g0289 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.413+3509G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422145 | |||||||
| chr12:422145 | G | GTTCCATT others(805): Show |
1 | a0001c0001t0001g0402 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.413+3509_413+3510i others(814): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422145 | |||||||
| chr12:422145 | G | GTTCCATT others(66): Show |
2 | a0001c0001t0001g0408 a0004c0004t0001g0095 |
2 | HG01167.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.413+3509_413+3510i others(75): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422145 | |||||||
| chr12:422146 | C | T | 75 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(72): Show |
75 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.413+3510C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422146 | |||||||
| chr12:422160 | T | A | 26 | a0001c0001t0002g0055 a0001c0001t0002g0293 a0001c0001t0002g0294 others(23): Show |
26 | HG00544.hp2 HG00621.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.413+3524T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422160 | |||||||
| chr12:422194 | AAT | A | 9 | a0001c0001t0006g0012 a0001c0001t0006g0388 a0001c0001t0006g0389 others(6): Show |
9 | HG00735.hp1 HG02155.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+3560_413+3561d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 422194 | ||||||
| chr12:422235 | T | A | 14 | a0001c0001t0001g0178 a0001c0001t0001g0406 a0001c0001t0001g0407 others(11): Show |
14 | HG00735.hp1 HG01168.hp1 HG01261.hp2 others(11): Show |
intron_variant | MODIFIER | c.413+3599T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422235 | |||||||
| chr12:422276 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.413+3640C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422276 | |||||||
| chr12:422298 | T | G | 1 | a0002c0002t0001g0190 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.413+3662T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422298 | |||||||
| chr12:422386 | A | G | 1 | a0001c0001t0001g0402 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.413+3750A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422386 | |||||||
| chr12:422419 | C | T | 1 | a0003c0003t0002g0249 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.413+3783C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422419 | |||||||
| chr12:422457 | C | T | 5 | a0003c0003t0002g0209 a0003c0003t0002g0213 a0003c0003t0002g0214 others(2): Show |
5 | NA18950.hp2 NA18952.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+3821C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422457 | |||||||
| chr12:422468 | A | G | 1 | a0001c0001t0002g0403 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.413+3832A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422468 | |||||||
| chr12:422524 | C | T | 2 | a0001c0001t0004g0317 a0001c0001t0004g0318 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.413+3888C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422524 | |||||||
| chr12:422593 | G | C | 1 | a0002c0002t0001g0134 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.413+3957G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422593 | |||||||
| chr12:422677 | C | G | 2 | a0002c0002t0001g0233 a0002c0002t0001g0234 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.413+4041C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422677 | |||||||
| chr12:422746 | G | A | 3 | a0001c0001t0002g0049 a0003c0003t0002g0068 a0003c0003t0002g0081 |
3 | NA18948.hp1 NA19002.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.413+4110G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422746 | |||||||
| chr12:422795 | G | A | 1 | a0001c0001t0002g0259 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.413+4159G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422795 | |||||||
| chr12:422815 | T | C | 1 | a0001c0001t0004g0244 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.413+4179T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422815 | |||||||
| chr12:423003 | A | G | 3 | a0001c0001t0001g0131 a0001c0001t0001g0146 a0001c0001t0001g0348 |
3 | HG01175.hp1 HG01993.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.413+4367A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423003 | |||||||
| chr12:423094 | C | CT | 10 | a0001c0001t0001g0245 a0001c0001t0001g0281 a0002c0002t0001g0322 others(7): Show |
10 | HG01346.hp2 HG02109.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.413+4468dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423094 | ||||||
| chr12:423094 | CT | C | 23 | a0001c0001t0002g0055 a0001c0001t0002g0293 a0001c0001t0002g0294 others(20): Show |
23 | HG00408.hp1 HG00423.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.413+4468delT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423094 | ||||||
| chr12:423105 | CTTT | C | 74 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(71): Show |
74 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.413+4471_413+4473d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423105 | ||||||
| chr12:423114 | C | CT | 62 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0013 others(59): Show |
68 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.413+4502dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423114 | ||||||
| chr12:423114 | C | CTT | 12 | a0001c0001t0001g0155 a0001c0001t0001g0211 a0001c0001t0002g0051 others(9): Show |
12 | HG01243.hp2 HG01943.hp1 HG02293.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+4501_413+4502d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423114 | ||||||
| chr12:423114 | C | CTTT | 55 | a0001c0001t0001g0025 a0001c0001t0001g0108 a0001c0001t0001g0132 others(52): Show |
55 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.413+4500_413+4502d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423114 | ||||||
| chr12:423114 | C | CTTTT | 14 | a0001c0001t0001g0024 a0001c0001t0001g0131 a0001c0001t0001g0143 others(11): Show |
14 | HG00438.hp1 HG00642.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.413+4499_413+4502d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423114 | ||||||
| chr12:423114 | CTT | C | 25 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(22): Show |
25 | HG01081.hp1 HG01106.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.413+4501_413+4502d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423114 | ||||||
| chr12:423114 | CTTTTTT | C | 9 | a0001c0001t0004g0399 a0005c0005t0005g0332 a0005c0005t0005g0409 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+4497_413+4502d others(8): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423114 | ||||||
| chr12:423129 | T | TC | 3 | a0001c0001t0004g0096 a0001c0001t0007g0016 a0004c0004t0001g0315 |
3 | HG03139.hp2 NA18942.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.413+4493_413+4494i others(3): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423129 | |||||||
| chr12:423129 | T | TTC | 93 | a0001c0001t0001g0151 a0001c0001t0001g0178 a0001c0001t0001g0241 others(90): Show |
95 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.413+4494_413+4495i others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423129 | ||||||
| chr12:423129 | T | TTTC | 114 | a0001c0001t0002g0004 a0001c0001t0002g0041 a0001c0001t0002g0049 others(111): Show |
118 | HG00408.hp1 HG00423.hp2 HG00609.hp2 others(115): Show |
intron_variant | MODIFIER | c.413+4495_413+4496i others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423129 | ||||||
| chr12:423145 | G | A | 9 | a0001c0001t0001g0167 a0001c0001t0001g0191 a0001c0001t0001g0192 others(6): Show |
9 | HG01071.hp1 HG02602.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.413+4509G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423145 | |||||||
| chr12:423182 | A | G | 215 | a0001c0001t0001g0151 a0001c0001t0001g0178 a0001c0001t0001g0241 others(212): Show |
221 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.413+4546A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423182 | |||||||
| chr12:423189 | T | C | 215 | a0001c0001t0001g0151 a0001c0001t0001g0178 a0001c0001t0001g0241 others(212): Show |
221 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.413+4553T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423189 | |||||||
| chr12:423191 | C | G | 215 | a0001c0001t0001g0151 a0001c0001t0001g0178 a0001c0001t0001g0241 others(212): Show |
221 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.413+4555C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423191 | |||||||
| chr12:423195 | A | C | 1 | a0007c0007t0005g0326 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.413+4559A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423195 | |||||||
| chr12:423290 | A | G | 9 | a0001c0001t0004g0246 a0001c0001t0004g0328 a0001c0001t0008g0170 others(6): Show |
9 | HG01081.hp1 HG01109.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.413+4654A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423290 | |||||||
| chr12:423294 | T | A | 1 | a0001c0001t0002g0049 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.413+4658T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423294 | |||||||
| chr12:423294 | T | TTA | 195 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(192): Show |
198 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.413+4672_413+4673d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423294 | ||||||
| chr12:423308 | A | AT | 11 | a0002c0002t0001g0303 a0002c0002t0001g0387 a0005c0005t0005g0332 others(8): Show |
11 | HG02145.hp1 HG02572.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.413+4684dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423308 | ||||||
| chr12:423308 | A | ATAT | 7 | a0001c0001t0001g0150 a0001c0001t0001g0220 a0001c0001t0001g0338 others(4): Show |
7 | HG00280.hp1 HG00423.hp1 HG00642.hp1 others(4): Show |
intron_variant | MODIFIER | c.413+4673_413+4674i others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423308 | ||||||
| chr12:423308 | A | ATT | 84 | a0001c0001t0001g0292 a0001c0001t0001g0396 a0001c0001t0002g0004 others(81): Show |
87 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.413+4683_413+4684d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423308 | ||||||
| chr12:423308 | A | T | 1 | a0001c0001t0002g0051 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.413+4672A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423308 | |||||||
| chr12:423309 | T | TA | 14 | a0001c0001t0002g0335 a0001c0001t0002g0346 a0001c0001t0002g0403 others(11): Show |
14 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.413+4673_413+4674i others(3): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423309 | |||||||
| chr12:423310 | T | A | 51 | a0001c0001t0001g0151 a0001c0001t0001g0178 a0001c0001t0001g0241 others(48): Show |
52 | HG00597.hp1 HG00673.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.413+4674T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423310 | |||||||
| chr12:423311 | T | A | 1 | a0003c0003t0001g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.413+4675T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423311 | |||||||
| chr12:423319 | T | G | 5 | a0001c0001t0001g0178 a0001c0001t0001g0406 a0001c0001t0001g0407 others(2): Show |
5 | HG01168.hp1 HG01261.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.413+4683T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423319 | |||||||
| chr12:423394 | C | A | 2 | a0001c0001t0002g0083 a0003c0003t0002g0380 |
2 | HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.413+4758C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423394 | |||||||
| chr12:423468 | GTGTTTTT others(17): Show |
G | 9 | a0001c0001t0004g0399 a0005c0005t0005g0332 a0005c0005t0005g0409 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+4841_413+4864d others(26): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423468 | ||||||
| chr12:423470 | G | GT | 10 | a0001c0001t0001g0151 a0001c0001t0001g0365 a0001c0001t0007g0015 others(7): Show |
10 | HG01346.hp1 HG02683.hp1 HG02698.hp1 others(7): Show |
intron_variant | MODIFIER | c.413+4840dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423470 | ||||||
| chr12:423470 | G | GTTT | 5 | a0001c0001t0001g0396 a0002c0002t0001g0109 a0002c0002t0001g0128 others(2): Show |
5 | HG02630.hp2 HG03942.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.413+4838_413+4840d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423470 | ||||||
