Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and 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 | copy fasta | chr12 | 396644 | 447642 |
| a0002 | 0/0 | 488 | 103 | 20 | 21 | 45 | 2 | 15 | 37 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0003 | 0/0 | 488 | 78 | 20 | 4 | 51 | 0 | 3 | 48 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0004 | 0/1 | 488 | 28 | 8 | 5 | 8 | 3 | 3 | 7 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0005 | 0/0 | 488 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0006 | 0/0 | 456 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0007 | 0/0 | 488 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0008 | 0/0 | 13 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0009 | 0/0 | 133 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0010 | 0/0 | 488 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0011 | 0/0 | 488 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 1467 | 205 | 30 | 47 | 93 | 7 | 27 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| c0002 | 0/0 | 1467 | 102 | 19 | 21 | 45 | 2 | 15 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| c0003 | 0/0 | 1467 | 78 | 20 | 4 | 51 | 0 | 3 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| c0004 | 0/1 | 1467 | 27 | 7 | 5 | 8 | 3 | 3 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| c0005 | 0/0 | 1467 | 7 | 7 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| c0006 | 0/0 | 1429 | 4 | 4 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| c0007 | 0/0 | 1467 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| c0008 | 0/0 | 1467 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| c0009 | 0/0 | 1467 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| c0010 | 0/0 | 1467 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| c0011 | 0/0 | 1467 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| c0012 | 0/0 | 1467 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| c0013 | 0/0 | 1467 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 834 | 202 | 41 | 50 | 65 | 8 | 37 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| t0002 | 0/0 | 834 | 109 | 12 | 12 | 75 | 4 | 6 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| t0003 | 0/0 | 834 | 47 | 0 | 5 | 38 | 0 | 4 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| t0004 | 0/0 | 834 | 34 | 17 | 8 | 9 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| t0005 | 0/0 | 834 | 11 | 11 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| t0006 | 0/0 | 834 | 9 | 0 | 1 | 8 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| t0007 | 1/0 | 834 | 5 | 1 | 1 | 2 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| t0008 | 0/0 | 834 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| t0009 | 0/0 | 834 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| t0010 | 0/0 | 834 | 2 | 0 | 1 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| t0011 | 0/0 | 818 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| t0012 | 0/0 | 818 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| t0013 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| t0014 | 0/0 | 834 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| t0015 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| t0016 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0187 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0358 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0386 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0387 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0390 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0391 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0393 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0394 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0398 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0399 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0401 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0405 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0406 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0407 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0408 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0409 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0410 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0411 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0412 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0413 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0414 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0415 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0416 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0417 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0418 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0419 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0420 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0421 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| g0422 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1467 | 205 | 30 | 47 | 93 | 7 | 27 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0002c0002 | 0/0 | 1467 | 102 | 19 | 21 | 45 | 2 | 15 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0002c0009 | 0/0 | 1467 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0003c0003 | 0/0 | 1467 | 78 | 20 | 4 | 51 | 0 | 3 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0004c0004 | 0/1 | 1467 | 27 | 7 | 5 | 8 | 3 | 3 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0004c0012 | 0/0 | 1467 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0005c0005 | 0/0 | 1467 | 7 | 7 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0006c0006 | 0/0 | 1429 | 4 | 4 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0007c0007 | 0/0 | 1467 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0008c0013 | 0/0 | 1467 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0009c0011 | 0/0 | 1467 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0010c0010 | 0/0 | 1467 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0011c0008 | 0/0 | 1467 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | 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 | copy fasta | chr12 | 396644 | 447642 |
| a0001c0001t0002 | 0/0 | 2300 | 46 | 6 | 12 | 21 | 4 | 3 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0001c0001t0003 | 0/0 | 2300 | 45 | 0 | 5 | 36 | 0 | 4 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0001c0001t0004 | 0/0 | 2300 | 28 | 13 | 6 | 9 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0001c0001t0006 | 0/0 | 2300 | 8 | 0 | 1 | 7 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0001c0001t0007 | 1/0 | 2300 | 3 | 0 | 0 | 2 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0001c0001t0008 | 0/0 | 2300 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0001c0001t0009 | 0/0 | 2300 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0001c0001t0010 | 0/0 | 2300 | 2 | 0 | 1 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0001c0001t0016 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0002c0002t0001 | 0/0 | 2300 | 92 | 18 | 21 | 36 | 2 | 15 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0002c0002t0002 | 0/0 | 2300 | 8 | 0 | 0 | 8 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0002c0002t0013 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0002c0002t0014 | 0/0 | 2300 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0002c0009t0001 | 0/0 | 2300 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0003c0003t0001 | 0/0 | 2300 | 19 | 8 | 2 | 9 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0003c0003t0002 | 0/0 | 2300 | 47 | 5 | 0 | 39 | 0 | 3 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0003c0003t0003 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0003c0003t0004 | 0/0 | 2300 | 5 | 4 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0003c0003t0006 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0003c0003t0007 | 0/0 | 2300 | 2 | 1 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0003c0003t0008 | 0/0 | 2300 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0003c0003t0009 | 0/0 | 2300 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0003c0003t0015 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0004c0004t0001 | 0/1 | 2300 | 20 | 5 | 5 | 3 | 3 | 3 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0004c0004t0002 | 0/0 | 2300 | 6 | 1 | 0 | 5 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0004c0004t0005 | 0/0 | 2300 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0004c0012t0001 | 0/0 | 2300 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0005c0005t0005 | 0/0 | 2300 | 7 | 7 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0006c0006t0011 | 0/0 | 2246 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0006c0006t0012 | 0/0 | 2246 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0007c0007t0005 | 0/0 | 2300 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0008c0013t0004 | 0/0 | 2300 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0009c0011t0002 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0010c0010t0003 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| a0011c0008t0002 | 0/0 | 2300 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | copy fasta | chr12 | 396644 | 447642 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0042 | 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 |
| a0001c0001t0001g0141 | 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 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0157 | 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 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0273 | 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 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0378 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0398 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0404 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0407 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0409 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0001g0410 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0058 | 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 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0116 | 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 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0338 | 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 |
| a0001c0001t0002g0348 | 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 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0388 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0400 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0002g0405 | 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 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| 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 |
| a0001c0001t0003g0044 | 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 | 0 | 1 | 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 |
| a0001c0001t0003g0050 | 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 |
| a0001c0001t0003g0053 | 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 |
| a0001c0001t0003g0055 | 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 |
| a0001c0001t0003g0059 | 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 |
| a0001c0001t0003g0077 | 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 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0320 | 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 |
| a0001c0001t0004g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0330 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0386 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0004g0401 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0004g0417 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0006g0395 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0006g0396 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0007g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0007g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0007g0358 | 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 |
| a0001c0001t0008g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0009g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0010g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0010g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0001c0001t0016g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0051 | 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 |
| a0002c0002t0001g0094 | 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 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0002c0002t0001g0143 | 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 |
| a0002c0002t0001g0152 | 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 |
| a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 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 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0321 | 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 |
| a0002c0002t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0354 | 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 |
| a0002c0002t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0373 | 0/0 | 1 | 0 | 1 | 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 |
| a0002c0002t0001g0389 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0402 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0001g0403 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0002g0083 | 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 |
| 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 |
| a0002c0002t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0013g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0002t0014g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0002c0009t0001g0406 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0003c0003t0001g0062 | 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 |
| a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0068 | 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 |
| a0003c0003t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0095 | 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 |
| a0003c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0001g0342 | 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 |
| a0003c0003t0001g0415 | 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 |
| a0003c0003t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0063 | 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 |
| a0003c0003t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0230 | 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 |
| a0003c0003t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0315 | 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 |
| a0003c0003t0002g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0381 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0382 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0002g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0004g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0004g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0004g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0004g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0006g0089 | 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 |
| a0003c0003t0007g0414 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0003c0003t0008g0276 | 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 |
| a0003c0003t0015g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0004c0004t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0096 | 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 |
| a0004c0004t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0187 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0004t0001g0375 | 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 |
| a0004c0004t0002g0307 | 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 |
| a0004c0004t0005g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0004c0012t0001g0416 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0005c0005t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0005c0005t0005g0411 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0005c0005t0005g0412 | 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 |
| a0005c0005t0005g0420 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0005c0005t0005g0421 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0005c0005t0005g0422 | 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 |
| a0007c0007t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0007c0007t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0007c0007t0005g0384 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0008c0013t0004g0419 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| a0009c0011t0002g0397 | 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 |
| a0011c0008t0002g0101 | 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 | g0306 | 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 | g0271 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00423 | hp2 | a0002 | c0002 | t0013 | g0363 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00544 | hp1 | a0003 | c0003 | t0002 | g0155 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0058 | 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 | g0116 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0067 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0299 | 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 | g0386 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0273 | 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 | g0380 | EAS | CHS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00735 | hp1 | a0001 | c0001 | t0006 | g0010 | 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 | g0026 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0362 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0038 | 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 | g0338 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0356 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01074 | hp2 | a0008 | c0013 | t0004 | g0419 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0330 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0172 | 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 | g0341 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01109 | hp1 | a0003 | c0003 | t0004 | g0365 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0316 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01167 | hp1 | a0004 | c0004 | t0001 | g0096 | 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 | g0408 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0153 | 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 | g0262 | 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 | g0297 | 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 | g0266 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01243 | hp1 | a0003 | c0003 | t0007 | g0414 | AMR | PUR | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0357 | 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 | g0141 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0143 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0221 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0410 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0122 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01346 | hp2 | a0003 | c0003 | t0001 | g0318 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0304 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01433 | hp1 | a0001 | c0001 | t0010 | g0281 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0280 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0269 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | IBS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0237 | EUR | IBS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | IBS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0009 | EUR | IBS | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0401 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01884 | hp2 | a0003 | c0003 | t0001 | g0188 | 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 | g0212 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01928 | hp2 | a0004 | c0004 | t0001 | g0071 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0033 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01934 | hp2 | a0002 | c0002 | t0001 | g0223 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0216 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0213 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0348 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0222 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01978 | hp1 | a0004 | c0004 | t0001 | g0072 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0373 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01981 | hp1 | a0004 | c0004 | t0001 | g0064 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0220 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0349 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0217 | 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 | g0226 | 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 | g0032 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0045 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0379 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | KHV | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02145 | hp1 | a0005 | c0005 | t0005 | g0334 | 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 | g0219 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0352 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | CDX | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02155 | hp2 | a0001 | c0001 | t0006 | g0391 | EAS | CDX | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02165 | hp1 | a0003 | c0003 | t0002 | g0201 | 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 | g0258 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0402 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0417 | 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 | g0235 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0295 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0404 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0283 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0218 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0361 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0215 | AMR | PEL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0407 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02451 | hp2 | a0002 | c0009 | t0001 | g0406 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0333 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02572 | hp2 | a0005 | c0005 | t0005 | g0422 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0409 | 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 | g0371 | 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 | g0381 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0398 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02647 | hp1 | a0003 | c0003 | t0002 | g0374 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02647 | hp2 | a0004 | c0012 | t0001 | g0416 | 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 | g0121 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02717 | hp1 | a0003 | c0003 | t0004 | g0331 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02723 | hp2 | a0003 | c0003 | t0001 | g0189 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02735 | hp1 | a0004 | c0004 | t0001 | g0207 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0377 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0378 | 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 | g0245 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0405 