Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 84660 |
|---|---|
| ensemblid | ENSG00000130783.14 |
| hgncid | 30723 |
| symbol | CCDC62 |
| name | coiled-coil domain containing 62 |
| refseq_nuc | NM_201435.5 |
| refseq_prot | NP_958843.2 |
| ensembl_nuc | ENST00000253079.11 |
| ensembl_prot | ENSP00000253079.6 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 122774572 |
| end | 122827528 |
| strand | + |
| ver | v1.2 |
| region | chr12:122774572-122827528 |
| region5000 | chr12:122769572-122832528 |
| regionname0 | CCDC62_chr12_122774572_122827528 |
| regionname5000 | CCDC62_chr12_122769572_122832528 |
| 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 | 1/1 | 684 | 270 | 64 | 49 | 113 | 11 | 31 | 79 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0002 | 0/0 | 684 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0003 | 0/0 | 684 | 7 | 4 | 0 | 0 | 0 | 3 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0004 | 0/0 | 684 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0005 | 0/0 | 684 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0006 | 0/0 | 684 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0007 | 0/0 | 292 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0008 | 0/0 | 684 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0009 | 0/0 | 684 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0010 | 0/0 | 684 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0011 | 0/0 | 684 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0012 | 0/0 | 684 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| 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 | 1/1 | 2055 | 259 | 55 | 48 | 113 | 11 | 30 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| c0002 | 0/0 | 2055 | 9 | 8 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| c0003 | 0/0 | 2055 | 7 | 4 | 0 | 0 | 0 | 3 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| c0004 | 0/0 | 2055 | 5 | 5 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| c0005 | 0/0 | 2055 | 4 | 4 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| c0006 | 0/0 | 2055 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| c0007 | 0/0 | 2055 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| c0008 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| c0009 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| c0010 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| c0011 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| c0012 | 0/0 | 2050 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| c0013 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| c0014 | 0/0 | 2055 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| c0015 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| c0016 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| 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 | 1248 | 190 | 43 | 40 | 80 | 9 | 17 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| t0002 | 0/0 | 1248 | 63 | 15 | 6 | 33 | 0 | 9 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| t0003 | 0/0 | 1248 | 21 | 16 | 0 | 0 | 1 | 4 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| t0004 | 1/0 | 1247 | 13 | 5 | 1 | 2 | 0 | 4 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| t0005 | 0/0 | 1248 | 4 | 0 | 2 | 0 | 2 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| t0006 | 0/0 | 1248 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| t0007 | 0/0 | 1248 | 2 | 0 | 1 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| t0008 | 0/0 | 1248 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| t0009 | 0/0 | 1248 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| t0010 | 0/0 | 1248 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| 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 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| 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 | 1/1 | 2055 | 259 | 55 | 48 | 113 | 11 | 30 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0001c0004 | 0/0 | 2055 | 5 | 5 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0001c0005 | 0/0 | 2055 | 4 | 4 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0001c0009 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0001c0014 | 0/0 | 2055 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0002c0002 | 0/0 | 2055 | 9 | 8 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0003c0003 | 0/0 | 2055 | 7 | 4 | 0 | 0 | 0 | 3 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0004c0006 | 0/0 | 2055 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0005c0007 | 0/0 | 2055 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0006c0015 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0007c0012 | 0/0 | 2050 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0008c0011 | 0/0 | 2055 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0009c0010 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0010c0008 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0011c0013 | 0/0 | 2055 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0012c0016 | 0/0 | 2055 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3302 | 170 | 29 | 39 | 78 | 9 | 14 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0001c0001t0002 | 0/0 | 3302 | 58 | 11 | 5 | 33 | 0 | 9 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0001c0001t0003 | 0/0 | 3302 | 9 | 8 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0001c0001t0004 | 1/0 | 3301 | 12 | 5 | 1 | 1 | 0 | 4 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0001c0001t0005 | 0/0 | 3302 | 4 | 0 | 2 | 0 | 2 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0001c0001t0006 | 0/0 | 3302 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0001c0001t0007 | 0/0 | 3302 | 2 | 0 | 1 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0001c0001t0008 | 0/0 | 3302 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0001c0001t0009 | 0/0 | 3302 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0001c0004t0003 | 0/0 | 3302 | 5 | 5 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0001c0005t0002 | 0/0 | 3302 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0001c0005t0003 | 0/0 | 3302 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0001c0009t0001 | 0/0 | 3302 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0001c0014t0002 | 0/0 | 3302 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0002c0002t0001 | 0/0 | 3302 | 9 | 8 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0003c0003t0001 | 0/0 | 3302 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0003c0003t0003 | 0/0 | 3302 | 5 | 2 | 0 | 0 | 0 | 3 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0004c0006t0001 | 0/0 | 3302 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0004c0006t0002 | 0/0 | 3302 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0005c0007t0001 | 0/0 | 3302 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0006c0015t0001 | 0/0 | 3302 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0007c0012t0004 | 0/0 | 3296 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0008c0011t0010 | 0/0 | 3302 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0009c0010t0001 | 0/0 | 3302 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0010c0008t0003 | 0/0 | 3302 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0011c0013t0001 | 0/0 | 3302 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| a0012c0016t0001 | 0/0 | 3302 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | copy fasta | chr12 | 122769572 | 122832528 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0166 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0004g0208 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0004g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0005g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0006g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0007g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0007g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0008g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0001t0009g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0004t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0004t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0004t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0004t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0004t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0005t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0005t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0005t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0005t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0009t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0001c0014t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0002c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0002c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0002c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0002c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0002c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0002c0002t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0002c0002t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0003c0003t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0003c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0003c0003t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0003c0003t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0003c0003t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0003c0003t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0003c0003t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0004c0006t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0004c0006t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0004c0006t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0005c0007t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0005c0007t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0006c0015t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0007c0012t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0008c0011t0010g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0009c0010t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0010c0008t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0011c0013t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| a0012c0016t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | FIN | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00280 | hp2 | a0010 | c0008 | t0003 | g0220 | EUR | FIN | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CHS | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | CHS | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | CHS | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0210 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01074 | hp1 | a0001 | c0001 | t0005 | g0043 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0180 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01109 | hp1 | a0001 | c0014 | t0002 | g0196 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01168 | hp1 | a0001 | c0001 | t0007 | g0117 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0294 | AMR | PUR | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | CLM | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01515 | hp1 | a0001 | c0001 | t0005 | g0112 | EUR | IBS | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0235 | EUR | IBS | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | IBS | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0111 | EUR | IBS | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01884 | hp1 | a0001 | c0005 | t0002 | g0283 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01934 | hp1 | a0001 | c0001 | t0005 | g0110 | AMR | PEL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | KHV | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0193 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | KHV | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | KHV | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | KHV | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02132 | hp2 | a0001 | c0001 | t0004 | g0050 | EAS | KHV | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02145 | hp1 | a0004 | c0006 | t0001 | g0014 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CDX | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CDX | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0290 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02280 | hp2 | a0001 | c0004 | t0003 | g0023 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02451 | hp1 | a0004 | c0006 | t0002 | g0141 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02451 | hp2 | a0001 | c0004 | t0003 | g0201 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02572 | hp1 | a0001 | c0005 | t0003 | g0280 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0203 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02602 | hp1 | a0003 | c0003 | t0003 | g0216 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0292 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0278 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0205 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0272 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0248 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02683 | hp2 | a0001 | c0001 | t0007 | g0086 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02717 | hp1 | a0001 | c0004 | t0003 | g0268 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02717 | hp2 | a0003 | c0003 | t0001 | g0184 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02735 | hp1 | a0006 | c0015 | t0001 | g0215 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0259 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02809 | hp1 | a0003 | c0003 | t0001 | g0195 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0194 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0221 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0206 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0295 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0213 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0296 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | ESN | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | ESN | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0279 | AFR | ESN | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | ESN | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0285 | AFR | ESN | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02976 | hp2 | a0003 | c0003 | t0003 | g0186 | AFR | ESN | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0207 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03041 | hp2 | a0001 | c0004 | t0003 | g0022 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | MSL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03098 | hp2 | a0004 | c0006 | t0001 | g0148 | AFR | MSL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03195 | hp1 | a0005 | c0007 | t0001 | g0271 | AFR | ESN | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03209 | hp1 | a0001 | c0005 | t0002 | g0282 | AFR | MSL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03225 | hp2 | a0001 | c0005 | t0002 | g0281 | AFR | MSL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03239 | hp1 | a0011 | c0013 | t0001 | g0168 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03453 | hp1 | a0003 | c0003 | t0003 | g0187 | AFR | MSL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | MSL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | MSL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0223 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03490 | hp2 | a0001 | c0001 | t0008 | g0068 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0066 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0284 | AFR | ESN | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0214 | AFR | ESN | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0265 | AFR | GWD | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03669 | hp1 | a0001 | c0009 | t0001 | g0183 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03669 | hp2 | a0003 | c0003 | t0003 | g0219 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0224 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | BEB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0260 | SAS | BEB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0229 | SAS | BEB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | STU | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0026 | SAS | STU | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0246 | SAS | STU | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0218 | SAS | STU | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | CHB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18906 | hp1 | a0001 | c0004 | t0003 | g0021 | AFR | YRI | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | YRI | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18965 | hp1 | a0001 | c0001 | t0009 | g0036 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18972 | hp1 | a0007 | c0012 | t0004 | g0020 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18977 | hp1 | a0012 | c0016 | t0001 | g0237 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19030 | hp2 | a0005 | c0007 | t0001 | g0270 | AFR | LWK | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0289 | AFR | LWK | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | LWK | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19054 | hp1 | a0009 | c0010 | t0001 | g0033 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0274 | AFR | YRI | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0291 | AFR | YRI | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ASW | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ASW | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | TSI | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | TSI | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0250 | SAS | GIH | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| NA20905 | hp2 | a0003 | c0003 | t0003 | g0209 | SAS | GIH | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0293 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02559 | hp1 | a0008 | c0011 | t0010 | g0199 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | ACB | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | MSL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0166 | REF | REF | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0208 | REF | REF | CCDC62_chr12_122769572_122832528 | CCDC62 | chr12 | 122769572 | 122832528 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:122777533
|
C | T | 1 | a0004 | 3 | HG02145.hp1 HG02451.hp1 HG03098.hp2 |
missense_variant | MODERATE | c.79C>T | p.Arg27Trp | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/13 | 178/3301 | 79/2055 | 27/684 | chr12 | 122777533 | ||
| chr12:122777642
|
A | G | 1 | a0012 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.188A>G | p.Gln63Arg | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/13 | 287/3301 | 188/2055 | 63/684 | chr12 | 122777642 | ||
| chr12:122781203
|
C | T | 1 | a0006 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.269C>T | p.Thr90Met | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/13 | 368/3301 | 269/2055 | 90/684 | chr12 | 122781203 | ||
| chr12:122785744
|
C | T | 1 | a0002 | 9 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(6): Show |
missense_variant | MODERATE | c.422C>T | p.Thr141Met | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/13 | 521/3301 | 422/2055 | 141/684 | chr12 | 122785744 | ||
| chr12:122788906
|
A | G | 1 | a0011 | 1 | HG03239.hp1 | missense_variant | MODERATE | c.647A>G | p.Lys216Arg | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/13 | 746/3301 | 647/2055 | 216/684 | chr12 | 122788906 | ||
| chr12:122798066
|
TTGTCAAT others(16): Show |
T | 1 | a0007 | 1 | NA18972.hp1 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.862-15_869delCAATA others(18): Show |
p.Ile288fs | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/13 | 862/2055 | 288/684 | INFO_REALIGN_3_PRIME | chr12 | 122798066 | ||
| chr12:122798161
|
A | T | 1 | a0008 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.938A>T | p.Tyr313Phe | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/13 | 1037/3301 | 938/2055 | 313/684 | chr12 | 122798161 | ||
| chr12:122801228
|
T | C | 1 | a0005 | 2 | HG03195.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.1082T>C | p.Met361Thr | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/13 | 1181/3301 | 1082/2055 | 361/684 | chr12 | 122801228 | ||
| chr12:122801300
|
C | T | 1 | a0009 | 1 | NA19054.hp1 | missense_variant | MODERATE | c.1154C>T | p.Thr385Ile | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/13 | 1253/3301 | 1154/2055 | 385/684 | chr12 | 122801300 | ||
| chr12:122801740
|
G | A | 1 | a0010 | 1 | HG00280.hp2 | missense_variant | MODERATE | c.1594G>A | p.Val532Met | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/13 | 1693/3301 | 1594/2055 | 532/684 | chr12 | 122801740 | ||
| chr12:122813355
|
C | T | 2 | a0003a0010 | 8 | HG00280.hp2 HG02602.hp1 HG02717.hp2 others(5): Show |
missense_variant | MODERATE | c.1937C>T | p.Thr646Met | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/13 | 2036/3301 | 1937/2055 | 646/684 | chr12 | 122813355 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:122781249
|
A | G | 1 | a0001c0014 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.315A>G | p.Thr105Thr | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/13 | 414/3301 | 315/2055 | 105/684 | chr12 | 122781249 | ||
| chr12:122788925
|
A | G | 1 | a0001c0005 | 4 | HG01884.hp1 HG02572.hp1 HG03209.hp1 others(1): Show |
synonymous_variant | LOW | c.666A>G | p.Leu222Leu | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/13 | 765/3301 | 666/2055 | 222/684 | chr12 | 122788925 | ||
| chr12:122801238
|
G | A | 1 | a0001c0004 | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
synonymous_variant | LOW | c.1092G>A | p.Gln364Gln | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/13 | 1191/3301 | 1092/2055 | 364/684 | chr12 | 122801238 | ||
| chr12:122813314
|
C | T | 1 | a0001c0009 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.1896C>T | p.Ser632Ser | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/13 | 1995/3301 | 1896/2055 | 632/684 | chr12 | 122813314 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:122774597
|
G | C | 1 | a0001c0001t0006 | 2 | HG02572.hp2 HG02622.hp2 |
5_prime_UTR_variant | MODIFIER | c.-74G>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/13 | 74 | chr12 | 122774597 | |||||
| chr12:122774616
|
G | T | 1 | a0001c0001t0007 | 2 | HG01168.hp1 HG02683.hp2 |
5_prime_UTR_variant | MODIFIER | c.-55G>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/13 | 55 | chr12 | 122774616 | |||||
| chr12:122826696
|
G | A | 1 | a0001c0001t0005 | 4 | HG01074.hp1 HG01515.hp1 HG01517.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*315G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 13/13 | 3277 | chr12 | 122826696 | |||||
| chr12:122826755
|
A | AC | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*377dupC | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 13/13 | 3340 | INFO_REALIGN_3_PRIME | chr12 | 122826755 | ||||
| chr12:122826810
|
C | A | 2 | a0001c0001t0007a0001c0001t0008 | 3 | HG01168.hp1 HG02683.hp2 HG03490.hp2 |
3_prime_UTR_variant | MODIFIER | c.*429C>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 13/13 | 3391 | chr12 | 122826810 | |||||
| chr12:122826915
|
G | T | 1 | a0008c0011t0010 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*534G>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 13/13 | 3496 | chr12 | 122826915 | |||||
| chr12:122826966
|
T | A | 1 | a0001c0001t0009 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*585T>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 13/13 | 3547 | chr12 | 122826966 | |||||
| chr12:122827306
|
