Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 51496 |
|---|---|
| ensemblid | ENSG00000137770.14 |
| hgncid | 26936 |
| symbol | CTDSPL2 |
| name | CTD small phosphatase like 2 |
| refseq_nuc | NM_016396.3 |
| refseq_prot | NP_057480.2 |
| ensembl_nuc | ENST00000260327.9 |
| ensembl_prot | ENSP00000260327.4 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 44427629 |
| end | 44529038 |
| strand | + |
| ver | v1.2 |
| region | chr15:44427629-44529038 |
| region5000 | chr15:44422629-44534038 |
| regionname0 | CTDSPL2_chr15_44427629_44529038 |
| regionname5000 | CTDSPL2_chr15_44422629_44534038 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 466 | 230 | 77 | 38 | 89 | 2 | 22 | 61 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0002 | 0/0 | 466 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0003 | 0/0 | 466 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0004 | 0/0 | 466 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1401 | 202 | 61 | 38 | 77 | 2 | 22 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| c0002 | 0/0 | 1401 | 18 | 6 | 0 | 12 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| c0003 | 0/0 | 1401 | 9 | 9 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| c0004 | 0/0 | 1401 | 2 | 2 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| c0005 | 0/0 | 1401 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| c0006 | 0/0 | 1401 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| c0007 | 0/0 | 1401 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 5033 | 90 | 37 | 17 | 22 | 1 | 11 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0002 | 0/0 | 5033 | 29 | 3 | 11 | 8 | 1 | 6 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0003 | 0/0 | 5031 | 20 | 6 | 1 | 11 | 0 | 2 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0004 | 0/0 | 5033 | 19 | 0 | 1 | 17 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0005 | 0/0 | 5033 | 18 | 6 | 0 | 12 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0006 | 0/0 | 5033 | 8 | 0 | 3 | 5 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0007 | 0/0 | 5030 | 8 | 0 | 2 | 6 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0008 | 0/0 | 5032 | 6 | 6 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0009 | 0/0 | 5032 | 4 | 4 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0010 | 0/0 | 5032 | 4 | 4 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0011 | 0/0 | 5032 | 4 | 4 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0012 | 0/0 | 5029 | 2 | 2 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0013 | 0/0 | 5033 | 2 | 2 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0014 | 0/0 | 5032 | 2 | 0 | 0 | 2 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0015 | 0/0 | 5033 | 2 | 0 | 0 | 2 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0016 | 0/0 | 5032 | 2 | 0 | 2 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0017 | 0/0 | 5034 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0018 | 0/0 | 5029 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0019 | 0/0 | 5033 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0020 | 0/0 | 5033 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0021 | 0/0 | 5033 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0022 | 0/0 | 5033 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0023 | 0/0 | 5033 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0024 | 0/0 | 5031 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0025 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0026 | 0/0 | 5031 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0027 | 0/0 | 5033 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0028 | 0/0 | 5033 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0029 | 0/0 | 5033 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| t0030 | 0/0 | 5031 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0222 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1401 | 202 | 61 | 38 | 77 | 2 | 22 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0002 | 0/0 | 1401 | 18 | 6 | 0 | 12 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0003 | 0/0 | 1401 | 9 | 9 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0005 | 0/0 | 1401 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0002c0004 | 0/0 | 1401 | 2 | 2 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0003c0006 | 0/0 | 1401 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0004c0007 | 0/0 | 1401 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6433 | 89 | 36 | 17 | 22 | 1 | 11 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0002 | 0/0 | 6433 | 28 | 3 | 11 | 7 | 1 | 6 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0003 | 0/0 | 6431 | 20 | 6 | 1 | 11 | 0 | 2 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0004 | 0/0 | 6433 | 19 | 0 | 1 | 17 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0006 | 0/0 | 6433 | 8 | 0 | 3 | 5 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0007 | 0/0 | 6430 | 8 | 0 | 2 | 6 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0009 | 0/0 | 6432 | 4 | 4 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0011 | 0/0 | 6432 | 4 | 4 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0012 | 0/0 | 6429 | 2 | 2 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0014 | 0/0 | 6432 | 2 | 0 | 0 | 2 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0015 | 0/0 | 6433 | 2 | 0 | 0 | 2 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0016 | 0/0 | 6432 | 2 | 0 | 2 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0017 | 0/0 | 6434 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0018 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0019 | 0/0 | 6433 