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0383 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02886 | hp2 | a0003 | c0003 | t0001 | g0342 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0319 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02895 | hp2 | a0005 | c0005 | t0005 | g0420 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02896 | hp1 | a0003 | c0003 | t0001 | g0415 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0227 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0284 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0320 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0183 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0092 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02970 | hp1 | a0005 | c0005 | t0005 | g0418 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02970 | hp2 | a0004 | c0004 | t0001 | g0375 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0399 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02976 | hp2 | a0005 | c0005 | t0005 | g0411 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03017 | hp2 | a0003 | c0003 | t0002 | g0210 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03041 | hp1 | a0003 | c0003 | t0001 | g0095 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0275 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0335 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03098 | hp2 | a0003 | c0003 | t0002 | g0370 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0329 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0389 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03139 | hp2 | a0004 | c0004 | t0001 | g0317 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03195 | hp1 | a0002 | c0002 | t0014 | g0323 | 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 | g0321 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03209 | hp2 | a0007 | c0007 | t0005 | g0384 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0336 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03225 | hp2 | a0007 | c0007 | t0005 | g0328 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0366 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0239 | 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 | g0214 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03486 | hp1 | a0003 | c0003 | t0008 | g0276 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0325 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0152 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0234 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03516 | hp2 | a0003 | c0003 | t0001 | g0413 | AFR | ESN | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0403 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0294 | AFR | GWD | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0388 | AFR | MSL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03579 | hp2 | a0005 | c0005 | t0005 | g0421 | 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 | g0041 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0247 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0364 | SAS | STU | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03688 | hp2 | a0004 | c0004 | t0001 | g0192 | SAS | STU | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03704 | hp2 | a0003 | c0003 | t0002 | g0205 | 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 | g0191 | SAS | PJL | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0261 | SAS | BEB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0254 | 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 | g0181 | 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 | g0337 | SAS | BEB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0236 | 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 | g0292 | 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 | g0260 | SAS | BEB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0259 | SAS | BEB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0094 | SAS | STU | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | STU | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0178 | 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 | g0268 | SAS | STU | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | STU | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0190 | EAS | CHB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0088 | EAS | CHB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18747 | hp1 | a0001 | c0001 | t0007 | g0013 | EAS | CHB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | CHB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18906 | hp1 | a0003 | c0003 | t0001 | g0289 | 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 | g0051 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18941 | hp2 | a0001 | c0001 | t0006 | g0392 | 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 | g0014 | 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 | g0296 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18945 | hp1 | a0003 | c0003 | t0002 | g0173 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0030 | 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 | g0395 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18949 | hp2 | a0001 | c0001 | t0004 | g0084 | 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 | g0230 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18951 | hp1 | a0003 | c0003 | t0002 | g0228 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0054 | 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 | g0229 | 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 | g0048 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0305 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0303 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18956 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0308 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18957 | hp2 | a0003 | c0003 | t0002 | g0285 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0068 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18960 | hp1 | a0003 | c0003 | t0002 | g0194 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18960 | hp2 | a0003 | c0003 | t0001 | g0017 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0367 | 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 | g0203 | 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 | g0307 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0256 | 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 | g0031 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0301 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0002 | 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 | g0355 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18971 | hp1 | a0003 | c0003 | t0002 | g0385 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18973 | hp1 | a0011 | 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 | g0006 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18977 | hp2 | a0003 | c0003 | t0002 | g0007 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0020 | 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 | g0291 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18980 | hp2 | a0003 | c0003 | t0002 | g0175 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18981 | hp1 | a0001 | c0001 | t0006 | g0393 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0052 | 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 | g0196 | 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 | g0204 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18985 | hp1 | a0003 | c0003 | t0002 | g0006 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18985 | hp2 | a0003 | c0003 | t0002 | g0232 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18986 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18988 | hp1 | a0003 | c0003 | t0002 | g0176 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0057 | 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 | g0199 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18991 | hp1 | a0003 | c0003 | t0002 | g0180 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18992 | hp1 | a0003 | c0003 | t0003 | g0069 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18992 | hp2 | a0003 | c0003 | t0002 | g0368 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18993 | hp2 | a0002 | c0002 | t0001 | g0243 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18995 | hp1 | a0003 | c0003 | t0002 | g0315 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0024 | 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 | g0302 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA18998 | hp2 | a0001 | c0001 | t0006 | g0394 | 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 | g0185 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19000 | hp1 | a0003 | c0003 | t0001 | g0073 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19000 | hp2 | a0003 | c0003 | t0001 | g0070 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19002 | hp1 | a0001 | c0001 | t0004 | g0086 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0040 | 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 | g0396 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19005 | hp1 | a0003 | c0003 | t0006 | g0089 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19006 | hp1 | a0003 | c0003 | t0002 | g0195 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19006 | hp2 | a0001 | c0001 | t0003 | g0053 | 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 | g0233 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19009 | hp1 | a0004 | c0004 | t0001 | g0177 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19009 | hp2 | a0003 | c0003 | t0002 | g0202 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19011 | hp1 | a0003 | c0003 | t0002 | g0007 | 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 | g0313 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0400 | AFR | LWK | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19030 | hp2 | a0004 | c0004 | t0005 | g0344 | AFR | LWK | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0387 | AFR | LWK | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0322 | AFR | LWK | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0060 | 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 | g0157 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0241 | 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 | g0372 | 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 | g0049 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0286 | 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 | g0248 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19065 | hp1 | a0009 | c0011 | t0002 | g0397 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0298 | 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 | g0015 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19067 | hp2 | a0003 | c0003 | t0015 | g0290 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19068 | hp2 | a0004 | c0004 | t0001 | g0065 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19070 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19072 | hp1 | a0001 | c0001 | t0004 | g0085 | 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 | g0264 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19074 | hp2 | a0003 | c0003 | t0002 | g0278 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19077 | hp2 | a0003 | c0003 | t0002 | g0200 | 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 | g0078 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19079 | hp1 | a0003 | c0003 | t0002 | g0193 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19079 | hp2 | a0003 | c0003 | t0002 | g0231 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19080 | hp1 | a0003 | c0003 | t0001 | g0066 | 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 | g0119 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19081 | hp2 | a0003 | c0003 | t0002 | g0376 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19082 | hp2 | a0003 | c0003 | t0002 | g0369 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0350 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19087 | hp1 | a0003 | c0003 | t0002 | g0063 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0244 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19088 | hp2 | a0003 | c0003 | t0002 | g0174 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19090 | hp2 | a0003 | c0003 | t0001 | g0062 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0123 | 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 | g0184 | 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 | g0279 | AFR | ASW | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA20752 | hp1 | a0004 | c0004 | t0001 | g0186 | 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 | g0340 | EUR | TSI | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA20905 | hp1 | a0001 | c0001 | t0010 | g0209 | SAS | GIH | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0242 | SAS | GIH | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0354 | AMR | CLM | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0359 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02109 | hp2 | a0004 | c0004 | t0001 | g0093 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0182 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02559 | hp1 | a0003 | c0003 | t0004 | g0339 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG02559 | hp2 | a0002 | c0002 | t0001 | g0326 | AFR | ACB | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| HG03471 | hp1 | a0003 | c0003 | t0002 | g0382 | 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 | g0412 | AFR | USA | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0224 | AFR | USA | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA21309 | hp1 | a0004 | c0004 | t0001 | g0345 | AFR | LWK | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| NA21309 | hp2 | a0002 | c0002 | t0001 | g0332 | AFR | LWK | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| homoSapiens_chm13v2 | hp1 | a0004 | c0004 | t0001 | g0187 | REF | REF | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0007 | g0358 | REF | REF | CCDC77_chr12_396644_447642 | CCDC77 | chr12 | 396644 | 447642 |
| 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 | a0003a0004a0005 | 113 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(110): 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 | a0009 | 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 | a0002a0004a0011 | 132 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(129): 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 | a0011 | 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 | a0005a0007 | 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 |
| 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 | a0005c0005a0007c0007 | 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 |
| 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 | a0001c0001t0008a0001c0001t0009a0003c0003t0008others(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 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(30): Show | 425 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(422): 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 | a0001c0001t0003a0003c0003t0003a0010c0010t0003 | 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 | a0001c0001t0002a0001c0001t0016a0002c0002t0002others(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 | a0001c0001t0006a0003c0003t0006 | 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 | a0004c0004t0005a0005c0005t0005a0007c0007t0005 | 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 | a0001c0001t0004a0001c0001t0008a0003c0003t0004others(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 |
| 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 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0006g0010 | 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 | a0001c0001t0007g0013a0001c0001t0007g0014 | 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 | 97 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0002g0003others(94): 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 | a0005c0005t0005g0420a0005c0005t0005g0421a0005c0005t0005g0422 | 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 | a0001c0001t0001g0398a0001c0001t0001g0404a0001c0001t0001g0407others(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 | a0001c0001t0006g0390a0001c0001t0006g0391a0001c0001t0006g0392others(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 | a0001c0001t0001g0108a0001c0001t0002g0116a0001c0001t0003g0125others(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 | a0001c0001t0002g0388a0001c0001t0004g0386a0002c0002t0001g0387others(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 | 93 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0002g0003others(90): 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 | a0001c0001t0004g0417a0003c0003t0001g0413a0003c0003t0001g0415others(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 | a0001c0001t0001g0131a0002c0002t0001g0130 | 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 | a0003c0003t0002g0385 | 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 | a0001c0001t0004g0383a0007c0007t0005g0384 | 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 | a0003c0003t0002g0381a0003c0003t0002g0382 | 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 | a0002c0002t0001g0109a0002c0002t0001g0110a0002c0002t0001g0111 | 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 | a0001c0001t0001g0404a0001c0001t0001g0407a0001c0001t0001g0408others(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 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0135 | 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 | 94 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0398others(91): 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 | a0001c0001t0002g0380 | 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 | a0001c0001t0001g0398 | 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 | 69 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0002g0003others(66): 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 | a0001c0001t0001g0398 | 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 | a0001c0001t0002g0136a0001c0001t0002g0137a0001c0001t0002g0138 | 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 | a0003c0003t0001g0140a0004c0004t0001g0139 | 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 | a0001c0001t0001g0408a0001c0001t0001g0409a0001c0001t0001g0410 | 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 | a0001c0001t0001g0398 | 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 | 73 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0377others(70): 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 | a0001c0001t0003g0080a0002c0002t0001g0079a0006c0006t0011g0103others(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 | a0001c0001t0001g0141a0001c0001t0002g0144a0001c0001t0004g0399others(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 | a0003c0003t0001g0015 | 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 | a0003c0003t0001g0015 | 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 | a0002c0002t0001g0373 | 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 | a0002c0002t0001g0372 | 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 | a0003c0003t0004g0371 | 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 | a0001c0001t0006g0390a0001c0001t0006g0391a0001c0001t0006g0392others(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 | 285 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0132others(282): Show | 293 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(290): 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 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0001t0001g0153others(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 | a0001c0001t0001g0398 | 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 | a0001c0001t0001g0378 | 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 | a0001c0001t0002g0003a0001c0001t0002g0074a0001c0001t0002g0075others(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 | a0001c0001t0006g0390a0001c0001t0006g0391a0001c0001t0006g0392others(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 | a0001c0001t0002g0329a0001c0001t0004g0159a0001c0001t0004g0160others(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 | a0011c0008t0002g0101 | 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 | a0002c0002t0001g0316 | 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 | a0003c0003t0001g0148a0003c0003t0002g0370 | 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 | 126 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0404others(123): 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 | a0003c0003t0001g0015a0003c0003t0001g0017a0003c0003t0001g0062others(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 | a0001c0001t0001g0407 | 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 | a0001c0001t0001g0108a0001c0001t0002g0116a0001c0001t0003g0125others(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 | 220 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0141others(217): Show | 226 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(223): 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 | a0003c0003t0002g0315 | 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 | a0003c0003t0001g0015a0003c0003t0001g0017a0003c0003t0001g0062others(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 | a0001c0001t0001g0151a0001c0001t0001g0367a0002c0002t0001g0163others(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 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 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 | a0001c0001t0001g0313a0001c0001t0001g0314a0002c0002t0001g0308others(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 | a0001c0001t0001g0366 | 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 | a0003c0003t0001g0148a0003c0003t0002g0370a0003c0003t0004g0365 | 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 | a0001c0001t0007g0013a0001c0001t0007g0014 | 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 | a0001c0001t0004g0417a0003c0003t0001g0413a0003c0003t0001g0415others(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 | a0001c0001t0001g0407a0001c0001t0002g0405a0002c0009t0001g0406 | 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 | a0004c0004t0001g0306 | 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 | a0001c0001t0001g0108a0001c0001t0001g0153a0001c0001t0001g0154others(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 | 244 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0131others(241): Show | 250 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(247): 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 | a0001c0001t0001g0147a0001c0001t0001g0298a0001c0001t0001g0377others(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 | a0003c0003t0002g0374 | 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 | a0001c0001t0002g0337 | 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 | a0001c0001t0002g0003a0001c0001t0002g0074a0001c0001t0002g0075 | 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 | 347 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0131others(344): Show | 355 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(352): 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 | a0001c0001t0002g0338 | 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 | a0001c0001t0001g0288 | 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 | 347 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0131others(344): Show | 355 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(352): Show |