A | G | 14 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(11): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*925A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 13/13 | 3887 | chr12 | 122827306 | |||||
| chr12:122827434
|
C | T | 5 | a0001c0001t0002a0001c0005t0002a0001c0014t0002others(2): Show | 64 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1053C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 13/13 | 4015 | chr12 | 122827434 | |||||
| chr12:122827504
|
C | T | 14 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(11): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*1123C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 13/13 | 4085 | chr12 | 122827504 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:122775062
|
C | T | 2 | a0001c0001t0001g0297a0001c0001t0001g0298 | 2 | HG00438.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.36+356C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122775062 | ||||||
| chr12:122775093
|
C | CA | 182 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(179): Show | 182 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.36+410dupA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 122775093 | |||||
| chr12:122775093
|
C | CAA | 19 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(16): Show | 19 | HG00140.hp1 HG00621.hp2 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.36+409_36+410dupAA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 122775093 | |||||
| chr12:122775093
|
CAAAAA | C | 10 | a0001c0001t0001g0287a0001c0001t0001g0288a0002c0002t0001g0289others(7): Show | 10 | HG01243.hp2 HG02055.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.36+406_36+410delAA others(3): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 122775093 | |||||
| chr12:122775131
|
T | G | 1 | a0001c0001t0003g0200 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.36+425T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122775131 | ||||||
| chr12:122775172
|
C | T | 1 | a0008c0011t0010g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.36+466C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122775172 | ||||||
| chr12:122775173
|
A | T | 1 | a0001c0001t0001g0286 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.36+467A>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122775173 | ||||||
| chr12:122775192
|
G | A | 1 | a0001c0004t0003g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.36+486G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122775192 | ||||||
| chr12:122775375
|
C | A | 1 | a0001c0001t0002g0202 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.36+669C>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122775375 | ||||||
| chr12:122775405
|
C | T | 2 | a0001c0001t0001g0197a0001c0001t0001g0198 | 2 | NA19066.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.36+699C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122775405 | ||||||
| chr12:122775673
|
C | G | 1 | a0001c0001t0002g0202 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.36+967C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122775673 | ||||||
| chr12:122775674
|
G | T | 26 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0277others(23): Show | 26 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.36+968G>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122775674 | ||||||
| chr12:122775738
|
A | G | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(270): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.36+1032A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122775738 | ||||||
| chr12:122775802
|
A | G | 2 | a0001c0001t0002g0275a0001c0001t0002g0276 | 2 | NA18980.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.36+1096A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122775802 | ||||||
| chr12:122776028
|
CT | C | 26 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0277others(23): Show | 26 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.36+1326delT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 122776028 | |||||
| chr12:122776155
|
G | A | 1 | a0001c0001t0001g0277 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.37-1336G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122776155 | ||||||
| chr12:122776205
|
A | G | 1 | a0001c0009t0001g0183 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.37-1286A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122776205 | ||||||
| chr12:122776438
|
A | G | 1 | a0001c0001t0002g0202 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.37-1053A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122776438 | ||||||
| chr12:122776554
|
G | A | 1 | a0001c0001t0002g0225 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.37-937G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122776554 | ||||||
| chr12:122776806
|
G | GT | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(184): Show | 187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.37-677dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr12 | 122776806 | |||||
| chr12:122776923
|
G | A | 3 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023 | 3 | HG02280.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.37-568G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122776923 | ||||||
| chr12:122776940
|
C | T | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.37-551C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122776940 | ||||||
| chr12:122776988
|
G | C | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.37-503G>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122776988 | ||||||
| chr12:122777044
|
C | A | 1 | a0009c0010t0001g0033 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.37-447C>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122777044 | ||||||
| chr12:122777113
|
T | G | 2 | a0001c0001t0002g0226a0001c0001t0002g0227 | 2 | HG00609.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.37-378T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122777113 | ||||||
| chr12:122777254
|
C | T | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.37-237C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122777254 | ||||||
| chr12:122777287
|
A | C | 1 | a0001c0001t0003g0224 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.37-204A>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122777287 | ||||||
| chr12:122777362
|
G | A | 2 | a0001c0001t0006g0001a0001c0001t0006g0203 | 2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.37-129G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122777362 | ||||||
| chr12:122777415
|
T | C | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.37-76T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 1/12 | chr12 | 122777415 | ||||||
| chr12:122777757
|
A | G | 3 | a0002c0002t0001g0294a0002c0002t0001g0295a0002c0002t0001g0296 | 3 | HG01243.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.229+74A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122777757 | ||||||
| chr12:122778204
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.229+521G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122778204 | ||||||
| chr12:122778269
|
G | A | 4 | a0001c0005t0002g0281a0001c0005t0002g0282a0001c0005t0002g0283others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.229+586G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122778269 | ||||||
| chr12:122778353
|
CA | C | 74 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(71): Show | 74 | HG00280.hp1 HG00621.hp2 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.229+688delA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 122778353 | |||||
| chr12:122778353
|
CAA | C | 80 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(77): Show | 80 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.229+687_229+688del others(2): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 122778353 | |||||
| chr12:122778400
|
A | G | 3 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023 | 3 | HG02280.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.229+717A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122778400 | ||||||
| chr12:122778563
|
T | G | 4 | a0001c0001t0001g0204a0001c0001t0001g0286a0001c0001t0004g0205others(1): Show | 4 | HG02630.hp1 HG02895.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.229+880T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122778563 | ||||||
| chr12:122778633
|
A | C | 1 | a0002c0002t0001g0293 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.229+950A>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122778633 | ||||||
| chr12:122778782
|
G | A | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.229+1099G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122778782 | ||||||
| chr12:122778874
|
G | A | 1 | a0001c0001t0001g0002 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.229+1191G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122778874 | ||||||
| chr12:122778889
|
GAAAC | G | 81 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(78): Show | 81 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.229+1214_229+1217d others(6): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 122778889 | |||||
| chr12:122778969
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.229+1286C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122778969 | ||||||
| chr12:122779259
|
G | A | 1 | a0001c0001t0004g0207 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.229+1576G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122779259 | ||||||
| chr12:122779483
|
A | AC | 26 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0277others(23): Show | 26 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.230-1680dupC | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 122779483 | |||||
| chr12:122779485
|
A | C | 26 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0277others(23): Show | 26 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.230-1679A>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122779485 | ||||||
| chr12:122779486
|
A | T | 26 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0277others(23): Show | 26 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.230-1678A>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122779486 | ||||||
| chr12:122779488
|
A | G | 26 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0277others(23): Show | 26 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.230-1676A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122779488 | ||||||
| chr12:122779634
|
G | A | 1 | a0001c0004t0003g0268 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.230-1530G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122779634 | ||||||
| chr12:122779898
|
ACT | A | 3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0003g0285 | 3 | HG02615.hp2 HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.230-1263_230-1262d others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 122779898 | |||||
| chr12:122779907
|
CA | C | 203 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(200): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.230-1232delA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 122779907 | |||||
| chr12:122779907
|
CAA | C | 70 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(67): Show | 70 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.230-1233_230-1232d others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 122779907 | |||||
| chr12:122779907
|
CAAA | C | 9 | a0001c0001t0001g0034a0001c0001t0001g0267a0001c0001t0002g0266others(6): Show | 9 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.230-1234_230-1232d others(5): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 122779907 | |||||
| chr12:122780135
|
C | T | 1 | a0002c0002t0001g0294 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.230-1029C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122780135 | ||||||
| chr12:122780162
|
A | T | 87 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(84): Show | 87 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.230-1002A>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122780162 | ||||||
| chr12:122780188
|
G | A | 2 | a0001c0004t0003g0201a0001c0004t0003g0268 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.230-976G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122780188 | ||||||
| chr12:122780259
|
C | T | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-905C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122780259 | ||||||
| chr12:122780266
|
G | C | 1 | a0001c0001t0001g0037 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.230-898G>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122780266 | ||||||
| chr12:122780379
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.230-785C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122780379 | ||||||
| chr12:122780429
|
C | T | 1 | a0001c0001t0002g0128 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.230-735C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122780429 | ||||||
| chr12:122780466
|
T | G | 1 | a0001c0001t0001g0038 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.230-698T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122780466 | ||||||
| chr12:122780531
|
G | A | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.230-633G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122780531 | ||||||
| chr12:122780536
|
C | A | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-628C>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122780536 | ||||||
| chr12:122780550
|
C | G | 5 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0127others(2): Show | 5 | HG01978.hp2 HG01981.hp2 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.230-614C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122780550 | ||||||
| chr12:122780563
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.230-601G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122780563 | ||||||
| chr12:122780583
|
C | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.230-581C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122780583 | ||||||
| chr12:122780614
|
A | AAAAAT | 46 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0118others(43): Show | 46 | HG00280.hp2 HG00621.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.230-495_230-491dup others(5): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 122780614 | |||||
| chr12:122780614
|
A | AAAAATAA others(3): Show |
4 | a0001c0001t0001g0286a0001c0001t0002g0180a0001c0001t0002g0222others(1): Show | 4 | HG01099.hp2 HG02895.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.230-500_230-491dup others(10): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 122780614 | |||||
| chr12:122780614
|
A | AAAAATAA others(8): Show |
1 | a0001c0001t0001g0003 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.230-505_230-491dup others(15): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 122780614 | |||||
| chr12:122780614
|
AAAAAT | A | 80 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0034others(77): Show | 80 | HG00438.hp1 HG00609.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.230-495_230-491del others(5): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 122780614 | |||||
| chr12:122780614
|
AAAAATAA others(3): Show |
A | 15 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0132others(12): Show | 15 | HG00735.hp1 HG01074.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.230-500_230-491del others(10): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 122780614 | |||||
| chr12:122780614
|
AAAAATAA others(8): Show |
A | 9 | a0001c0001t0001g0004a0001c0001t0001g0039a0001c0001t0001g0040others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.230-505_230-491del others(15): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 122780614 | |||||
| chr12:122780614
|
AAAAATAA others(18): Show |
A | 2 | a0001c0004t0003g0201a0001c0004t0003g0268 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.230-515_230-491del others(25): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr12 | 122780614 | |||||
| chr12:122780730
|
G | A | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.230-434G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122780730 | ||||||
| chr12:122780863
|
C | T | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(272): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.230-301C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122780863 | ||||||
| chr12:122780956
|
C | T | 1 | a0001c0001t0004g0214 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.230-208C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122780956 | ||||||
| chr12:122781060
|
T | C | 1 | a0001c0001t0002g0180 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.230-104T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122781060 | ||||||
| chr12:122781141
|
A | G | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.230-23A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 2/12 | chr12 | 122781141 | ||||||
| chr12:122781399
|
G | A | 4 | a0001c0005t0002g0281a0001c0005t0002g0282a0001c0005t0002g0283others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.396+69G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122781399 | ||||||
| chr12:122781405
|
A | G | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(270): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.396+75A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122781405 | ||||||
| chr12:122781502
|
G | A | 1 | a0008c0011t0010g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.396+172G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122781502 | ||||||
| chr12:122781541
|
C | T | 13 | a0001c0001t0001g0164a0001c0001t0001g0169a0001c0001t0001g0171others(10): Show | 13 | HG01099.hp2 HG01891.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.396+211C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122781541 | ||||||
| chr12:122781641
|
C | T | 2 | a0001c0001t0002g0226a0001c0001t0002g0227 | 2 | HG00609.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.396+311C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122781641 | ||||||
| chr12:122781685
|
CA | C | 88 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(85): Show | 88 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.396+366delA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 122781685 | |||||
| chr12:122781780
|
T | C | 1 | a0001c0001t0002g0128 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.396+450T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122781780 | ||||||
| chr12:122781788
|
CTTTG | C | 82 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(79): Show | 82 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.396+463_396+466del others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 122781788 | |||||
| chr12:122781836
|
A | G | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.396+506A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122781836 | ||||||
| chr12:122782025
|
C | CA | 89 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0031others(86): Show | 89 | HG00423.hp1 HG00609.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.396+713dupA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 122782025 | |||||
| chr12:122782025
|
C | CAA | 9 | a0001c0001t0001g0277a0001c0001t0002g0024a0001c0001t0002g0236others(6): Show | 9 | HG00438.hp1 HG01109.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.396+712_396+713dup others(2): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 122782025 | |||||
| chr12:122782045
|
C | T | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG00639.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.396+715C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122782045 | ||||||
| chr12:122782107
|
G | A | 1 | a0001c0001t0004g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.396+777G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122782107 | ||||||
| chr12:122782172
|
A | C | 1 | a0001c0001t0001g0116 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.396+842A>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122782172 | ||||||
| chr12:122782212
|
C | T | 1 | a0002c0002t0001g0292 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.396+882C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122782212 | ||||||
| chr12:122782388
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.396+1058T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122782388 | ||||||
| chr12:122782461
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.396+1131T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122782461 | ||||||
| chr12:122782473
|
T | C | 26 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0277others(23): Show | 26 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.396+1143T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122782473 | ||||||
| chr12:122782576
|
A | G | 4 | a0001c0005t0002g0281a0001c0005t0002g0282a0001c0005t0002g0283others(1): Show | 4 | HG01884.hp1 HG02572.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.396+1246A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122782576 | ||||||
| chr12:122782590
|
C | T | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.396+1260C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122782590 | ||||||
| chr12:122782843
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.396+1513C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122782843 | ||||||
| chr12:122782874
|
G | A | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.396+1544G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122782874 | ||||||
| chr12:122782879
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.396+1549G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122782879 | ||||||
| chr12:122783100
|
C | T | 1 | a0001c0001t0004g0223 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.396+1770C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122783100 | ||||||
| chr12:122783121
|
A | AT | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.396+1798dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr12 | 122783121 | |||||
| chr12:122783122
|
T | G | 1 | a0001c0001t0002g0239 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.396+1792T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122783122 | ||||||
| chr12:122783251
|
G | A | 2 | a0001c0001t0006g0001a0001c0001t0006g0203 | 2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.396+1921G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122783251 | ||||||
| chr12:122783299
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.396+1969C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122783299 | ||||||
| chr12:122783309
|
G | A | 10 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0002g0018others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.396+1979G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122783309 | ||||||
| chr12:122783319
|
C | A | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.396+1989C>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122783319 | ||||||
| chr12:122783377
|
G | A | 1 | a0001c0001t0009g0036 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.396+2047G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122783377 | ||||||
| chr12:122783453
|
C | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.396+2123C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122783453 | ||||||
| chr12:122783516
|
G | A | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.396+2186G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122783516 | ||||||
| chr12:122783559
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.397-2160C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122783559 | ||||||
| chr12:122783594
|
G | A | 1 | a0008c0011t0010g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.397-2125G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122783594 | ||||||
| chr12:122783613
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.397-2106G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122783613 | ||||||
| chr12:122783634
|