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0020 | 0/0 | 6433 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0021 | 0/0 | 6433 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0022 | 0/0 | 6433 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0023 | 0/0 | 6433 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0024 | 0/0 | 6431 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0025 | 0/0 | 6431 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0026 | 0/0 | 6431 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0027 | 0/0 | 6433 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0028 | 0/0 | 6433 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0029 | 0/0 | 6433 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0001t0030 | 0/0 | 6431 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0002t0005 | 0/0 | 6433 | 18 | 6 | 0 | 12 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0003t0008 | 0/0 | 6432 | 6 | 6 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0003t0010 | 0/0 | 6432 | 3 | 3 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0001c0005t0001 | 0/0 | 6433 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0002c0004t0013 | 0/0 | 6433 | 2 | 2 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0003c0006t0010 | 0/0 | 6432 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| a0004c0007t0002 | 0/0 | 6433 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | copy fasta | chr15 | 44422629 | 44534038 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0222 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0226 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0006g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0006g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0007g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0007g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0007g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0007g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0007g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0007g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0007g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0009g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0009g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0009g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0009g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0011g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0011g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0011g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0011g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0012g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0012g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0014g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0014g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0015g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0015g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0016g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0016g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0017g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0018g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0019g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0020g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0021g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0022g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0023g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0024g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0025g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0026g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0027g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0028g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0029g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0001t0030g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0002t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0002t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0002t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0002t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0002t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0002t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0002t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0002t0005g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0002t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0002t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0002t0005g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0002t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0002t0005g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0002t0005g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0002t0005g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0002t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0002t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0002t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0003t0008g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0003t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0003t0008g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0003t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0003t0008g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0003t0008g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0003t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0003t0010g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0003t0010g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0001c0005t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0002c0004t0013g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0002c0004t0013g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0003c0006t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| a0004c0007t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | CHS | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0168 | EAS | CHS | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG00423 | hp1 | a0001 | c0001 | t0024 | g0010 | EAS | CHS | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG00423 | hp2 | a0001 | c0001 | t0007 | g0194 | EAS | CHS | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | CHS | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0172 | EAS | CHS | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG00673 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | CHS | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG00738 | hp2 | a0001 | c0001 | t0016 | g0189 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01071 | hp1 | a0001 | c0001 | t0016 | g0188 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01074 | hp2 | a0001 | c0001 | t0021 | g0142 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01167 | hp2 | a0001 | c0001 | t0006 | g0113 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01891 | hp1 | a0001 | c0001 | t0026 | g0024 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01891 | hp2 | a0001 | c0001 | t0012 | g0066 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01928 | hp1 | a0001 | c0001 | t0007 | g0185 | AMR | PEL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01928 | hp2 | a0001 | c0001 | t0006 | g0102 | AMR | PEL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01978 | hp2 | a0001 | c0001 | t0007 | g0071 | AMR | PEL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0133 | AMR | PEL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0192 | EAS | KHV | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02040 | hp1 | a0001 | c0002 | t0005 | g0049 | EAS | KHV | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02040 | hp2 | a0001 | c0001 | t0019 | g0079 | EAS | KHV | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0028 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0150 | EAS | KHV | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0146 | EAS | KHV | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | KHV | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | PEL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02155 | hp1 | a0001 | c0001 | t0006 | g0084 | EAS | CDX | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02155 | hp2 | a0001 | c0002 | t0005 | g0050 | EAS | CDX | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CDX | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02165 | hp2 | a0001 | c0001 | t0007 | g0077 | EAS | CDX | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02257 | hp1 | a0001 | c0002 | t0005 | g0031 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02258 | hp2 | a0001 | c0003 | t0008 | g0060 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02293 | hp1 | a0001 | c0001 | t0006 | g0094 | AMR | PEL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02451 | hp2 | a0001 | c0002 | t0005 | g0034 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02523 | hp1 | a0001 | c0002 | t0005 | g0047 | EAS | KHV | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | KHV | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02572 | hp1 | a0001 | c0001 | t0009 | g0027 | AFR | GWD | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0152 | SAS | PJL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02615 | hp2 | a0001 | c0003 | t0008 | g0059 | AFR | GWD | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02630 | hp2 | a0001 | c0003 | t0008 | g0061 | AFR | GWD | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02723 | hp1 | a0001 | c0005 | t0001 | g0161 | AFR | GWD | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02809 | hp1 | a0001 | c0001 | t0027 | g0201 | AFR | GWD | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02886 | hp1 | a0001 | c0003 | t0008 | g0062 | AFR | GWD | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0026 | AFR | GWD | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02922 | hp2 | a0001 | c0002 | t0005 | g0033 | AFR | ESN | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02965 | hp1 | a0003 | c0006 | t0010 | g0056 | AFR | ESN | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ESN | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02970 | hp2 | a0001 | c0001 | t0011 | g0052 | AFR | ESN | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | MSL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03098 | hp2 | a0001 | c0001 | t0011 | g0054 | AFR | MSL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03130 | hp1 | a0001 | c0001 | t0011 | g0053 | AFR | ESN | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03130 | hp2 | a0001 | c0001 | t0012 | g0065 | AFR | ESN | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03139 | hp1 | a0001 | c0001 | t0011 | g0051 | AFR | ESN | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03195 | hp1 | a0002 | c0004 | t0013 | g0199 | AFR | ESN | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | MSL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | MSL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03453 | hp1 | a0001 | c0002 | t0005 | g0035 | AFR | MSL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | MSL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0029 | AFR | MSL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03516 | hp1 | a0001 | c0002 | t0005 | g0036 | AFR | ESN | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03516 | hp2 | a0001 | c0003 | t0010 | g0064 | AFR | ESN | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03654 | hp1 | a0001 | c0001 | t0023 | g0083 | SAS | PJL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | STU | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03704 | hp1 | a0001 | c0001 | t0020 | g0167 | SAS | PJL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0006 | SAS | BEB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0140 | SAS | BEB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | BEB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | STU | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | STU | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | STU | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | STU | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | YRI | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | YRI | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18906 | hp2 | a0001 | c0003 | t0010 | g0057 | AFR | YRI | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18951 | hp1 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18951 | hp2 | a0001 | c0002 | t0005 | g0042 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18952 | hp2 | a0001 | c0001 | t0028 | g0100 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18953 | hp2 | a0001 | c0001 | t0007 | g0206 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18960 | hp2 | a0001 | c0002 | t0005 | g0039 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18962 | hp2 | a0001 | c0001 | t0006 | g0138 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18965 | hp1 | a0001 | c0002 | t0005 | g0046 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18966 | hp2 | a0001 | c0002 | t0005 | g0045 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18971 | hp1 | a0001 | c0002 | t0005 | g0040 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18971 | hp2 | a0001 | c0001 | t0007 | g0169 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18975 | hp1 | a0001 | c0001 | t0007 | g0131 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18986 | hp1 | a0001 | c0002 | t0005 | g0043 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18986 | hp2 | a0001 | c0001 | t0015 | g0104 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18990 | hp1 | a0001 | c0002 | t0005 | g0041 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18990 | hp2 | a0001 | c0001 | t0029 | g0234 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18992 | hp1 | a0001 | c0001 | t0015 | g0224 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18995 | hp1 | a0001 | c0001 | t0014 | g0225 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0089 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0210 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19001 | hp2 | a0004 | c0007 | t0002 | g0076 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19004 | hp2 | a0001 | c0002 | t0005 | g0048 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | LWK | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | LWK | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | LWK | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19043 | hp2 | a0001 | c0001 | t0018 | g0030 | AFR | LWK | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19055 | hp1 | a0001 | c0001 | t0004 | g0190 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19055 | hp2 | a0001 | c0001 | t0030 | g0008 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19063 | hp2 | a0001 | c0002 | t0005 | g0044 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19064 | hp2 | a0001 | c0001 | t0006 | g0135 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19074 | hp1 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19090 | hp1 | a0001 | c0001 | t0006 | g0101 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | ASW | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ASW | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0080 | EUR | TSI | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | TSI | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02109 | hp1 | a0001 | c0001 | t0025 | g0025 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02109 | hp2 | a0001 | c0001 | t0017 | g0001 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG02559 | hp2 | a0001 | c0002 | t0005 | g0032 | AFR | ACB | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG03471 | hp2 | a0001 | c0003 | t0008 | g0063 | AFR | MSL | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG06807 | hp1 | a0001 | c0003 | t0010 | g0055 | AFR | USA | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| HG06807 | hp2 | a0002 | c0004 | t0013 | g0200 | AFR | USA | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18955 | hp1 | a0001 | c0001 | t0007 | g0129 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA18955 | hp2 | a0001 | c0001 | t0014 | g0038 | EAS | JPT | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA20300 | hp1 | a0001 | c0003 | t0008 | g0058 | AFR | USA | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA20300 | hp2 | a0001 | c0001 | t0022 | g0114 | AFR | USA | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | LWK | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | LWK | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0226 | REF | REF | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0222 | REF | REF | CTDSPL2_chr15_44422629_44534038 | CTDSPL2 | chr15 | 44422629 | 44534038 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:44490976
|
A | G | 1 | a0004 | 1 | NA19001.hp2 | missense_variant | MODERATE | c.668A>G | p.Asn223Ser | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/13 | 836/6433 | 668/1401 | 223/466 | chr15 | 44490976 | ||
| chr15:44496419
|
C | T | 1 | a0003 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.731C>T | p.Ala244Val | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 6/13 | 899/6433 | 731/1401 | 244/466 | chr15 | 44496419 | ||