intron_variant | MODIFIER | c.-16-1013G>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 2/12 | chr12 | 408355 | ||||||
| chr12:408398
|
TA | T | 69 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0002g0003others(66): 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 | a0002c0002t0013g0363 | 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 | a0008c0013t0004g0419 | 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 | a0003c0003t0004g0339a0005c0005t0005g0420a0005c0005t0005g0421others(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 | a0001c0001t0007g0013a0001c0001t0007g0014 | 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 | a0001c0001t0001g0286a0001c0001t0001g0287 | 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 | a0003c0003t0001g0289 | 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 | 315 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0131others(312): Show | 323 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(320): 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0404others(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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0172 | 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 | a0001c0001t0003g0099a0001c0001t0004g0082a0001c0001t0004g0084others(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 | 69 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0002g0003others(66): 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 | 311 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0131others(308): Show | 319 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(316): 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 | a0003c0003t0002g0006a0003c0003t0002g0155a0003c0003t0002g0173others(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 | 72 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0002g0003others(69): 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 | 378 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(375): Show | 386 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(383): 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 | a0003c0003t0003g0069 | 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 | 301 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0131others(298): Show | 309 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(306): 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 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0377others(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 | a0001c0001t0002g0329a0001c0001t0002g0388a0001c0001t0004g0159others(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 | a0002c0002t0001g0336 | 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 | a0004c0004t0001g0340 | 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 | 417 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(414): Show | 427 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(424): 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 | a0001c0001t0003g0053 | 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 | a0001c0001t0004g0386a0002c0002t0001g0387a0003c0003t0004g0365 | 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 | a0001c0001t0002g0388a0002c0002t0001g0389 | 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 | a0003c0003t0004g0339a0005c0005t0005g0420a0005c0005t0005g0421others(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 | 207 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0141others(204): Show | 213 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(210): 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 | 104 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0002g0003others(101): 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 | a0003c0003t0002g0382 | 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 | a0001c0001t0002g0388a0002c0002t0001g0389 | 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 | a0001c0001t0001g0282a0001c0001t0010g0281a0002c0002t0001g0280 | 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 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0001t0001g0132others(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 | a0001c0001t0002g0329a0001c0001t0004g0159a0001c0001t0004g0160others(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 | a0002c0002t0001g0283 | 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 | a0001c0001t0001g0404a0001c0001t0002g0400a0001c0001t0004g0401 | 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 | a0001c0001t0002g0329a0001c0001t0004g0159a0001c0001t0004g0160others(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 | a0001c0001t0001g0404a0001c0001t0002g0400a0001c0001t0004g0359others(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 | a0003c0003t0004g0339a0005c0005t0005g0420a0005c0005t0005g0421others(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 | a0003c0003t0002g0381a0003c0003t0002g0382a0003c0003t0009g0168 | 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 | 265 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0131others(262): Show | 269 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(266): 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 | a0001c0001t0002g0338 | 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 | a0001c0001t0002g0144a0001c0001t0006g0390a0001c0001t0006g0391others(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 | a0002c0002t0001g0051a0002c0002t0001g0149 | 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 | a0001c0001t0002g0144a0001c0001t0006g0390a0001c0001t0006g0391others(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 | a0001c0001t0004g0319a0001c0001t0004g0320 | 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 | a0003c0003t0002g0278 | 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 | a0001c0001t0004g0333 | 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 | a0001c0001t0001g0398a0001c0001t0004g0213a0001c0001t0008g0214others(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 | a0001c0001t0001g0277 | 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 | a0001c0001t0002g0116 | 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 | a0001c0001t0004g0333 | 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 | a0001c0001t0003g0050 | 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 | a0001c0001t0001g0407a0004c0004t0001g0096 | 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 | a0001c0001t0002g0405 | 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 | a0004c0004t0002g0307 | 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 | a0002c0002t0014g0323a0003c0003t0001g0188a0003c0003t0001g0189others(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 | a0005c0005t0005g0411 | 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 | a0001c0001t0001g0407 | 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 | a0001c0001t0001g0211a0001c0001t0002g0304a0001c0001t0004g0275others(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 | 272 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0131others(269): Show | 277 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(274): 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 | a0002c0002t0014g0323a0003c0003t0001g0188a0003c0003t0001g0189others(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 | 35 | a0001c0001t0004g0159a0001c0001t0004g0160a0001c0001t0004g0319others(32): 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 | a0003c0003t0002g0210 | 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 | a0002c0002t0001g0004a0002c0002t0001g0124a0002c0002t0001g0143others(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 | a0002c0002t0001g0296 | 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 | a0001c0001t0004g0399 | 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 | a0001c0001t0004g0399 | 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 | a0003c0003t0002g0374a0003c0003t0004g0212 | 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 | a0001c0001t0002g0003a0001c0001t0002g0049a0001c0001t0002g0074others(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 | 197 | a0001c0001t0001g0042a0001c0001t0001g0131a0001c0001t0001g0132others(194): Show | 200 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.270+1556C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 413534 | ||||||
| chr12:413535
|
G | A | 34 | a0001c0001t0004g0159a0001c0001t0004g0160a0001c0001t0004g0319others(31): 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 | 36 | a0001c0001t0001g0131a0001c0001t0001g0185a0001c0001t0001g0272others(33): Show | 36 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(33): 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 | a0002c0002t0014g0323a0003c0003t0001g0188a0003c0003t0001g0189others(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 | a0001c0001t0004g0159a0001c0001t0004g0160a0001c0001t0004g0319others(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 | a0001c0001t0004g0092a0003c0003t0004g0339a0005c0005t0005g0334others(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 | a0001c0001t0007g0013a0001c0001t0007g0014 | 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 | a0001c0001t0001g0185a0001c0001t0004g0082a0001c0001t0004g0084others(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 | a0001c0001t0002g0405 | 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 | a0001c0001t0001g0108a0001c0001t0001g0349a0001c0001t0001g0408others(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 | a0001c0001t0002g0011a0001c0001t0002g0012 | 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 | a0001c0001t0001g0185a0001c0001t0004g0082a0001c0001t0004g0084others(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 | 147 | a0001c0001t0001g0141a0001c0001t0001g0185a0001c0001t0001g0206others(144): Show | 148 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(145): 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 | 20 | a0002c0002t0001g0051a0002c0002t0001g0109a0002c0002t0001g0110others(17): 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 | a0001c0001t0004g0399 | 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 | a0002c0002t0001g0296 | 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 | a0001c0001t0001g0185a0001c0001t0003g0020a0001c0001t0004g0082others(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 | a0001c0001t0010g0209 | 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 | a0004c0004t0001g0093 | 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 | a0001c0001t0001g0349a0001c0001t0001g0408a0001c0001t0001g0409others(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 | a0001c0001t0003g0020 | 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 | a0001c0001t0001g0282a0001c0001t0009g0294a0003c0003t0001g0289 | 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 | a0001c0001t0007g0013a0001c0001t0007g0014a0001c0001t0008g0214others(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 | a0001c0001t0001g0298 | 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 | a0004c0004t0002g0307 | 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 | a0001c0001t0008g0170a0002c0009t0001g0406a0003c0003t0001g0095others(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 | a0001c0001t0001g0404a0001c0001t0004g0359a0003c0003t0002g0382others(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 | a0001c0001t0001g0270a0001c0001t0002g0304a0001c0001t0004g0269others(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 | a0001c0001t0003g0125a0001c0001t0006g0390a0001c0001t0006g0391others(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 | 41 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0267others(38): 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 | 94 | a0001c0001t0001g0108a0001c0001t0001g0211a0001c0001t0001g0265others(91): Show | 94 | HG00280.hp2 HG00408.hp1 HG00609.hp2 others(91): 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 | a0001c0001t0004g0359a0003c0003t0002g0370a0003c0003t0002g0381 | 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 | a0001c0001t0003g0031a0001c0001t0003g0040 | 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 | a0001c0001t0001g0265 | 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 | a0001c0001t0001g0409a0001c0001t0001g0410 | 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 | a0001c0001t0001g0408 | 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 | a0001c0001t0002g0405a0001c0001t0004g0213a0001c0001t0006g0010others(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 | a0001c0001t0001g0407a0001c0001t0006g0396 | 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 | a0003c0003t0001g0188a0003c0003t0001g0189a0003c0003t0001g0341others(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 | a0002c0002t0001g0389 | 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 | a0003c0003t0004g0339 | 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 | a0001c0001t0004g0386 | 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 | a0001c0001t0002g0049 | 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 | a0001c0001t0004g0082a0001c0001t0004g0088a0001c0001t0004g0102 | 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 | a0001c0001t0002g0049 | 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 | a0002c0002t0001g0283 | 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 | a0001c0001t0004g0159a0001c0001t0004g0160a0001c0001t0004g0319others(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 | 225 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(222): Show | 228 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(225): 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 | a0001c0001t0001g0282a0001c0001t0001g0404a0001c0001t0002g0197others(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 | a0001c0001t0004g0417 | 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 | a0001c0001t0004g0386 | 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 | a0004c0004t0001g0317 | 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 | a0001c0001t0002g0041 | 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 | 56 | a0001c0001t0001g0270a0001c0001t0002g0003a0001c0001t0002g0074others(53): 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 | 121 | a0001c0001t0001g0398a0001c0001t0002g0003a0001c0001t0002g0037others(118): Show | 124 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.271-3173A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 415321 | ||||||
| chr12:415324
|
C | T | 231 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0131others(228): Show | 234 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(231): 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 | a0002c0002t0002g0083a0002c0002t0002g0113a0002c0002t0002g0145others(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 | a0001c0001t0002g0304a0002c0002t0001g0184a0002c0002t0002g0100others(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 | a0001c0001t0001g0164a0003c0003t0002g0381 | 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 | a0001c0001t0002g0008 | 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 | a0001c0001t0002g0032a0001c0001t0002g0056a0001c0001t0002g0058others(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 | a0001c0001t0004g0330 | 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 | a0001c0001t0001g0270a0002c0002t0001g0114a0002c0002t0001g0129others(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 | a0001c0001t0002g0049 | 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 | a0001c0001t0002g0049a0002c0002t0001g0111 | 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 | 152 | a0001c0001t0001g0151a0001c0001t0001g0154a0001c0001t0001g0185others(149): Show | 155 | HG00280.hp2 HG00423.hp2 HG00597.hp1 others(152): 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 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0041others(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 | a0001c0001t0001g0147a0001c0001t0001g0211a0002c0002t0001g0183others(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 | a0001c0001t0002g0009a0001c0001t0002g0161a0001c0001t0002g0346others(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 | a0005c0005t0005g0411 | 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 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0001t0001g0238others(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 | a0003c0003t0007g0327a0003c0003t0007g0414 | 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 | a0003c0003t0007g0327a0003c0003t0007g0414 | 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 | 113 | a0001c0001t0001g0398a0001c0001t0002g0003a0001c0001t0002g0037others(110): Show | 116 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(113): 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 | a0003c0003t0007g0327a0003c0003t0007g0414a0005c0005t0005g0411 | 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 | a0001c0001t0001g0042a0001c0001t0001g0132a0001c0001t0001g0151others(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 | a0001c0001t0001g0146a0001c0001t0001g0154 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0002g0136a0001c0001t0002g0197a0001c0001t0004g0401others(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 | a0001c0001t0003g0055 | 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 | 113 | a0001c0001t0001g0398a0001c0001t0002g0003a0001c0001t0002g0037others(110): Show | 116 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(113): 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 | a0005c0005t0005g0411 | 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 | a0003c0003t0007g0327a0003c0003t0007g0414 | 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 | a0001c0001t0002g0049a0001c0001t0002g0304a0001c0001t0004g0084others(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 | a0001c0001t0002g0197a0001c0001t0004g0401a0001c0001t0010g0209others(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 | a0001c0001t0004g0084a0001c0001t0004g0090a0003c0003t0007g0327others(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 | a0005c0005t0005g0411 | 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 | a0001c0001t0002g0197a0001c0001t0004g0401a0001c0001t0010g0209others(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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(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 | a0003c0003t0007g0327a0003c0003t0007g0414 | 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 | a0003c0003t0007g0327a0003c0003t0007g0414 | 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 | a0001c0001t0002g0197a0001c0001t0004g0401a0001c0001t0010g0209others(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 | a0002c0002t0001g0301 | 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 | a0001c0001t0002g0091a0001c0001t0007g0013a0001c0001t0007g0014others(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 | a0001c0001t0004g0084a0001c0001t0004g0090 | 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 | a0001c0001t0004g0084a0001c0001t0004g0090 | 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 | a0001c0001t0004g0084a0001c0001t0004g0090 | 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 | a0001c0001t0002g0091 | 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 | a0001c0001t0007g0013a0001c0001t0007g0014 | 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 | a0003c0003t0002g0233 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0008g0170a0003c0003t0004g0365a0006c0006t0011g0103others(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 | 133 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0001t0001g0238others(130): Show | 136 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(133): 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 | a0001c0001t0004g0275a0001c0001t0004g0330a0003c0003t0004g0331 | 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 | a0001c0001t0001g0257a0001c0001t0004g0084a0001c0001t0004g0090 | 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 | a0003c0003t0004g0365a0006c0006t0011g0103a0006c0006t0011g0106 | 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 | a0001c0001t0002g0197a0001c0001t0004g0084a0001c0001t0004g0090others(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 | a0002c0002t0001g0296a0005c0005t0005g0418 | 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 | a0001c0001t0004g0386 | 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 | a0001c0001t0004g0386 | 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 | 34 | a0001c0001t0002g0009a0001c0001t0002g0037a0002c0002t0001g0038others(31): 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 | a0001c0001t0004g0092a0001c0001t0004g0159a0001c0001t0004g0160others(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 | a0001c0001t0002g0197a0001c0001t0004g0084a0001c0001t0004g0090others(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 | a0001c0001t0002g0091 | 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 | a0001c0001t0002g0197a0001c0001t0004g0084a0001c0001t0004g0090others(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 | a0002c0002t0001g0152a0002c0002t0001g0234a0002c0002t0001g0235others(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 | a0001c0001t0003g0022a0001c0001t0003g0055a0001c0001t0003g0181others(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 | a0001c0001t0004g0082a0001c0001t0004g0085a0001c0001t0004g0086others(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 | a0003c0003t0002g0203a0003c0003t0002g0204 | 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 | a0002c0002t0001g0224 | 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 | a0001c0001t0003g0048 | 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 | a0003c0003t0001g0015a0003c0003t0001g0062a0003c0003t0001g0066others(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 | 335 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(332): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(336): 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 | a0001c0001t0001g0147a0001c0001t0001g0211a0002c0002t0001g0326others(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 | a0003c0003t0001g0015a0003c0003t0001g0062a0003c0003t0001g0066others(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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0282others(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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0002g0304a0001c0001t0002g0388a0001c0001t0002g0400others(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 | a0002c0002t0001g0163a0002c0002t0001g0372 | 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 | 345 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(342): Show | 349 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(346): 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 | a0007c0007t0005g0328 | 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 | a0001c0001t0004g0275a0001c0001t0004g0330a0001c0001t0008g0170others(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 | 285 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(282): Show | 289 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(286): 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 | 152 | a0001c0001t0001g0398a0001c0001t0002g0003a0001c0001t0002g0037others(149): Show | 156 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(153): 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 | a0001c0001t0002g0075a0002c0002t0001g0038a0002c0002t0001g0117others(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 | a0001c0001t0003g0247 | 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 | a0001c0001t0002g0091a0001c0001t0004g0159a0001c0001t0004g0160others(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 | a0001c0001t0004g0269 | 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 | a0001c0001t0002g0075a0002c0002t0001g0038a0002c0002t0001g0117others(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 | a0001c0001t0004g0090a0001c0001t0004g0092a0001c0001t0004g0098others(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 | a0001c0001t0001g0151a0001c0001t0001g0367a0001c0001t0002g0116others(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 | a0001c0001t0001g0042a0001c0001t0001g0141a0001c0001t0001g0185others(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 | a0001c0001t0001g0030a0001c0001t0001g0108a0001c0001t0001g0131others(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 | a0001c0001t0001g0172a0001c0001t0001g0178a0003c0003t0002g0370 | 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 | a0001c0001t0003g0031a0001c0001t0003g0040a0001c0001t0003g0125 | 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 | 44 | a0001c0001t0002g0003a0001c0001t0002g0049a0001c0001t0002g0074others(41): 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 | a0001c0001t0004g0084 | 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 | a0001c0001t0002g0075a0002c0002t0001g0038a0002c0002t0001g0117others(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 | a0001c0001t0002g0037a0002c0002t0001g0182a0002c0002t0001g0264others(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 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0256others(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 | 83 | a0001c0001t0001g0398a0001c0001t0004g0084a0001c0001t0004g0386others(80): Show | 85 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(82): 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 | a0002c0002t0001g0117a0002c0002t0001g0118a0002c0002t0001g0119others(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 | a0001c0001t0002g0075a0002c0002t0001g0183 | 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 | 116 | a0001c0001t0001g0398a0001c0001t0002g0032a0001c0001t0002g0056others(113): Show | 118 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(115): 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 | a0001c0001t0002g0011a0001c0001t0002g0137a0003c0003t0002g0202others(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 | a0001c0001t0004g0269a0003c0003t0009g0168a0004c0004t0001g0093 | 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 | a0001c0001t0004g0090a0001c0001t0004g0092a0001c0001t0004g0098others(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 | a0001c0001t0003g0247 | 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 | a0001c0001t0001g0151a0001c0001t0001g0367a0001c0001t0004g0085others(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 | a0004c0004t0002g0307 | 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 | a0001c0001t0001g0185a0001c0001t0004g0082a0001c0001t0004g0102 | 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 | a0001c0001t0004g0386a0002c0002t0001g0372a0002c0002t0002g0100others(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 | a0001c0001t0003g0247 | 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 | a0002c0002t0001g0021a0002c0002t0001g0079a0002c0002t0001g0107 | 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 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0111others(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 | a0001c0001t0001g0398a0002c0002t0001g0124a0002c0002t0001g0133others(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 | a0002c0002t0001g0043a0002c0002t0001g0130a0002c0002t0001g0243others(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 | a0002c0002t0001g0134a0002c0002t0001g0135a0002c0002t0001g0332others(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 | a0002c0002t0001g0094 | 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 | a0002c0002t0001g0284a0002c0002t0001g0301 | 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 | a0004c0004t0001g0306 | 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 | a0002c0002t0001g0321 | 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 | 75 | a0001c0001t0001g0398a0001c0001t0004g0386a0002c0002t0001g0004others(72): 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 | a0004c0004t0001g0340 | 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 | a0002c0009t0001g0406 | 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 | 89 | a0001c0001t0001g0398a0001c0001t0004g0386a0002c0002t0001g0004others(86): Show | 91 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(88): 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 | a0002c0002t0001g0354 | 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 | a0001c0001t0003g0247 | 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 | 100 | a0001c0001t0001g0398a0001c0001t0004g0386a0002c0002t0001g0004others(97): Show | 102 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.271-2135G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416359 | ||||||
| chr12:416361
|
G | A | 106 | a0001c0001t0001g0398a0001c0001t0002g0037a0001c0001t0004g0084others(103): Show | 108 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(105): 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 | a0001c0001t0001g0298 | 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 | 115 | a0001c0001t0001g0398a0001c0001t0002g0037a0001c0001t0004g0084others(112): Show | 117 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(114): 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 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0256others(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 | a0003c0003t0002g0381 | 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 | a0003c0003t0001g0017 | 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 | 112 | a0001c0001t0001g0398a0001c0001t0002g0037a0001c0001t0004g0084others(109): Show | 114 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.271-2129G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416365 | ||||||
| chr12:416367
|
G | A | 120 | a0001c0001t0001g0398a0001c0001t0002g0037a0001c0001t0004g0084others(117): Show | 122 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(119): 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 | a0001c0001t0004g0213a0003c0003t0002g0374a0003c0003t0004g0212others(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 | a0004c0004t0001g0317 | 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 | a0002c0002t0001g0402 | 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 | 115 | a0001c0001t0001g0398a0001c0001t0002g0037a0001c0001t0004g0084others(112): Show | 117 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(114): 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 | a0003c0003t0001g0188a0003c0003t0001g0189a0003c0003t0001g0341others(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 | a0001c0001t0004g0359 | 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 | a0004c0004t0001g0096 | 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 | 113 | a0001c0001t0001g0398a0001c0001t0002g0037a0001c0001t0004g0084others(110): Show | 115 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(112): 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 | a0001c0001t0002g0032a0001c0001t0002g0058a0003c0003t0002g0278 | 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 | a0001c0001t0002g0300 | 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 | a0001c0001t0002g0091a0003c0003t0002g0382 | 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 | a0002c0002t0001g0389 | 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 | 106 | a0001c0001t0002g0032a0001c0001t0002g0037a0001c0001t0002g0056others(103): 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 | a0003c0003t0002g0006a0003c0003t0002g0285 | 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 | a0003c0003t0002g0175a0003c0003t0002g0368a0003c0003t0015g0290 | 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 | a0003c0003t0002g0174 | 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 | a0003c0003t0002g0173a0003c0003t0002g0199 | 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 | a0001c0001t0001g0211a0004c0004t0001g0093 | 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 | a0001c0001t0001g0147a0001c0001t0001g0270a0002c0002t0001g0326others(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 | a0001c0001t0001g0282a0001c0001t0001g0408a0001c0001t0001g0409others(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 | 149 | a0001c0001t0001g0151a0001c0001t0001g0367a0001c0001t0001g0398others(146): Show | 152 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(149): 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 | a0001c0001t0002g0198a0001c0001t0002g0279a0001c0001t0002g0346others(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 | a0001c0001t0002g0136a0001c0001t0002g0293a0001c0001t0002g0357others(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 | a0003c0003t0002g0155 | 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 | a0001c0001t0002g0012a0001c0001t0002g0197a0006c0006t0012g0105 | 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 | a0001c0001t0006g0010a0001c0001t0006g0390a0001c0001t0006g0391others(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 | a0001c0001t0002g0041 | 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 | a0001c0001t0004g0275a0001c0001t0008g0170a0003c0003t0004g0331others(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 | 225 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(222): Show | 234 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(231): 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 | a0001c0001t0002g0008 | 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 | a0003c0003t0002g0176 | 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 | a0001c0001t0001g0131a0001c0001t0001g0167a0001c0001t0001g0179others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0141a0001c0001t0001g0206a0001c0001t0001g0265others(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 | a0003c0003t0006g0089 | 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 | a0003c0003t0004g0365 | 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 | a0001c0001t0004g0330 | 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 | a0001c0001t0001g0172a0001c0001t0001g0178a0001c0001t0002g0337others(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 | a0002c0002t0001g0117a0002c0002t0001g0118a0002c0002t0001g0119others(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 | a0003c0003t0009g0168a0004c0004t0001g0207 | 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 | a0002c0002t0001g0169a0002c0002t0001g0182 | 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 | a0001c0001t0002g0361a0003c0003t0001g0148 | 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 | a0002c0002t0001g0216 | 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 | a0002c0002t0001g0152a0002c0002t0001g0234 | 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 | a0001c0001t0004g0401a0001c0001t0010g0209a0001c0001t0010g0281others(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 | a0002c0002t0001g0183 | 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 | a0004c0004t0001g0340 | 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 | 50 | a0001c0001t0002g0003a0001c0001t0002g0049a0001c0001t0002g0074others(47): 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 | a0003c0003t0001g0289a0003c0003t0001g0318 | 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 | 63 | a0001c0001t0002g0003a0001c0001t0002g0049a0001c0001t0002g0074others(60): 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 | a0002c0002t0001g0227 | 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 | 95 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(92): Show | 97 | HG00423.hp2 HG00438.hp2 HG00639.hp1 others(94): 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 | a0002c0002t0001g0227 | 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 | a0001c0001t0004g0386a0004c0004t0002g0097 | 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 | a0001c0001t0002g0032a0001c0001t0002g0056a0001c0001t0002g0058others(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 | 85 | a0001c0001t0001g0398a0001c0001t0004g0084a0001c0001t0004g0324others(82): Show | 87 | HG00423.hp2 HG00438.hp2 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.271-2075C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 416419 | ||||||
| chr12:416419
|
CTT | C | 198 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(195): 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 | 84 | a0001c0001t0001g0398a0001c0001t0004g0084a0001c0001t0004g0324others(81): Show | 86 | HG00423.hp2 HG00438.hp2 HG00741.hp2 others(83): 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 | a0002c0002t0001g0227 | 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 | a0007c0007t0005g0328 | 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 | 174 | a0001c0001t0001g0398a0001c0001t0002g0003a0001c0001t0002g0037others(171): Show | 178 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(175): 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 | a0001c0001t0004g0275a0001c0001t0004g0330a0001c0001t0008g0170others(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 | a0001c0001t0006g0010a0001c0001t0006g0390a0001c0001t0006g0391others(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 | a0005c0005t0005g0418 | 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 | 285 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(282): Show | 289 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(286): Show |
intron_variant | MODIFIER | c.271-1440G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 4/12 | chr12 | 417054 | ||||||
| chr12:417132
|
C | CA | 330 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(327): Show | 339 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(336): 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 | a0001c0001t0001g0146a0001c0001t0001g0377a0001c0001t0001g0378others(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 | a0001c0001t0001g0211a0001c0001t0001g0270a0002c0002t0001g0326others(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 | 346 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(343): Show | 350 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(347): 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 | a0001c0001t0002g0405 | 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 | a0001c0001t0010g0209a0001c0001t0010g0281 | 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 | a0001c0001t0001g0349 | 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 | a0001c0001t0004g0333 | 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 | a0001c0001t0006g0010a0001c0001t0006g0390a0001c0001t0006g0391others(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 | a0001c0001t0003g0031a0001c0001t0003g0040 | 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 | a0003c0003t0001g0188a0003c0003t0001g0189a0003c0003t0001g0341others(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 | a0002c0002t0002g0113a0004c0004t0002g0307a0004c0004t0002g0309others(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 | a0001c0001t0004g0401a0001c0001t0010g0209a0001c0001t0010g0281others(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 | a0001c0001t0006g0010a0001c0001t0006g0390a0001c0001t0006g0391others(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 | a0001c0001t0001g0349 | 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 | a0001c0001t0004g0092a0001c0001t0004g0159a0001c0001t0004g0160others(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 | a0001c0001t0006g0010a0001c0001t0006g0390a0001c0001t0006g0391others(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 | a0001c0001t0001g0267 | 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 | 48 | a0001c0001t0002g0003a0001c0001t0002g0049a0001c0001t0002g0074others(45): 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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0001g0408a0001c0001t0001g0409a0001c0001t0001g0410others(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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0006g0010a0001c0001t0006g0390a0001c0001t0006g0391others(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 | a0002c0002t0001g0354 | 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 | a0001c0001t0006g0010a0001c0001t0006g0390a0001c0001t0006g0391others(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 | a0002c0002t0001g0038 | 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 | a0001c0001t0004g0401 | 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 | a0002c0002t0001g0326a0002c0002t0001g0387a0004c0004t0001g0093 | 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 | a0003c0003t0004g0365 | 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 | a0001c0001t0002g0008 | 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 | a0001c0001t0010g0209a0001c0001t0010g0281a0005c0005t0005g0411 | 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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0001g0282a0001c0001t0001g0408a0001c0001t0001g0409others(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 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166 | 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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0005c0005t0005g0334a0005c0005t0005g0412a0005c0005t0005g0420others(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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0002g0008a0001c0001t0004g0213a0001c0001t0004g0275others(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 | a0001c0001t0001g0147a0001c0001t0001g0164a0001c0001t0001g0165others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0238 | 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 | a0002c0002t0001g0389 | 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 | a0002c0002t0001g0295a0003c0003t0001g0148 | 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 | a0001c0001t0004g0325a0002c0002t0001g0216 | 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 | 314 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(311): Show | 319 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(316): 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 | a0001c0001t0001g0239 | 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 | 25 | a0001c0001t0004g0092a0001c0001t0004g0269a0001c0001t0004g0399others(22): Show | 25 | HG00408.hp1 HG00423.hp2 HG01496.hp1 others(22): 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 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0208others(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 | 149 | a0001c0001t0001g0398a0001c0001t0002g0003a0001c0001t0002g0037others(146): 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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(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 | a0002c0002t0002g0083 | 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 | 25 | a0001c0001t0004g0092a0001c0001t0004g0269a0001c0001t0004g0399others(22): Show | 25 | HG00408.hp1 HG00423.hp2 HG01496.hp1 others(22): 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 | 25 | a0001c0001t0004g0092a0001c0001t0004g0269a0001c0001t0004g0399others(22): Show | 25 | HG00408.hp1 HG00423.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.413+895G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419531 | ||||||
| chr12:419532
|
T | A | 25 | a0001c0001t0004g0092a0001c0001t0004g0269a0001c0001t0004g0399others(22): Show | 25 | HG00408.hp1 HG00423.hp2 HG01496.hp1 others(22): 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 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0004g0213others(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 | a0001c0001t0002g0032a0001c0001t0002g0041a0001c0001t0002g0056others(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 | 26 | a0001c0001t0001g0238a0001c0001t0004g0092a0001c0001t0004g0269others(23): Show | 26 | HG00408.hp1 HG00423.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.413+900C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419536 | ||||||
| chr12:419551
|
C | A | 33 | a0001c0001t0001g0167a0001c0001t0001g0239a0001c0001t0002g0008others(30): Show | 34 | HG00408.hp1 HG00423.hp2 HG01069.hp2 others(31): 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 | a0001c0001t0001g0167a0001c0001t0002g0008a0005c0005t0005g0334others(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 | 116 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(113): Show | 116 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(113): 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 | a0001c0001t0010g0209a0001c0001t0010g0281a0005c0005t0005g0411 | 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 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0208others(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 | 32 | a0001c0001t0002g0136a0001c0001t0004g0092a0001c0001t0004g0269others(29): Show | 32 | HG00408.hp1 HG00423.hp2 HG01109.hp1 others(29): 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 | a0001c0001t0002g0011a0001c0001t0002g0012 | 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 | a0003c0003t0001g0188a0003c0003t0001g0189a0003c0003t0001g0341others(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 | a0003c0003t0007g0327a0006c0006t0011g0103a0006c0006t0011g0106 | 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 | a0001c0001t0004g0330 | 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 | a0001c0001t0004g0213a0001c0001t0004g0275a0001c0001t0008g0170others(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 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0208others(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 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0208others(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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0004g0092a0001c0001t0004g0399a0007c0007t0005g0328 | 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 | 69 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0211others(66): Show | 71 | HG00408.hp1 HG00423.hp2 HG00735.hp1 others(68): 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 | a0001c0001t0001g0167a0002c0002t0001g0216a0002c0002t0001g0295 | 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 | a0002c0002t0001g0216a0002c0002t0001g0295a0002c0002t0002g0351 | 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 | a0001c0001t0001g0147a0001c0001t0001g0178a0001c0001t0001g0179others(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 | a0005c0005t0005g0418 | 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 | 81 | a0001c0001t0001g0147a0001c0001t0001g0178a0001c0001t0001g0179others(78): Show | 81 | HG00408.hp1 HG00423.hp2 HG00735.hp1 others(78): 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 | a0001c0001t0008g0170a0003c0003t0004g0331 | 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 | 76 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0208others(73): Show | 76 | HG00408.hp1 HG00423.hp2 HG00735.hp1 others(73): Show |
intron_variant | MODIFIER | c.413+1063A>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 419699 | ||||||
| chr12:419707
|