C | T | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.397-2085C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122783634 | ||||||
| chr12:122783801
|
A | C | 4 | a0001c0001t0005g0043a0001c0001t0005g0110a0001c0001t0005g0111others(1): Show | 4 | HG01074.hp1 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.397-1918A>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122783801 | ||||||
| chr12:122783992
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.397-1727A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122783992 | ||||||
| chr12:122784095
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.397-1624C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122784095 | ||||||
| chr12:122784096
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.397-1623G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122784096 | ||||||
| chr12:122784179
|
T | C | 1 | a0001c0001t0004g0206 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.397-1540T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122784179 | ||||||
| chr12:122784186
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.397-1533A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122784186 | ||||||
| chr12:122784187
|
C | T | 87 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(84): Show | 87 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.397-1532C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122784187 | ||||||
| chr12:122784230
|
A | T | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(270): Show | 273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.397-1489A>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122784230 | ||||||
| chr12:122784293
|
C | T | 13 | a0001c0001t0001g0164a0001c0001t0001g0169a0001c0001t0001g0171others(10): Show | 13 | HG01099.hp2 HG01891.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.397-1426C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122784293 | ||||||
| chr12:122784294
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG03017.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.397-1425G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122784294 | ||||||
| chr12:122784337
|
A | G | 87 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(84): Show | 87 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.397-1382A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122784337 | ||||||
| chr12:122784860
|
G | C | 11 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0002g0018others(8): Show | 11 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.397-859G>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122784860 | ||||||
| chr12:122784876
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG00140.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.397-843C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122784876 | ||||||
| chr12:122784894
|
T | C | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.397-825T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122784894 | ||||||
| chr12:122784936
|
C | T | 1 | a0001c0001t0004g0066 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.397-783C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122784936 | ||||||
| chr12:122784954
|
C | T | 1 | a0011c0013t0001g0168 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.397-765C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122784954 | ||||||
| chr12:122785044
|
C | T | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.397-675C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122785044 | ||||||
| chr12:122785107
|
A | C | 1 | a0001c0001t0001g0105 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.397-612A>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122785107 | ||||||
| chr12:122785121
|
G | A | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.397-598G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122785121 | ||||||
| chr12:122785211
|
G | A | 26 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0277others(23): Show | 26 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.397-508G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122785211 | ||||||
| chr12:122785212
|
A | G | 5 | a0002c0002t0001g0272a0002c0002t0001g0289a0002c0002t0001g0290others(2): Show | 5 | HG02257.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.397-507A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122785212 | ||||||
| chr12:122785267
|
A | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.397-452A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122785267 | ||||||
| chr12:122785330
|
A | G | 9 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0002g0018others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.397-389A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122785330 | ||||||
| chr12:122785477
|
G | A | 1 | a0001c0001t0008g0068 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.397-242G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122785477 | ||||||
| chr12:122785588
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.397-131A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 3/12 | chr12 | 122785588 | ||||||
| chr12:122785897
|
G | A | 1 | a0001c0001t0002g0240 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.498+77G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122785897 | ||||||
| chr12:122786109
|
C | T | 7 | a0001c0001t0006g0001a0001c0001t0006g0203a0001c0004t0003g0021others(4): Show | 7 | HG02280.hp2 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.498+289C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786109 | ||||||
| chr12:122786142
|
G | GT | 6 | a0001c0001t0001g0159a0001c0004t0003g0021a0001c0004t0003g0022others(3): Show | 6 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.498+330dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 122786142 | |||||
| chr12:122786170
|
C | T | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.498+350C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786170 | ||||||
| chr12:122786179
|
GCT | G | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.498+362_498+363del others(2): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 122786179 | |||||
| chr12:122786186
|
G | C | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.498+366G>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786186 | ||||||
| chr12:122786187
|
G | A | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.498+367G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786187 | ||||||
| chr12:122786209
|
T | G | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.498+389T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786209 | ||||||
| chr12:122786211
|
C | G | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.498+391C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786211 | ||||||
| chr12:122786212
|
G | A | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.498+392G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786212 | ||||||
| chr12:122786214
|
C | T | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.498+394C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786214 | ||||||
| chr12:122786217
|
A | G | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.498+397A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786217 | ||||||
| chr12:122786222
|
G | A | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.498+402G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786222 | ||||||
| chr12:122786251
|
C | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.498+431C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786251 | ||||||
| chr12:122786306
|
C | T | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.498+486C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786306 | ||||||
| chr12:122786308
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.498+488C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786308 | ||||||
| chr12:122786314
|
A | AT | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.498+501dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 122786314 | |||||
| chr12:122786394
|
C | G | 1 | a0001c0001t0001g0104 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.498+574C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786394 | ||||||
| chr12:122786417
|
G | A | 4 | a0003c0003t0001g0184a0003c0003t0001g0195a0003c0003t0003g0186others(1): Show | 4 | HG02717.hp2 HG02809.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.498+597G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786417 | ||||||
| chr12:122786447
|
C | CG | 82 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(79): Show | 82 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.498+627_498+628ins others(1): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786447 | ||||||
| chr12:122786745
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.498+925G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786745 | ||||||
| chr12:122786833
|
G | T | 26 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0277others(23): Show | 26 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.498+1013G>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786833 | ||||||
| chr12:122786944
|
C | T | 1 | a0002c0002t0001g0291 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.498+1124C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122786944 | ||||||
| chr12:122787176
|
C | T | 2 | a0001c0001t0002g0238a0001c0001t0002g0262 | 2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.498+1356C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122787176 | ||||||
| chr12:122787198
|
A | C | 2 | a0001c0001t0006g0001a0001c0001t0006g0203 | 2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.498+1378A>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122787198 | ||||||
| chr12:122787207
|
G | T | 1 | a0001c0001t0001g0011 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.498+1387G>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122787207 | ||||||
| chr12:122787228
|
G | A | 11 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0105others(8): Show | 11 | HG00408.hp2 HG00438.hp2 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.498+1408G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122787228 | ||||||
| chr12:122787375
|
C | T | 1 | a0001c0001t0003g0200 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.499-1383C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122787375 | ||||||
| chr12:122787450
|
C | CA | 8 | a0001c0001t0001g0217a0001c0001t0002g0222a0001c0001t0004g0218others(5): Show | 8 | HG00280.hp2 HG02602.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.499-1292dupA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 122787450 | |||||
| chr12:122787450
|
CA | C | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(269): Show | 272 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.499-1292delA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 122787450 | |||||
| chr12:122787476
|
T | G | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(272): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.499-1282T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122787476 | ||||||
| chr12:122787566
|
A | G | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.499-1192A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122787566 | ||||||
| chr12:122787750
|
G | GA | 7 | a0001c0001t0001g0015a0001c0001t0001g0123a0001c0001t0001g0124others(4): Show | 7 | HG00639.hp1 HG00735.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.499-994dupA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr12 | 122787750 | |||||
| chr12:122787940
|
T | C | 1 | a0001c0001t0001g0004 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.499-818T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122787940 | ||||||
| chr12:122788659
|
G | A | 89 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(86): Show | 89 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.499-99G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 4/12 | chr12 | 122788659 | ||||||
| chr12:122789026
|
A | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0122 | 2 | HG00639.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.670+97A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122789026 | ||||||
| chr12:122789189
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.670+260C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122789189 | ||||||
| chr12:122789278
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.670+349G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122789278 | ||||||
| chr12:122789283
|
A | T | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.670+354A>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122789283 | ||||||
| chr12:122789361
|
C | T | 2 | a0001c0001t0005g0111a0001c0001t0005g0112 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.670+432C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122789361 | ||||||
| chr12:122789380
|
C | T | 9 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0002g0018others(6): Show | 9 | HG02055.hp1 HG02109.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.670+451C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122789380 | ||||||
| chr12:122789452
|
C | T | 2 | a0001c0001t0006g0001a0001c0001t0006g0203 | 2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.670+523C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122789452 | ||||||
| chr12:122789612
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.670+683T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122789612 | ||||||
| chr12:122789854
|
G | A | 3 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023 | 3 | HG02280.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.670+925G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122789854 | ||||||
| chr12:122789930
|
GCTACA | G | 9 | a0002c0002t0001g0272a0002c0002t0001g0289a0002c0002t0001g0290others(6): Show | 9 | HG01243.hp2 HG02257.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.670+1004_670+1008d others(7): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 122789930 | |||||
| chr12:122789933
|
A | G | 2 | a0001c0001t0001g0102a0001c0001t0001g0103 | 2 | HG01175.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.670+1004A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122789933 | ||||||
| chr12:122789936
|
C | T | 1 | a0001c0001t0006g0203 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.670+1007C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122789936 | ||||||
| chr12:122790097
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.670+1168C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122790097 | ||||||
| chr12:122790355
|
C | CT | 274 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(271): Show | 274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.670+1435dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 122790355 | |||||
| chr12:122790483
|
T | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.671-1537T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122790483 | ||||||
| chr12:122790582
|
A | G | 1 | a0001c0001t0001g0273 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.671-1438A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122790582 | ||||||
| chr12:122790675
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.671-1345A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122790675 | ||||||
| chr12:122790922
|
TTC | T | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.671-1095_671-1094d others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr12 | 122790922 | |||||
| chr12:122791008
|
C | T | 7 | a0001c0001t0006g0001a0001c0001t0006g0203a0001c0004t0003g0021others(4): Show | 7 | HG02280.hp2 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.671-1012C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122791008 | ||||||
| chr12:122791009
|
G | A | 11 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0002g0018others(8): Show | 11 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.671-1011G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122791009 | ||||||
| chr12:122791062
|
G | A | 89 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(86): Show | 89 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.671-958G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122791062 | ||||||
| chr12:122791204
|
G | A | 7 | a0001c0001t0006g0001a0001c0001t0006g0203a0001c0004t0003g0021others(4): Show | 7 | HG02280.hp2 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.671-816G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122791204 | ||||||
| chr12:122791224
|
C | T | 89 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(86): Show | 89 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.671-796C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122791224 | ||||||
| chr12:122791226
|
C | T | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.671-794C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122791226 | ||||||
| chr12:122791322
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.671-698A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122791322 | ||||||
| chr12:122791358
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.671-662C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122791358 | ||||||
| chr12:122791405
|
T | C | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.671-615T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122791405 | ||||||
| chr12:122791695
|
C | T | 3 | a0001c0005t0002g0281a0001c0005t0002g0282a0001c0005t0002g0283 | 3 | HG01884.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.671-325C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122791695 | ||||||
| chr12:122791731
|
G | A | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.671-289G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122791731 | ||||||
| chr12:122791810
|
G | C | 1 | a0001c0001t0001g0073 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.671-210G>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122791810 | ||||||
| chr12:122791841
|
G | A | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.671-179G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 5/12 | chr12 | 122791841 | ||||||
| chr12:122792141
|
G | A | 1 | a0003c0003t0003g0209 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.772+20G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122792141 | ||||||
| chr12:122792202
|
G | GT | 85 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0010others(82): Show | 85 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.772+100dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 122792202 | |||||
| chr12:122792202
|
G | GTT | 13 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0070others(10): Show | 13 | HG01891.hp1 HG01891.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.772+99_772+100dupT others(1): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 122792202 | |||||
| chr12:122792202
|
GT | G | 7 | a0001c0001t0001g0067a0001c0001t0007g0117a0001c0005t0002g0281others(4): Show | 7 | HG01168.hp1 HG01168.hp2 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.772+100delT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 122792202 | |||||
| chr12:122792202
|
GTT | G | 22 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0277others(19): Show | 22 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.772+99_772+100delT others(1): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 122792202 | |||||
| chr12:122792215
|
TTTTTTTG others(10): Show |
T | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0011others(4): Show | 7 | HG00642.hp1 HG02293.hp1 NA18957.hp1 others(4): Show |
intron_variant | MODIFIER | c.772+114_772+130del others(17): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 122792215 | |||||
| chr12:122792216
|
TTTTTTGA others(9): Show |
T | 1 | a0001c0001t0001g0129 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.772+101_772+116del others(16): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 122792216 | |||||
| chr12:122792377
|
C | T | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.772+256C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122792377 | ||||||
| chr12:122792378
|
G | A | 26 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0277others(23): Show | 26 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.772+257G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122792378 | ||||||
| chr12:122792432
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.772+311G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122792432 | ||||||
| chr12:122792584
|
T | G | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.772+463T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122792584 | ||||||
| chr12:122792623
|
G | A | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(272): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.772+502G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122792623 | ||||||
| chr12:122792666
|
A | G | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(272): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.772+545A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122792666 | ||||||
| chr12:122792670
|
T | C | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.772+549T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122792670 | ||||||
| chr12:122792739
|
G | A | 1 | a0006c0015t0001g0215 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.772+618G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122792739 | ||||||
| chr12:122792755
|
T | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0053others(4): Show | 7 | HG02293.hp1 NA18957.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.772+634T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122792755 | ||||||
| chr12:122792800
|
G | A | 26 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0277others(23): Show | 26 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.772+679G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122792800 | ||||||
| chr12:122792986
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.772+865C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122792986 | ||||||
| chr12:122793150
|
G | T | 3 | a0001c0001t0001g0137a0001c0001t0001g0166a0001c0001t0001g0181 | 3 | HG00741.hp2 HG01074.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.772+1029G>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122793150 | ||||||
| chr12:122793194
|
C | T | 57 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(54): Show | 57 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.772+1073C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122793194 | ||||||
| chr12:122793418
|
A | C | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.772+1297A>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122793418 | ||||||
| chr12:122793451
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.772+1330A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122793451 | ||||||
| chr12:122793539
|
G | GA | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(291): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.772+1424dupA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 122793539 | |||||
| chr12:122793592
|
C | T | 26 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0277others(23): Show | 26 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.772+1471C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122793592 | ||||||
| chr12:122793777
|
A | C | 1 | a0002c0002t0001g0293 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.772+1656A>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122793777 | ||||||
| chr12:122793913
|
A | T | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.772+1792A>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122793913 | ||||||
| chr12:122794262
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.772+2141G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122794262 | ||||||
| chr12:122794298
|