| chr12:423470 | G | GTTTTT | 11 | a0001c0001t0004g0098 a0001c0001t0004g0246 a0001c0001t0004g0328 others(8): Show |
11 | HG01081.hp1 HG01109.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.413+4836_413+4840d others(7): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423470 | ||||||
| chr12:423470 | G | GTTTTTTT others(5): Show |
1 | a0002c0002t0001g0117 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.413+4840_413+4841i others(14): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423470 | ||||||
| chr12:423470 | GTTTTTTG others(16): Show |
G | 1 | a0005c0005t0005g0410 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.413+4835_413+4857d others(25): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423470 | |||||||
| chr12:423470 | GTTTTTTG others(24): Show |
G | 1 | a0003c0003t0001g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.413+4841_413+4871d others(33): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423470 | ||||||
| chr12:423471 | T | G | 1 | a0002c0002t0001g0387 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.413+4835T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423471 | |||||||
| chr12:423471 | TTTTTTGT others(16): Show |
T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0218 a0001c0001t0001g0237 others(1): Show |
4 | HG01192.hp2 HG02698.hp2 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+4841_413+4863d others(25): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423471 | ||||||
| chr12:423472 | T | G | 47 | a0001c0001t0001g0178 a0001c0001t0001g0406 a0001c0001t0001g0407 others(44): Show |
48 | HG00438.hp2 HG00621.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.413+4836T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423472 | |||||||
| chr12:423472 | TTTTTGTG others(15): Show |
T | 67 | a0001c0001t0001g0024 a0001c0001t0001g0108 a0001c0001t0001g0132 others(64): Show |
67 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.413+4841_413+4862d others(24): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423472 | ||||||
| chr12:423473 | TTTTGTG | T | 30 | a0001c0001t0002g0075 a0001c0001t0003g0002 a0001c0001t0003g0003 others(27): Show |
31 | HG00738.hp1 HG01496.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.413+4841_413+4846d others(8): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423473 | ||||||
| chr12:423473 | TTTTGTGT others(9): Show |
T | 2 | a0001c0001t0003g0125 a0004c0004t0001g0095 |
2 | HG01167.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.413+4841_413+4856d others(18): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423473 | ||||||
| chr12:423473 | TTTTGTGT others(14): Show |
T | 24 | a0001c0001t0001g0131 a0001c0001t0001g0178 a0001c0001t0001g0348 others(21): Show |
24 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.413+4841_413+4861d others(23): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423473 | ||||||
| chr12:423474 | T | G | 1 | a0002c0002t0001g0179 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.413+4838T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423474 | |||||||
| chr12:423474 | TTTGTG | T | 20 | a0001c0001t0002g0004 a0001c0001t0002g0041 a0001c0001t0003g0002 others(17): Show |
21 | HG00609.hp2 HG01934.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.413+4841_413+4845d others(7): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423474 | ||||||
| chr12:423474 | TTTGTGTT others(8): Show |
T | 10 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(7): Show |
10 | HG01192.hp1 HG01346.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.413+4841_413+4855d others(17): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423474 | ||||||
| chr12:423474 | TTTGTGTT others(13): Show |
T | 12 | a0001c0001t0001g0152 a0001c0001t0001g0217 a0001c0001t0004g0333 others(9): Show |
12 | HG00735.hp1 HG01168.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.413+4841_413+4860d others(22): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423474 | ||||||
| chr12:423475 | TTG | T | 31 | a0001c0001t0001g0241 a0001c0001t0004g0087 a0002c0002t0001g0005 others(28): Show |
32 | HG00423.hp1 HG00741.hp2 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.413+4843_413+4844d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423475 | ||||||
| chr12:423475 | TTGTGTTT others(7): Show |
T | 1 | a0003c0003t0001g0411 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.413+4841_413+4854d others(16): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423475 | ||||||
| chr12:423475 | TTGTGTTT others(12): Show |
T | 21 | a0001c0001t0004g0357 a0001c0001t0004g0384 a0001c0001t0006g0393 others(18): Show |
21 | HG00408.hp1 HG00423.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.413+4841_413+4859d others(21): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 423475 | ||||||
| chr12:423476 | TG | T | 32 | a0001c0001t0007g0016 a0002c0002t0001g0023 a0002c0002t0001g0124 others(29): Show |
32 | HG00280.hp2 HG00438.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.413+4841delG | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423476 | |||||||
| chr12:423476 | TGTG | T | 9 | a0001c0001t0003g0045 a0001c0001t0004g0086 a0001c0001t0004g0088 others(6): Show |
9 | HG01884.hp2 HG02080.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.413+4841_413+4843d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423476 | |||||||
| chr12:423476 | TGTGTTTT others(6): Show |
T | 3 | a0002c0002t0001g0050 a0004c0004t0001g0067 a0004c0004t0001g0069 |
3 | HG00741.hp1 HG01981.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.413+4841_413+4853d others(15): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423476 | |||||||
| chr12:423476 | TGTGTTTT others(11): Show |
T | 3 | a0002c0002t0001g0006 a0002c0002t0002g0082 a0004c0004t0002g0310 |
4 | HG02818.hp1 HG03130.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+4841_413+4858d others(20): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423476 | |||||||
| chr12:423477 | G | T | 43 | a0001c0001t0001g0151 a0001c0001t0001g0365 a0001c0001t0001g0396 others(40): Show |
44 | HG00621.hp2 HG00673.hp1 HG01346.hp1 others(41): Show |
intron_variant | MODIFIER | c.413+4841G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423477 | |||||||
| chr12:423479 | G | T | 116 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(113): Show |
118 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.413+4843G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423479 | |||||||
| chr12:423486 | T | G | 4 | a0002c0002t0001g0199 a0002c0002t0001g0233 a0002c0002t0001g0298 others(1): Show |
4 | HG01109.hp2 HG01175.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+4850T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423486 | |||||||
| chr12:423487 | T | G | 16 | a0002c0002t0001g0090 a0002c0002t0001g0130 a0002c0002t0001g0154 others(13): Show |
16 | HG00423.hp1 HG00741.hp2 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.413+4851T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423487 | |||||||
| chr12:423488 | T | TTGTTTGT others(3): Show |
4 | a0001c0001t0004g0246 a0003c0003t0004g0329 a0006c0006t0011g0103 others(1): Show |
4 | HG01891.hp1 HG02145.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.413+4852_413+4853i others(12): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423488 | |||||||
| chr12:423488 | T | TTTTTTGT others(3): Show |
3 | a0001c0001t0008g0170 a0003c0003t0007g0327 a0003c0003t0007g0412 |
3 | HG01243.hp1 NA18906.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.413+4852_413+4853i others(12): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423488 | |||||||
| chr12:423488 | T | TTTTTTTT others(3): Show |
2 | a0001c0001t0004g0328 a0003c0003t0004g0363 |
2 | HG01081.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.413+4852_413+4853i others(12): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423488 | |||||||
| chr12:423488 | TGTTTTG | T | 4 | a0001c0001t0003g0127 a0002c0002t0001g0400 a0004c0004t0001g0072 others(1): Show |
4 | HG01928.hp2 HG01978.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.413+4853_413+4858d others(8): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423488 | |||||||
| chr12:423489 | G | T | 175 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(172): Show |
180 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.413+4853G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423489 | |||||||
| chr12:423494 | G | T | 184 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0241 others(181): Show |
189 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(186): Show |
intron_variant | MODIFIER | c.413+4858G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423494 | |||||||
| chr12:423495 | T | G | 9 | a0001c0001t0004g0399 a0005c0005t0005g0332 a0005c0005t0005g0409 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.413+4859T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423495 | |||||||
| chr12:423499 | T | G | 5 | a0001c0001t0001g0405 a0001c0001t0002g0335 a0001c0001t0002g0353 others(2): Show |
5 | HG00738.hp2 HG02148.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.413+4863T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423499 | |||||||
| chr12:423504 | T | G | 2 | a0001c0001t0001g0405 a0002c0002t0001g0401 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.413+4868T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423504 | |||||||
| chr12:423553 | C | T | 1 | a0004c0004t0001g0315 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.413+4917C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423553 | |||||||
| chr12:423562 | C | T | 1 | a0003c0003t0001g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.413+4926C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423562 | |||||||
| chr12:423630 | G | T | 1 | a0001c0001t0002g0254 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.413+4994G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423630 | |||||||
| chr12:423671 | A | G | 1 | a0001c0001t0006g0393 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.413+5035A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423671 | |||||||
| chr12:423890 | C | G | 1 | a0001c0001t0002g0014 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.414-4879C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423890 | |||||||
| chr12:423932 | A | G | 3 | a0002c0002t0001g0118 a0002c0002t0001g0221 a0002c0002t0001g0222 |
3 | HG02698.hp1 HG03831.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.414-4837A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423932 | |||||||
| chr12:424017 | C | T | 1 | a0003c0003t0004g0337 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.414-4752C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 424017 | |||||||
| chr12:424083 | A | C | 3 | a0001c0001t0004g0176 a0003c0003t0002g0372 a0003c0003t0004g0175 |
3 | HG01891.hp2 HG01952.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.414-4686A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 424083 | |||||||
| chr12:424093 | C | T | 2 | a0002c0002t0001g0141 a0002c0002t0001g0183 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.414-4676C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 424093 | |||||||
| chr12:424405 | G | T | 33 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(30): Show |
33 | HG00597.hp1 HG01167.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.414-4364G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 424405 | |||||||
| chr12:424656 | A | G | 33 | a0001c0001t0002g0049 a0002c0002t0001g0050 a0002c0002t0001g0053 others(30): Show |
34 | HG00673.hp1 HG00741.hp1 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.414-4113A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 424656 | |||||||
| chr12:424783 | C | T | 8 | a0001c0001t0001g0402 a0001c0001t0004g0246 a0001c0001t0008g0170 others(5): Show |
8 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.414-3986C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 424783 | |||||||
| chr12:424919 | C | CT | 20 | a0001c0001t0001g0151 a0001c0001t0001g0200 a0001c0001t0001g0201 others(17): Show |
20 | HG01167.hp2 HG02258.hp1 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.414-3833dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 424919 | ||||||
| chr12:424919 | CT | C | 14 | a0001c0001t0001g0338 a0001c0001t0002g0059 a0001c0001t0004g0086 others(11): Show |