T | C | 69 | a0001c0001t0001g0147a0001c0001t0001g0178a0001c0001t0001g0179others(66): Show | 69 | HG00408.hp1 HG00423.hp2 HG01071.hp1 others(66): 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 | a0003c0003t0007g0414 | 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 | a0001c0001t0001g0273 | 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 | 99 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(96): Show | 99 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(96): 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 | a0003c0003t0001g0289 | 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 | a0001c0001t0001g0166a0003c0003t0001g0017 | 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 | a0001c0001t0001g0147a0001c0001t0001g0166a0001c0001t0001g0211others(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 | a0001c0001t0001g0147a0001c0001t0001g0166a0001c0001t0001g0167others(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 | a0001c0001t0006g0010a0001c0001t0006g0391a0001c0001t0006g0392others(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 | a0001c0001t0001g0164a0001c0001t0001g0165 | 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 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0208others(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 | a0001c0001t0001g0147a0001c0001t0001g0167a0001c0001t0001g0178others(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 | a0003c0003t0002g0229 | 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 | a0001c0001t0001g0272 | 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 | a0003c0003t0001g0073 | 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 | a0002c0002t0001g0387 | 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 | 130 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(127): Show | 130 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(127): 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 | a0002c0002t0014g0323 | 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 | a0003c0003t0004g0339 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0002c0002t0014g0323 | 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 | a0001c0001t0004g0213a0003c0003t0002g0374a0003c0003t0004g0212 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0003c0003t0001g0148a0005c0005t0005g0334a0005c0005t0005g0412others(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 | a0002c0002t0001g0389 | 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 | a0002c0002t0001g0402 | 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 | a0001c0001t0001g0282a0001c0001t0001g0408a0001c0001t0001g0409others(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 | a0002c0002t0001g0326a0004c0004t0001g0093 | 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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0167others(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 | a0001c0001t0001g0282a0001c0001t0001g0408a0001c0001t0001g0409others(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 | a0001c0001t0001g0146a0001c0001t0001g0167a0001c0001t0001g0238others(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 | a0002c0002t0001g0296 | 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(511): Show |
T | 1 | a0004c0004t0001g0187 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.413+1293_413+1810d 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 | a0003c0003t0002g0201 | 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 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(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 | a0003c0003t0001g0017 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0258a0001c0001t0001g0404 | 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 | a0002c0002t0001g0259 | 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 | a0001c0001t0001g0364a0001c0001t0001g0366 | 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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0008g0170a0003c0003t0004g0331 | 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 | a0001c0001t0001g0132a0001c0001t0001g0147a0001c0001t0001g0211others(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 | a0001c0001t0006g0390a0001c0001t0010g0209a0001c0001t0010g0281others(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 | a0002c0002t0001g0259 | 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 | a0001c0001t0001g0132a0001c0001t0001g0146a0001c0001t0001g0167others(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 | a0001c0001t0001g0132a0001c0001t0001g0146a0001c0001t0001g0147others(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 | a0001c0001t0004g0401 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0282a0001c0001t0001g0408a0001c0001t0001g0409others(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 | a0001c0001t0001g0132a0001c0001t0001g0251a0001c0001t0001g0252others(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 | 154 | a0001c0001t0001g0282a0001c0001t0001g0398a0001c0001t0001g0408others(151): 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 | a0001c0001t0001g0165a0001c0001t0001g0178a0001c0001t0001g0179others(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 | a0001c0001t0001g0165a0001c0001t0001g0178a0001c0001t0001g0179others(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 | a0003c0003t0002g0228 | 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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0002c0002t0002g0100a0002c0002t0002g0113a0002c0002t0013g0363others(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 | a0001c0001t0004g0159a0001c0001t0004g0160a0001c0001t0004g0319others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0004g0275 | 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 | a0001c0001t0001g0132a0001c0001t0001g0146a0001c0001t0001g0166others(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 | 255 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(252): 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 | a0003c0003t0002g0229 | 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 | a0002c0002t0001g0244 | 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 | a0001c0001t0002g0405a0003c0003t0002g0370a0003c0003t0002g0381 | 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 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0266others(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 | a0001c0001t0001g0166a0001c0001t0001g0282a0001c0001t0001g0408others(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 | a0002c0002t0001g0402a0002c0002t0002g0145a0002c0002t0002g0162others(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 | a0004c0004t0001g0096 | 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 | a0004c0004t0001g0096 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0003c0003t0001g0289 | 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 | a0001c0001t0002g0032a0001c0001t0002g0041a0001c0001t0002g0056others(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 | a0001c0001t0001g0132a0001c0001t0001g0167a0001c0001t0001g0239others(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 | a0001c0001t0001g0147a0001c0001t0001g0166a0001c0001t0001g0211others(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 | a0001c0001t0004g0401 | 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 | a0002c0002t0014g0323 | 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 | a0001c0001t0002g0136a0001c0001t0004g0269a0001c0001t0004g0325others(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 | a0001c0001t0004g0330a0003c0003t0007g0414 | 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 | a0001c0001t0001g0146a0001c0001t0001g0272a0003c0003t0001g0073 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0208others(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 | a0001c0001t0004g0092a0001c0001t0004g0399 | 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 | a0002c0002t0001g0216 | 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 | a0001c0001t0004g0325 | 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 | a0002c0002t0001g0402 | 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 | a0002c0002t0001g0402 | 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 | 225 | a0001c0001t0001g0132a0001c0001t0001g0147a0001c0001t0001g0165others(222): 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 | a0001c0001t0001g0146a0001c0001t0001g0272a0003c0003t0001g0073 | 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 | a0001c0001t0002g0011a0001c0001t0002g0012 | 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 | a0002c0002t0001g0295 | 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 | a0001c0001t0001g0157a0001c0001t0001g0240a0001c0001t0001g0257others(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 | a0001c0001t0001g0132a0001c0001t0001g0147a0001c0001t0001g0165others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0410 | 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 | a0001c0001t0010g0209a0001c0001t0010g0281 | 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 | 228 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(225): 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 | a0001c0001t0001g0404 | 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 | a0003c0003t0004g0339 | 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 | 204 | a0001c0001t0001g0166a0001c0001t0001g0178a0001c0001t0001g0179others(201): 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 | a0001c0001t0001g0166a0001c0001t0001g0366a0002c0002t0002g0351 | 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 | a0001c0001t0001g0030a0001c0001t0001g0108a0001c0001t0001g0131others(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 | a0001c0001t0008g0170a0003c0003t0004g0331 | 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 | a0001c0001t0001g0042a0001c0001t0001g0147a0001c0001t0001g0150others(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 | 259 | a0001c0001t0001g0030a0001c0001t0001g0108a0001c0001t0001g0131others(256): 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 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0208others(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 | a0001c0001t0008g0170a0003c0003t0004g0331 | 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 | a0001c0001t0001g0172a0001c0001t0001g0356 | 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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0356 | 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 | 209 | a0001c0001t0001g0030a0001c0001t0001g0108a0001c0001t0001g0131others(206): 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 | 202 | a0001c0001t0001g0282a0001c0001t0001g0398a0001c0001t0001g0404others(199): 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 | a0005c0005t0005g0334a0005c0005t0005g0412a0005c0005t0005g0420others(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 | a0001c0001t0001g0030a0001c0001t0001g0132a0001c0001t0001g0141others(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 | a0003c0003t0001g0188a0003c0003t0001g0189a0003c0003t0001g0341others(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 | a0003c0003t0007g0327a0006c0006t0011g0103a0006c0006t0011g0106 | 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 | 172 | a0001c0001t0001g0042a0001c0001t0001g0150a0001c0001t0001g0164others(169): 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 | a0001c0001t0001g0042a0001c0001t0001g0150a0001c0001t0001g0164others(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 | a0002c0002t0001g0244 | 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 | a0001c0001t0001g0267a0001c0001t0001g0377a0001c0001t0002g0198others(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 | a0007c0007t0005g0328 | 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 | a0001c0001t0001g0356a0001c0001t0001g0410a0001c0001t0002g0032others(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 | 284 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(281): 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 | a0002c0002t0001g0387 | 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 | a0001c0001t0002g0388 | 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 | a0001c0001t0001g0267 | 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 | a0003c0003t0001g0073 | 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 | a0001c0001t0002g0198a0003c0003t0009g0168 | 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 | a0002c0002t0001g0387 | 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 | a0001c0001t0001g0377 | 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 | 230 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(227): 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 | a0001c0001t0003g0247 | 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 | 185 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0208others(182): 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 | a0001c0001t0001g0030a0001c0001t0001g0108a0001c0001t0001g0131others(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 | a0002c0002t0001g0308 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0267 | 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 | a0002c0002t0001g0259 | 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 | a0001c0001t0004g0159a0001c0001t0004g0160a0001c0001t0004g0269others(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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(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 | 178 | a0001c0001t0001g0146a0001c0001t0001g0272a0001c0001t0001g0282others(175): 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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0238 | 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 | a0001c0001t0001g0408 | 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 | a0001c0001t0001g0404 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | 215 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0001t0001g0185others(212): 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 | 210 | a0001c0001t0001g0238a0001c0001t0001g0272a0001c0001t0001g0273others(207): 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 | a0001c0001t0001g0377 | 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 | 77 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0001t0001g0178others(74): Show | 79 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.413+1751A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420387 | ||||||
| chr12:420419
|
TA | T | 70 | a0001c0001t0001g0147a0001c0001t0001g0151a0001c0001t0001g0178others(67): Show | 70 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(67): 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 | a0001c0001t0004g0275 | 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 | a0001c0001t0004g0330 | 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 | a0003c0003t0007g0414 | 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 | 257 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0151others(254): Show | 261 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(258): 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 | a0002c0002t0001g0326a0004c0004t0001g0093 | 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 | a0002c0002t0001g0403 | 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 | 272 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(269): 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 | a0002c0002t0001g0243 | 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 | 50 | a0001c0001t0001g0146a0001c0001t0001g0258a0001c0001t0001g0272others(47): Show | 52 | HG00408.hp1 HG00423.hp2 HG00642.hp2 others(49): 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 | a0002c0002t0001g0295 | 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 | a0001c0001t0001g0273a0003c0003t0001g0073a0003c0003t0004g0339 | 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 | 171 | a0001c0001t0001g0282a0001c0001t0001g0398a0001c0001t0001g0408others(168): 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 | 152 | a0001c0001t0001g0282a0001c0001t0001g0398a0001c0001t0001g0409others(149): 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 | a0001c0001t0001g0147a0001c0001t0001g0178a0001c0001t0001g0179others(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 | a0002c0002t0001g0326a0004c0004t0001g0093 | 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 | a0001c0001t0001g0410 | 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 | a0002c0002t0014g0323 | 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 | 159 | a0001c0001t0001g0147a0001c0001t0001g0151a0001c0001t0001g0178others(156): Show | 161 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(158): 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 | a0001c0001t0001g0258 | 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 | a0001c0001t0002g0329 | 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 | 175 | a0001c0001t0001g0282a0001c0001t0001g0398a0001c0001t0001g0409others(172): 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 | a0002c0002t0001g0389 | 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 | a0001c0001t0001g0258 | 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 | 192 | a0001c0001t0001g0146a0001c0001t0001g0178a0001c0001t0001g0179others(189): 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0404 | 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 | a0001c0001t0008g0170a0003c0003t0004g0331 | 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 | 35 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0208others(32): Show | 35 | HG00408.hp1 HG00423.hp2 HG01167.hp1 others(32): 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 | a0002c0002t0002g0145a0002c0002t0002g0162a0002c0002t0002g0350others(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 | a0001c0001t0002g0299 | 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 | a0001c0001t0001g0146a0001c0001t0001g0150a0001c0001t0001g0270others(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 | a0001c0001t0001g0211a0002c0002t0001g0387a0003c0003t0001g0095others(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 | a0001c0001t0004g0275 | 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 | a0001c0001t0001g0251a0001c0001t0001g0252 | 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 | a0001c0001t0004g0330 | 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 | a0003c0003t0001g0415 | 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 | 202 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0150others(199): 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 | a0001c0001t0001g0157a0001c0001t0001g0298 | 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 | a0001c0001t0001g0267 | 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 | a0001c0001t0004g0401a0005c0005t0005g0418 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | 245 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(242): 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 | a0003c0003t0004g0365 | 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 | a0003c0003t0007g0414 | 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 | a0001c0001t0001g0238a0001c0001t0001g0251a0001c0001t0001g0252 | 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 | 52 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0267others(49): Show | 52 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(49): 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 | a0001c0001t0001g0408a0001c0001t0001g0410a0002c0002t0001g0402 | 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 | a0001c0001t0001g0146a0001c0001t0001g0258a0001c0001t0001g0273others(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 | a0001c0001t0002g0198 | 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 | a0003c0003t0004g0339 | 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 | a0002c0002t0002g0100a0002c0002t0002g0113a0002c0002t0013g0363others(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 | a0001c0001t0001g0132a0001c0001t0001g0313a0003c0003t0002g0230others(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 | a0001c0001t0001g0157a0001c0001t0001g0167a0001c0001t0001g0238others(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 | 187 | a0001c0001t0001g0132a0001c0001t0001g0146a0001c0001t0001g0157others(184): Show | 192 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(189): 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 | a0008c0013t0004g0419 | 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 | a0001c0001t0001g0178 | 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 | a0001c0001t0001g0378 | 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 | a0001c0001t0004g0092a0001c0001t0004g0159a0001c0001t0004g0160others(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 | 50 | a0001c0001t0002g0003a0001c0001t0002g0049a0001c0001t0002g0074others(47): 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 | 248 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(245): 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 | 222 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(219): Show | 227 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(224): 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 | a0001c0001t0002g0032a0001c0001t0002g0041a0001c0001t0002g0056others(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 | a0001c0001t0002g0338 | 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 | a0001c0001t0001g0146a0003c0003t0002g0229 | 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 | 192 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0273others(189): 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 | a0001c0001t0006g0010a0001c0001t0006g0391a0001c0001t0006g0392others(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 | 69 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(66): Show | 69 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(66): 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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0132a0001c0001t0001g0157a0001c0001t0001g0167others(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 | a0001c0001t0001g0238 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0147a0001c0001t0001g0151a0001c0001t0001g0185others(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 | a0001c0001t0008g0170a0003c0003t0004g0331a0003c0003t0007g0327others(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 | a0003c0003t0002g0229 | 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 | a0001c0001t0001g0132a0001c0001t0001g0151a0001c0001t0001g0179others(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 | a0001c0001t0001g0356a0003c0003t0004g0339 | 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 | 14 | a0001c0001t0001g0272a0001c0001t0001g0282a0001c0001t0002g0008others(11): Show | 16 | HG00735.hp2 HG01069.hp2 HG01071.hp2 others(13): 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 | a0005c0005t0005g0334a0005c0005t0005g0412a0005c0005t0005g0420others(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 | 236 | a0001c0001t0001g0131a0001c0001t0001g0146a0001c0001t0001g0150others(233): 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 | a0001c0001t0001g0409 | 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 | a0001c0001t0001g0258 | 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 | a0002c0002t0001g0403 | 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 | a0001c0001t0010g0209a0001c0001t0010g0281 | 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 | a0001c0001t0001g0408a0001c0001t0001g0410a0003c0003t0004g0339 | 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 | a0001c0001t0001g0132a0001c0001t0001g0251a0001c0001t0001g0252others(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 | a0003c0003t0001g0017 | 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 | 207 | a0001c0001t0001g0131a0001c0001t0001g0146a0001c0001t0001g0150others(204): 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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0003c0003t0001g0066 | 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 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0156others(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 | a0001c0001t0001g0030 | 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 | a0001c0001t0001g0146a0001c0001t0001g0157a0001c0001t0001g0167others(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 | a0001c0001t0001g0282a0001c0001t0009g0294 | 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 | a0003c0003t0007g0414 | 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 | a0001c0001t0001g0141a0001c0001t0001g0165a0001c0001t0001g0172others(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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(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 | a0001c0001t0001g0208 | 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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(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 | 208 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0178others(205): 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 | a0001c0001t0001g0408a0001c0001t0001g0410 | 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 | a0001c0001t0001g0377 | 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 | a0002c0002t0001g0296 | 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 | a0003c0003t0002g0228 | 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 | a0001c0001t0001g0273 | 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 | a0001c0001t0004g0275 | 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 | a0001c0001t0001g0141a0001c0001t0001g0164a0001c0001t0001g0172others(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 | a0001c0001t0001g0165a0001c0001t0001g0263a0001c0001t0001g0265others(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 | a0001c0001t0002g0329 | 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 | a0001c0001t0001g0404 | 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 | a0001c0001t0001g0250 | 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 | 205 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0178others(202): 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 | ||||||