G | A | 26 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0277others(23): Show | 26 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.772+2177G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122794298 | ||||||
| chr12:122794467
|
C | T | 26 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0001g0277others(23): Show | 26 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.772+2346C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122794467 | ||||||
| chr12:122794483
|
A | T | 10 | a0001c0001t0001g0185a0001c0001t0001g0188a0001c0001t0002g0018others(7): Show | 10 | HG01109.hp1 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.772+2362A>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122794483 | ||||||
| chr12:122794534
|
C | T | 1 | a0003c0003t0003g0187 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.772+2413C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122794534 | ||||||
| chr12:122794581
|
T | G | 1 | a0001c0001t0002g0242 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.772+2460T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122794581 | ||||||
| chr12:122794611
|
A | G | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(272): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.772+2490A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122794611 | ||||||
| chr12:122794680
|
A | G | 1 | a0001c0001t0002g0259 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.772+2559A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122794680 | ||||||
| chr12:122794783
|
A | C | 2 | a0001c0001t0001g0140a0001c0001t0003g0274 | 2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.773-2524A>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122794783 | ||||||
| chr12:122795005
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.773-2302T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795005 | ||||||
| chr12:122795017
|
G | A | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.773-2290G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795017 | ||||||
| chr12:122795041
|
C | T | 1 | a0001c0001t0001g0154 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.773-2266C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795041 | ||||||
| chr12:122795113
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.773-2194C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795113 | ||||||
| chr12:122795239
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.773-2068C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795239 | ||||||
| chr12:122795298
|
G | T | 2 | a0001c0001t0002g0178a0001c0001t0002g0180 | 2 | HG01099.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.773-2009G>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795298 | ||||||
| chr12:122795302
|
C | T | 2 | a0001c0001t0001g0065a0001c0001t0002g0258 | 2 | HG01952.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.773-2005C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795302 | ||||||
| chr12:122795315
|
T | C | 56 | a0001c0001t0001g0029a0001c0001t0001g0031a0001c0001t0001g0032others(53): Show | 56 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.773-1992T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795315 | ||||||
| chr12:122795486
|
T | C | 268 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(265): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.773-1821T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795486 | ||||||
| chr12:122795524
|
T | C | 5 | a0001c0001t0001g0003a0001c0001t0001g0047a0001c0001t0001g0051others(2): Show | 5 | HG02818.hp1 HG03831.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.773-1783T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795524 | ||||||
| chr12:122795578
|
C | T | 1 | a0001c0001t0003g0278 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.773-1729C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795578 | ||||||
| chr12:122795596
|
T | C | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.773-1711T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795596 | ||||||
| chr12:122795611
|
A | T | 1 | a0001c0001t0001g0097 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.773-1696A>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795611 | ||||||
| chr12:122795614
|
T | C | 9 | a0001c0001t0001g0061a0001c0001t0001g0097a0001c0001t0001g0109others(6): Show | 9 | HG00609.hp2 HG00639.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.773-1693T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795614 | ||||||
| chr12:122795645
|
T | C | 2 | a0001c0001t0001g0037a0001c0001t0002g0229 | 2 | HG02074.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.773-1662T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795645 | ||||||
| chr12:122795649
|
T | C | 268 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(265): Show | 268 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.773-1658T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795649 | ||||||
| chr12:122795703
|
C | T | 1 | a0001c0001t0003g0200 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.773-1604C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795703 | ||||||
| chr12:122795923
|
A | G | 9 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0178others(6): Show | 9 | HG01099.hp2 HG01884.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.773-1384A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795923 | ||||||
| chr12:122795969
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.773-1338T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122795969 | ||||||
| chr12:122796178
|
G | C | 11 | a0001c0001t0001g0204a0001c0001t0001g0277a0002c0002t0001g0272others(8): Show | 11 | HG01243.hp2 HG02257.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.773-1129G>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122796178 | ||||||
| chr12:122796206
|
G | A | 2 | a0001c0001t0001g0243a0012c0016t0001g0237 | 2 | NA18945.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.773-1101G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122796206 | ||||||
| chr12:122796316
|
AT | A | 51 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.773-983delT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 122796316 | |||||
| chr12:122796488
|
C | CTGTTAAC others(17): Show |
1 | a0007c0012t0004g0020 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.773-817_773-794dup others(24): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 122796488 | |||||
| chr12:122796505
|
A | G | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.773-802A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122796505 | ||||||
| chr12:122796579
|
C | T | 2 | a0003c0003t0003g0186a0003c0003t0003g0187 | 2 | HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.773-728C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122796579 | ||||||
| chr12:122796620
|
G | A | 51 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.773-687G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122796620 | ||||||
| chr12:122796628
|
C | T | 51 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.773-679C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122796628 | ||||||
| chr12:122796715
|
G | A | 51 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.773-592G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122796715 | ||||||
| chr12:122796824
|
A | G | 1 | a0001c0001t0002g0030 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.773-483A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122796824 | ||||||
| chr12:122796874
|
C | CT | 4 | a0001c0001t0002g0202a0001c0001t0002g0239a0001c0001t0002g0259others(1): Show | 4 | HG01069.hp2 HG01099.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.773-431dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 122796874 | |||||
| chr12:122796874
|
C | CTT | 43 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0231others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.773-432_773-431dup others(2): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 122796874 | |||||
| chr12:122796874
|
C | CTTT | 4 | a0001c0001t0001g0034a0001c0001t0002g0030a0001c0001t0002g0230others(1): Show | 4 | HG00642.hp2 NA18979.hp2 NA18987.hp1 others(1): Show |
intron_variant | MODIFIER | c.773-431_773-430ins others(3): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 122796874 | |||||
| chr12:122796874
|
CTTCTT | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(182): Show | 185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.773-430_773-426del others(5): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 122796874 | |||||
| chr12:122796877
|
C | T | 51 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.773-430C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122796877 | ||||||
| chr12:122796877
|
CT | C | 38 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(35): Show | 38 | HG00280.hp2 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.773-411delT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr12 | 122796877 | |||||
| chr12:122796965
|
C | T | 2 | a0001c0001t0006g0001a0001c0001t0006g0203 | 2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.773-342C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122796965 | ||||||
| chr12:122797097
|
C | T | 1 | a0001c0001t0004g0206 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.773-210C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122797097 | ||||||
| chr12:122797197
|
A | T | 51 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.773-110A>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 6/12 | chr12 | 122797197 | ||||||
| chr12:122797420
|
G | A | 257 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(254): Show | 257 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.861+25G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 7/12 | chr12 | 122797420 | ||||||
| chr12:122797564
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.861+169G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 7/12 | chr12 | 122797564 | ||||||
| chr12:122797610
|
G | A | 1 | a0001c0001t0003g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.861+215G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 7/12 | chr12 | 122797610 | ||||||
| chr12:122797615
|
A | G | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.861+220A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 7/12 | chr12 | 122797615 | ||||||
| chr12:122797643
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.861+248C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 7/12 | chr12 | 122797643 | ||||||
| chr12:122797694
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.861+299C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 7/12 | chr12 | 122797694 | ||||||
| chr12:122797728
|
G | C | 51 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.861+333G>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 7/12 | chr12 | 122797728 | ||||||
| chr12:122797745
|
T | C | 51 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.862-340T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 7/12 | chr12 | 122797745 | ||||||
| chr12:122797843
|
A | G | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.862-242A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 7/12 | chr12 | 122797843 | ||||||
| chr12:122797858
|
T | C | 2 | a0001c0001t0006g0001a0001c0001t0006g0203 | 2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.862-227T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 7/12 | chr12 | 122797858 | ||||||
| chr12:122797985
|
G | A | 196 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.862-100G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 7/12 | chr12 | 122797985 | ||||||
| chr12:122798264
|
C | T | 2 | a0001c0001t0006g0001a0001c0001t0006g0203 | 2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.977+64C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122798264 | ||||||
| chr12:122798379
|
G | A | 51 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(48): Show | 51 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.977+179G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122798379 | ||||||
| chr12:122798439
|
C | T | 1 | a0001c0001t0001g0054 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.977+239C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122798439 | ||||||
| chr12:122798441
|
A | G | 1 | a0001c0001t0001g0243 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.977+241A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122798441 | ||||||
| chr12:122798508
|
C | G | 10 | a0001c0001t0001g0034a0001c0001t0002g0025a0001c0001t0002g0030others(7): Show | 10 | HG00438.hp1 HG02129.hp1 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.977+308C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122798508 | ||||||
| chr12:122798777
|
G | A | 2 | a0001c0001t0006g0001a0001c0001t0006g0203 | 2 | HG02572.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.977+577G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122798777 | ||||||
| chr12:122798990
|
G | A | 3 | a0001c0001t0001g0013a0001c0001t0001g0118a0001c0001t0001g0122 | 3 | HG00639.hp2 HG01516.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.977+790G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122798990 | ||||||
| chr12:122799037
|
G | A | 1 | a0001c0001t0003g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.977+837G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122799037 | ||||||
| chr12:122799294
|
A | G | 84 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(81): Show | 84 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.977+1094A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122799294 | ||||||
| chr12:122799317
|
C | T | 52 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(49): Show | 52 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.977+1117C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122799317 | ||||||
| chr12:122799398
|
C | T | 25 | a0001c0001t0001g0286a0001c0001t0002g0018a0001c0001t0002g0170others(22): Show | 25 | HG01099.hp2 HG01109.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.977+1198C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122799398 | ||||||
| chr12:122799628
|
A | G | 2 | a0001c0004t0003g0201a0001c0004t0003g0268 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.977+1428A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122799628 | ||||||
| chr12:122799848
|
C | T | 50 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.978-1276C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122799848 | ||||||
| chr12:122799925
|
G | A | 49 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.978-1199G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122799925 | ||||||
| chr12:122800096
|
C | T | 7 | a0001c0001t0001g0204a0002c0002t0001g0272a0002c0002t0001g0289others(4): Show | 7 | HG02257.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.978-1028C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122800096 | ||||||
| chr12:122800133
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.978-991G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122800133 | ||||||
| chr12:122800164
|
C | CT | 32 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0011others(29): Show | 32 | HG00438.hp2 HG00642.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.978-936dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 122800164 | |||||
| chr12:122800164
|
CT | C | 39 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0114others(36): Show | 39 | HG00423.hp1 HG00642.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.978-936delT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 122800164 | |||||
| chr12:122800164
|
CTTTTTTT | C | 8 | a0001c0001t0002g0222a0001c0001t0003g0019a0001c0004t0003g0201others(5): Show | 8 | HG00280.hp2 HG02451.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.978-942_978-936del others(7): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 122800164 | |||||
| chr12:122800178
|
T | C | 1 | a0001c0001t0001g0125 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.978-946T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122800178 | ||||||
| chr12:122800190
|
T | G | 1 | a0001c0001t0001g0004 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.978-934T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122800190 | ||||||
| chr12:122800427
|
A | AT | 11 | a0001c0001t0001g0011a0001c0001t0001g0042a0001c0001t0001g0070others(8): Show | 11 | HG00642.hp1 HG01175.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.978-681dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 122800427 | |||||
| chr12:122800427
|
A | T | 7 | a0001c0001t0006g0001a0001c0001t0006g0203a0001c0004t0003g0021others(4): Show | 7 | HG02280.hp2 HG02451.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.978-697A>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122800427 | ||||||
| chr12:122800490
|
C | T | 4 | a0002c0002t0001g0272a0002c0002t0001g0289a0002c0002t0001g0290others(1): Show | 4 | HG02257.hp1 HG02647.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.978-634C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122800490 | ||||||
| chr12:122800563
|
G | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0055 | 2 | HG00140.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.978-561G>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122800563 | ||||||
| chr12:122800577
|
G | A | 49 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.978-547G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122800577 | ||||||
| chr12:122800584
|
C | T | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(192): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.978-540C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122800584 | ||||||
| chr12:122800647
|
G | A | 2 | a0001c0001t0001g0231a0001c0001t0001g0232 | 2 | NA18944.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.978-477G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122800647 | ||||||
| chr12:122800722
|
C | T | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.978-402C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122800722 | ||||||
| chr12:122800736
|
AT | A | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.978-380delT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 122800736 | |||||
| chr12:122800737
|
T | A | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.978-387T>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122800737 | ||||||
| chr12:122800774
|
AAGAG | A | 200 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(197): Show | 200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.978-345_978-342del others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr12 | 122800774 | |||||
| chr12:122801095
|
C | G | 1 | a0001c0001t0001g0179 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.978-29C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 8/12 | chr12 | 122801095 | ||||||
| chr12:122801915
|
A | T | 1 | a0001c0001t0001g0092 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1706+63A>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122801915 | ||||||
| chr12:122801931
|
C | T | 49 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1706+79C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122801931 | ||||||
| chr12:122801944
|
A | G | 50 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(47): Show | 50 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1706+92A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122801944 | ||||||
| chr12:122802227
|
C | T | 49 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1706+375C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122802227 | ||||||
| chr12:122802233
|
C | T | 197 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(194): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1706+381C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122802233 | ||||||
| chr12:122802410
|
C | CT | 24 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0091others(21): Show | 24 | HG00280.hp2 HG02602.hp1 HG02615.hp2 others(21): Show |
intron_variant | MODIFIER | c.1706+578dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 122802410 | |||||
| chr12:122802411
|
T | A | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1706+559T>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122802411 | ||||||
| chr12:122802482
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1706+630T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122802482 | ||||||
| chr12:122802682
|
G | A | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1706+830G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122802682 | ||||||
| chr12:122802782
|
C | G | 49 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1706+930C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122802782 | ||||||
| chr12:122802871
|
A | T | 2 | a0001c0001t0001g0122a0001c0001t0003g0194 | 2 | HG01516.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1706+1019A>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122802871 | ||||||
| chr12:122802898
|
C | T | 3 | a0001c0001t0002g0238a0001c0001t0002g0242a0001c0001t0002g0262 | 3 | HG00642.hp2 HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.1706+1046C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122802898 | ||||||
| chr12:122803156
|
G | A | 1 | a0001c0001t0002g0030 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1706+1304G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122803156 | ||||||
| chr12:122803161
|
C | T | 49 | a0001c0001t0001g0029a0001c0001t0001g0032a0001c0001t0001g0034others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1706+1309C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122803161 | ||||||
| chr12:122803586
|
T | C | 3 | a0001c0001t0003g0278a0001c0001t0003g0279a0001c0001t0003g0285 | 3 | HG02615.hp2 HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1706+1734T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122803586 | ||||||
| chr12:122803600
|
C | T | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1706+1748C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122803600 | ||||||
| chr12:122803766
|
T | C | 49 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0002g0024others(46): Show | 49 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.1706+1914T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122803766 | ||||||
| chr12:122803892
|
A | G | 209 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(206): Show | 209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.1706+2040A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122803892 | ||||||
| chr12:122804048
|
C | A | 6 | a0001c0001t0003g0019a0001c0004t0003g0021a0001c0004t0003g0022others(3): Show | 6 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1707-2103C>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122804048 | ||||||
| chr12:122804073
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1707-2078G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122804073 | ||||||
| chr12:122804075
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1707-2076G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122804075 | ||||||
| chr12:122804192
|
C | G | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1707-1959C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122804192 | ||||||
| chr12:122804344
|
G | A | 8 | a0001c0001t0003g0194a0001c0004t0003g0021a0001c0004t0003g0022others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1707-1807G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122804344 | ||||||
| chr12:122804438
|
G | T | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1707-1713G>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122804438 | ||||||
| chr12:122804456
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1707-1695C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122804456 | ||||||
| chr12:122804719
|
T | G | 9 | a0001c0001t0003g0194a0001c0001t0003g0274a0001c0001t0006g0001others(6): Show | 9 | HG02280.hp2 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1707-1432T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122804719 | ||||||