14 | HG01074.hp1 HG01256.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.414-3833delT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 424919 | ||||||
| chr12:424962 | C | T | 1 | a0005c0005t0005g0409 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.414-3807C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 424962 | |||||||
| chr12:424994 | G | A | 10 | a0001c0001t0004g0399 a0005c0005t0005g0332 a0005c0005t0005g0409 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.414-3775G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 424994 | |||||||
| chr12:425000 | G | A | 17 | a0002c0002t0001g0149 a0002c0002t0002g0082 a0002c0002t0002g0100 others(14): Show |
17 | HG00408.hp1 HG00423.hp2 HG02165.hp2 others(14): Show |
intron_variant | MODIFIER | c.414-3769G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 425000 | |||||||
| chr12:425065 | G | A | 1 | a0002c0002t0001g0179 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.414-3704G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 425065 | |||||||
| chr12:425177 | C | T | 1 | a0001c0001t0004g0331 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.414-3592C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 425177 | |||||||
| chr12:425200 | G | A | 10 | a0001c0001t0004g0399 a0005c0005t0005g0332 a0005c0005t0005g0409 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.414-3569G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 425200 | |||||||
| chr12:425221 | G | A | 1 | a0004c0004t0001g0315 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.414-3548G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 425221 | |||||||
| chr12:425223 | A | G | 215 | a0001c0001t0001g0151 a0001c0001t0001g0178 a0001c0001t0001g0241 others(212): Show |
221 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.414-3546A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 425223 | |||||||
| chr12:425297 | C | CAGAAGCT others(3204): Show |
1 | a0005c0005t0005g0418 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.414-3458_414-3457i others(3213): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425297 | ||||||
| chr12:425297 | C | CAGAAGCT others(2798): Show |
1 | a0007c0007t0005g0382 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2807): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425297 | ||||||
| chr12:425297 | C | CAGAAGCT others(2841): Show |
1 | a0005c0005t0005g0409 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2850): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425297 | ||||||
| chr12:425297 | C | CAGAAGCT others(2847): Show |
3 | a0005c0005t0005g0332 a0005c0005t0005g0416 a0005c0005t0005g0419 |
3 | HG02145.hp1 HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.414-3458_414-3457i others(2856): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425297 | ||||||
| chr12:425297 | C | CAGAAGCT others(3206): Show |
1 | a0005c0005t0005g0420 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.414-3458_414-3457i others(3215): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425297 | ||||||
| chr12:425297 | C | CAGAAGCT others(2848): Show |
1 | a0007c0007t0005g0197 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2857): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425297 | ||||||
| chr12:425297 | C | CAGAAGCT others(2670): Show |
1 | a0005c0005t0005g0410 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2679): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425297 | ||||||
| chr12:425297 | C | CAGAAGCT others(2845): Show |
1 | a0001c0001t0004g0399 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2854): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425297 | ||||||
| chr12:425297 | C | CAGAAGCT others(2507): Show |
1 | a0001c0001t0006g0394 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2516): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425297 | ||||||
| chr12:425297 | C | CAGAAGCT others(2507): Show |
1 | a0001c0001t0006g0388 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2516): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425297 | ||||||
| chr12:425297 | C | CAGAAGCT others(2458): Show |
1 | a0003c0003t0006g0084 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2467): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425297 | ||||||
| chr12:425297 | C | CAGAAGCT others(2507): Show |
3 | a0001c0001t0006g0012 a0001c0001t0006g0389 a0001c0001t0006g0390 |
3 | HG00735.hp1 NA18941.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.414-3458_414-3457i others(2516): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425297 | ||||||
| chr12:425297 | C | CAGAAGCT others(2507): Show |
2 | a0001c0001t0006g0391 a0001c0001t0006g0392 |
2 | NA18981.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.414-3458_414-3457i others(2516): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425297 | ||||||
| chr12:425297 | C | CAGAAGCT others(2509): Show |
1 | a0001c0001t0006g0393 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2518): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425297 | ||||||
| chr12:425298 | A | AGAAGCTG others(2481): Show |
1 | a0003c0003t0001g0411 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2490): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425298 | A | AGAAGCTG others(2482): Show |
1 | a0001c0001t0001g0281 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2491): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425298 | A | AGAAGCTG others(2331): Show |
1 | a0003c0003t0004g0329 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2340): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425298 | A | AGAAGCTG others(2562): Show |
1 | a0003c0003t0004g0363 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2571): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425298 | A | AGAAGCTG others(2332): Show |
6 | a0001c0001t0004g0246 a0001c0001t0008g0170 a0003c0003t0007g0327 others(3): Show |
6 | HG01243.hp1 HG01891.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-3458_414-3457i others(2341): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425298 | A | AGAAGCTG others(2511): Show |
1 | a0001c0001t0004g0328 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2520): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425298 | A | AGAAGCTG others(2482): Show |
1 | a0003c0003t0001g0094 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2491): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425298 | A | AGAAGCTG others(2490): Show |
1 | a0003c0003t0001g0316 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2499): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425298 | A | AGAAGCTG others(2483): Show |
2 | a0001c0001t0001g0245 a0003c0003t0001g0413 |
2 | HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.414-3458_414-3457i others(2492): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425298 | A | AGAAGCTG others(2489): Show |
4 | a0002c0002t0001g0322 a0002c0002t0001g0385 a0003c0003t0001g0287 others(1): Show |
4 | HG02109.hp2 HG02559.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-3458_414-3457i others(2498): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425298 | A | AGAAGCTG others(2492): Show |
1 | a0001c0001t0001g0147 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2501): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425298 | A | AGAAGCTG others(2840): Show |
1 | a0003c0003t0004g0175 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2849): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425298 | A | AGAAGCTG others(2840): Show |
1 | a0001c0001t0004g0176 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2849): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425298 | A | AGAAGCTG others(2841): Show |
1 | a0003c0003t0002g0372 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2850): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425298 | A | AGAAGCTG others(2829): Show |
1 | a0003c0003t0001g0250 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2838): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425298 | A | AGAAGCTG others(2841): Show |
1 | a0002c0002t0001g0387 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2850): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425298 | A | AGAAGCTG others(2618): Show |
1 | a0002c0002t0014g0321 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2627): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425298 | A | AGAAGCTG others(2881): Show |
1 | a0003c0003t0001g0251 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.414-3458_414-3457i others(2890): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425298 | A | AGAAGCTG others(2830): Show |
2 | a0003c0003t0001g0341 a0003c0003t0001g0342 |
2 | HG01106.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.414-3458_414-3457i others(2839): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425298 | ||||||
| chr12:425380 | C | CT | 9 | a0001c0001t0001g0178 a0001c0001t0001g0406 a0001c0001t0001g0407 others(6): Show |
9 | HG01167.hp1 HG01168.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-3387dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 425380 | ||||||
| chr12:425444 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0001g0365 |
2 | NA18961.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.414-3325C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 425444 | |||||||
| chr12:425503 | C | T | 1 | a0001c0001t0003g0046 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.414-3266C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 425503 | |||||||
| chr12:425506 | C | T | 5 | a0001c0001t0001g0178 a0001c0001t0001g0406 a0001c0001t0001g0407 others(2): Show |
5 | HG01168.hp1 HG01261.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.414-3263C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 425506 | |||||||
| chr12:425779 | G | A | 9 | a0001c0001t0006g0012 a0001c0001t0006g0388 a0001c0001t0006g0389 others(6): Show |
9 | HG00735.hp1 HG02155.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-2990G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 425779 | |||||||
| chr12:425791 | G | A | 76 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(73): Show |
76 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(73): Show |
intron_variant | MODIFIER | c.414-2978G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 425791 | |||||||
| chr12:425793 | G | A | 9 | a0001c0001t0006g0012 a0001c0001t0006g0388 a0001c0001t0006g0389 others(6): Show |
9 | HG00735.hp1 HG02155.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-2976G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 425793 | |||||||
| chr12:425819 | C | T | 29 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(26): Show |
29 | HG01081.hp1 HG01106.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.414-2950C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 425819 | |||||||
| chr12:425898 | T | A | 75 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(72): Show |
75 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.414-2871T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 425898 | |||||||
| chr12:425932 | G | A | 1 | a0001c0001t0002g0041 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.414-2837G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 425932 | |||||||
| chr12:425985 | C | G | 1 | a0001c0001t0002g0013 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.414-2784C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 425985 | |||||||
| chr12:426008 | C | T | 3 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 |
3 | NA18961.hp1 NA18997.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.414-2761C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 426008 | |||||||
| chr12:426080 | G | A | 1 | a0001c0001t0002g0013 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.414-2689G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 426080 | |||||||
| chr12:426154 | C | T | 1 | a0003c0003t0004g0337 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.414-2615C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 426154 | |||||||
| chr12:426174 | A | G | 1 | a0007c0007t0005g0197 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.414-2595A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 426174 | |||||||
| chr12:426374 | A | G | 49 | a0001c0001t0002g0004 a0001c0001t0002g0041 a0001c0001t0002g0074 others(46): Show |
52 | HG00609.hp2 HG00738.hp1 HG01496.hp2 others(49): Show |
intron_variant | MODIFIER | c.414-2395A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 426374 | |||||||