| chr12:420867
|
C | T | 1 | a0004c0004t0001g0187 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.413+2231C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420867 | ||||||
| chr12:420880
|
C | A | 46 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | 67 | a0001c0001t0001g0131a0001c0001t0001g0146a0001c0001t0001g0147others(64): Show | 68 | HG00280.hp1 HG00735.hp1 HG00735.hp2 others(65): 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 | 63 | a0001c0001t0001g0132a0001c0001t0001g0141a0001c0001t0001g0146others(60): Show | 64 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(61): 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0132a0001c0001t0001g0238a0001c0001t0001g0251others(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 | a0003c0003t0001g0188a0003c0003t0001g0341 | 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 | a0003c0003t0001g0189a0003c0003t0001g0342 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0254 | 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 | a0001c0001t0001g0258 | 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 | a0003c0003t0002g0229 | 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 | a0001c0001t0001g0141a0001c0001t0001g0164a0001c0001t0001g0165others(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 | a0001c0001t0001g0248a0003c0003t0001g0140 | 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 | a0001c0001t0001g0249a0001c0001t0001g0286a0001c0001t0001g0287 | 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 | a0001c0001t0001g0153a0001c0001t0001g0255a0001c0001t0001g0262others(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 | a0001c0001t0001g0274 | 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 | a0001c0001t0001g0154 | 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 | 171 | a0001c0001t0001g0398a0001c0001t0002g0003a0001c0001t0002g0037others(168): 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 | a0001c0001t0001g0157 | 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 | 29 | a0001c0001t0001g0150a0001c0001t0001g0178a0001c0001t0001g0179others(26): Show | 29 | HG00280.hp1 HG00642.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.413+2303C>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 420939 | ||||||
| chr12:420941
|
C | T | 171 | a0001c0001t0001g0398a0001c0001t0002g0003a0001c0001t0002g0037others(168): 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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(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 | a0001c0001t0001g0270a0002c0002t0001g0387 | 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 | a0003c0003t0004g0331 | 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 | a0001c0001t0001g0298 | 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 | a0003c0003t0001g0017 | 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 | a0001c0001t0001g0132a0001c0001t0001g0141a0001c0001t0001g0147others(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 | a0001c0001t0001g0253 | 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 | 12 | a0001c0001t0001g0167a0001c0001t0001g0172a0001c0001t0001g0239others(9): Show | 13 | HG00323.hp1 HG00642.hp2 HG00735.hp2 others(10): 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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(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 | a0001c0001t0001g0131a0001c0001t0001g0141a0001c0001t0001g0146others(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 | a0001c0001t0001g0211a0003c0003t0001g0095a0003c0003t0001g0289others(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 | a0002c0002t0001g0326a0004c0004t0001g0093 | 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 | a0001c0001t0008g0170a0006c0006t0011g0106 | 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 | a0001c0001t0001g0257 | 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 | a0001c0001t0006g0010a0001c0001t0006g0391a0001c0001t0006g0392others(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 | a0001c0001t0001g0253a0001c0001t0001g0407a0003c0003t0001g0017others(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 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0141others(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 | a0003c0003t0001g0073 | 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(290): Show |
T | 1 | a0004c0004t0001g0187 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.413+2400_413+2696d others(2): 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 | a0001c0001t0003g0031 | 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 | 267 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(264): 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0238a0001c0001t0001g0409a0003c0003t0001g0062 | 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 | 200 | a0001c0001t0001g0132a0001c0001t0001g0165a0001c0001t0001g0167others(197): 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 | a0001c0001t0001g0157a0001c0001t0001g0178a0001c0001t0001g0208others(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 | 48 | a0001c0001t0002g0003a0001c0001t0002g0049a0001c0001t0002g0074others(45): 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 | a0001c0001t0001g0282a0001c0001t0009g0294 | 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 | a0001c0001t0002g0009a0001c0001t0002g0329a0001c0001t0002g0347others(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 | a0001c0001t0001g0409 | 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 | 119 | a0001c0001t0001g0179a0001c0001t0001g0398a0001c0001t0002g0037others(116): 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 | a0001c0001t0004g0330 | 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 | a0001c0001t0001g0157a0001c0001t0001g0208a0001c0001t0001g0238others(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 | a0001c0001t0001g0132a0001c0001t0001g0147a0001c0001t0001g0238others(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 | a0001c0001t0001g0131a0001c0001t0001g0141a0001c0001t0001g0146others(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 | a0003c0003t0001g0148a0005c0005t0005g0418 | 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 | a0001c0001t0004g0401a0001c0001t0010g0209a0001c0001t0010g0281 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0150a0001c0001t0001g0238a0001c0001t0001g0256others(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 | a0001c0001t0003g0023a0001c0001t0003g0024a0001c0001t0003g0039 | 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 | a0001c0001t0001g0157a0001c0001t0001g0172a0001c0001t0001g0211others(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 | a0001c0001t0001g0239 | 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 | a0001c0001t0008g0170a0003c0003t0007g0414a0006c0006t0011g0106 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0004g0330 | 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 | a0001c0001t0001g0178 | 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 | a0005c0005t0005g0411 | 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 | a0007c0007t0005g0245 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0239 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0146others(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 | a0001c0001t0001g0157a0001c0001t0001g0172a0001c0001t0001g0408others(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 | a0001c0001t0006g0010a0001c0001t0006g0390a0001c0001t0006g0391others(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 | a0001c0001t0002g0011a0001c0001t0002g0012 | 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 | a0001c0001t0001g0132a0001c0001t0001g0251a0001c0001t0001g0252others(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 | a0001c0001t0001g0366 | 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 | a0002c0002t0014g0323 | 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 | a0001c0001t0001g0364 | 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 | a0002c0002t0001g0296 | 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 | a0001c0001t0004g0275 | 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 | a0003c0003t0004g0365 | 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 | a0001c0001t0001g0253 | 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 | a0001c0001t0001g0131a0001c0001t0001g0141a0001c0001t0001g0146others(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 | a0001c0001t0004g0213a0003c0003t0002g0374a0003c0003t0004g0212 | 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 | a0001c0001t0001g0167a0001c0001t0001g0250a0001c0001t0001g0273others(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 | a0001c0001t0001g0208a0002c0002t0002g0083 | 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 | a0001c0001t0001g0147a0001c0001t0001g0253a0001c0001t0001g0364others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0004g0330 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0132a0001c0001t0001g0251a0001c0001t0001g0252others(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 | a0001c0001t0001g0167a0001c0001t0001g0250a0001c0001t0001g0273others(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 | a0001c0001t0002g0329 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0131a0001c0001t0001g0141a0001c0001t0001g0146others(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 | a0001c0001t0001g0147a0001c0001t0001g0150a0001c0001t0001g0157others(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 | a0001c0001t0001g0238 | 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 | a0001c0001t0001g0141a0001c0001t0001g0164a0001c0001t0001g0206others(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 | a0001c0001t0002g0041a0001c0001t0002g0136a0001c0001t0002g0137others(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 | a0001c0001t0001g0377a0001c0001t0001g0404a0002c0002t0001g0402others(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 | a0003c0003t0004g0331 | 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 | a0003c0003t0007g0414 | 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 | a0001c0001t0001g0165a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0164others(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 | a0003c0003t0007g0414 | 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 | a0001c0001t0001g0258a0003c0003t0004g0331a0003c0003t0007g0327others(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 | a0001c0001t0001g0377 | 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 | a0001c0001t0001g0258 | 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 | a0001c0001t0001g0404 | 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 | 143 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0208others(140): 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 | 181 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0150others(178): Show | 185 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(182): 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 | a0001c0001t0001g0147a0001c0001t0001g0178a0001c0001t0001g0211others(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 | a0001c0001t0001g0211 | 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 | a0002c0002t0001g0326a0004c0004t0001g0093 | 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 | a0001c0001t0001g0147a0001c0001t0001g0178a0001c0001t0001g0250others(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 | a0001c0001t0001g0178a0001c0001t0001g0250a0001c0001t0001g0256others(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 | a0002c0002t0001g0259 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0002g0357 | 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 | a0001c0001t0001g0410a0001c0001t0002g0008a0002c0002t0002g0083others(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 | a0001c0001t0001g0178a0001c0001t0001g0250a0004c0004t0002g0097 | 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 | a0001c0001t0001g0157a0001c0001t0001g0172a0001c0001t0001g0178others(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 | a0001c0001t0001g0147a0001c0001t0001g0150a0001c0001t0001g0157others(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 | a0001c0001t0001g0366a0001c0001t0001g0410 | 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 | a0001c0001t0001g0167a0001c0001t0001g0238a0001c0001t0001g0239 | 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 | a0001c0001t0001g0178a0001c0001t0001g0250a0001c0001t0001g0377others(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 | a0001c0001t0001g0270a0002c0002t0001g0387a0003c0003t0001g0095others(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 | a0003c0003t0001g0289 | 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 | a0001c0001t0001g0410a0001c0001t0004g0325a0004c0004t0001g0096others(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 | a0001c0001t0001g0257 | 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 | a0001c0001t0001g0131a0001c0001t0001g0146a0001c0001t0001g0274others(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 | 65 | a0001c0001t0001g0270a0001c0001t0001g0366a0001c0001t0001g0377others(62): 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 | a0001c0001t0001g0165a0001c0001t0001g0270a0001c0001t0001g0366others(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 | 128 | a0001c0001t0001g0179a0001c0001t0001g0208a0001c0001t0001g0258others(125): Show | 130 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.413+2843G>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421479 | ||||||
| chr12:421480
|
T | C | 207 | a0001c0001t0001g0147a0001c0001t0001g0165a0001c0001t0001g0179others(204): Show | 212 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(209): 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0132others(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 | a0001c0001t0001g0167a0001c0001t0001g0238a0001c0001t0001g0239others(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 | 102 | a0001c0001t0001g0398a0001c0001t0002g0037a0001c0001t0003g0024others(99): Show | 104 | HG00280.hp2 HG00438.hp2 HG00639.hp1 others(101): 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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(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 | a0001c0001t0001g0157a0001c0001t0001g0172a0001c0001t0001g0253others(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 | a0002c0002t0001g0403 | 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 | a0003c0003t0001g0066 | 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 | a0001c0001t0001g0366a0001c0001t0001g0408a0004c0004t0001g0317 | 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 | a0001c0001t0002g0116 | 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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0164a0001c0001t0001g0263a0001c0001t0001g0314others(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 | a0001c0001t0001g0248 | 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 | a0003c0003t0002g0228 | 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 | a0001c0001t0001g0288 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0132others(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 | a0001c0001t0001g0249a0001c0001t0001g0286a0001c0001t0001g0287 | 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 | a0001c0001t0001g0265 | 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 | a0001c0001t0001g0141a0001c0001t0001g0206 | 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 | a0002c0002t0001g0259 | 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 | 20 | a0001c0001t0001g0404a0001c0001t0001g0407a0002c0002t0001g0111others(17): 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 | a0003c0003t0002g0230a0003c0003t0002g0231a0003c0003t0002g0232others(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 | a0003c0003t0002g0278 | 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 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0001t0001g0146others(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 | 26 | a0001c0001t0001g0282a0001c0001t0001g0377a0001c0001t0001g0407others(23): 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 | a0003c0003t0007g0327a0003c0003t0007g0414 | 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 | a0001c0001t0004g0275 | 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 | a0001c0001t0001g0150a0001c0001t0001g0151a0001c0001t0001g0157others(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 | a0001c0001t0001g0282a0001c0001t0001g0377a0001c0001t0001g0409others(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 | 53 | a0001c0001t0001g0147a0001c0001t0001g0179a0001c0001t0001g0208others(50): 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 | 19 | a0002c0002t0001g0111a0002c0002t0001g0244a0002c0002t0002g0083others(16): 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0132others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0132others(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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0282others(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 | a0003c0003t0004g0365a0006c0006t0011g0106 | 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 | a0001c0001t0003g0023 | 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0001g0147a0002c0002t0001g0326a0004c0004t0001g0093 | 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 | 220 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(217): 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 | 108 | a0001c0001t0001g0141a0001c0001t0001g0150a0001c0001t0001g0172others(105): 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 | 79 | a0001c0001t0001g0172a0001c0001t0001g0178a0001c0001t0001g0250others(76): 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 | 100 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0001t0001g0146others(97): 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 | a0001c0001t0001g0408 | 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 | a0003c0003t0004g0331 | 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 | a0001c0001t0001g0178 | 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 | 88 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0001t0001g0146others(85): 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 | a0002c0002t0001g0244 | 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 | a0001c0001t0006g0010a0001c0001t0006g0390a0001c0001t0006g0391others(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 | a0001c0001t0001g0172a0001c0001t0001g0179a0001c0001t0001g0208others(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 | a0001c0001t0004g0325 | 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 | 53 | a0001c0001t0002g0003a0001c0001t0002g0049a0001c0001t0002g0074others(50): 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0132others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0003c0003t0001g0066a0004c0004t0001g0096 | 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 | a0001c0001t0001g0147a0001c0001t0001g0211a0002c0002t0001g0326others(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 | a0002c0002t0014g0323 | 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 | a0002c0002t0002g0083 | 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 | 3 | a0002c0002t0001g0111a0004c0004t0001g0191a0004c0004t0001g0192 | 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 | a0001c0001t0001g0157a0001c0001t0001g0253a0001c0001t0001g0377others(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 | a0005c0005t0005g0411 | 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 | 58 | a0001c0001t0001g0141a0001c0001t0001g0150a0001c0001t0001g0206others(55): 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 | 107 | a0001c0001t0001g0141a0001c0001t0001g0147a0001c0001t0001g0150others(104): 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 | a0001c0001t0004g0401a0001c0001t0010g0209a0001c0001t0010g0281 | 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 | a0001c0001t0001g0179a0001c0001t0001g0208a0001c0001t0001g0378 | 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 | 159 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(156): 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 | a0005c0005t0005g0418 | 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 | a0003c0003t0001g0062 | 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 | a0001c0001t0001g0146a0001c0001t0001g0167a0001c0001t0001g0238others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0132others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0132others(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 | a0001c0001t0001g0157a0001c0001t0001g0258a0001c0001t0001g0273others(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 | a0002c0002t0002g0113a0002c0002t0002g0145a0002c0002t0002g0162others(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 | 52 | a0001c0001t0002g0003a0001c0001t0002g0049a0001c0001t0002g0074others(49): 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 | a0001c0001t0001g0172a0002c0002t0001g0402a0003c0003t0007g0414 | 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 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0001t0001g0257others(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 | 3 | a0002c0002t0001g0111a0004c0004t0001g0191a0004c0004t0001g0192 | 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 | a0003c0003t0001g0188a0003c0003t0001g0189a0003c0003t0001g0342 | 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 | a0001c0001t0001g0253 | 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 | a0002c0002t0001g0389 | 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 | a0003c0003t0001g0341 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0132others(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 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0167others(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 | a0005c0005t0005g0334a0005c0005t0005g0412a0005c0005t0005g0420others(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 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0001t0001g0253others(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 | a0001c0001t0001g0141a0001c0001t0001g0206a0001c0001t0001g0256others(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 | a0004c0004t0001g0096 | 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 | a0001c0001t0001g0258a0001c0001t0001g0273 | 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 | a0003c0003t0007g0414 | 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 | a0001c0001t0001g0256a0001c0001t0001g0298a0001c0001t0001g0356others(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 | a0001c0001t0001g0141a0001c0001t0001g0206 | 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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0007c0007t0005g0245 | 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 | a0001c0001t0003g0023a0004c0004t0002g0097a0006c0006t0012g0105 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0132others(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 | a0001c0001t0001g0147a0001c0001t0001g0150a0001c0001t0001g0157others(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 | a0003c0003t0004g0365 | 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 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0001t0001g0146others(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 | a0001c0001t0001g0150a0001c0001t0001g0407a0004c0004t0001g0096 | 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 | a0001c0001t0001g0250a0001c0001t0004g0213a0003c0003t0002g0374others(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 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0001t0001g0146others(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 | a0003c0003t0001g0066 | 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 | a0001c0001t0001g0404 | 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 | a0001c0001t0004g0092a0001c0001t0004g0159a0001c0001t0004g0160others(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 | a0004c0004t0001g0317 | 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 | a0003c0003t0001g0066 | 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 | a0001c0001t0001g0407 | 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 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0001t0001g0146others(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 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0001t0001g0146others(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 | 150 | a0001c0001t0001g0150a0001c0001t0001g0250a0001c0001t0001g0282others(147): Show | 152 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(149): 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 | a0001c0001t0001g0250 | 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 | 123 | a0001c0001t0001g0282a0001c0001t0001g0398a0001c0001t0001g0407others(120): Show | 125 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.413+3303A>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 421939 | ||||||