| chr12:122804848
|
A | G | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1707-1303A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122804848 | ||||||
| chr12:122804882
|
AT | A | 191 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(188): Show | 191 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.1707-1250delT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 122804882 | |||||
| chr12:122804882
|
ATT | A | 10 | a0001c0001t0001g0047a0001c0001t0001g0056a0001c0001t0001g0076others(7): Show | 10 | HG00544.hp1 HG00544.hp2 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.1707-1251_1707-125 others(6): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 122804882 | |||||
| chr12:122804927
|
C | T | 1 | a0001c0001t0001g0007 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1707-1224C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122804927 | ||||||
| chr12:122804947
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1707-1204C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122804947 | ||||||
| chr12:122805029
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1707-1122C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122805029 | ||||||
| chr12:122805031
|
C | T | 1 | a0001c0001t0004g0050 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1707-1120C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122805031 | ||||||
| chr12:122805187
|
C | CT | 201 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 201 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(198): Show |
intron_variant | MODIFIER | c.1707-942dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 122805187 | |||||
| chr12:122805187
|
C | CTT | 39 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(36): Show | 39 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1707-943_1707-942d others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 122805187 | |||||
| chr12:122805187
|
CT | C | 35 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(32): Show | 35 | HG00280.hp2 HG01099.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.1707-942delT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 122805187 | |||||
| chr12:122805287
|
T | C | 1 | a0001c0001t0002g0228 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1707-864T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122805287 | ||||||
| chr12:122805343
|
C | CT | 9 | a0001c0001t0001g0034a0001c0001t0001g0061a0001c0001t0001g0140others(6): Show | 9 | HG02055.hp1 HG02135.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1707-789dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 122805343 | |||||
| chr12:122805343
|
CT | C | 99 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(96): Show | 99 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.1707-789delT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 122805343 | |||||
| chr12:122805509
|
C | CT | 172 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0008others(169): Show | 172 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.1707-619dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 122805509 | |||||
| chr12:122805509
|
C | CTT | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(60): Show | 63 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.1707-620_1707-619d others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 122805509 | |||||
| chr12:122805509
|
C | CTTT | 13 | a0001c0001t0001g0034a0001c0001t0002g0024a0001c0001t0002g0030others(10): Show | 13 | HG00609.hp1 HG00642.hp2 HG02071.hp1 others(10): Show |
intron_variant | MODIFIER | c.1707-621_1707-619d others(5): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 122805509 | |||||
| chr12:122805509
|
CT | C | 9 | a0001c0001t0002g0018a0001c0001t0002g0189a0001c0001t0002g0190others(6): Show | 9 | HG02055.hp1 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1707-619delT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr12 | 122805509 | |||||
| chr12:122805539
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1707-612G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122805539 | ||||||
| chr12:122805540
|
A | G | 3 | a0001c0001t0004g0213a0001c0001t0004g0214a0001c0001t0004g0221 | 3 | HG02895.hp1 HG02897.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1707-611A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122805540 | ||||||
| chr12:122805715
|
C | T | 1 | a0001c0001t0002g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1707-436C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122805715 | ||||||
| chr12:122805753
|
G | A | 2 | a0001c0001t0003g0274a0001c0001t0006g0001 | 2 | HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1707-398G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122805753 | ||||||
| chr12:122805888
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1707-263C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122805888 | ||||||
| chr12:122805968
|
T | C | 1 | a0002c0002t0001g0291 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1707-183T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 9/12 | chr12 | 122805968 | ||||||
| chr12:122806404
|
G | GT | 8 | a0001c0001t0001g0286a0001c0001t0002g0191a0001c0001t0002g0192others(5): Show | 8 | HG00280.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1851+128dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122806404 | |||||
| chr12:122806404
|
GT | G | 7 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0096others(4): Show | 7 | HG00741.hp1 HG01261.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1851+128delT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122806404 | |||||
| chr12:122806404
|
GTT | G | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.1851+127_1851+128d others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122806404 | |||||
| chr12:122806409
|
T | TA | 3 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023 | 3 | HG02280.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1851+114_1851+115i others(3): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122806409 | ||||||
| chr12:122806410
|
T | G | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1851+115T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122806410 | ||||||
| chr12:122806538
|
G | A | 48 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0002g0024others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1851+243G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122806538 | ||||||
| chr12:122806543
|
A | G | 3 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023 | 3 | HG02280.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1851+248A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122806543 | ||||||
| chr12:122806737
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1851+442C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122806737 | ||||||
| chr12:122806808
|
AT | A | 203 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(200): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.1851+527delT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122806808 | |||||
| chr12:122806959
|
C | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1851+664C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122806959 | ||||||
| chr12:122807047
|
A | G | 1 | a0001c0001t0001g0090 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1851+752A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122807047 | ||||||
| chr12:122807069
|
T | C | 1 | a0001c0001t0002g0230 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1851+774T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122807069 | ||||||
| chr12:122807105
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1851+810G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122807105 | ||||||
| chr12:122807195
|
C | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1851+900C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122807195 | ||||||
| chr12:122807251
|
G | A | 4 | a0001c0001t0001g0015a0001c0001t0001g0056a0001c0001t0001g0143others(1): Show | 4 | HG00544.hp1 HG02040.hp2 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.1851+956G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122807251 | ||||||
| chr12:122807270
|
G | C | 1 | a0001c0001t0002g0228 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1851+975G>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122807270 | ||||||
| chr12:122807271
|
C | G | 1 | a0001c0001t0002g0228 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1851+976C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122807271 | ||||||
| chr12:122807446
|
G | A | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1851+1151G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122807446 | ||||||
| chr12:122807529
|
C | CA | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 175 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1851+1253dupA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122807529 | |||||
| chr12:122807529
|
C | CAA | 68 | a0001c0001t0001g0017a0001c0001t0001g0029a0001c0001t0001g0034others(65): Show | 68 | HG00423.hp1 HG00544.hp2 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.1851+1252_1851+125 others(6): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122807529 | |||||
| chr12:122807550
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1851+1255G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122807550 | ||||||
| chr12:122807632
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1851+1337A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122807632 | ||||||
| chr12:122807639
|
T | G | 48 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0002g0024others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1851+1344T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122807639 | ||||||
| chr12:122807714
|
G | T | 1 | a0001c0001t0001g0035 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1851+1419G>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122807714 | ||||||
| chr12:122807717
|
A | T | 1 | a0001c0001t0001g0035 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1851+1422A>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122807717 | ||||||
| chr12:122807718
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1851+1423C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122807718 | ||||||
| chr12:122807934
|
T | G | 7 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0048others(4): Show | 7 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1851+1639T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122807934 | ||||||
| chr12:122807947
|
T | C | 1 | a0001c0001t0003g0284 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1851+1652T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122807947 | ||||||
| chr12:122807956
|
A | C | 42 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(39): Show | 42 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(39): Show |
intron_variant | MODIFIER | c.1851+1661A>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122807956 | ||||||
| chr12:122807961
|
C | CCTATTGT others(9): Show |
1 | a0001c0001t0002g0228 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1851+1667_1851+168 others(20): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122807961 | |||||
| chr12:122808063
|
G | A | 1 | a0005c0007t0001g0271 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1851+1768G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122808063 | ||||||
| chr12:122808102
|
G | T | 1 | a0001c0001t0001g0150 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1851+1807G>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122808102 | ||||||
| chr12:122808112
|
C | T | 2 | a0001c0001t0002g0026a0001c0001t0002g0250 | 2 | HG04199.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1851+1817C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122808112 | ||||||
| chr12:122808368
|
T | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1851+2073T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122808368 | ||||||
| chr12:122808375
|
G | A | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1851+2080G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122808375 | ||||||
| chr12:122808446
|
G | A | 9 | a0001c0001t0003g0194a0001c0001t0003g0274a0001c0001t0006g0001others(6): Show | 9 | HG02280.hp2 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1851+2151G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122808446 | ||||||
| chr12:122808501
|
C | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1851+2206C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122808501 | ||||||
| chr12:122808514
|
T | G | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1851+2219T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122808514 | ||||||
| chr12:122808576
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1851+2281G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122808576 | ||||||
| chr12:122808625
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1851+2330C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122808625 | ||||||
| chr12:122808755
|
T | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1851+2460T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122808755 | ||||||
| chr12:122808808
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1851+2513C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122808808 | ||||||
| chr12:122808860
|
C | A | 1 | a0001c0001t0001g0076 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1851+2565C>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122808860 | ||||||
| chr12:122808862
|
A | C | 1 | a0001c0001t0001g0076 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1851+2567A>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122808862 | ||||||
| chr12:122808887
|
G | A | 1 | a0001c0001t0002g0276 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1851+2592G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122808887 | ||||||
| chr12:122808943
|
A | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0116 | 2 | NA18989.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1851+2648A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122808943 | ||||||
| chr12:122808945
|
A | G | 1 | a0001c0001t0001g0298 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1851+2650A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122808945 | ||||||
| chr12:122808992
|
A | G | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1851+2697A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122808992 | ||||||
| chr12:122809012
|
T | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1851+2717T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122809012 | ||||||
| chr12:122809031
|
C | T | 2 | a0003c0003t0001g0184a0003c0003t0001g0195 | 2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1851+2736C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122809031 | ||||||
| chr12:122809109
|
G | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1851+2814G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122809109 | ||||||
| chr12:122809221
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1851+2926G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122809221 | ||||||
| chr12:122809260
|
T | C | 253 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(250): Show | 253 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.1851+2965T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122809260 | ||||||
| chr12:122809261
|
G | C | 1 | a0001c0001t0001g0076 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1851+2966G>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122809261 | ||||||
| chr12:122809707
|
T | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1851+3412T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122809707 | ||||||
| chr12:122809740
|
G | A | 1 | a0008c0011t0010g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1851+3445G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122809740 | ||||||
| chr12:122809768
|
A | G | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1851+3473A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122809768 | ||||||
| chr12:122809969
|
C | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1852-3301C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122809969 | ||||||
| chr12:122809987
|
T | C | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1852-3283T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122809987 | ||||||
| chr12:122809998
|
C | T | 1 | a0001c0005t0003g0280 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1852-3272C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122809998 | ||||||
| chr12:122810001
|
C | T | 13 | a0001c0001t0003g0200a0001c0001t0003g0278a0001c0001t0003g0279others(10): Show | 13 | HG00280.hp2 HG02602.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.1852-3269C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122810001 | ||||||
| chr12:122810099
|
A | G | 1 | a0001c0005t0002g0281 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1852-3171A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122810099 | ||||||
| chr12:122810163
|
G | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1852-3107G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122810163 | ||||||
| chr12:122810246
|
G | A | 9 | a0001c0001t0003g0194a0001c0001t0003g0274a0001c0001t0006g0001others(6): Show | 9 | HG02280.hp2 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1852-3024G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122810246 | ||||||
| chr12:122810251
|
A | C | 1 | a0001c0001t0002g0260 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1852-3019A>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122810251 | ||||||
| chr12:122810279
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1852-2991A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122810279 | ||||||
| chr12:122810462
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1852-2808A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122810462 | ||||||
| chr12:122810524
|
G | A | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | HG00735.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1852-2746G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122810524 | ||||||
| chr12:122810555
|
C | CTTTTACA others(2): Show |
244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1852-2714_1852-270 others(13): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122810555 | |||||
| chr12:122810917
|
A | G | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852-2353A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122810917 | ||||||
| chr12:122810948
|
C | T | 1 | a0001c0001t0002g0228 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1852-2322C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122810948 | ||||||
| chr12:122811027
|
G | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1852-2243G>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122811027 | ||||||
| chr12:122811118
|
A | G | 1 | a0001c0001t0001g0235 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1852-2152A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122811118 | ||||||
| chr12:122811210
|
C | CT | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(237): Show | 240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1852-2042dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122811210 | |||||
| chr12:122811210
|
C | CTT | 12 | a0001c0001t0001g0040a0001c0001t0001g0042a0001c0001t0001g0057others(9): Show | 12 | HG00741.hp2 HG01175.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.1852-2043_1852-204 others(6): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122811210 | |||||
| chr12:122811229
|
C | G | 254 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(251): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1852-2041C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122811229 | ||||||
| chr12:122811298
|
G | A | 1 | a0001c0001t0002g0229 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1852-1972G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122811298 | ||||||
| chr12:122811315
|
G | A | 1 | a0001c0001t0004g0050 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1852-1955G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122811315 | ||||||
| chr12:122811330
|
G | A | 1 | a0001c0001t0003g0284 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1852-1940G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122811330 | ||||||
| chr12:122811369
|
G | A | 1 | a0008c0011t0010g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1852-1901G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122811369 | ||||||
| chr12:122811437
|
C | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0211 | 3 | HG01175.hp2 HG02148.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1852-1833C>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122811437 | ||||||
| chr12:122811526
|
T | TA | 193 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(190): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.1852-1729dupA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122811526 | |||||
| chr12:122811526
|
T | TAA | 45 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0136others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1852-1730_1852-172 others(6): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122811526 | |||||
| chr12:122811526
|
TA | T | 9 | a0001c0001t0003g0194a0001c0001t0003g0274a0001c0001t0006g0001others(6): Show | 9 | HG01109.hp1 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1852-1729delA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122811526 | |||||
| chr12:122811571
|
G | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1852-1699G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122811571 | ||||||
| chr12:122811617
|
C | T | 7 | a0001c0001t0001g0204a0002c0002t0001g0272a0002c0002t0001g0289others(4): Show | 7 | HG02257.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1852-1653C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122811617 | ||||||
| chr12:122811649
|
G | A | 6 | a0001c0001t0002g0229a0001c0001t0002g0244a0001c0001t0002g0245others(3): Show | 6 | HG02040.hp1 HG02132.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.1852-1621G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122811649 | ||||||
| chr12:122811657
|
G | A | 20 | a0001c0001t0001g0013a0001c0001t0001g0046a0001c0001t0001g0063others(17): Show | 20 | HG00639.hp2 HG00738.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1852-1613G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122811657 | ||||||
| chr12:122811715
|
GA | G | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852-1554delA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122811715 | ||||||
| chr12:122811747
|
G | A | 104 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(101): Show | 104 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1852-1523G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122811747 | ||||||
| chr12:122811802
|
C | T | 1 | a0001c0001t0002g0258 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1852-1468C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122811802 | ||||||
| chr12:122811821
|
C | CA | 53 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0038others(50): Show | 53 | HG00423.hp1 HG00438.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1852-1417dupA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122811821 | |||||
| chr12:122811821
|
C | CAA | 8 | a0001c0001t0001g0046a0001c0001t0001g0138a0001c0001t0002g0230others(5): Show | 8 | HG01081.hp1 HG01978.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1852-1418_1852-141 others(6): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122811821 | |||||
| chr12:122811821
|
CA | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(102): Show | 105 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.1852-1417delA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122811821 | |||||