| chr12:426410 | CTCTTA | C | 3 | a0001c0001t0004g0176 a0003c0003t0002g0372 a0003c0003t0004g0175 |
3 | HG01891.hp2 HG01952.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.414-2354_414-2350d others(7): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 426410 | ||||||
| chr12:426646 | G | A | 215 | a0001c0001t0001g0151 a0001c0001t0001g0178 a0001c0001t0001g0241 others(212): Show |
221 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.414-2123G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 426646 | |||||||
| chr12:426724 | C | T | 33 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(30): Show |
33 | HG00597.hp1 HG01167.hp2 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.414-2045C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 426724 | |||||||
| chr12:426842 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.414-1927G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 426842 | |||||||
| chr12:426870 | A | T | 4 | a0002c0002t0001g0133 a0002c0002t0001g0134 a0002c0002t0001g0135 others(1): Show |
4 | NA18962.hp2 NA19054.hp2 NA19057.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-1899A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 426870 | |||||||
| chr12:426890 | G | A | 74 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(71): Show |
74 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.414-1879G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 426890 | |||||||
| chr12:426891 | A | C | 37 | a0001c0001t0004g0093 a0001c0001t0004g0159 a0001c0001t0004g0160 others(34): Show |
37 | HG00735.hp1 HG01081.hp1 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.414-1878A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 426891 | |||||||
| chr12:426910 | C | T | 2 | a0001c0001t0010g0277 a0001c0001t0010g0278 |
2 | HG01433.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.414-1859C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 426910 | |||||||
| chr12:426998 | C | T | 1 | a0002c0002t0001g0006 | 2 | HG02818.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.414-1771C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 426998 | |||||||
| chr12:427008 | T | A | 1 | a0001c0001t0003g0030 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.414-1761T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 427008 | |||||||
| chr12:427061 | A | C | 1 | a0004c0004t0001g0279 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.414-1708A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 427061 | |||||||
| chr12:427066 | G | A | 1 | a0001c0001t0002g0403 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.414-1703G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 427066 | |||||||
| chr12:427106 | A | G | 4 | a0001c0001t0003g0127 a0002c0002t0001g0199 a0002c0002t0001g0298 others(1): Show |
4 | HG01175.hp2 HG02809.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-1663A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 427106 | |||||||
| chr12:427115 | T | G | 1 | a0001c0001t0001g0164 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.414-1654T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 427115 | |||||||
| chr12:427117 | C | T | 1 | a0001c0001t0003g0034 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.414-1652C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 427117 | |||||||
| chr12:427137 | C | T | 14 | a0001c0001t0003g0018 a0001c0001t0003g0054 a0001c0001t0003g0099 others(11): Show |
14 | HG00735.hp1 HG01496.hp2 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.414-1632C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 427137 | |||||||
| chr12:427176 | C | T | 1 | a0003c0003t0004g0369 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.414-1593C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 427176 | |||||||
| chr12:427200 | A | G | 6 | a0001c0001t0002g0299 a0001c0001t0002g0386 a0001c0001t0002g0398 others(3): Show |
6 | HG01358.hp2 HG02809.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-1569A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 427200 | |||||||
| chr12:427206 | T | C | 6 | a0001c0001t0002g0299 a0001c0001t0002g0386 a0001c0001t0002g0398 others(3): Show |
6 | HG01358.hp2 HG02809.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.414-1563T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 427206 | |||||||
| chr12:427209 | C | T | 1 | a0001c0001t0002g0138 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.414-1560C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 427209 | |||||||
| chr12:427232 | G | A | 117 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(114): Show |
117 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.414-1537G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 427232 | |||||||
| chr12:427250 | GA | G | 189 | a0001c0001t0001g0151 a0001c0001t0001g0178 a0001c0001t0001g0241 others(186): Show |
195 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(192): Show |
intron_variant | MODIFIER | c.414-1508delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 427250 | ||||||
| chr12:427293 | T | A | 11 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(8): Show |
11 | HG01192.hp1 HG01346.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.414-1476T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 427293 | |||||||
| chr12:427405 | C | T | 71 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0013 others(68): Show |
77 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.414-1364C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 427405 | |||||||
| chr12:427475 | A | AT | 23 | a0001c0001t0001g0147 a0001c0001t0002g0335 a0001c0001t0006g0012 others(20): Show |
23 | HG00735.hp1 HG01192.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.414-1277dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 427475 | ||||||
| chr12:427475 | AT | A | 106 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(103): Show |
106 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.414-1277delT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 427475 | ||||||
| chr12:427475 | ATT | A | 21 | a0001c0001t0004g0093 a0001c0001t0004g0159 a0001c0001t0004g0160 others(18): Show |
21 | HG01106.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.414-1278_414-1277d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 427475 | ||||||
| chr12:427624 | G | A | 1 | a0001c0001t0003g0127 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.414-1145G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 427624 | |||||||
| chr12:427719 | G | A | 1 | a0001c0001t0002g0254 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.414-1050G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 427719 | |||||||
| chr12:427789 | C | T | 2 | a0001c0001t0001g0405 a0002c0002t0001g0401 |
2 | HG02451.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.414-980C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 427789 | |||||||
| chr12:428126 | C | T | 1 | a0003c0003t0002g0068 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.414-643C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428126 | |||||||
| chr12:428239 | G | A | 1 | a0001c0001t0001g0402 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.414-530G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428239 | |||||||
| chr12:428250 | C | T | 1 | a0004c0004t0001g0304 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.414-519C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428250 | |||||||
| chr12:428251 | G | C | 7 | a0001c0001t0004g0176 a0002c0002t0001g0387 a0003c0003t0001g0250 others(4): Show |
7 | HG01106.hp2 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.414-518G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428251 | |||||||
| chr12:428279 | G | A | 9 | a0001c0001t0006g0012 a0001c0001t0006g0388 a0001c0001t0006g0389 others(6): Show |
9 | HG00735.hp1 HG02155.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.414-490G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428279 | |||||||
| chr12:428339 | T | C | 1 | a0001c0001t0004g0357 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.414-430T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428339 | |||||||
| chr12:428367 | C | T | 5 | a0001c0001t0001g0406 a0001c0001t0001g0407 a0001c0001t0001g0408 others(2): Show |
5 | HG01168.hp1 HG01261.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.414-402C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428367 | |||||||
| chr12:428372 | A | G | 3 | a0001c0001t0003g0003 a0001c0001t0003g0030 a0001c0001t0003g0034 |
4 | HG02074.hp1 HG02155.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.414-397A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428372 | |||||||
| chr12:428381 | G | C | 3 | a0001c0001t0003g0003 a0001c0001t0003g0030 a0001c0001t0003g0034 |
4 | HG02074.hp1 HG02155.hp1 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.414-388G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428381 | |||||||
| chr12:428438 | C | G | 4 | a0001c0001t0001g0178 a0001c0001t0004g0246 a0001c0001t0008g0170 others(1): Show |
4 | HG02717.hp2 HG03041.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.414-331C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428438 | |||||||
| chr12:428447 | G | C | 11 | a0001c0001t0004g0246 a0003c0003t0001g0148 a0003c0003t0002g0009 others(8): Show |
12 | HG00544.hp1 HG03041.hp2 HG03453.hp1 others(9): Show |
intron_variant | MODIFIER | c.414-322G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428447 | |||||||
| chr12:428447 | G | T | 2 | a0001c0001t0001g0131 a0001c0001t0001g0348 |
2 | HG01175.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.414-322G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428447 | |||||||
| chr12:428460 | A | G | 13 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(10): Show |
13 | HG01192.hp1 HG01346.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.414-309A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428460 | |||||||
| chr12:428464 | C | T | 1 | a0001c0001t0004g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.414-305C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428464 | |||||||
| chr12:428465 | C | T | 1 | a0001c0001t0004g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.414-304C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428465 | |||||||
| chr12:428466 | G | A | 10 | a0001c0001t0006g0012 a0001c0001t0006g0388 a0001c0001t0006g0389 others(7): Show |
10 | HG00735.hp1 HG01978.hp2 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.414-303G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428466 | |||||||
| chr12:428468 | A | G | 1 | a0001c0001t0004g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.414-301A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428468 | |||||||
| chr12:428472 | T | C | 7 | a0001c0001t0002g0347 a0001c0001t0004g0246 a0003c0003t0007g0327 others(4): Show |
7 | HG00735.hp2 HG01243.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.414-297T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428472 | |||||||
| chr12:428485 | T | C | 1 | a0002c0002t0001g0291 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.414-284T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428485 | |||||||
| chr12:428485 | T | G | 1 | a0004c0004t0001g0304 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.414-284T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428485 | |||||||
| chr12:428488 | A | G | 3 | a0001c0001t0004g0246 a0002c0002t0001g0291 a0004c0004t0001g0304 |
3 | HG00280.hp2 HG03041.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.414-281A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428488 | |||||||
| chr12:428490 | A | C | 1 | a0001c0001t0004g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.414-279A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428490 | |||||||
| chr12:428491 | A | G | 1 | a0002c0002t0001g0291 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.414-278A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428491 | |||||||
| chr12:428497 | C | T | 1 | a0002c0002t0001g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.414-272C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428497 | |||||||
| chr12:428510 | C | CA | 24 | a0001c0001t0001g0147 a0001c0001t0002g0137 a0001c0001t0002g0138 others(21): Show |
24 | HG01192.hp1 HG01358.hp2 HG02071.hp1 others(21): Show |