| chr12:421943
|
CTGTG | C | 104 | a0001c0001t0001g0398a0001c0001t0002g0037a0001c0001t0003g0023others(101): Show | 106 | HG00280.hp2 HG00438.hp2 HG00639.hp1 others(103): 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 | a0001c0001t0004g0092a0001c0001t0004g0159a0001c0001t0004g0160others(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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0132others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0132others(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 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0001t0001g0146others(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 | a0002c0002t0001g0403 | 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 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0001t0001g0146others(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 | 203 | a0001c0001t0001g0147a0001c0001t0001g0150a0001c0001t0001g0157others(200): Show | 207 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.413+3377T>A | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 422013 | ||||||
| chr12:422045
|
T | TA | 164 | a0001c0001t0001g0282a0001c0001t0001g0398a0001c0001t0001g0409others(161): Show | 168 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(165): 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 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0001t0001g0146others(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 | a0001c0001t0004g0330 | 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 | a0001c0001t0001g0250a0001c0001t0004g0092a0001c0001t0004g0159others(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 | a0001c0001t0001g0151a0001c0001t0001g0178a0001c0001t0001g0185others(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 | a0001c0001t0001g0408 | 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 | 167 | a0001c0001t0001g0282a0001c0001t0001g0398a0001c0001t0001g0409others(164): Show | 171 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(168): 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 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0001t0001g0146others(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 | a0001c0001t0001g0141a0001c0001t0001g0206 | 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 | a0001c0001t0001g0356 | 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 | a0003c0003t0001g0017 | 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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0256a0001c0001t0001g0298 | 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 | a0001c0001t0001g0377 | 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0002g0116 | 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 | a0001c0001t0001g0251a0001c0001t0001g0252a0001c0001t0001g0253 | 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 | a0001c0001t0001g0314 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0132others(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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0267 | 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 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0266 | 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 | a0003c0003t0001g0015 | 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 | a0001c0001t0001g0156a0001c0001t0001g0240 | 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 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0248others(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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(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 | a0001c0001t0001g0404 | 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 | a0001c0001t0001g0282a0001c0001t0001g0409a0001c0001t0009g0294others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | 304 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(301): Show | 308 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(305): 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 | a0001c0001t0001g0282a0001c0001t0001g0409a0001c0001t0009g0294others(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 | a0001c0001t0001g0404 | 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 | a0001c0001t0001g0410a0004c0004t0001g0096 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0002g0058a0001c0001t0002g0299a0001c0001t0002g0300others(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 | a0001c0001t0006g0010a0001c0001t0006g0390a0001c0001t0006g0391others(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 | a0001c0001t0001g0282a0001c0001t0001g0408a0001c0001t0001g0409others(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 | a0002c0002t0001g0271 | 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 | a0001c0001t0001g0404 | 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 | a0003c0003t0002g0278 | 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 | a0003c0003t0002g0229a0003c0003t0002g0230a0003c0003t0002g0231others(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 | a0001c0001t0002g0405 | 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 | a0001c0001t0004g0319a0001c0001t0004g0320 | 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 | a0002c0002t0001g0227a0002c0002t0001g0284 | 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 | a0001c0001t0002g0037a0003c0003t0002g0063a0003c0003t0002g0081 | 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 | a0001c0001t0002g0197 | 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 | a0001c0001t0004g0269 | 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 | a0001c0001t0001g0131a0001c0001t0001g0146a0001c0001t0001g0349 | 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 | a0001c0001t0001g0211a0001c0001t0001g0270a0002c0002t0001g0326others(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 | a0001c0001t0002g0058a0001c0001t0002g0299a0001c0001t0002g0300others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0011others(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 | a0001c0001t0001g0156a0001c0001t0001g0251a0001c0001t0002g0041others(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 | a0001c0001t0001g0030a0001c0001t0001g0108a0001c0001t0001g0132others(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 | a0001c0001t0001g0042a0001c0001t0001g0131a0001c0001t0001g0141others(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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0004g0401a0005c0005t0005g0334a0005c0005t0005g0411others(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 | a0001c0001t0004g0090a0001c0001t0007g0014a0004c0004t0001g0317 | 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 | 94 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0282others(91): Show | 96 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(93): 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 | 116 | a0001c0001t0002g0003a0001c0001t0002g0037a0001c0001t0002g0049others(113): 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 | a0001c0001t0001g0167a0001c0001t0001g0178a0001c0001t0001g0179others(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 | 218 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0282others(215): Show | 222 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.413+4546A>G | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423182 | ||||||
| chr12:423189
|
T | C | 218 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0282others(215): Show | 222 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.413+4553T>C | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423189 | ||||||
| chr12:423191
|
C | G | 218 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0282others(215): Show | 222 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(219): 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 | a0007c0007t0005g0328 | 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 | a0001c0001t0004g0275a0001c0001t0004g0330a0001c0001t0008g0170others(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 | a0001c0001t0002g0037 | 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 | 197 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(194): 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 | a0002c0002t0001g0305a0002c0002t0001g0389a0005c0005t0005g0334others(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 | a0001c0001t0001g0150a0001c0001t0001g0253a0001c0001t0001g0356others(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 | 85 | a0001c0001t0001g0298a0001c0001t0001g0398a0001c0001t0002g0003others(82): Show | 88 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(85): 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 | a0001c0001t0002g0041 | 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 | a0001c0001t0002g0337a0001c0001t0002g0346a0001c0001t0002g0405others(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 | 52 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0282others(49): 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 | a0001c0001t0001g0282a0001c0001t0001g0408a0001c0001t0001g0409others(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 | a0001c0001t0002g0091a0003c0003t0002g0382 | 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 | a0001c0001t0004g0401a0005c0005t0005g0334a0005c0005t0005g0411others(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 | a0001c0001t0001g0151a0001c0001t0001g0367a0001c0001t0007g0013others(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 | a0001c0001t0001g0398a0002c0002t0001g0109a0002c0002t0001g0128others(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 | a0001c0001t0004g0098a0001c0001t0004g0275a0001c0001t0004g0330others(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 | a0002c0002t0001g0115 | 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 | a0005c0005t0005g0412 | 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 | a0002c0002t0001g0389 | 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 | a0001c0001t0001g0030a0001c0001t0001g0255a0001c0001t0001g0266others(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 | a0001c0001t0001g0282a0001c0001t0001g0408a0001c0001t0001g0409others(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 | a0001c0001t0001g0042a0001c0001t0001g0108a0001c0001t0001g0132others(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 | a0001c0001t0002g0075a0001c0001t0003g0002a0001c0001t0003g0016others(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 | a0001c0001t0003g0125a0004c0004t0001g0096 | 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 | a0001c0001t0001g0131a0001c0001t0001g0282a0001c0001t0001g0349others(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 | a0002c0002t0001g0217 | 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 | a0001c0001t0002g0003a0001c0001t0002g0049a0001c0001t0003g0019others(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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0001g0153a0001c0001t0001g0262a0001c0001t0004g0335others(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 | a0001c0001t0001g0185a0001c0001t0004g0087a0002c0002t0001g0004others(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 | a0003c0003t0001g0413 | 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 | a0001c0001t0004g0359a0001c0001t0004g0386a0001c0001t0006g0395others(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 | 33 | a0001c0001t0007g0014a0002c0002t0001g0043a0002c0002t0001g0124others(30): Show | 33 | HG00280.hp2 HG00438.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.413+4841delG | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423476 | ||||||
| chr12:423476
|
TGTG | T | 9 | a0001c0001t0003g0034a0001c0001t0004g0082a0001c0001t0004g0084others(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 | a0002c0002t0001g0038a0004c0004t0001g0064a0004c0004t0001g0065 | 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 | a0002c0002t0001g0005a0002c0002t0002g0083a0004c0004t0002g0310 | 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 | 44 | a0001c0001t0001g0151a0001c0001t0001g0367a0001c0001t0001g0398others(41): 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 | 118 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(115): Show | 119 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(116): 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 | a0002c0002t0001g0236a0002c0002t0001g0284a0002c0002t0001g0297others(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 | a0002c0002t0001g0094a0002c0002t0001g0130a0002c0002t0001g0152others(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 | a0001c0001t0004g0275a0003c0003t0004g0331a0006c0006t0011g0103others(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 | a0001c0001t0008g0170a0003c0003t0007g0327a0003c0003t0007g0414 | 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 | a0001c0001t0004g0330a0003c0003t0004g0365 | 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 | a0001c0001t0003g0127a0002c0002t0001g0402a0004c0004t0001g0071others(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 | 178 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(175): Show | 181 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.413+4853G>T | CCDC77 | ENSG00000120647.10 | transcript | ENST00000239830.9 | protein_coding | 5/12 | chr12 | 423489 | ||||||
| chr12:423494
|
G | T | 187 | a0001c0001t0001g0147a0001c0001t0001g0151a0001c0001t0001g0185others(184): Show | 190 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(187): 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 | a0001c0001t0004g0401a0005c0005t0005g0334a0005c0005t0005g0411others(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 | a0001c0001t0001g0407a0001c0001t0002g0337a0001c0001t0002g0352others(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 | a0001c0001t0001g0407a0002c0002t0001g0403 | 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 | a0004c0004t0001g0317 | 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 | a0001c0001t0002g0279 | 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 | a0001c0001t0006g0395 | 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 | a0001c0001t0002g0012 | 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 | a0002c0002t0001g0121a0002c0002t0001g0260a0002c0002t0001g0261 | 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 | a0003c0003t0004g0339 | 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 | a0001c0001t0004g0213a0003c0003t0002g0374a0003c0003t0004g0212 | 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 | a0002c0002t0001g0143a0002c0002t0001g0221 | 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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(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 | 34 | a0001c0001t0002g0037a0002c0002t0001g0038a0002c0002t0001g0051others(31): 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 | a0001c0001t0001g0404a0001c0001t0004g0275a0001c0001t0008g0170others(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 | a0001c0001t0001g0151a0001c0001t0001g0248a0001c0001t0001g0249others(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 | a0001c0001t0001g0356a0001c0001t0002g0056a0001c0001t0004g0085others(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 | a0005c0005t0005g0411 | 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 | a0001c0001t0004g0401a0005c0005t0005g0334a0005c0005t0005g0411others(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 | a0002c0002t0001g0149a0002c0002t0002g0083a0002c0002t0002g0100others(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 | a0002c0002t0001g0217 | 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 | a0001c0001t0004g0333 | 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 | a0001c0001t0004g0401a0005c0005t0005g0334a0005c0005t0005g0411others(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 | a0004c0004t0001g0317 | 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 | 218 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0282others(215): Show | 222 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(219): 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 | a0005c0005t0005g0420 | 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 | a0007c0007t0005g0384 | 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 | a0005c0005t0005g0411 | 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 | a0005c0005t0005g0334a0005c0005t0005g0418a0005c0005t0005g0421 | 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 | a0005c0005t0005g0422 | 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 | a0007c0007t0005g0245 | 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 | a0005c0005t0005g0412 | 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 | a0001c0001t0004g0401 | 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 | a0001c0001t0006g0396 | 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 | a0001c0001t0006g0391 | 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 | a0003c0003t0006g0089 | 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 | a0001c0001t0006g0010a0001c0001t0006g0390a0001c0001t0006g0392 | 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 | a0001c0001t0006g0393a0001c0001t0006g0394 | 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 | a0001c0001t0006g0395 | 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 | a0003c0003t0001g0413 | 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 | a0001c0001t0001g0211 | 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 | a0003c0003t0004g0331 | 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 | a0003c0003t0004g0365 | 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 | a0001c0001t0004g0275a0001c0001t0008g0170a0003c0003t0007g0327others(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 | a0001c0001t0004g0330 | 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 | a0003c0003t0001g0095 | 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 | a0003c0003t0001g0318 | 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 | a0001c0001t0001g0270a0003c0003t0001g0415 | 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 | a0002c0002t0001g0326a0002c0002t0001g0387a0003c0003t0001g0289others(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 | a0003c0003t0004g0212 | 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 | a0001c0001t0004g0213 | 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 | a0003c0003t0002g0374 | 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 | a0003c0003t0001g0188 | 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 | a0002c0002t0001g0389 | 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 | a0002c0002t0014g0323 | 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 | a0003c0003t0001g0189 | 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 | a0003c0003t0001g0341a0003c0003t0001g0342 | 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 | a0001c0001t0001g0282a0001c0001t0001g0408a0001c0001t0001g0409others(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 | a0001c0001t0001g0151a0001c0001t0001g0367 | 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 | a0001c0001t0003g0033 | 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 | a0001c0001t0001g0282a0001c0001t0001g0408a0001c0001t0001g0409others(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 | a0001c0001t0006g0010a0001c0001t0006g0390a0001c0001t0006g0391others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0006g0010a0001c0001t0006g0390a0001c0001t0006g0391others(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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0002g0049 | 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 | a0001c0001t0002g0011 | 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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367 | 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 | a0001c0001t0002g0011 | 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 | a0003c0003t0004g0339 | 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 | a0007c0007t0005g0245 | 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 | 50 | a0001c0001t0002g0003a0001c0001t0002g0049a0001c0001t0002g0074others(47): 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 | a0001c0001t0004g0213a0003c0003t0002g0374a0003c0003t0004g0212 | 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 | 218 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0282others(215): Show | 222 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(219): 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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(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 | a0001c0001t0001g0274 | 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 | a0002c0002t0001g0133a0002c0002t0001g0134a0002c0002t0001g0135others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0004g0092a0001c0001t0004g0159a0001c0001t0004g0160others(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 | a0001c0001t0010g0209a0001c0001t0010g0281 | 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 | a0002c0002t0001g0005 | 