| chr15:44521360
|
A | G | 1 | a0002 | 2 | HG03195.hp1 HG06807.hp2 |
missense_variant | MODERATE | c.1289A>G | p.Asn430Ser | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/13 | 1457/6433 | 1289/1401 | 430/466 | chr15 | 44521360 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:44459152
|
C | T | 1 | a0001c0002 | 18 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(15): Show |
synonymous_variant | LOW | c.138C>T | p.Thr46Thr | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/13 | 306/6433 | 138/1401 | 46/466 | chr15 | 44459152 | ||
| chr15:44490806
|
A | G | 1 | a0001c0003 | 9 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
synonymous_variant | LOW | c.498A>G | p.Pro166Pro | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/13 | 666/6433 | 498/1401 | 166/466 | chr15 | 44490806 | ||
| chr15:44519178
|
T | A | 1 | a0001c0005 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.1122T>A | p.Leu374Leu | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/13 | 1290/6433 | 1122/1401 | 374/466 | chr15 | 44519178 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:44427674
|
G | T | 1 | a0001c0001t0011 | 4 | HG02970.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-123G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/13 | 31341 | chr15 | 44427674 | |||||
| chr15:44427700
|
G | A | 3 | a0001c0001t0012a0001c0001t0017a0001c0001t0018 | 4 | HG01891.hp2 HG02109.hp2 HG03130.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-97G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/13 | 31315 | chr15 | 44427700 | |||||
| chr15:44427734
|
C | T | 1 | a0001c0001t0030 | 1 | NA19055.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/13 | chr15 | 44427734 | ||||||
| chr15:44427736
|
C | T | 1 | a0001c0001t0029 | 1 | NA18990.hp2 | 5_prime_UTR_variant | MODIFIER | c.-61C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/13 | 31279 | chr15 | 44427736 | |||||
| chr15:44524695
|
A | G | 1 | a0001c0001t0028 | 1 | NA18952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*521A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 521 | chr15 | 44524695 | |||||
| chr15:44525317
|
C | G | 3 | a0001c0003t0008a0001c0003t0010a0003c0006t0010 | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1143C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 1143 | chr15 | 44525317 | |||||
| chr15:44525339
|
A | T | 1 | a0001c0001t0011 | 4 | HG02970.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1165A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 1165 | chr15 | 44525339 | |||||
| chr15:44525766
|
G | A | 1 | a0002c0004t0013 | 2 | HG03195.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1592G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 1592 | chr15 | 44525766 | |||||
| chr15:44525975
|
C | CA | 3 | a0001c0001t0017a0001c0001t0018a0001c0002t0005 | 20 | HG02040.hp1 HG02109.hp2 HG02155.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1811dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 1812 | INFO_REALIGN_3_PRIME | chr15 | 44525975 | ||||
| chr15:44525977
|
A | G | 1 | a0001c0001t0027 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1803A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 1803 | chr15 | 44525977 | |||||
| chr15:44526916
|
C | T | 2 | a0001c0001t0025a0001c0001t0026 | 2 | HG01891.hp1 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2742C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 2742 | chr15 | 44526916 | |||||
| chr15:44526940
|
C | G | 1 | a0001c0002t0005 | 18 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*2766C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 2766 | chr15 | 44526940 | |||||
| chr15:44526995
|
AGTT | A | 1 | a0001c0001t0007 | 8 | HG00423.hp2 HG01928.hp1 HG01978.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2825_*2827delGTT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 2825 | INFO_REALIGN_3_PRIME | chr15 | 44526995 | ||||
| chr15:44527216
|
TG | T | 1 | a0001c0001t0016 | 2 | HG00738.hp2 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3043delG | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 3043 | chr15 | 44527216 | |||||
| chr15:44527266
|
GGTT | G | 2 | a0001c0001t0012a0001c0001t0018 | 3 | HG01891.hp2 HG03130.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3096_*3098delGTT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 3096 | INFO_REALIGN_3_PRIME | chr15 | 44527266 | ||||
| chr15:44527277
|
GT | G | 5 | a0001c0001t0012a0001c0001t0014a0001c0001t0018others(2): Show | 7 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3112delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 3112 | INFO_REALIGN_3_PRIME | chr15 | 44527277 | ||||
| chr15:44527315
|
A | T | 4 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(1): Show | 56 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*3141A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 3141 | chr15 | 44527315 | |||||
| chr15:44527348
|
T | C | 1 | a0001c0001t0025 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3174T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 3174 | chr15 | 44527348 | |||||
| chr15:44527351
|
A | G | 1 | a0001c0001t0024 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3177A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 3177 | chr15 | 44527351 | |||||
| chr15:44527383
|
C | T | 3 | a0001c0001t0003a0001c0001t0024a0001c0001t0030 | 22 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3209C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 3209 | chr15 | 44527383 | |||||
| chr15:44527469
|
G | A | 5 | a0001c0001t0012a0001c0001t0014a0001c0001t0018others(2): Show | 7 | HG01891.hp1 HG01891.hp2 HG02109.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3295G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 3295 | chr15 | 44527469 | |||||