| chr12:122811821
|
CAAAAAAA others(4): Show |
C | 2 | a0001c0004t0003g0201a0001c0004t0003g0268 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1852-1427_1852-141 others(15): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122811821 | |||||
| chr12:122811821
|
CAAAAAAA others(5): Show |
C | 7 | a0001c0001t0003g0194a0001c0001t0003g0274a0001c0001t0006g0001others(4): Show | 7 | HG02280.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1852-1428_1852-141 others(16): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122811821 | |||||
| chr12:122811821
|
CAAAAAAA others(9): Show |
C | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1852-1432_1852-141 others(20): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122811821 | |||||
| chr12:122811943
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0078 | 2 | NA18979.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.1852-1327C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122811943 | ||||||
| chr12:122812214
|
G | A | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852-1056G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812214 | ||||||
| chr12:122812268
|
C | G | 1 | a0001c0001t0002g0265 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1852-1002C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812268 | ||||||
| chr12:122812279
|
C | T | 1 | a0008c0011t0010g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1852-991C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812279 | ||||||
| chr12:122812302
|
T | C | 245 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(242): Show | 245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.1852-968T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812302 | ||||||
| chr12:122812311
|
G | A | 2 | a0001c0001t0002g0025a0001c0001t0002g0266 | 2 | NA18946.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.1852-959G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812311 | ||||||
| chr12:122812325
|
G | A | 8 | a0003c0003t0001g0184a0003c0003t0001g0195a0003c0003t0003g0186others(5): Show | 8 | HG00280.hp2 HG02602.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1852-945G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812325 | ||||||
| chr12:122812442
|
CA | C | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(245): Show | 248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1852-814delA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812442 | |||||
| chr12:122812481
|
T | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1852-789T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812481 | ||||||
| chr12:122812506
|
T | C | 254 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(251): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.1852-764T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812506 | ||||||
| chr12:122812560
|
G | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1852-710G>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812560 | ||||||
| chr12:122812585
|
C | CA | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1852-676dupA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812585 | |||||
| chr12:122812616
|
T | C | 3 | a0001c0001t0003g0274a0001c0001t0006g0001a0001c0001t0006g0203 | 3 | HG02572.hp2 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1852-654T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812616 | ||||||
| chr12:122812646
|
A | AGGCAGGA others(15): Show |
10 | a0001c0001t0003g0019a0001c0001t0003g0194a0001c0001t0003g0274others(7): Show | 10 | HG02280.hp2 HG02451.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1852-622_1852-621i others(24): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812646 | |||||
| chr12:122812647
|
G | GGCAGGAG others(15): Show |
2 | a0001c0001t0001g0115a0001c0001t0001g0288 | 2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1852-622_1852-621i others(24): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812647 | |||||
| chr12:122812647
|
G | GGCAGGAG others(15): Show |
243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1852-622_1852-621i others(24): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812647 | |||||
| chr12:122812676
|
G | C | 284 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(281): Show | 284 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.1852-594G>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812676 | ||||||
| chr12:122812721
|
C | CA | 7 | a0001c0001t0002g0018a0001c0001t0002g0189a0001c0001t0002g0190others(4): Show | 7 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1852-534dupA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812721 | |||||
| chr12:122812733
|
A | G | 194 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(191): Show | 194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1852-537A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812733 | ||||||
| chr12:122812739
|
A | G | 48 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(45): Show | 48 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.1852-531A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812739 | ||||||
| chr12:122812756
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1852-514G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812756 | ||||||
| chr12:122812756
|
G | GA | 3 | a0001c0001t0001g0042a0001c0001t0001g0076a0002c0002t0001g0294 | 3 | HG01175.hp1 HG01243.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1852-514_1852-513i others(3): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812756 | ||||||
| chr12:122812756
|
G | GAGA | 5 | a0001c0001t0001g0056a0001c0001t0001g0120a0001c0001t0002g0027others(2): Show | 5 | HG00544.hp1 HG03540.hp2 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.1852-514_1852-513i others(5): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812756 | ||||||
| chr12:122812756
|
G | GGA | 3 | a0001c0001t0002g0177a0003c0003t0003g0187a0008c0011t0010g0199 | 3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1852-491_1852-490d others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812756 | |||||
| chr12:122812756
|
G | GGAGA | 3 | a0001c0001t0002g0178a0001c0001t0004g0206a0001c0005t0003g0280 | 3 | HG02572.hp1 HG02895.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1852-493_1852-490d others(6): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812756 | |||||
| chr12:122812756
|
GGA | G | 13 | a0001c0001t0001g0029a0001c0001t0001g0053a0001c0001t0002g0028others(10): Show | 13 | HG00642.hp2 HG01069.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.1852-491_1852-490d others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812756 | |||||
| chr12:122812756
|
GGAGA | G | 38 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(35): Show | 38 | HG00280.hp1 HG00609.hp2 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.1852-493_1852-490d others(6): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812756 | |||||
| chr12:122812756
|
GGAGAGA | G | 3 | a0001c0001t0002g0254a0001c0001t0002g0263a0001c0001t0002g0276 | 3 | HG02132.hp1 NA18959.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.1852-495_1852-490d others(8): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812756 | |||||
| chr12:122812767
|
GAGAGAGA others(15): Show |
G | 5 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(2): Show | 5 | HG02280.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852-499_1852-478d others(24): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812767 | |||||
| chr12:122812767
|
GAGAGAGA others(19): Show |
G | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1852-499_1852-474d others(28): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812767 | |||||
| chr12:122812769
|
G | A | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1852-501G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812769 | ||||||
| chr12:122812769
|
GAGAGAGA others(5): Show |
G | 1 | a0002c0002t0001g0292 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1852-497_1852-486d others(14): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812769 | |||||
| chr12:122812771
|
GAGAGAGA others(3): Show |
G | 3 | a0001c0001t0002g0229a0001c0001t0002g0244a0001c0001t0002g0245 | 3 | HG02040.hp1 HG04184.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1852-495_1852-486d others(12): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812771 | |||||
| chr12:122812773
|
G | A | 7 | a0001c0001t0001g0046a0001c0001t0001g0153a0001c0001t0002g0265others(4): Show | 7 | HG01978.hp1 HG02040.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1852-497G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812773 | ||||||
| chr12:122812773
|
G | GAA | 6 | a0001c0001t0001g0160a0001c0001t0002g0128a0001c0001t0002g0225others(3): Show | 6 | HG01261.hp2 HG02027.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.1852-496_1852-495i others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812773 | |||||
| chr12:122812773
|
G | GAAAGAA | 5 | a0001c0001t0002g0024a0001c0001t0002g0239a0001c0001t0002g0259others(2): Show | 5 | HG01099.hp1 HG02735.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852-496_1852-495i others(8): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812773 | |||||
| chr12:122812773
|
G | GAAAGAAA others(3): Show |
3 | a0001c0001t0001g0056a0001c0001t0001g0120a0001c0001t0002g0248 | 3 | HG00544.hp1 HG02683.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1852-496_1852-495i others(12): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812773 | |||||
| chr12:122812773
|
G | GAAAGAAA others(7): Show |
1 | a0001c0001t0002g0240 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1852-496_1852-495i others(16): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812773 | |||||
| chr12:122812773
|
G | GAGAA | 31 | a0001c0001t0001g0011a0001c0001t0001g0013a0001c0001t0001g0041others(28): Show | 31 | HG00639.hp2 HG00642.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.1852-494_1852-493i others(6): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812773 | |||||
| chr12:122812773
|
G | GAGAAAGA others(1): Show |
24 | a0001c0001t0001g0009a0001c0001t0001g0039a0001c0001t0001g0044others(21): Show | 24 | HG00621.hp1 HG00735.hp1 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.1852-494_1852-493i others(10): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812773 | |||||
| chr12:122812773
|
G | GAGAAAGA others(5): Show |
8 | a0001c0001t0001g0003a0001c0001t0001g0040a0001c0001t0001g0058others(5): Show | 8 | HG00408.hp1 HG00408.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1852-494_1852-493i others(14): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812773 | |||||
| chr12:122812773
|
G | GAGAAAGA others(9): Show |
3 | a0001c0001t0001g0002a0001c0001t0001g0089a0001c0001t0004g0050 | 3 | HG00140.hp1 HG00738.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.1852-494_1852-493i others(18): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812773 | |||||
| chr12:122812773
|
G | GAGAAAGA others(13): Show |
2 | a0001c0001t0001g0016a0001c0001t0001g0061 | 2 | HG02135.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1852-494_1852-493i others(22): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812773 | |||||
| chr12:122812773
|
G | GAGAAAGA others(17): Show |
3 | a0001c0001t0001g0015a0001c0001t0001g0140a0001c0001t0001g0197 | 3 | HG03041.hp1 NA19012.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1852-494_1852-493i others(26): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812773 | |||||
| chr12:122812773
|
G | GAGAAAGA others(21): Show |
1 | a0001c0001t0001g0198 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1852-494_1852-493i others(30): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812773 | |||||
| chr12:122812773
|
G | GAGAAAGA others(29): Show |
1 | a0001c0001t0001g0146 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1852-494_1852-493i others(38): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812773 | |||||
| chr12:122812773
|
GAGAGAGA others(1): Show |
G | 13 | a0001c0001t0001g0004a0001c0001t0001g0032a0001c0001t0001g0098others(10): Show | 13 | HG00438.hp2 HG00639.hp1 HG00735.hp2 others(10): Show |
intron_variant | MODIFIER | c.1852-493_1852-486d others(10): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812773 | |||||
| chr12:122812773
|
GAGAGAGA others(5): Show |
G | 8 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0094others(5): Show | 8 | HG01515.hp2 HG02004.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1852-493_1852-482d others(14): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812773 | |||||
| chr12:122812773
|
GAGAGAGA others(9): Show |
G | 12 | a0001c0001t0001g0070a0001c0001t0001g0082a0001c0001t0001g0100others(9): Show | 12 | HG00733.hp1 HG00741.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1852-493_1852-478d others(18): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812773 | |||||
| chr12:122812777
|
G | A | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(145): Show | 148 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1852-493G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812777 | ||||||
| chr12:122812777
|
G | GAAAGAA | 10 | a0001c0001t0001g0034a0001c0001t0002g0025a0001c0001t0002g0030others(7): Show | 10 | HG00438.hp1 HG00609.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1852-492_1852-491i others(8): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812777 | |||||
| chr12:122812777
|
G | GAAAGAAA others(3): Show |
1 | a0001c0001t0002g0241 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1852-492_1852-491i others(12): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812777 | |||||
| chr12:122812777
|
G | GAAAGAAA others(7): Show |
3 | a0001c0001t0002g0226a0001c0001t0002g0257a0001c0001t0002g0264 | 3 | HG00423.hp1 NA18612.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1852-492_1852-491i others(16): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812777 | |||||
| chr12:122812777
|
G | GAGAAAGA others(1): Show |
5 | a0001c0001t0002g0230a0001c0001t0002g0256a0001c0001t0004g0207others(2): Show | 5 | HG03017.hp1 HG03516.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.1852-447_1852-440d others(10): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812777 | |||||
| chr12:122812777
|
G | GAGAAAGA others(9): Show |
1 | a0001c0001t0004g0223 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1852-455_1852-440d others(18): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812777 | |||||
| chr12:122812777
|
G | GAGAGAGA others(5): Show |
1 | a0001c0001t0004g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1852-490_1852-489i others(14): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812777 | |||||
| chr12:122812777
|
G | GAGAGAGA others(5): Show |
1 | a0001c0001t0002g0190 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1852-490_1852-489i others(14): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812777 | |||||
| chr12:122812777
|
G | GAGAGAGA others(13): Show |
1 | a0001c0001t0002g0193 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1852-490_1852-489i others(22): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812777 | |||||
| chr12:122812777
|
G | GAGAGAGA others(7): Show |
1 | a0001c0001t0002g0189 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1852-490_1852-489i others(16): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812777 | |||||
| chr12:122812777
|
G | GAGAGAGA others(11): Show |
3 | a0001c0001t0002g0018a0001c0001t0002g0191a0004c0006t0002g0141 | 3 | HG02451.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1852-490_1852-489i others(20): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812777 | |||||
| chr12:122812777
|
G | GAGAGAGA others(17): Show |
1 | a0001c0001t0002g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1852-490_1852-489i others(26): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812777 | |||||
| chr12:122812777
|
GAGAA | G | 4 | a0001c0001t0003g0224a0001c0001t0003g0284a0001c0001t0004g0210others(1): Show | 4 | HG00733.hp2 HG03516.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.1852-443_1852-440d others(6): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812777 | |||||
| chr12:122812777
|
GAGAAAGA others(5): Show |
G | 3 | a0001c0001t0003g0285a0001c0001t0004g0213a0001c0001t0004g0221 | 3 | HG02895.hp1 HG02897.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1852-451_1852-440d others(14): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812777 | |||||
| chr12:122812777
|
GAGAAAGA others(13): Show |
G | 3 | a0001c0005t0002g0281a0001c0005t0002g0282a0001c0005t0002g0283 | 3 | HG01884.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1852-459_1852-440d others(22): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812777 | |||||
| chr12:122812779
|
GAAAGAAA others(11): Show |
G | 1 | a0001c0014t0002g0196 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1852-489_1852-472d others(20): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812779 | |||||
| chr12:122812781
|
A | G | 9 | a0001c0001t0002g0170a0001c0001t0002g0177a0003c0003t0001g0184others(6): Show | 9 | HG00280.hp2 HG02559.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1852-489A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812781 | ||||||
| chr12:122812785
|
A | G | 1 | a0001c0001t0003g0284 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1852-485A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812785 | ||||||
| chr12:122812793
|
A | G | 1 | a0001c0001t0003g0285 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1852-477A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812793 | ||||||
| chr12:122812801
|
A | G | 3 | a0001c0005t0002g0281a0001c0005t0002g0282a0001c0005t0002g0283 | 3 | HG01884.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1852-469A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812801 | ||||||
| chr12:122812805
|
AAG | A | 8 | a0003c0003t0001g0184a0003c0003t0001g0195a0003c0003t0003g0186others(5): Show | 8 | HG00280.hp2 HG02602.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1852-463_1852-462d others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812805 | |||||
| chr12:122812817
|
A | G | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1852-453A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812817 | ||||||
| chr12:122812821
|
AAG | A | 4 | a0001c0001t0001g0035a0001c0001t0003g0274a0001c0001t0006g0001others(1): Show | 4 | HG01361.hp1 HG02572.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1852-447_1852-446d others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122812821 | |||||
| chr12:122812872
|
A | T | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1852-398A>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812872 | ||||||
| chr12:122812965
|
A | T | 1 | a0001c0001t0003g0194 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1852-305A>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812965 | ||||||
| chr12:122812986
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1852-284C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122812986 | ||||||
| chr12:122813022
|
A | C | 1 | a0001c0001t0001g0204 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1852-248A>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122813022 | ||||||
| chr12:122813035
|
C | CAA | 241 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(238): Show | 241 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(238): Show |
intron_variant | MODIFIER | c.1852-226_1852-225d others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr12 | 122813035 | |||||
| chr12:122813077
|
C | T | 3 | a0001c0001t0003g0274a0001c0001t0006g0001a0001c0001t0006g0203 | 3 | HG02572.hp2 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1852-193C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122813077 | ||||||
| chr12:122813143
|
A | G | 1 | a0008c0011t0010g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1852-127A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122813143 | ||||||
| chr12:122813162
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1852-108G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122813162 | ||||||
| chr12:122813170
|
G | A | 7 | a0001c0001t0002g0018a0001c0001t0002g0189a0001c0001t0002g0190others(4): Show | 7 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1852-100G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122813170 | ||||||
| chr12:122813171
|
T | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1852-99T>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 10/12 | chr12 | 122813171 | ||||||
| chr12:122813422
|
A | C | 1 | a0001c0004t0003g0021 | 1 | NA18906.hp1 | splice_region_variant&intron_variant | LOW | c.2001+3A>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122813422 | ||||||
| chr12:122813504
|
G | A | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2001+85G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122813504 | ||||||
| chr12:122813589
|
A | G | 8 | a0001c0001t0002g0018a0001c0001t0002g0189a0001c0001t0002g0190others(5): Show | 8 | HG01109.hp1 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2001+170A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122813589 | ||||||
| chr12:122813673
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2001+254G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122813673 | ||||||
| chr12:122813674
|
G | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.2001+255G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122813674 | ||||||
| chr12:122813936
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2001+517C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122813936 | ||||||
| chr12:122814009
|
T | C | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.2001+590T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122814009 | ||||||
| chr12:122814053
|
G | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.2001+634G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122814053 | ||||||
| chr12:122814072
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.2001+653A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122814072 | ||||||
| chr12:122814080
|
A | G | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.2001+661A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122814080 | ||||||
| chr12:122814174
|
G | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.2001+755G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122814174 | ||||||
| chr12:122814195
|
T | C | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.2001+776T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122814195 | ||||||
| chr12:122814206
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2001+787C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122814206 | ||||||
| chr12:122814207
|
G | A | 4 | a0001c0001t0005g0043a0001c0001t0005g0110a0001c0001t0005g0111others(1): Show | 4 | HG01074.hp1 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.2001+788G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122814207 | ||||||
| chr12:122814279
|
C | CA | 8 | a0001c0001t0001g0286a0001c0001t0002g0018a0001c0001t0002g0189others(5): Show | 8 | HG02055.hp1 HG02451.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.2001+882dupA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122814279 | |||||
| chr12:122814285
|
A | G | 1 | a0001c0001t0001g0243 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2001+866A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122814285 | ||||||
| chr12:122814295
|
AAAAAAAG others(4): Show |
A | 1 | a0001c0001t0002g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2001+878_2001+888d others(13): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122814295 | |||||
| chr12:122814297
|
AAAAAGAG | A | 179 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(176): Show | 179 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.2001+880_2001+886d others(9): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122814297 | |||||
| chr12:122814297
|
AAAAAGAG others(4): Show |