intron_variant | MODIFIER | c.414-233dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 428510 | ||||||
| chr12:428510 | C | CAAAAA | 9 | a0001c0001t0004g0093 a0001c0001t0004g0159 a0001c0001t0004g0160 others(6): Show |
9 | HG01167.hp2 HG01169.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.414-237_414-233dup others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 428510 | ||||||
| chr12:428510 | C | CAAAAAAA others(3): Show |
6 | a0001c0001t0001g0241 a0001c0001t0004g0089 a0001c0001t0004g0096 others(3): Show |
6 | HG00597.hp1 HG02257.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.414-242_414-233dup others(10): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 428510 | ||||||
| chr12:428510 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0007g0015 a0001c0001t0007g0016 a0004c0004t0001g0315 others(1): Show |
4 | HG02145.hp2 HG03139.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.414-243_414-233dup others(11): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 428510 | ||||||
| chr12:428510 | C | CAAAAAAA others(6): Show |
3 | a0003c0003t0001g0148 a0003c0003t0007g0327 a0006c0006t0011g0106 |
3 | HG01891.hp1 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.414-245_414-233dup others(13): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 428510 | ||||||
| chr12:428510 | C | CAAAAAAA others(7): Show |
1 | a0003c0003t0007g0412 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.414-246_414-233dup others(14): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 428510 | ||||||
| chr12:428510 | CA | C | 199 | a0001c0001t0001g0025 a0001c0001t0001g0108 a0001c0001t0001g0131 others(196): Show |
205 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.414-233delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 428510 | ||||||
| chr12:428510 | CAAAA | C | 12 | a0001c0001t0004g0088 a0001c0001t0004g0091 a0001c0001t0004g0328 others(9): Show |
12 | HG00735.hp1 HG01081.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.414-236_414-233del others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 428510 | ||||||
| chr12:428510 | CAAAAA | C | 12 | a0001c0001t0001g0178 a0001c0001t0001g0406 a0001c0001t0001g0407 others(9): Show |
12 | HG01109.hp1 HG01167.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.414-237_414-233del others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 428510 | ||||||
| chr12:428595 | C | G | 1 | a0002c0002t0001g0186 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.414-174C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428595 | |||||||
| chr12:428654 | A | T | 1 | a0001c0001t0004g0098 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.414-115A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428654 | |||||||
| chr12:428656 | T | A | 1 | a0001c0001t0004g0098 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.414-113T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428656 | |||||||
| chr12:428659 | G | T | 1 | a0001c0001t0004g0098 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.414-110G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428659 | |||||||
| chr12:428662 | G | T | 75 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(72): Show |
75 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.414-107G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 428662 | |||||||
| chr12:428675 | T | TA | 337 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(334): Show |
343 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(340): Show |
intron_variant | MODIFIER | c.414-84dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 428675 | ||||||
| chr12:428948 | C | T | 1 | a0003c0003t0002g0249 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.510+83C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 428948 | |||||||
| chr12:428949 | G | A | 2 | a0001c0001t0004g0176 a0003c0003t0004g0175 |
2 | HG01891.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.510+84G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 428949 | |||||||
| chr12:429128 | A | G | 324 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(321): Show |
329 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(326): Show |
intron_variant | MODIFIER | c.510+263A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 429128 | |||||||
| chr12:429305 | T | C | 19 | a0001c0001t0004g0399 a0002c0002t0002g0082 a0002c0002t0002g0100 others(16): Show |
19 | HG00408.hp1 HG00423.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.510+440T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 429305 | |||||||
| chr12:429307 | T | C | 16 | a0001c0001t0004g0176 a0001c0001t0006g0012 a0001c0001t0006g0388 others(13): Show |
16 | HG00735.hp1 HG01106.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.510+442T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 429307 | |||||||
| chr12:429308 | A | G | 1 | a0001c0001t0002g0358 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.510+443A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 429308 | |||||||
| chr12:429342 | A | G | 1 | a0001c0001t0002g0049 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.510+477A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 429342 | |||||||
| chr12:429345 | G | A | 2 | a0001c0001t0002g0137 a0001c0001t0002g0138 |
2 | NA18963.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.510+480G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 429345 | |||||||
| chr12:429418 | G | C | 4 | a0003c0003t0001g0250 a0003c0003t0001g0251 a0003c0003t0001g0341 others(1): Show |
4 | HG01106.hp2 HG01884.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.510+553G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 429418 | |||||||
| chr12:429463 | C | CT | 180 | a0001c0001t0001g0396 a0001c0001t0002g0049 a0001c0001t0003g0002 others(177): Show |
185 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.510+613dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 429463 | ||||||
| chr12:429514 | G | A | 1 | a0003c0003t0001g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.510+649G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 429514 | |||||||
| chr12:429531 | C | T | 2 | a0002c0002t0001g0400 a0004c0004t0001g0095 |
2 | HG01167.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.510+666C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 429531 | |||||||
| chr12:429678 | C | T | 1 | a0002c0002t0001g0122 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.510+813C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 429678 | |||||||
| chr12:429702 | G | A | 1 | a0002c0002t0001g0319 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.510+837G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 429702 | |||||||
| chr12:429756 | C | A | 1 | a0001c0001t0002g0259 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.510+891C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 429756 | |||||||
| chr12:429798 | A | T | 1 | a0004c0004t0001g0095 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.511-866A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 429798 | |||||||
| chr12:429872 | G | C | 334 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(331): Show |
339 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(336): Show |
intron_variant | MODIFIER | c.511-792G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 429872 | |||||||
| chr12:429974 | TTTTG | T | 6 | a0002c0002t0002g0113 a0004c0004t0002g0305 a0004c0004t0002g0309 others(3): Show |
6 | HG00408.hp1 HG02165.hp2 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.511-686_511-683del others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 429974 | ||||||
| chr12:430056 | C | T | 11 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(8): Show |
11 | HG01192.hp1 HG01346.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.511-608C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 430056 | |||||||
| chr12:430201 | T | C | 61 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(58): Show |
61 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(58): Show |
intron_variant | MODIFIER | c.511-463T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 430201 | |||||||
| chr12:430488 | G | A | 1 | a0002c0002t0001g0235 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.511-176G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 430488 | |||||||
| chr12:430551 | A | AT | 15 | a0002c0002t0001g0005 a0002c0002t0001g0124 a0002c0002t0001g0141 others(12): Show |
16 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.511-112dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 430551 | ||||||
| chr12:430620 | C | T | 1 | a0002c0002t0001g0182 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.511-44C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 6/12 | chr12 | 430620 | |||||||
| chr12:430818 | C | T | 171 | a0001c0001t0001g0396 a0001c0001t0002g0049 a0001c0001t0003g0002 others(168): Show |
176 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(173): Show |
intron_variant | MODIFIER | c.583+82C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | chr12 | 430818 | |||||||
| chr12:430849 | T | C | 1 | a0001c0001t0002g0051 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.583+113T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | chr12 | 430849 | |||||||
| chr12:430876 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.583+140C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | chr12 | 430876 | |||||||
| chr12:430933 | A | G | 22 | a0001c0001t0004g0399 a0002c0002t0002g0082 a0002c0002t0002g0100 others(19): Show |
22 | HG00408.hp1 HG00423.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.583+197A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | chr12 | 430933 | |||||||
| chr12:430937 | G | A | 1 | a0002c0002t0001g0122 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.583+201G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | chr12 | 430937 | |||||||
| chr12:430940 | TG | T | 3 | a0004c0004t0001g0171 a0004c0004t0001g0339 a0004c0004t0005g0340 |
3 | HG02258.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.583+205delG | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | chr12 | 430940 | |||||||
| chr12:430944 | G | A | 75 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(72): Show |
75 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.583+208G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | chr12 | 430944 | |||||||
| chr12:430957 | G | A | 33 | a0001c0001t0002g0049 a0002c0002t0001g0050 a0002c0002t0001g0053 others(30): Show |
34 | HG00673.hp1 HG00741.hp1 HG01346.hp1 others(31): Show |
intron_variant | MODIFIER | c.583+221G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | chr12 | 430957 | |||||||
| chr12:431011 | C | T | 1 | a0003c0003t0002g0313 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.583+275C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | chr12 | 431011 | |||||||
| chr12:431045 | G | A | 7 | a0001c0001t0004g0176 a0002c0002t0001g0387 a0003c0003t0001g0250 others(4): Show |
7 | HG01106.hp2 HG01884.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.583+309G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | chr12 | 431045 | |||||||
| chr12:431066 | C | CA | 162 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(159): Show |
162 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.583+349dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 431066 | ||||||
| chr12:431066 | C | CAA | 17 | a0001c0001t0001g0131 a0001c0001t0001g0191 a0001c0001t0001g0220 others(14): Show |
17 | HG00438.hp2 HG00642.hp1 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.583+348_583+349dup others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 431066 | ||||||
| chr12:431066 | CA | C | 76 | a0001c0001t0001g0396 a0001c0001t0001g0405 a0001c0001t0002g0004 others(73): Show |
83 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.583+349delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 431066 | ||||||
| chr12:431098 | T | C | 9 | a0001c0001t0004g0086 a0001c0001t0004g0087 a0001c0001t0004g0088 others(6): Show |
9 | HG00597.hp1 HG02080.hp1 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.583+362T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | chr12 | 431098 | |||||||
| chr12:431210 | TTC | T | 71 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(68): Show |
71 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.583+476_583+477del others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 431210 | ||||||