| chr15:44527856
|
A | G | 2 | a0001c0001t0006a0001c0001t0028 | 9 | HG01167.hp2 HG01928.hp2 HG02155.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3682A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 3682 | chr15 | 44527856 | |||||
| chr15:44528023
|
T | C | 1 | a0001c0001t0019 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3849T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 3849 | chr15 | 44528023 | |||||
| chr15:44528085
|
T | C | 2 | a0001c0001t0025a0001c0001t0026 | 2 | HG01891.hp1 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3911T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 3911 | chr15 | 44528085 | |||||
| chr15:44528099
|
C | T | 1 | a0001c0001t0015 | 2 | NA18986.hp2 NA18992.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3925C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 3925 | chr15 | 44528099 | |||||
| chr15:44528138
|
T | G | 1 | a0001c0001t0020 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3964T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 3964 | chr15 | 44528138 | |||||
| chr15:44528165
|
G | C | 1 | a0001c0001t0021 | 1 | HG01074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3991G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 3991 | chr15 | 44528165 | |||||
| chr15:44528212
|
G | C | 1 | a0001c0001t0022 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4038G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 4038 | chr15 | 44528212 | |||||
| chr15:44528240
|
C | T | 1 | a0001c0003t0008 | 6 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4066C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 4066 | chr15 | 44528240 | |||||
| chr15:44528323
|
C | T | 1 | a0001c0001t0017 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4149C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 4149 | chr15 | 44528323 | |||||
| chr15:44528337
|
CT | C | 12 | a0001c0001t0003a0001c0001t0009a0001c0001t0011others(9): Show | 61 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*4174delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 4174 | INFO_REALIGN_3_PRIME | chr15 | 44528337 | ||||
| chr15:44528508
|
GT | G | 3 | a0001c0001t0003a0001c0001t0024a0001c0001t0030 | 22 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4347delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 4347 | INFO_REALIGN_3_PRIME | chr15 | 44528508 | ||||
| chr15:44528675
|
G | A | 1 | a0001c0001t0023 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4501G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 4501 | chr15 | 44528675 | |||||
| chr15:44528764
|
A | G | 1 | a0001c0001t0004 | 19 | HG00408.hp2 HG00597.hp2 HG00673.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*4590A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 4590 | chr15 | 44528764 | |||||
| chr15:44528848
|
C | T | 1 | a0002c0004t0013 | 2 | HG03195.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4674C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 13/13 | 4674 | chr15 | 44528848 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:44427809
|
A | G | 6 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0232others(3): Show | 6 | HG02015.hp2 NA18949.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+37A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44427809 | ||||||
| chr15:44427813
|
C | T | 3 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0001g0228 | 3 | HG01081.hp2 HG03471.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-25+41C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44427813 | ||||||
| chr15:44427835
|
C | T | 1 | a0001c0001t0014g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-25+63C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44427835 | ||||||
| chr15:44428117
|
CT | C | 67 | a0001c0001t0001g0037a0001c0001t0003g0002a0001c0001t0003g0003others(64): Show | 67 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.-25+352delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44428117 | |||||
| chr15:44428296
|
G | T | 1 | a0001c0001t0001g0228 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-25+524G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44428296 | ||||||
| chr15:44428313
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0004g0068a0001c0001t0004g0069 | 3 | NA18965.hp2 NA19074.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-25+541G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44428313 | ||||||
| chr15:44428320
|
TAGTAAAG others(3): Show |
T | 1 | a0001c0001t0015g0224 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-25+552_-25+561del others(10): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44428320 | |||||
| chr15:44428347
|
G | C | 67 | a0001c0001t0001g0037a0001c0001t0003g0002a0001c0001t0003g0003others(64): Show | 67 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.-25+575G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44428347 | ||||||
| chr15:44428645
|
A | G | 2 | a0001c0001t0012g0065a0001c0001t0012g0066 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-25+873A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44428645 | ||||||
| chr15:44428674
|
C | G | 1 | a0001c0001t0015g0224 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-25+902C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44428674 | ||||||
| chr15:44428682
|
A | G | 1 | a0001c0001t0015g0224 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-25+910A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44428682 | ||||||
| chr15:44428683
|
G | A | 1 | a0001c0001t0015g0224 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-25+911G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44428683 | ||||||