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 | a0001c0001t0003g0028 | 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 | a0004c0004t0001g0207 | 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 | a0001c0001t0002g0405 | 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 | a0001c0001t0003g0127a0002c0002t0001g0236a0002c0002t0001g0297others(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 | a0001c0001t0003g0027 | 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 | a0001c0001t0003g0016a0001c0001t0003g0053a0001c0001t0003g0099others(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 | a0003c0003t0004g0371 | 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 | a0001c0001t0002g0304a0001c0001t0002g0388a0001c0001t0002g0400others(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 | a0001c0001t0002g0304a0001c0001t0002g0388a0001c0001t0002g0400others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | 191 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0282others(188): 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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0002g0008a0001c0001t0002g0009a0001c0001t0002g0011others(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 | a0001c0001t0001g0147a0001c0001t0002g0337a0001c0001t0006g0010others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0004g0092a0001c0001t0004g0159a0001c0001t0004g0160others(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 | a0001c0001t0002g0279 | 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 | a0001c0001t0001g0407a0002c0002t0001g0403 | 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 | a0003c0003t0002g0063 | 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 | a0001c0001t0001g0404 | 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 | a0004c0004t0001g0306 | 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 | a0001c0001t0004g0213a0002c0002t0001g0389a0003c0003t0001g0188others(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 | a0001c0001t0006g0010a0001c0001t0006g0390a0001c0001t0006g0391others(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 | a0001c0001t0004g0359 | 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 | a0001c0001t0001g0408a0001c0001t0001g0409a0001c0001t0001g0410others(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 | a0001c0001t0003g0002a0001c0001t0003g0027a0001c0001t0003g0028 | 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 | a0001c0001t0003g0002a0001c0001t0003g0027a0001c0001t0003g0028 | 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 | a0001c0001t0001g0282a0001c0001t0004g0275a0001c0001t0008g0170others(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 | a0001c0001t0004g0275a0003c0003t0001g0148a0003c0003t0002g0006others(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 | a0001c0001t0001g0131a0001c0001t0001g0349 | 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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0004g0275 | 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 | a0001c0001t0004g0275 | 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 | a0001c0001t0006g0010a0001c0001t0006g0390a0001c0001t0006g0391others(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 | a0001c0001t0004g0275 | 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 | a0001c0001t0002g0347a0001c0001t0004g0275a0003c0003t0007g0327others(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 | a0002c0002t0001g0296 | 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 | a0004c0004t0001g0306 | 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 | a0001c0001t0004g0275a0002c0002t0001g0296a0004c0004t0001g0306 | 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 | a0001c0001t0004g0275 | 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 | a0002c0002t0001g0296 | 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 | a0001c0001t0001g0147a0001c0001t0002g0137a0001c0001t0002g0138others(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 | a0001c0001t0004g0092a0001c0001t0004g0159a0001c0001t0004g0160others(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 | a0001c0001t0001g0185a0001c0001t0004g0084a0001c0001t0004g0090others(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 | a0001c0001t0007g0013a0001c0001t0007g0014a0004c0004t0001g0317others(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 | a0003c0003t0001g0148a0003c0003t0007g0327a0006c0006t0011g0106 | 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 | a0003c0003t0007g0414 | 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 | 201 | a0001c0001t0001g0030a0001c0001t0001g0108a0001c0001t0001g0131others(198): Show | 206 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(203): 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 | a0001c0001t0004g0086a0001c0001t0004g0088a0001c0001t0004g0330others(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 | a0001c0001t0001g0282a0001c0001t0001g0408a0001c0001t0001g0409others(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 | a0002c0002t0001g0216 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | 340 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(337): Show | 344 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(341): 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 | a0003c0003t0002g0278 | 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 | a0001c0001t0004g0213a0003c0003t0004g0212 | 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 | 327 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(324): Show | 330 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(327): 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 | a0001c0001t0004g0401a0002c0002t0002g0083a0002c0002t0002g0100others(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 | a0001c0001t0004g0213a0001c0001t0006g0010a0001c0001t0006g0390others(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 | a0001c0001t0002g0361 | 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 | a0001c0001t0002g0037 | 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 | a0001c0001t0002g0137a0001c0001t0002g0138 | 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 | a0003c0003t0001g0188a0003c0003t0001g0189a0003c0003t0001g0341others(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 | 183 | a0001c0001t0001g0398a0001c0001t0002g0037a0001c0001t0003g0002others(180): Show | 186 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(183): 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 | a0002c0002t0001g0402a0004c0004t0001g0096 | 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 | a0002c0002t0001g0123 | 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 | a0002c0002t0001g0321 | 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 | a0001c0001t0002g0197 | 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 | a0004c0004t0001g0096 | 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 | 337 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(334): Show | 340 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(337): 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 | a0002c0002t0002g0113a0004c0004t0002g0307a0004c0004t0002g0309others(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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0002c0002t0001g0264 | 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 | a0002c0002t0001g0004a0002c0002t0001g0124a0002c0002t0001g0143others(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 | a0002c0002t0001g0220 | 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 | 174 | a0001c0001t0001g0398a0001c0001t0002g0037a0001c0001t0003g0002others(171): Show | 177 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(174): 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 | a0001c0001t0002g0041 | 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 | a0001c0001t0004g0401a0002c0002t0002g0083a0002c0002t0002g0100others(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 | a0002c0002t0001g0123 | 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 | a0004c0004t0001g0171a0004c0004t0001g0345a0004c0004t0005g0344 | 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | 34 | a0001c0001t0002g0037a0002c0002t0001g0038a0002c0002t0001g0051others(31): 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 | a0003c0003t0002g0315 | 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 | a0001c0001t0004g0213a0002c0002t0001g0389a0003c0003t0001g0188others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0131a0001c0001t0001g0239a0001c0001t0001g0253others(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 | a0001c0001t0001g0398a0001c0001t0001g0407a0001c0001t0002g0003others(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 | a0001c0001t0004g0082a0001c0001t0004g0084a0001c0001t0004g0085others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0001c0001t0001g0404a0005c0005t0005g0334a0005c0005t0005g0411others(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 | a0001c0001t0001g0147a0001c0001t0001g0270a0001c0001t0001g0407others(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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0282others(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 | 179 | a0001c0001t0001g0398a0001c0001t0002g0037a0001c0001t0003g0002others(176): Show | 182 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(179): 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 | a0001c0001t0002g0091a0003c0003t0002g0374a0003c0003t0002g0382 | 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 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | 338 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(335): Show | 341 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(338): 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 | a0001c0001t0002g0405a0003c0003t0002g0370a0003c0003t0002g0381 | 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 | a0001c0001t0001g0042a0001c0001t0001g0263 | 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 | a0002c0002t0001g0389 | 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 | 181 | a0001c0001t0001g0282a0001c0001t0001g0398a0001c0001t0001g0408others(178): Show | 184 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(181): 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 | a0003c0003t0002g0278 | 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 | a0002c0002t0001g0402a0004c0004t0001g0096 | 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 | a0002c0002t0002g0083a0002c0002t0002g0145a0002c0002t0002g0162others(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 | a0004c0004t0001g0171a0004c0004t0001g0345a0004c0004t0005g0344 | 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 | a0001c0001t0006g0010a0001c0001t0006g0390a0001c0001t0006g0391others(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 | a0002c0002t0001g0389a0003c0003t0001g0188a0003c0003t0001g0189others(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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(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 | a0001c0001t0001g0147a0001c0001t0001g0211a0002c0002t0001g0326others(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 | a0003c0003t0002g0176 | 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 | a0001c0001t0004g0275a0001c0001t0004g0330a0001c0001t0008g0170others(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 | a0001c0001t0003g0048a0001c0001t0006g0010a0001c0001t0006g0390others(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 | a0001c0001t0004g0275a0001c0001t0004g0330a0001c0001t0008g0170others(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 | a0002c0002t0014g0323 | 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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0266others(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 | a0001c0001t0004g0092a0001c0001t0004g0159a0001c0001t0004g0160others(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 | a0001c0001t0001g0178a0001c0001t0002g0405a0001c0001t0003g0059others(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 | a0002c0002t0001g0389a0003c0003t0001g0188a0003c0003t0001g0189others(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 | a0001c0001t0004g0401a0002c0002t0002g0083a0002c0002t0002g0100others(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 | a0002c0002t0001g0402a0004c0004t0001g0096 | 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 | 180 | a0001c0001t0001g0282a0001c0001t0001g0398a0001c0001t0001g0408others(177): Show | 183 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(180): 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 | a0004c0004t0001g0317 | 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 | a0002c0002t0001g0224 | 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 | a0001c0001t0002g0329 | 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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | 45 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0018others(42): 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 | a0002c0002t0001g0004a0002c0002t0001g0124a0002c0002t0001g0143others(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 | a0001c0001t0001g0349 | 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 | a0002c0002t0001g0402a0004c0004t0001g0096 | 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 | 179 | a0001c0001t0001g0282a0001c0001t0001g0398a0001c0001t0001g0408others(176): Show | 182 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(179): 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 | a0001c0001t0002g0009a0001c0001t0002g0357 | 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 | a0001c0001t0004g0275a0001c0001t0004g0330a0001c0001t0008g0170others(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 | a0001c0001t0001g0404 | 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 | a0001c0001t0002g0091 | 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 | a0003c0003t0004g0331 | 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 | a0001c0001t0003g0028 | 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 | a0003c0003t0002g0200 | 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 | a0004c0004t0001g0093 | 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 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0367others(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 | 152 | a0001c0001t0001g0042a0001c0001t0001g0150a0001c0001t0001g0263others(149): Show | 155 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(152): 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 | 51 | a0001c0001t0001g0151a0001c0001t0001g0185a0001c0001t0001g0298others(48): 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 | a0001c0001t0001g0154a0001c0001t0001g0266a0001c0001t0001g0282others(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 | a0001c0001t0004g0359a0001c0001t0004g0386a0008c0013t0004g0419 | 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 | a0001c0001t0001g0132a0001c0001t0001g0313a0001c0001t0001g0314 | 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 | a0001c0001t0001g0272a0001c0001t0003g0077 | 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 | a0001c0001t0002g0304a0001c0001t0002g0388a0001c0001t0002g0400others(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 | a0001c0001t0003g0125a0002c0002t0001g0308 | 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 | a0002c0002t0001g0280 | 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 | a0001c0001t0002g0041a0003c0003t0001g0148 | 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 | a0002c0002t0001g0280 | 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 | a0002c0002t0014g0323a0004c0004t0001g0171a0004c0004t0001g0345others(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 | a0002c0002t0014g0323a0004c0004t0001g0171a0004c0004t0001g0345others(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 | a0002c0002t0001g0280 | 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 | a0002c0002t0001g0402a0004c0004t0001g0096 | 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 | a0001c0001t0004g0085a0001c0001t0004g0213a0001c0001t0010g0209others(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 | a0001c0001t0004g0084a0001c0001t0004g0085a0001c0001t0004g0087others(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 | a0001c0001t0004g0269a0004c0004t0002g0097 | 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 | a0001c0001t0004g0269a0004c0004t0002g0097 | 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 | a0001c0001t0001g0282a0001c0001t0001g0408a0001c0001t0001g0409others(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 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0009others(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 | a0001c0001t0001g0282a0001c0001t0001g0408a0001c0001t0001g0409others(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 | 158 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(155): 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 | a0001c0001t0001g0407 | 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 | 205 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(202): 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 | a0001c0001t0001g0398a0001c0001t0004g0275a0001c0001t0004g0330others(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 | a0001c0001t0001g0132a0001c0001t0001g0313a0001c0001t0001g0314others(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 | a0001c0001t0001g0251a0001c0001t0001g0252 | 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 | a0001c0001t0001g0253 | 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 | a0001c0001t0001g0172 | 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 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0266others(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 | 214 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(211): 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 | a0001c0001t0002g0388a0001c0001t0002g0400a0003c0003t0002g0343others(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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | 162 | a0001c0001t0001g0151a0001c0001t0001g0211a0001c0001t0002g0293others(159): Show | 165 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(162): 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 | a0002c0002t0001g0296a0002c0002t0014g0323a0003c0003t0003g0069others(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 | a0002c0002t0002g0083a0002c0002t0002g0100a0002c0002t0002g0113others(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 | a0001c0001t0003g0046a0001c0001t0003g0077 | 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 | a0001c0001t0001g0377 | 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 | 415 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(412): Show | 425 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(422): 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 | a0001c0001t0001g0165a0001c0001t0001g0166 | 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 | a0001c0001t0001g0407a0001c0001t0002g0003a0001c0001t0002g0008others(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 | a0001c0001t0002g0380 | 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 | a0001c0001t0002g0008 | 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 | a0001c0001t0001g0147a0001c0001t0001g0178a0001c0001t0001g0211others(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 | a0001c0001t0001g0398a0001c0001t0004g0082a0001c0001t0004g0086others(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 | a0001c0001t0002g0058a0001c0001t0002g0299a0001c0001t0002g0300 | 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 | a0003c0003t0004g0339 | 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 | a0001c0001t0016g0078 | 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 | a0004c0004t0001g0171a0004c0004t0001g0345a0004c0004t0005g0344 | 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 | 48 | a0001c0001t0003g0002a0001c0001t0003g0016a0001c0001t0003g0018others(45): 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 | 33 | a0002c0002t0001g0038a0002c0002t0001g0051a0002c0002t0001g0109others(30): 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 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(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 | a0003c0003t0002g0200 | 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 | a0001c0001t0001g0407a0001c0001t0002g0003a0001c0001t0002g0008others(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 | a0001c0001t0004g0082a0001c0001t0004g0084a0001c0001t0004g0085others(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 | 131 | a0001c0001t0004g0213a0001c0001t0016g0078a0002c0002t0001g0004others(128): Show | 133 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(130): 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 | a0001c0001t0002g0091a0001c0001t0002g0329a0003c0003t0002g0374others(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 | a0001c0001t0001g0254 | 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 | a0002c0002t0001g0402 | 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 | a0001c0001t0002g0091a0001c0001t0002g0329a0003c0003t0002g0374others(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 | a0001c0001t0002g0197 | 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 | a0003c0003t0002g0202 | 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 | a0001c0001t0004g0082a0001c0001t0004g0084a0001c0001t0004g0085others(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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0282a0001c0001t0001g0408a0001c0001t0001g0409others(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 | a0001c0001t0001g0407a0001c0001t0002g0003a0001c0001t0002g0008others(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 | a0002c0002t0001g0152a0002c0002t0001g0234 | 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 | 116 | a0001c0001t0002g0032a0001c0001t0002g0037a0001c0001t0002g0056others(113): Show | 119 | HG00280.hp2 HG00423.hp1 HG00438.hp2 others(116): 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 | 415 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(412): Show | 425 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(422): 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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0002g0400a0003c0003t0002g0343a0006c0006t0012g0105 | 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 | 33 | a0002c0002t0001g0038a0002c0002t0001g0051a0002c0002t0001g0109others(30): 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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | a0001c0001t0002g0405 | 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 | 165 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0266others(162): 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 | a0001c0001t0003g0181 | 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 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0266 | 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 | a0003c0003t0015g0290 | 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 | a0001c0001t0001g0398a0001c0001t0004g0082a0001c0001t0004g0084others(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 | a0001c0001t0001g0147a0001c0001t0001g0211a0001c0001t0001g0270others(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 | 217 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0108others(214): 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 | a0001c0001t0001g0257a0001c0001t0001g0367a0001c0001t0001g0407others(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 | a0003c0003t0015g0290 | 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 | a0003c0003t0015g0290 | 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 | a0003c0003t0015g0290 | 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 |