| chr12:431211 | TC | T | 11 | a0001c0001t0001g0402 a0005c0005t0005g0332 a0005c0005t0005g0409 others(8): Show |
11 | HG02145.hp1 HG02280.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.583+476delC | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | chr12 | 431211 | |||||||
| chr12:431212 | C | CT | 102 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0405 others(99): Show |
109 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.583+494dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 431212 | ||||||
| chr12:431212 | CT | C | 49 | a0001c0001t0001g0151 a0001c0001t0001g0178 a0001c0001t0001g0241 others(46): Show |
49 | HG00597.hp1 HG00639.hp1 HG01074.hp2 others(46): Show |
intron_variant | MODIFIER | c.583+494delT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 431212 | ||||||
| chr12:431212 | CTT | C | 176 | a0001c0001t0001g0396 a0001c0001t0002g0049 a0001c0001t0003g0002 others(173): Show |
181 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.583+493_583+494del others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr12 | 431212 | ||||||
| chr12:431265 | C | G | 3 | a0001c0001t0002g0083 a0003c0003t0002g0372 a0003c0003t0002g0380 |
3 | HG02647.hp1 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.583+529C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | chr12 | 431265 | |||||||
| chr12:431378 | C | G | 45 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0011 others(42): Show |
51 | HG00323.hp1 HG00673.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.584-488C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | chr12 | 431378 | |||||||
| chr12:431723 | G | A | 26 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0245 others(23): Show |
26 | HG01106.hp2 HG01167.hp1 HG01168.hp1 others(23): Show |
intron_variant | MODIFIER | c.584-143G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | chr12 | 431723 | |||||||
| chr12:431828 | A | G | 335 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(332): Show |
340 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(337): Show |
intron_variant | MODIFIER | c.584-38A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 7/12 | chr12 | 431828 | |||||||
| chr12:431985 | G | A | 3 | a0001c0001t0002g0403 a0003c0003t0002g0368 a0003c0003t0002g0379 |
3 | HG02630.hp1 HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.672+31G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 8/12 | chr12 | 431985 | |||||||
| chr12:432072 | C | T | 2 | a0001c0001t0001g0024 a0001c0001t0001g0210 |
2 | HG00438.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.672+118C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 8/12 | chr12 | 432072 | |||||||
| chr12:432363 | T | C | 1 | a0002c0002t0001g0387 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.672+409T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 8/12 | chr12 | 432363 | |||||||
| chr12:432417 | C | T | 178 | a0001c0001t0001g0178 a0001c0001t0001g0396 a0001c0001t0001g0406 others(175): Show |
183 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.672+463C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 8/12 | chr12 | 432417 | |||||||
| chr12:432567 | C | G | 1 | a0003c0003t0001g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.673-607C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 8/12 | chr12 | 432567 | |||||||
| chr12:432726 | C | A | 1 | a0003c0003t0002g0249 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.673-448C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 8/12 | chr12 | 432726 | |||||||
| chr12:433345 | C | T | 2 | a0002c0002t0001g0400 a0004c0004t0001g0095 |
2 | HG01167.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.821+23C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 433345 | |||||||
| chr12:433350 | C | T | 8 | a0002c0002t0002g0082 a0002c0002t0002g0145 a0002c0002t0002g0162 others(5): Show |
8 | HG00423.hp2 NA18967.hp2 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.821+28C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 433350 | |||||||
| chr12:433468 | C | G | 3 | a0004c0004t0001g0171 a0004c0004t0001g0339 a0004c0004t0005g0340 |
3 | HG02258.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.821+146C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 433468 | |||||||
| chr12:433526 | G | A | 9 | a0001c0001t0006g0012 a0001c0001t0006g0388 a0001c0001t0006g0389 others(6): Show |
9 | HG00735.hp1 HG02155.hp2 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.821+204G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 433526 | |||||||
| chr12:433625 | C | T | 5 | a0002c0002t0001g0387 a0003c0003t0001g0250 a0003c0003t0001g0251 others(2): Show |
5 | HG01106.hp2 HG01884.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.821+303C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 433625 | |||||||
| chr12:433651 | C | CA | 18 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0245 others(15): Show |
18 | HG01168.hp1 HG01192.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.821+344dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 433651 | ||||||
| chr12:433651 | CA | C | 40 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(37): Show |
40 | HG00597.hp1 HG01167.hp1 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.821+344delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 433651 | ||||||
| chr12:433785 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.821+463C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 433785 | |||||||
| chr12:433809 | G | A | 39 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(36): Show |
39 | HG00597.hp1 HG01167.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.821+487G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 433809 | |||||||
| chr12:434040 | C | T | 38 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(35): Show |
38 | HG00597.hp1 HG01167.hp2 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.821+718C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 434040 | |||||||
| chr12:434051 | C | T | 10 | a0001c0001t0001g0147 a0001c0001t0001g0281 a0002c0002t0001g0322 others(7): Show |
10 | HG01192.hp1 HG01346.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.821+729C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 434051 | |||||||
| chr12:434074 | C | T | 1 | a0003c0003t0002g0270 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.821+752C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 434074 | |||||||
| chr12:434162 | T | TA | 17 | a0001c0001t0004g0246 a0001c0001t0004g0328 a0001c0001t0008g0170 others(14): Show |
17 | HG01081.hp1 HG01109.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.821+850dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 434162 | ||||||
| chr12:434162 | TA | T | 10 | a0001c0001t0003g0040 a0001c0001t0006g0012 a0001c0001t0006g0388 others(7): Show |
10 | HG00735.hp1 HG02155.hp2 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.821+850delA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 434162 | ||||||
| chr12:434271 | A | G | 15 | a0001c0001t0004g0246 a0001c0001t0004g0328 a0001c0001t0008g0170 others(12): Show |
15 | HG01081.hp1 HG01109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.821+949A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 434271 | |||||||
| chr12:434316 | G | T | 1 | a0002c0002t0014g0321 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.821+994G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 434316 | |||||||
| chr12:434353 | C | CT | 30 | a0001c0001t0001g0151 a0001c0001t0001g0237 a0001c0001t0001g0241 others(27): Show |
31 | HG00597.hp1 HG01069.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.821+1047dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 434353 | ||||||
| chr12:434353 | C | CTT | 16 | a0001c0001t0004g0093 a0001c0001t0004g0159 a0001c0001t0004g0160 others(13): Show |
16 | HG01167.hp2 HG01169.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.821+1046_821+1047d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 434353 | ||||||
| chr12:434353 | CT | C | 8 | a0001c0001t0001g0224 a0001c0001t0002g0403 a0001c0001t0003g0057 others(5): Show |
8 | HG02071.hp2 HG02630.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.821+1047delT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 434353 | ||||||
| chr12:434422 | G | A | 5 | a0002c0002t0001g0387 a0003c0003t0001g0250 a0003c0003t0001g0251 others(2): Show |
5 | HG01106.hp2 HG01884.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.821+1100G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 434422 | |||||||
| chr12:434490 | T | A | 17 | a0001c0001t0004g0399 a0002c0002t0002g0082 a0002c0002t0002g0100 others(14): Show |
17 | HG00408.hp1 HG00423.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.821+1168T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 434490 | |||||||
| chr12:434541 | G | A | 1 | a0003c0003t0001g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.821+1219G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 434541 | |||||||
| chr12:434546 | G | T | 2 | a0002c0002t0001g0400 a0004c0004t0001g0095 |
2 | HG01167.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.821+1224G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 434546 | |||||||
| chr12:434598 | C | T | 177 | a0001c0001t0001g0178 a0001c0001t0001g0396 a0001c0001t0001g0406 others(174): Show |
182 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.821+1276C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 434598 | |||||||
| chr12:434618 | C | T | 1 | a0004c0004t0001g0315 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.821+1296C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 434618 | |||||||
| chr12:434643 | C | T | 1 | a0002c0002t0001g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.821+1321C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 434643 | |||||||
| chr12:434719 | G | T | 1 | a0001c0001t0002g0325 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.821+1397G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 434719 | |||||||
| chr12:434849 | A | G | 11 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(8): Show |
11 | HG01192.hp1 HG01346.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.821+1527A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 434849 | |||||||
| chr12:434929 | A | G | 75 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(72): Show |
75 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.821+1607A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 434929 | |||||||
| chr12:434938 | T | C | 44 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0018 others(41): Show |
46 | HG00609.hp2 HG00738.hp1 HG01496.hp2 others(43): Show |
intron_variant | MODIFIER | c.821+1616T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 434938 | |||||||
| chr12:434947 | C | T | 15 | a0002c0002t0001g0005 a0002c0002t0001g0124 a0002c0002t0001g0141 others(12): Show |
16 | HG01257.hp1 HG01258.hp1 HG01934.hp2 others(13): Show |
intron_variant | MODIFIER | c.821+1625C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 434947 | |||||||
| chr12:434969 | T | TTTTCATC others(72): Show |
1 | a0001c0001t0001g0348 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.821+1726_821+1804d others(81): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 434969 | ||||||
| chr12:434969 | TTTTCATC others(72): Show |
T | 2 | a0002c0002t0001g0400 a0004c0004t0001g0095 |
2 | HG01167.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.821+1726_821+1804d others(81): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 434969 | ||||||
| chr12:435048 | GTTTCATC others(72): Show |
G | 176 | a0001c0001t0001g0178 a0001c0001t0001g0396 a0001c0001t0001g0406 others(173): Show |
181 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.821+1760_821+1838d others(81): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 435048 | ||||||
| chr12:435077 | ATTCCGTT others(71): Show |
A | 1 | a0002c0002t0001g0128 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.821+1756_821+1833d others(80): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 435077 | |||||||
| chr12:435161 | A | ATTTCCAA others(72): Show |
2 | a0001c0001t0002g0011 a0001c0001t0002g0352 |
3 | HG01243.hp2 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.821+1907_821+1985d others(81): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 435161 | ||||||
| chr12:435253 | C | T | 15 | a0001c0001t0004g0246 a0001c0001t0004g0328 a0001c0001t0008g0170 others(12): Show |