| chr15:44428706
|
C | T | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+934C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44428706 | ||||||
| chr15:44428810
|
A | AT | 4 | a0001c0001t0011g0051a0001c0001t0011g0052a0001c0001t0011g0053others(1): Show | 4 | HG02970.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+1044dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44428810 | |||||
| chr15:44428821
|
T | C | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-25+1049T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44428821 | ||||||
| chr15:44428889
|
T | A | 230 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0070others(227): Show | 230 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.-25+1117T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44428889 | ||||||
| chr15:44428907
|
AATTGTTC | A | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.-25+1138_-25+1144d others(9): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44428907 | |||||
| chr15:44429004
|
C | T | 1 | a0001c0002t0005g0050 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-25+1232C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44429004 | ||||||
| chr15:44429018
|
A | T | 1 | a0001c0001t0015g0224 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-25+1246A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44429018 | ||||||
| chr15:44429022
|
T | A | 1 | a0001c0001t0015g0224 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-25+1250T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44429022 | ||||||
| chr15:44429154
|
A | G | 1 | a0001c0001t0001g0220 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-25+1382A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44429154 | ||||||
| chr15:44429318
|
C | T | 2 | a0001c0001t0012g0065a0001c0001t0012g0066 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-25+1546C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44429318 | ||||||
| chr15:44429412
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-25+1640G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44429412 | ||||||
| chr15:44429441
|
G | A | 2 | a0001c0001t0003g0020a0001c0001t0003g0021 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-25+1669G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44429441 | ||||||
| chr15:44429442
|
T | C | 1 | a0001c0001t0007g0071 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-25+1670T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44429442 | ||||||
| chr15:44429671
|
G | A | 4 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+1899G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44429671 | ||||||
| chr15:44429722
|
C | T | 5 | a0001c0002t0005g0045a0001c0002t0005g0046a0001c0002t0005g0047others(2): Show | 5 | HG02040.hp1 HG02523.hp1 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1950C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44429722 | ||||||
| chr15:44429824
|
C | G | 25 | a0001c0001t0001g0037a0001c0001t0003g0020a0001c0001t0003g0021others(22): Show | 25 | HG02027.hp2 HG02040.hp1 HG02155.hp2 others(22): Show |
intron_variant | MODIFIER | c.-25+2052C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44429824 | ||||||
| chr15:44429959
|
T | G | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-25+2187T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44429959 | ||||||
| chr15:44430117
|
T | G | 2 | a0001c0002t0005g0031a0001c0002t0005g0032 | 2 | HG02257.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.-25+2345T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44430117 | ||||||
| chr15:44430170
|
C | T | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+2398C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44430170 | ||||||
| chr15:44430263
|
ATTTATT | A | 12 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(9): Show | 12 | HG02040.hp1 HG02155.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.-25+2507_-25+2512d others(8): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44430263 | |||||
| chr15:44430300
|
C | G | 1 | a0001c0001t0001g0219 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-25+2528C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44430300 | ||||||
| chr15:44430342
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-25+2570C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44430342 | ||||||
| chr15:44430541
|
C | T | 42 | a0001c0001t0001g0037a0001c0001t0003g0003a0001c0001t0003g0004others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-25+2769C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44430541 | ||||||
| chr15:44430646
|
A | G | 4 | a0001c0001t0011g0051a0001c0001t0011g0052a0001c0001t0011g0053others(1): Show | 4 | HG02970.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+2874A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44430646 | ||||||
| chr15:44430820
|
CT | C | 18 | a0001c0002t0005g0031a0001c0002t0005g0032a0001c0002t0005g0033others(15): Show | 18 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-25+3058delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44430820 | |||||
| chr15:44431012
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-25+3240G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44431012 | ||||||
| chr15:44431083
|
A | G | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.-25+3311A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44431083 | ||||||
| chr15:44431150
|
G | A | 1 | a0001c0001t0001g0073 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-25+3378G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44431150 | ||||||
| chr15:44431604
|
A | G | 42 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-25+3832A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44431604 | ||||||