A | 4 | a0001c0001t0001g0164a0001c0001t0001g0169a0001c0001t0001g0172others(1): Show | 4 | HG02622.hp1 HG02630.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2001+880_2001+890d others(13): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122814297 | |||||
| chr12:122814298
|
AAAAGAG | A | 54 | a0001c0001t0001g0015a0001c0001t0001g0029a0001c0001t0001g0034others(51): Show | 54 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.2001+881_2001+886d others(8): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122814298 | |||||
| chr12:122814302
|
G | A | 30 | a0001c0001t0002g0018a0001c0001t0002g0189a0001c0001t0002g0190others(27): Show | 30 | HG00280.hp2 HG01109.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.2001+883G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122814302 | ||||||
| chr12:122814385
|
G | A | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.2001+966G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122814385 | ||||||
| chr12:122814432
|
G | GAGTGAAT | 244 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(241): Show | 244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.2001+1013_2001+101 others(11): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122814432 | ||||||
| chr12:122814504
|
A | AT | 50 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0058others(47): Show | 50 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.2001+1104dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122814504 | |||||
| chr12:122814504
|
AT | A | 98 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0015others(95): Show | 98 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.2001+1104delT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122814504 | |||||
| chr12:122814504
|
ATT | A | 8 | a0001c0001t0003g0194a0001c0001t0003g0274a0001c0001t0006g0001others(5): Show | 8 | HG02280.hp2 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2001+1103_2001+110 others(6): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122814504 | |||||
| chr12:122814689
|
T | G | 254 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(251): Show | 254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
intron_variant | MODIFIER | c.2001+1270T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122814689 | ||||||
| chr12:122814759
|
T | C | 277 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(274): Show | 277 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.2001+1340T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122814759 | ||||||
| chr12:122814796
|
C | A | 1 | a0001c0001t0003g0284 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2001+1377C>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122814796 | ||||||
| chr12:122814978
|
C | T | 243 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(240): Show | 243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.2001+1559C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122814978 | ||||||
| chr12:122815239
|
C | T | 2 | a0001c0001t0002g0257a0001c0001t0002g0261 | 2 | NA19009.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.2001+1820C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122815239 | ||||||
| chr12:122815445
|
G | GT | 95 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(92): Show | 95 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.2001+2037dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122815445 | |||||
| chr12:122815484
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2001+2065C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122815484 | ||||||
| chr12:122815571
|
C | G | 1 | a0001c0001t0003g0284 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2001+2152C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122815571 | ||||||
| chr12:122815616
|
T | G | 1 | a0003c0003t0003g0187 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2001+2197T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122815616 | ||||||
| chr12:122815694
|
G | A | 1 | a0001c0001t0004g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2001+2275G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122815694 | ||||||
| chr12:122815906
|
C | G | 40 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(37): Show | 40 | HG00280.hp2 HG01099.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.2001+2487C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122815906 | ||||||
| chr12:122816024
|
C | T | 40 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(37): Show | 40 | HG00280.hp2 HG01099.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.2001+2605C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122816024 | ||||||
| chr12:122816261
|
G | A | 30 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(27): Show | 30 | HG01099.hp2 HG01109.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.2001+2842G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122816261 | ||||||
| chr12:122816337
|
T | C | 14 | a0001c0001t0003g0200a0001c0001t0003g0278a0001c0001t0003g0279others(11): Show | 14 | HG00280.hp2 HG02559.hp1 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.2001+2918T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122816337 | ||||||
| chr12:122816385
|
T | G | 39 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(36): Show | 39 | HG00280.hp2 HG01099.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.2001+2966T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122816385 | ||||||
| chr12:122816546
|
A | G | 38 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(35): Show | 38 | HG00280.hp2 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2001+3127A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122816546 | ||||||
| chr12:122816547
|
A | G | 38 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(35): Show | 38 | HG00280.hp2 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2001+3128A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122816547 | ||||||
| chr12:122816573
|
A | T | 6 | a0001c0001t0001g0004a0001c0001t0001g0045a0001c0001t0001g0048others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2001+3154A>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122816573 | ||||||
| chr12:122816643
|
G | A | 16 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(13): Show | 16 | HG01099.hp2 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2001+3224G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122816643 | ||||||
| chr12:122816794
|
A | G | 38 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(35): Show | 38 | HG00280.hp2 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2001+3375A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122816794 | ||||||
| chr12:122816803
|
GT | G | 38 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(35): Show | 38 | HG00280.hp2 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2001+3392delT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122816803 | |||||
| chr12:122816804
|
T | G | 1 | a0001c0001t0002g0276 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2001+3385T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122816804 | ||||||
| chr12:122816811
|
T | A | 41 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0211others(38): Show | 41 | HG00280.hp2 HG01099.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.2001+3392T>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122816811 | ||||||
| chr12:122816818
|
T | C | 1 | a0001c0001t0001g0071 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2001+3399T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122816818 | ||||||
| chr12:122817042
|
T | TTTTATTT others(5): Show |
14 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0178others(11): Show | 14 | HG01099.hp2 HG01884.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.2001+3634_2001+364 others(16): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122817042 | |||||
| chr12:122817042
|
T | TTTTATTT others(9): Show |
10 | a0001c0001t0003g0274a0001c0001t0003g0284a0001c0001t0006g0001others(7): Show | 10 | HG00280.hp2 HG02572.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.2001+3630_2001+364 others(20): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122817042 | |||||
| chr12:122817042
|
T | TTTTATTT others(13): Show |
8 | a0001c0001t0002g0018a0001c0001t0002g0189a0001c0001t0002g0190others(5): Show | 8 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2001+3626_2001+364 others(24): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122817042 | |||||
| chr12:122817042
|
T | TTTTATTT others(17): Show |
4 | a0001c0001t0003g0019a0001c0001t0003g0194a0001c0001t0003g0285others(1): Show | 4 | HG01109.hp1 HG02818.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2001+3645_2001+364 others(28): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122817042 | |||||
| chr12:122817042
|
T | TTTTATTT others(21): Show |
2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2001+3645_2001+364 others(32): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122817042 | |||||
| chr12:122817144
|
C | T | 16 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(13): Show | 16 | HG01099.hp2 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2001+3725C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122817144 | ||||||
| chr12:122817218
|
A | AT | 196 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(193): Show | 196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.2001+3814dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122817218 | |||||
| chr12:122817218
|
A | ATTTTTTT | 11 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0178others(8): Show | 11 | HG01099.hp2 HG01109.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.2001+3808_2001+381 others(11): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122817218 | |||||
| chr12:122817218
|
A | ATTTTTTT others(3): Show |
15 | a0001c0001t0003g0200a0001c0001t0003g0274a0001c0001t0003g0284others(12): Show | 15 | HG00280.hp2 HG02280.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.2001+3805_2001+381 others(14): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122817218 | |||||
| chr12:122817218
|
A | ATTTTTTT others(4): Show |
4 | a0001c0001t0003g0278a0001c0001t0003g0279a0003c0003t0003g0216others(1): Show | 4 | HG02602.hp1 HG02615.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2001+3804_2001+381 others(15): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122817218 | |||||
| chr12:122817307
|
G | A | 38 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(35): Show | 38 | HG00280.hp2 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2001+3888G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122817307 | ||||||
| chr12:122817311
|
C | T | 3 | a0001c0001t0001g0015a0001c0001t0003g0019a0001c0001t0003g0194 | 3 | HG02818.hp2 HG03471.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.2001+3892C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122817311 | ||||||
| chr12:122817312
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2001+3893G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122817312 | ||||||
| chr12:122817343
|
A | G | 1 | a0001c0014t0002g0196 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2001+3924A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122817343 | ||||||
| chr12:122817435
|
T | C | 38 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(35): Show | 38 | HG00280.hp2 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2001+4016T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122817435 | ||||||
| chr12:122817547
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2001+4128C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122817547 | ||||||
| chr12:122817599
|
C | T | 2 | a0001c0001t0004g0205a0001c0001t0004g0206 | 2 | HG02630.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2001+4180C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122817599 | ||||||
| chr12:122817619
|
T | C | 38 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(35): Show | 38 | HG00280.hp2 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2001+4200T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122817619 | ||||||
| chr12:122817633
|
G | A | 295 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(292): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.2001+4214G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122817633 | ||||||
| chr12:122817699
|
T | G | 1 | a0002c0002t0001g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2001+4280T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122817699 | ||||||
| chr12:122817822
|
G | A | 38 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(35): Show | 38 | HG00280.hp2 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2001+4403G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122817822 | ||||||
| chr12:122817882
|
G | A | 6 | a0003c0003t0003g0186a0003c0003t0003g0187a0003c0003t0003g0209others(3): Show | 6 | HG00280.hp2 HG02602.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2001+4463G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122817882 | ||||||
| chr12:122818227
|
C | T | 199 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(196): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.2001+4808C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122818227 | ||||||
| chr12:122818385
|
G | A | 1 | a0003c0003t0001g0184 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2001+4966G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122818385 | ||||||
| chr12:122818400
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2002-4966C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122818400 | ||||||
| chr12:122818431
|
T | C | 38 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(35): Show | 38 | HG00280.hp2 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2002-4935T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122818431 | ||||||
| chr12:122818452
|
C | CA | 21 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0076others(18): Show | 21 | HG00741.hp1 HG01175.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.2002-4892dupA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122818452 | |||||
| chr12:122818452
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0003g0278 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2002-4901_2002-489 others(14): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122818452 | |||||
| chr12:122818452
|
CA | C | 30 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0001g0075others(27): Show | 30 | HG00280.hp2 HG01081.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.2002-4892delA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122818452 | |||||
| chr12:122818452
|
CAA | C | 7 | a0001c0001t0002g0189a0001c0001t0002g0190a0001c0001t0002g0191others(4): Show | 7 | HG01109.hp1 HG02055.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.2002-4893_2002-489 others(6): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122818452 | |||||
| chr12:122818528
|
G | C | 1 | a0001c0001t0001g0155 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2002-4838G>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122818528 | ||||||
| chr12:122818532
|
G | A | 38 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(35): Show | 38 | HG00280.hp2 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2002-4834G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122818532 | ||||||
| chr12:122818539
|
G | A | 1 | a0001c0001t0001g0007 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2002-4827G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122818539 | ||||||
| chr12:122818594
|
C | T | 38 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(35): Show | 38 | HG00280.hp2 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2002-4772C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122818594 | ||||||
| chr12:122818660
|
C | T | 6 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023others(3): Show | 6 | HG02280.hp2 HG02451.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2002-4706C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122818660 | ||||||
| chr12:122818668
|
ATCCT | A | 20 | a0001c0001t0003g0200a0001c0001t0003g0274a0001c0001t0003g0278others(17): Show | 20 | HG00280.hp2 HG02280.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.2002-4697_2002-469 others(8): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122818668 | ||||||
| chr12:122818743
|
T | C | 1 | a0001c0001t0003g0284 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2002-4623T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122818743 | ||||||
| chr12:122818856
|
G | A | 1 | a0001c0001t0002g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2002-4510G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122818856 | ||||||
| chr12:122818962
|
T | A | 38 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(35): Show | 38 | HG00280.hp2 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2002-4404T>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122818962 | ||||||
| chr12:122819039
|
A | G | 69 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0015others(66): Show | 69 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(66): Show |
intron_variant | MODIFIER | c.2002-4327A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122819039 | ||||||
| chr12:122819072
|
A | G | 38 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(35): Show | 38 | HG00280.hp2 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2002-4294A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122819072 | ||||||
| chr12:122819162
|
C | T | 3 | a0001c0001t0001g0053a0001c0001t0001g0273a0012c0016t0001g0237 | 3 | NA18957.hp1 NA18977.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.2002-4204C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122819162 | ||||||
| chr12:122819213
|
G | A | 2 | a0001c0001t0003g0019a0001c0001t0003g0194 | 2 | HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2002-4153G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122819213 | ||||||
| chr12:122819214
|
C | A | 2 | a0001c0001t0003g0019a0001c0001t0003g0194 | 2 | HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2002-4152C>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122819214 | ||||||
| chr12:122819319
|
C | A | 20 | a0001c0001t0003g0200a0001c0001t0003g0274a0001c0001t0003g0278others(17): Show | 20 | HG00280.hp2 HG02280.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.2002-4047C>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122819319 | ||||||
| chr12:122819398
|
C | A | 38 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(35): Show | 38 | HG00280.hp2 HG01099.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2002-3968C>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122819398 | ||||||
| chr12:122819449
|
C | T | 3 | a0001c0005t0002g0281a0001c0005t0002g0282a0001c0005t0002g0283 | 3 | HG01884.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2002-3917C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122819449 | ||||||
| chr12:122819642
|
G | A | 16 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(13): Show | 16 | HG01099.hp2 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2002-3724G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122819642 | ||||||
| chr12:122819940
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2002-3426T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122819940 | ||||||
| chr12:122820031
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2002-3335C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122820031 | ||||||
| chr12:122820061
|
C | CA | 19 | a0001c0001t0001g0010a0001c0001t0001g0047a0001c0001t0001g0063others(16): Show | 19 | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.2002-3283dupA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122820061 | |||||
| chr12:122820061
|
C | CAA | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.2002-3284_2002-328 others(6): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122820061 | |||||
| chr12:122820061
|
C | CAAA | 19 | a0001c0001t0001g0008a0001c0001t0001g0042a0001c0001t0001g0061others(16): Show | 19 | HG00639.hp1 HG01175.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.2002-3285_2002-328 others(7): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122820061 | |||||
| chr12:122820061
|
C | CAAAA | 48 | a0001c0001t0001g0051a0001c0001t0002g0024a0001c0001t0002g0025others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.2002-3286_2002-328 others(8): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122820061 | |||||
| chr12:122820061
|
C | CAAAAA | 10 | a0001c0001t0002g0128a0001c0001t0002g0225a0001c0001t0002g0239others(7): Show | 10 | HG02027.hp1 HG02071.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2002-3287_2002-328 others(9): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122820061 | |||||
| chr12:122820061
|
C | CAAAAAA | 6 | a0001c0001t0003g0284a0003c0003t0003g0187a0003c0003t0003g0209others(3): Show | 6 | HG00280.hp2 HG02602.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.2002-3288_2002-328 others(10): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122820061 | |||||
| chr12:122820205
|
C | T | 2 | a0001c0005t0002g0282a0001c0005t0002g0283 | 2 | HG01884.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2002-3161C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122820205 | ||||||
| chr12:122820338
|
G | T | 1 | a0001c0001t0002g0276 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2002-3028G>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122820338 | ||||||
| chr12:122820375
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2002-2991G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122820375 | ||||||
| chr12:122820427
|
G | A | 16 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(13): Show | 16 | HG01099.hp2 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2002-2939G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122820427 | ||||||
| chr12:122820772
|
C | T | 7 | a0001c0001t0002g0018a0001c0001t0002g0189a0001c0001t0002g0190others(4): Show | 7 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2002-2594C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122820772 | ||||||
| chr12:122820789
|
C | T | 4 | a0001c0001t0001g0061a0001c0001t0001g0131a0001c0001t0001g0146others(1): Show | 4 | HG02056.hp1 HG02135.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.2002-2577C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122820789 | ||||||
| chr12:122820824
|
G | C | 1 | a0001c0009t0001g0183 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2002-2542G>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122820824 | ||||||
| chr12:122820840
|
CA | C | 31 | a0001c0001t0001g0012a0001c0001t0001g0096a0001c0001t0001g0106others(28): Show | 31 | HG00280.hp2 HG00735.hp1 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.2002-2507delA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122820840 | |||||
| chr12:122820840
|
CAA | C | 205 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(202): Show | 205 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.2002-2508_2002-250 others(6): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122820840 | |||||
| chr12:122820840
|
CAAA | C | 49 | a0001c0001t0001g0107a0001c0001t0001g0175a0001c0001t0001g0232others(46): Show | 49 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.2002-2509_2002-250 others(7): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122820840 | |||||
| chr12:122820905
|
A | G | 2 | a0001c0001t0003g0278a0001c0001t0003g0279 | 2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2002-2461A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122820905 | ||||||
| chr12:122820918
|
C | G | 3 | a0001c0004t0003g0021a0001c0004t0003g0022a0001c0004t0003g0023 | 3 | HG02280.hp2 HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2002-2448C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122820918 | ||||||
| chr12:122820968
|