15 | HG01081.hp1 HG01109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.821+1931C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 435253 | |||||||
| chr12:435306 | T | G | 1 | a0001c0001t0001g0402 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.821+1984T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 435306 | |||||||
| chr12:435308 | T | A | 1 | a0001c0001t0002g0083 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.821+1986T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 435308 | |||||||
| chr12:435450 | C | G | 1 | a0004c0004t0002g0311 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.821+2128C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 435450 | |||||||
| chr12:435836 | G | A | 1 | a0003c0003t0004g0329 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.822-2499G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 435836 | |||||||
| chr12:435848 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.822-2487C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 435848 | |||||||
| chr12:435868 | C | T | 1 | a0003c0003t0002g0261 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.822-2467C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 435868 | |||||||
| chr12:435928 | T | A | 1 | a0004c0004t0001g0085 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.822-2407T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 435928 | |||||||
| chr12:436020 | A | G | 38 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0365 others(35): Show |
38 | HG00597.hp1 HG01167.hp2 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.822-2315A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436020 | |||||||
| chr12:436115 | C | CT | 150 | a0001c0001t0001g0024 a0001c0001t0001g0150 a0001c0001t0001g0210 others(147): Show |
154 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.822-2200dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 436115 | ||||||
| chr12:436115 | C | CTT | 50 | a0001c0001t0001g0151 a0001c0001t0001g0241 a0001c0001t0001g0292 others(47): Show |
51 | HG00597.hp1 HG00621.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.822-2201_822-2200d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 436115 | ||||||
| chr12:436115 | CT | C | 40 | a0001c0001t0001g0153 a0001c0001t0001g0178 a0001c0001t0001g0237 others(37): Show |
40 | HG00735.hp1 HG01081.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.822-2200delT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 436115 | ||||||
| chr12:436158 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.822-2177T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436158 | |||||||
| chr12:436168 | A | AGTG | 3 | a0001c0001t0004g0357 a0001c0001t0004g0384 a0008c0013t0004g0417 |
3 | HG00639.hp1 HG01074.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.822-2166_822-2164d others(5): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 436168 | ||||||
| chr12:436171 | G | A | 3 | a0001c0001t0001g0132 a0001c0001t0001g0307 a0001c0001t0001g0308 |
3 | HG00408.hp2 NA18959.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.822-2164G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436171 | |||||||
| chr12:436210 | C | T | 2 | a0001c0001t0001g0203 a0001c0001t0003g0078 |
2 | HG01261.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.822-2125C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436210 | |||||||
| chr12:436212 | G | C | 6 | a0001c0001t0002g0299 a0001c0001t0002g0386 a0001c0001t0002g0398 others(3): Show |
6 | HG01358.hp2 HG02809.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.822-2123G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436212 | |||||||
| chr12:436218 | T | C | 2 | a0001c0001t0003g0125 a0002c0002t0001g0306 |
2 | HG04204.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.822-2117T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436218 | |||||||
| chr12:436253 | G | A | 1 | a0002c0002t0001g0276 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.822-2082G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436253 | |||||||
| chr12:436262 | C | T | 2 | a0001c0001t0002g0051 a0003c0003t0001g0148 |
2 | HG03453.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.822-2073C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436262 | |||||||
| chr12:436263 | G | A | 1 | a0002c0002t0001g0276 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.822-2072G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436263 | |||||||
| chr12:436267 | A | G | 4 | a0002c0002t0014g0321 a0004c0004t0001g0171 a0004c0004t0001g0339 others(1): Show |
4 | HG02258.hp2 HG03195.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.822-2068A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436267 | |||||||
| chr12:436274 | C | T | 4 | a0002c0002t0014g0321 a0004c0004t0001g0171 a0004c0004t0001g0339 others(1): Show |
4 | HG02258.hp2 HG03195.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.822-2061C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436274 | |||||||
| chr12:436275 | G | A | 1 | a0002c0002t0001g0276 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.822-2060G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436275 | |||||||
| chr12:436279 | G | A | 2 | a0002c0002t0001g0400 a0004c0004t0001g0095 |
2 | HG01167.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.822-2056G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436279 | |||||||
| chr12:436284 | AT | A | 7 | a0001c0001t0004g0086 a0001c0001t0004g0176 a0001c0001t0010g0277 others(4): Show |
7 | HG01433.hp1 HG01891.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.822-2039delT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 436284 | ||||||
| chr12:436303 | A | G | 4 | a0001c0001t0004g0086 a0001c0001t0004g0087 a0001c0001t0004g0089 others(1): Show |
4 | NA18949.hp2 NA18982.hp2 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.822-2032A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436303 | |||||||
| chr12:436318 | A | G | 2 | a0001c0001t0004g0244 a0004c0004t0002g0097 |
2 | HG01496.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.822-2017A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436318 | |||||||
| chr12:436319 | A | G | 2 | a0001c0001t0004g0244 a0004c0004t0002g0097 |
2 | HG01496.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.822-2016A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436319 | |||||||
| chr12:436323 | T | A | 1 | a0004c0004t0002g0097 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.822-2012T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436323 | |||||||
| chr12:436519 | C | T | 11 | a0001c0001t0001g0178 a0001c0001t0001g0406 a0001c0001t0001g0407 others(8): Show |
11 | HG01106.hp2 HG01168.hp1 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.822-1816C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436519 | |||||||
| chr12:436616 | A | G | 1 | a0002c0002t0001g0130 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.822-1719A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436616 | |||||||
| chr12:436698 | T | C | 1 | a0002c0002t0001g0133 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.822-1637T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436698 | |||||||
| chr12:436724 | C | T | 69 | a0001c0001t0002g0004 a0001c0001t0002g0010 a0001c0001t0002g0011 others(66): Show |
76 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.822-1611C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436724 | |||||||
| chr12:436734 | G | A | 1 | a0001c0001t0006g0390 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.822-1601G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436734 | |||||||
| chr12:436735 | T | C | 5 | a0001c0001t0001g0178 a0001c0001t0001g0406 a0001c0001t0001g0407 others(2): Show |
5 | HG01168.hp1 HG01261.hp2 HG02602.hp2 others(2): Show |
intron_variant | MODIFIER | c.822-1600T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436735 | |||||||
| chr12:436847 | A | G | 157 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(154): Show |
159 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.822-1488A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436847 | |||||||
| chr12:436864 | C | T | 1 | a0001c0001t0001g0405 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.822-1471C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436864 | |||||||
| chr12:436870 | G | C | 204 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(201): Show |
206 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.822-1465G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436870 | |||||||
| chr12:436936 | G | C | 16 | a0001c0001t0001g0396 a0001c0001t0004g0246 a0001c0001t0004g0328 others(13): Show |
16 | HG01081.hp1 HG01109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.822-1399G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 436936 | |||||||
| chr12:437127 | A | G | 10 | a0001c0001t0001g0132 a0001c0001t0001g0307 a0001c0001t0001g0308 others(7): Show |
10 | HG00408.hp2 NA18950.hp2 NA18951.hp1 others(7): Show |
intron_variant | MODIFIER | c.822-1208A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 437127 | |||||||
| chr12:437534 | A | AGGAAGTT others(334): Show |
2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG00639.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.822-787_822-786ins others(341): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 437534 | ||||||
| chr12:437534 | A | AGGAAGTT others(335): Show |
1 | a0001c0001t0001g0220 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.822-787_822-786ins others(342): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 437534 | ||||||
| chr12:437534 | A | AGGAAGTT others(339): Show |
1 | a0001c0001t0001g0223 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.822-787_822-786ins others(346): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 437534 | ||||||
| chr12:437670 | C | G | 38 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0237 others(35): Show |
38 | HG00597.hp1 HG01081.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.822-665C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 437670 | |||||||
| chr12:437674 | A | G | 213 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(210): Show |
215 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(212): Show |
intron_variant | MODIFIER | c.822-661A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 437674 | |||||||
| chr12:437838 | C | G | 4 | a0001c0001t0002g0386 a0001c0001t0002g0398 a0003c0003t0002g0343 others(1): Show |
4 | HG02809.hp1 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.822-497C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 437838 | |||||||
| chr12:437845 | T | TA | 221 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(218): Show |
228 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.822-470dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 437845 | ||||||
| chr12:437845 | T | TAA | 159 | a0001c0001t0001g0151 a0001c0001t0001g0281 a0001c0001t0002g0288 others(156): Show |
164 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.822-471_822-470dup others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 437845 | ||||||
| chr12:437845 | T | TAAA | 16 | a0002c0002t0001g0291 a0002c0002t0014g0321 a0003c0003t0003g0065 others(13): Show |
16 | HG02145.hp1 HG02258.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.822-472_822-470dup others(3): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 437845 | ||||||
| chr12:437845 | T | TAAAA | 11 | a0002c0002t0002g0082 a0002c0002t0002g0100 a0002c0002t0002g0113 others(8): Show |
11 | HG00408.hp1 HG02165.hp2 NA18973.hp1 others(8): Show |
intron_variant | MODIFIER | c.822-473_822-470dup others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 437845 | ||||||
| chr12:437870 | T | G | 1 | a0002c0002t0001g0128 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.822-465T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 437870 | |||||||
| chr12:438059 | T | G | 2 | a0001c0001t0003g0036 a0001c0001t0003g0078 |
2 | NA18994.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.822-276T>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 438059 | |||||||
| chr12:438119 | G | A | 1 | a0001c0001t0001g0375 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.822-216G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 438119 | |||||||
| chr12:438159 | A | G | 412 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(409): Show |
424 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(421): Show |
intron_variant | MODIFIER | c.822-176A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 438159 | |||||||
| chr12:438163 | A | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | HG00323.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.822-172A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 438163 | |||||||
| chr12:438166 | A | G | 86 | a0001c0001t0001g0405 a0001c0001t0002g0004 a0001c0001t0002g0010 others(83): Show |
93 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.822-169A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 438166 | |||||||
| chr12:438277 | T | C | 1 | a0003c0003t0001g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.822-58T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 438277 | |||||||
| chr12:438288 | G | A | 1 | a0001c0001t0002g0378 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.822-47G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 9/12 | chr12 | 438288 | |||||||
| chr12:438847 | T | C | 1 | a0003c0003t0001g0148 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1041+293T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 438847 | |||||||
| chr12:438888 | G | A | 1 | a0001c0001t0002g0010 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1041+334G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 438888 | |||||||
| chr12:438895 | C | T | 1 | a0001c0001t0003g0061 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1041+341C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 438895 | |||||||
| chr12:438912 | C | CA | 38 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0224 others(35): Show |
38 | HG00738.hp1 HG01167.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.1041+374dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 438912 | ||||||
| chr12:438912 | C | CAA | 13 | a0001c0001t0001g0396 a0001c0001t0004g0087 a0001c0001t0004g0088 others(10): Show |
13 | HG00597.hp1 HG01081.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1041+373_1041+374d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 438912 | ||||||
| chr12:438966 | T | C | 3 | a0001c0001t0002g0055 a0001c0001t0002g0293 a0001c0001t0002g0294 |
3 | HG00544.hp2 HG00621.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1041+412T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 438966 | |||||||
| chr12:439064 | C | T | 1 | a0003c0003t0004g0337 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1041+510C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 439064 | |||||||
| chr12:439082 | C | A | 1 | a0001c0001t0016g0077 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1041+528C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 439082 | |||||||
| chr12:439107 | A | C | 3 | a0004c0004t0001g0171 a0004c0004t0001g0339 a0004c0004t0005g0340 |
3 | HG02258.hp2 NA19030.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1041+553A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 439107 | |||||||
| chr12:439194 | A | G | 47 | a0001c0001t0003g0002 a0001c0001t0003g0003 a0001c0001t0003g0018 others(44): Show |
49 | HG00609.hp2 HG00738.hp1 HG01433.hp1 others(46): Show |
intron_variant | MODIFIER | c.1041+640A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 439194 | |||||||
| chr12:439255 | C | G | 32 | a0002c0002t0001g0050 a0002c0002t0001g0053 a0002c0002t0001g0109 others(29): Show |
33 | HG00673.hp1 HG00741.hp1 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.1041+701C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 439255 | |||||||
| chr12:439291 | G | A | 73 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(70): Show |
73 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.1041+737G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 439291 | |||||||
| chr12:439444 | C | T | 1 | a0003c0003t0002g0261 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1041+890C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 439444 | |||||||
| chr12:439492 | C | T | 86 | a0001c0001t0001g0405 a0001c0001t0002g0004 a0001c0001t0002g0010 others(83): Show |
93 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1041+938C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 439492 | |||||||
| chr12:439518 | T | C | 9 | a0001c0001t0004g0086 a0001c0001t0004g0087 a0001c0001t0004g0088 others(6): Show |
9 | HG00597.hp1 HG02080.hp1 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.1041+964T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 439518 | |||||||
| chr12:439519 | C | CA | 129 | a0001c0001t0004g0176 a0001c0001t0016g0077 a0002c0002t0001g0005 others(126): Show |
132 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1041+977dupA | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 439519 | ||||||
| chr12:439569 | A | G | 4 | a0001c0001t0002g0083 a0001c0001t0002g0325 a0003c0003t0002g0372 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1041+1015A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 439569 | |||||||
| chr12:439649 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1042-968G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 439649 | |||||||
| chr12:439678 | G | A | 1 | a0002c0002t0001g0400 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1042-939G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 439678 | |||||||
| chr12:439728 | C | T | 4 | a0001c0001t0002g0083 a0001c0001t0002g0325 a0003c0003t0002g0372 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1042-889C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 439728 | |||||||
| chr12:439734 | C | T | 1 | a0001c0001t0002g0259 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1042-883C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 439734 | |||||||
| chr12:439737 | G | A | 1 | a0004c0004t0002g0311 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1042-880G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 439737 | |||||||
| chr12:439782 | A | G | 1 | a0003c0003t0002g0268 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1042-835A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 439782 | |||||||
| chr12:439789 | AAAAG | A | 30 | a0001c0001t0004g0086 a0001c0001t0004g0087 a0001c0001t0004g0088 others(27): Show |
30 | HG00597.hp1 HG01081.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1042-824_1042-821d others(6): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 439789 | ||||||
| chr12:439818 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1042-799G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 439818 | |||||||
| chr12:439903 | ACT | A | 7 | a0001c0001t0001g0178 a0001c0001t0001g0406 a0001c0001t0001g0407 others(4): Show |
7 | HG01168.hp1 HG01261.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1042-709_1042-708d others(4): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 439903 | ||||||
| chr12:440077 | G | A | 86 | a0001c0001t0001g0405 a0001c0001t0002g0004 a0001c0001t0002g0010 others(83): Show |
93 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1042-540G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 440077 | |||||||
| chr12:440078 | T | C | 2 | a0002c0002t0001g0154 a0002c0002t0001g0225 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1042-539T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 440078 | |||||||
| chr12:440102 | A | T | 115 | a0001c0001t0002g0044 a0001c0001t0002g0049 a0001c0001t0002g0055 others(112): Show |
118 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1042-515A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 440102 | |||||||
| chr12:440352 | G | C | 1 | a0002c0002t0001g0110 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1042-265G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 440352 | |||||||
| chr12:440374 | G | C | 412 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(409): Show |
424 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(421): Show |
intron_variant | MODIFIER | c.1042-243G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 10/12 | chr12 | 440374 | |||||||
| chr12:440788 | G | T | 15 | a0001c0001t0001g0147 a0001c0001t0001g0178 a0001c0001t0001g0245 others(12): Show |
15 | HG01168.hp1 HG01192.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.1167+46G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 11/12 | chr12 | 440788 | |||||||
| chr12:440791 | G | A | 3 | a0001c0001t0002g0398 a0003c0003t0002g0343 a0006c0006t0012g0105 |
3 | HG02809.hp1 HG03471.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1167+49G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 11/12 | chr12 | 440791 | |||||||
| chr12:440801 | C | T | 32 | a0002c0002t0001g0050 a0002c0002t0001g0053 a0002c0002t0001g0109 others(29): Show |
33 | HG00673.hp1 HG00741.hp1 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.1168-43C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 11/12 | chr12 | 440801 | |||||||
| chr12:440837 | T | C | 8 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(5): Show |
8 | HG01192.hp1 HG01346.hp2 HG02486.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.1168-7T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 11/12 | chr12 | 440837 | |||||||
| chr12:441150 | A | T | 1 | a0002c0002t0002g0100 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1320+154A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 12/12 | chr12 | 441150 | |||||||
| chr12:441248 | C | CAAGAAGT others(336): Show |
1 | a0001c0001t0002g0403 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1320+268_1320+269i others(345): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 441248 | ||||||
| chr12:441430 | C | T | 164 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0237 others(161): Show |
173 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(170): Show |
intron_variant | MODIFIER | c.1321-344C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 12/12 | chr12 | 441430 | |||||||
| chr12:441434 | T | TGCTTTCA others(29): Show |
1 | a0001c0001t0003g0228 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1321-306_1321-271d others(38): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 441434 | ||||||
| chr12:441494 | C | G | 3 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0237 |
3 | HG01192.hp2 HG02698.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1321-280C>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 12/12 | chr12 | 441494 | |||||||
| chr12:441499 | A | T | 1 | a0003c0003t0015g0301 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1321-275A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 12/12 | chr12 | 441499 | |||||||
| chr12:441730 | A | G | 31 | a0001c0001t0001g0396 a0001c0001t0004g0086 a0001c0001t0004g0087 others(28): Show |
31 | HG00597.hp1 HG01081.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1321-44A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 12/12 | chr12 | 441730 | |||||||
| chr12:441745 | C | CT | 20 | a0001c0001t0001g0147 a0001c0001t0001g0245 a0001c0001t0001g0281 others(17): Show |
20 | HG00735.hp1 HG01192.hp1 HG01346.hp2 others(17): Show |
intron_variant | MODIFIER | c.1321-12dupT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 441745 | ||||||
| chr12:441745 | CT | C | 216 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0108 others(213): Show |
222 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.1321-12delT | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 441745 | ||||||
| chr12:441745 | CTT | C | 11 | a0001c0001t0001g0198 a0001c0001t0001g0365 a0001c0001t0001g0405 others(8): Show |
13 | HG00323.hp1 HG00735.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1321-13_1321-12del others(2): Show |
CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 441745 | ||||||
| chr12:441758 | T | C | 1 | a0002c0002t0001g0130 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1321-16T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 12/12 | chr12 | 441758 | |||||||
| chr12:441762 | T | C | 1 | a0003c0003t0015g0301 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1321-12T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 12/12 | chr12 | 441762 | |||||||
| chr12:441763 | C | A | 1 | a0003c0003t0015g0301 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1321-11C>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 12/12 | chr12 | 441763 | |||||||
| chr12:441766 | A | C | 1 | a0003c0003t0015g0301 | 1 | NA19067.hp2 | splice_region_variant&intron_variant | LOW | c.1321-8A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 12/12 | chr12 | 441766 |