C | T | 13 | a0001c0001t0001g0123a0001c0001t0003g0019a0001c0001t0003g0194others(10): Show | 13 | HG00639.hp1 HG02280.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.2002-2398C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122820968 | ||||||
| chr12:122821308
|
T | C | 3 | a0001c0005t0002g0281a0001c0005t0002g0282a0001c0005t0002g0283 | 3 | HG01884.hp1 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2002-2058T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122821308 | ||||||
| chr12:122821351
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2002-2015C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122821351 | ||||||
| chr12:122821423
|
T | C | 2 | a0001c0001t0001g0063a0006c0015t0001g0215 | 2 | HG02735.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.2002-1943T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122821423 | ||||||
| chr12:122821488
|
C | T | 62 | a0001c0001t0002g0018a0001c0001t0002g0024a0001c0001t0002g0025others(59): Show | 62 | HG00438.hp1 HG00609.hp1 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.2002-1878C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122821488 | ||||||
| chr12:122821616
|
AT | A | 64 | a0001c0001t0002g0018a0001c0001t0002g0024a0001c0001t0002g0025others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.2002-1741delT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122821616 | |||||
| chr12:122821981
|
C | A | 1 | a0001c0001t0002g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2002-1385C>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122821981 | ||||||
| chr12:122822000
|
A | G | 64 | a0001c0001t0002g0018a0001c0001t0002g0024a0001c0001t0002g0025others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.2002-1366A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822000 | ||||||
| chr12:122822011
|
G | A | 48 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.2002-1355G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822011 | ||||||
| chr12:122822060
|
A | AAACACAC others(6): Show |
1 | a0001c0001t0002g0239 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2002-1305_2002-130 others(17): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122822060 | |||||
| chr12:122822060
|
A | AAC | 6 | a0001c0001t0003g0194a0001c0001t0003g0200a0001c0001t0003g0284others(3): Show | 6 | HG02602.hp1 HG02818.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2002-1277_2002-127 others(6): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122822060 | |||||
| chr12:122822060
|
A | AACAC | 10 | a0001c0001t0003g0019a0001c0001t0003g0278a0001c0001t0003g0279others(7): Show | 10 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.2002-1279_2002-127 others(8): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122822060 | |||||
| chr12:122822060
|
A | AACACACA others(1): Show |
12 | a0001c0001t0001g0005a0001c0001t0001g0135a0001c0001t0001g0138others(9): Show | 12 | HG01081.hp1 HG01099.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2002-1283_2002-127 others(12): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122822060 | |||||
| chr12:122822060
|
A | AACACACA others(3): Show |
44 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0035others(41): Show | 44 | HG00140.hp1 HG00609.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.2002-1285_2002-127 others(14): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122822060 | |||||
| chr12:122822060
|
A | AACACACA others(5): Show |
67 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0015others(64): Show | 67 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.2002-1287_2002-127 others(16): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122822060 | |||||
| chr12:122822060
|
A | AACACACA others(7): Show |
58 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0011others(55): Show | 58 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(55): Show |
intron_variant | MODIFIER | c.2002-1289_2002-127 others(18): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122822060 | |||||
| chr12:122822060
|
A | AACACACA others(9): Show |
50 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0029others(47): Show | 50 | HG00140.hp2 HG00438.hp2 HG01168.hp1 others(47): Show |
intron_variant | MODIFIER | c.2002-1291_2002-127 others(20): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122822060 | |||||
| chr12:122822060
|
A | AACACACA others(11): Show |
17 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0032others(14): Show | 17 | HG00738.hp2 HG01069.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.2002-1293_2002-127 others(22): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122822060 | |||||
| chr12:122822060
|
A | AACACACA others(13): Show |
1 | a0001c0001t0001g0040 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2002-1295_2002-127 others(24): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122822060 | |||||
| chr12:122822060
|
A | ACACACAC others(6): Show |
3 | a0001c0001t0001g0269a0001c0001t0001g0277a0001c0001t0002g0261 | 3 | HG02257.hp2 HG02647.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.2002-1306_2002-130 others(17): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822060 | ||||||
| chr12:122822060
|
A | ACACACAC others(8): Show |
4 | a0001c0001t0001g0017a0001c0001t0001g0071a0001c0001t0001g0144others(1): Show | 4 | HG00621.hp2 HG01981.hp1 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.2002-1306_2002-130 others(19): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822060 | ||||||
| chr12:122822060
|
A | ACACACAC others(10): Show |
1 | a0001c0001t0001g0114 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2002-1306_2002-130 others(21): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822060 | ||||||
| chr12:122822060
|
AAC | A | 3 | a0001c0001t0003g0274a0001c0001t0006g0001a0001c0001t0006g0203 | 3 | HG02572.hp2 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2002-1277_2002-127 others(6): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122822060 | |||||
| chr12:122822089
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0002g0242 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2002-1276_2002-127 others(15): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122822089 | |||||
| chr12:122822103
|
CT | C | 234 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(231): Show | 234 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.2002-1245delT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122822103 | |||||
| chr12:122822103
|
CTT | C | 45 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0073others(42): Show | 45 | HG00280.hp2 HG01099.hp2 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.2002-1246_2002-124 others(6): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122822103 | |||||
| chr12:122822235
|
C | T | 5 | a0001c0001t0003g0224a0003c0003t0003g0209a0003c0003t0003g0216others(2): Show | 5 | HG00280.hp2 HG02602.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.2002-1131C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822235 | ||||||
| chr12:122822350
|
T | C | 4 | a0001c0001t0002g0170a0001c0001t0002g0177a0001c0001t0002g0178others(1): Show | 4 | HG01099.hp2 HG02818.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2002-1016T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822350 | ||||||
| chr12:122822355
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2002-1011C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822355 | ||||||
| chr12:122822379
|
C | T | 2 | a0001c0001t0005g0111a0001c0001t0005g0112 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.2002-987C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822379 | ||||||
| chr12:122822539
|
A | T | 16 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(13): Show | 16 | HG01099.hp2 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2002-827A>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822539 | ||||||
| chr12:122822574
|
A | AT | 89 | a0001c0001t0001g0059a0001c0001t0001g0069a0001c0001t0001g0095others(86): Show | 89 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.2002-775dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122822574 | |||||
| chr12:122822574
|
A | ATT | 195 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(192): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.2002-776_2002-775d others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr12 | 122822574 | |||||
| chr12:122822601
|
T | A | 2 | a0001c0001t0003g0019a0001c0001t0003g0194 | 2 | HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2002-765T>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822601 | ||||||
| chr12:122822603
|
T | C | 3 | a0001c0001t0003g0274a0001c0001t0006g0001a0001c0001t0006g0203 | 3 | HG02572.hp2 HG02622.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2002-763T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822603 | ||||||
| chr12:122822634
|
T | C | 64 | a0001c0001t0002g0018a0001c0001t0002g0024a0001c0001t0002g0025others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.2002-732T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822634 | ||||||
| chr12:122822636
|
C | G | 64 | a0001c0001t0002g0018a0001c0001t0002g0024a0001c0001t0002g0025others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.2002-730C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822636 | ||||||
| chr12:122822642
|
T | C | 64 | a0001c0001t0002g0018a0001c0001t0002g0024a0001c0001t0002g0025others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.2002-724T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822642 | ||||||
| chr12:122822652
|
T | C | 63 | a0001c0001t0002g0018a0001c0001t0002g0024a0001c0001t0002g0025others(60): Show | 63 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.2002-714T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822652 | ||||||
| chr12:122822675
|
A | G | 63 | a0001c0001t0002g0018a0001c0001t0002g0024a0001c0001t0002g0025others(60): Show | 63 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.2002-691A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822675 | ||||||
| chr12:122822680
|
T | TCTCCTGC others(184): Show |
16 | a0001c0001t0002g0018a0001c0001t0002g0170a0001c0001t0002g0177others(13): Show | 16 | HG01099.hp2 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2002-686_2002-685i others(193): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822680 | ||||||
| chr12:122822680
|
T | TCTCCTGC others(184): Show |
1 | a0001c0001t0002g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2002-686_2002-685i others(193): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822680 | ||||||
| chr12:122822680
|
T | TCTCCTGC others(184): Show |
46 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(43): Show | 46 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.2002-686_2002-685i others(193): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822680 | ||||||
| chr12:122822697
|
A | G | 5 | a0001c0001t0001g0044a0001c0001t0001g0119a0001c0001t0001g0231others(2): Show | 5 | HG00621.hp1 NA18939.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.2002-669A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822697 | ||||||
| chr12:122822757
|
G | T | 1 | a0001c0001t0004g0050 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2002-609G>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822757 | ||||||
| chr12:122822764
|
A | G | 2 | a0001c0001t0001g0080a0001c0001t0001g0088 | 2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.2002-602A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822764 | ||||||
| chr12:122822991
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2002-375C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122822991 | ||||||
| chr12:122823189
|
G | T | 64 | a0001c0001t0002g0018a0001c0001t0002g0024a0001c0001t0002g0025others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.2002-177G>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122823189 | ||||||
| chr12:122823207
|
C | T | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.2002-159C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122823207 | ||||||
| chr12:122823208
|
A | G | 285 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(282): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.2002-158A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122823208 | ||||||
| chr12:122823316
|
A | C | 1 | a0010c0008t0003g0220 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2002-50A>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 11/12 | chr12 | 122823316 | ||||||
| chr12:122823616
|
G | C | 1 | a0001c0001t0002g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*40+157G>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122823616 | ||||||
| chr12:122823693
|
C | A | 1 | a0001c0001t0002g0202 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.*40+234C>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122823693 | ||||||
| chr12:122823703
|
TA | T | 64 | a0001c0001t0001g0057a0001c0001t0001g0059a0001c0001t0002g0018others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.*40+261delA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 122823703 | |||||
| chr12:122823720
|
A | AG | 4 | a0001c0001t0001g0045a0001c0001t0001g0052a0001c0001t0001g0136others(1): Show | 4 | HG02109.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.*40+263dupG | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 122823720 | |||||
| chr12:122823724
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0055 | 2 | HG00140.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.*40+265C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122823724 | ||||||
| chr12:122823729
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.*40+270G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122823729 | ||||||
| chr12:122823733
|
T | C | 1 | a0003c0003t0003g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.*40+274T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122823733 | ||||||
| chr12:122823849
|
G | A | 1 | a0001c0001t0004g0205 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.*40+390G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122823849 | ||||||
| chr12:122823979
|
C | T | 1 | a0001c0001t0003g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.*40+520C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122823979 | ||||||
| chr12:122824068
|
A | G | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.*40+609A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122824068 | ||||||
| chr12:122824382
|
C | T | 1 | a0003c0003t0003g0187 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*40+923C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122824382 | ||||||
| chr12:122824428
|
C | CA | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.*40+975dupA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 122824428 | |||||
| chr12:122824462
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.*40+1003G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122824462 | ||||||
| chr12:122824519
|
T | G | 1 | a0001c0001t0002g0222 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.*40+1060T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122824519 | ||||||
| chr12:122824607
|
TTATCCAT others(18): Show |
T | 48 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.*40+1149_*40+1173d others(27): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122824607 | ||||||
| chr12:122824613
|
A | G | 10 | a0001c0001t0003g0200a0001c0001t0003g0224a0001c0001t0003g0284others(7): Show | 10 | HG00280.hp2 HG02602.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.*40+1154A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122824613 | ||||||
| chr12:122824636
|
C | T | 64 | a0001c0001t0002g0018a0001c0001t0002g0024a0001c0001t0002g0025others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.*40+1177C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122824636 | ||||||
| chr12:122824649
|
T | C | 285 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(282): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.*40+1190T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122824649 | ||||||
| chr12:122824682
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.*40+1223A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122824682 | ||||||
| chr12:122824843
|
G | A | 1 | a0001c0001t0001g0004 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.*40+1384G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122824843 | ||||||
| chr12:122824851
|
G | A | 23 | a0001c0001t0003g0019a0001c0001t0003g0194a0001c0001t0003g0200others(20): Show | 23 | HG00280.hp2 HG02280.hp2 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.*40+1392G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122824851 | ||||||
| chr12:122824875
|
G | A | 48 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.*40+1416G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122824875 | ||||||
| chr12:122824928
|
T | C | 198 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(195): Show | 198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.*40+1469T>C | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122824928 | ||||||
| chr12:122824997
|
A | G | 48 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(45): Show | 48 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.*41-1425A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122824997 | ||||||
| chr12:122825018
|
G | A | 2 | a0001c0001t0003g0019a0001c0001t0003g0194 | 2 | HG02818.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.*41-1404G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122825018 | ||||||
| chr12:122825120
|
G | GA | 7 | a0001c0001t0003g0224a0003c0003t0003g0186a0003c0003t0003g0187others(4): Show | 7 | HG00280.hp2 HG02602.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.*41-1294dupA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 122825120 | |||||
| chr12:122825147
|
C | G | 1 | a0001c0001t0002g0024 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.*41-1275C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122825147 | ||||||
| chr12:122825197
|
T | A | 285 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(282): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.*41-1225T>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122825197 | ||||||
| chr12:122825238
|
C | G | 1 | a0001c0001t0001g0211 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.*41-1184C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122825238 | ||||||
| chr12:122825332
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0056a0001c0001t0001g0143 | 3 | HG00544.hp1 HG02165.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.*41-1090C>T | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122825332 | ||||||
| chr12:122825333
|
A | G | 285 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(282): Show | 285 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.*41-1089A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122825333 | ||||||
| chr12:122825342
|
A | AT | 97 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0016others(94): Show | 97 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.*41-1059dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 122825342 | |||||
| chr12:122825342
|
A | ATT | 12 | a0001c0001t0001g0011a0001c0001t0001g0017a0001c0001t0001g0069others(9): Show | 12 | HG00408.hp2 HG00621.hp2 HG00642.hp1 others(9): Show |
intron_variant | MODIFIER | c.*41-1060_*41-1059d others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 122825342 | |||||
| chr12:122825342
|
A | ATTT | 6 | a0001c0001t0001g0015a0001c0001t0001g0034a0001c0001t0001g0056others(3): Show | 6 | HG00544.hp1 HG02040.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.*41-1061_*41-1059d others(5): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 122825342 | |||||
| chr12:122825342
|
ATT | A | 59 | a0001c0001t0002g0018a0001c0001t0002g0024a0001c0001t0002g0025others(56): Show | 59 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.*41-1060_*41-1059d others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 122825342 | |||||
| chr12:122825347
|
T | G | 4 | a0001c0001t0002g0234a0001c0001t0002g0242a0001c0001t0002g0247others(1): Show | 4 | HG00642.hp2 HG02735.hp2 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.*41-1075T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122825347 | ||||||
| chr12:122825348
|
T | G | 43 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(40): Show | 43 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.*41-1074T>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122825348 | ||||||
| chr12:122825513
|
A | AT | 83 | a0001c0001t0002g0018a0001c0001t0002g0024a0001c0001t0002g0025others(80): Show | 83 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.*41-895dupT | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 122825513 | |||||
| chr12:122825513
|
A | ATTT | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 186 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.*41-897_*41-895dup others(3): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 122825513 | |||||
| chr12:122825513
|
A | ATTTT | 10 | a0001c0001t0001g0011a0001c0001t0001g0029a0001c0001t0001g0037others(7): Show | 10 | HG00140.hp2 HG00642.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.*41-898_*41-895dup others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 122825513 | |||||
| chr12:122825652
|
A | G | 262 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(259): Show | 262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.*41-770A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122825652 | ||||||
| chr12:122825800
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.*41-622A>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122825800 | ||||||
| chr12:122825807
|
G | A | 1 | a0002c0002t0001g0294 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.*41-615G>A | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122825807 | ||||||
| chr12:122825832
|
C | CAA | 182 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.*41-580_*41-579dup others(2): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 122825832 | |||||
| chr12:122825832
|
C | CAAA | 14 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0077others(11): Show | 14 | HG00544.hp2 HG00741.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.*41-581_*41-579dup others(3): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 122825832 | |||||
| chr12:122825974
|
C | G | 51 | a0001c0001t0001g0002a0001c0001t0001g0015a0001c0001t0001g0016others(48): Show | 51 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(48): Show |
intron_variant | MODIFIER | c.*41-448C>G | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | chr12 | 122825974 | ||||||
| chr12:122825993
|
C | CA | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.*41-409dupA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 122825993 | |||||
| chr12:122825993
|
CA | C | 61 | a0001c0001t0001g0080a0001c0001t0002g0018a0001c0001t0002g0024others(58): Show | 61 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(58): Show |
intron_variant | MODIFIER | c.*41-409delA | CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 122825993 | |||||
| chr12:122825993
|
CAAA | C | 14 | a0001c0001t0003g0019a0001c0001t0003g0194a0001c0001t0003g0274others(11): Show | 14 | HG02280.hp2 HG02451.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.*41-411_*41-409del others(3): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 122825993 | |||||
| chr12:122825993
|
CAAAA | C | 9 | a0001c0001t0003g0200a0001c0001t0003g0224a0001c0001t0003g0284others(6): Show | 9 | HG00280.hp2 HG02602.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.*41-412_*41-409del others(4): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 122825993 | |||||
| chr12:122825993
|
CAAAAAAA others(2): Show |
C | 17 | a0001c0001t0001g0046a0001c0001t0001g0089a0001c0001t0001g0094others(14): Show | 17 | HG00738.hp1 HG00741.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.*41-417_*41-409del others(9): Show |
CCDC62 | ENSG00000130783.14 | transcript | ENST00000253079.11 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr12 | 122825993 |