| chr15:44431621
|
A | G | 18 | a0001c0002t0005g0031a0001c0002t0005g0032a0001c0002t0005g0033others(15): Show | 18 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.-25+3849A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44431621 | ||||||
| chr15:44431715
|
TG | T | 3 | a0001c0001t0012g0065a0001c0001t0012g0066a0001c0001t0017g0001 | 3 | HG01891.hp2 HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-25+3944delG | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44431715 | ||||||
| chr15:44431716
|
G | T | 44 | a0001c0001t0002g0217a0001c0001t0003g0002a0001c0001t0003g0003others(41): Show | 44 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.-25+3944G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44431716 | ||||||
| chr15:44431716
|
GT | G | 9 | a0001c0001t0001g0067a0001c0001t0001g0130a0001c0001t0001g0229others(6): Show | 9 | HG00741.hp2 HG02165.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25+3963delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44431716 | |||||
| chr15:44431716
|
GTT | G | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+3962_-25+3963d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44431716 | |||||
| chr15:44431718
|
T | TG | 3 | a0001c0001t0003g0002a0001c0002t0005g0036a0001c0002t0005g0044 | 3 | HG03516.hp1 NA19030.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.-25+3946_-25+3947i others(3): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44431718 | ||||||
| chr15:44431719
|
T | G | 39 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(36): Show | 39 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.-25+3947T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44431719 | ||||||
| chr15:44431719
|
T | TG | 2 | a0001c0001t0001g0073a0001c0001t0001g0128 | 2 | HG03688.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.-25+3947_-25+3948i others(3): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44431719 | ||||||
| chr15:44431720
|
T | G | 65 | a0001c0001t0001g0037a0001c0001t0001g0070a0001c0001t0001g0074others(62): Show | 65 | HG00642.hp2 HG00738.hp1 HG01081.hp2 others(62): Show |
intron_variant | MODIFIER | c.-25+3948T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44431720 | ||||||
| chr15:44431721
|
T | G | 1 | a0001c0001t0007g0077 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-25+3949T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44431721 | ||||||
| chr15:44431722
|
T | G | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+3950T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44431722 | ||||||
| chr15:44431724
|
T | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0218others(1): Show | 4 | HG00738.hp1 HG03139.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25+3952T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44431724 | ||||||
| chr15:44431726
|
T | G | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+3954T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44431726 | ||||||
| chr15:44431754
|
T | C | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-25+3982T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44431754 | ||||||
| chr15:44431863
|
G | A | 16 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(13): Show | 16 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.-25+4091G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44431863 | ||||||
| chr15:44432089
|
C | T | 7 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(4): Show | 7 | HG00735.hp1 HG01167.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.-25+4317C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44432089 | ||||||
| chr15:44432300
|
ATATTATT others(19): Show |
A | 4 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+4540_-25+4565d others(28): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44432300 | |||||
| chr15:44432310
|
TTTA | T | 211 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0070others(208): Show | 211 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.-25+4562_-25+4564d others(5): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44432310 | |||||
| chr15:44432402
|
C | G | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+4630C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44432402 | ||||||
| chr15:44432405
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+4633C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44432405 | ||||||
| chr15:44432424
|
A | G | 2 | a0001c0001t0004g0210a0001c0001t0004g0211 | 2 | NA18998.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-25+4652A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44432424 | ||||||
| chr15:44432461
|
AGGC | A | 42 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-25+4690_-25+4692d others(5): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44432461 | ||||||
| chr15:44432464
|
C | T | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-25+4692C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44432464 | ||||||
| chr15:44432468
|
C | T | 42 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-25+4696C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44432468 | ||||||
| chr15:44432532
|
G | A | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+4760G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44432532 | ||||||
| chr15:44432574
|
C | T | 1 | a0001c0001t0001g0128 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-25+4802C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44432574 | ||||||
| chr15:44432660
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-25+4888C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44432660 | ||||||
| chr15:44432858
|
A | G | 2 | a0001c0001t0003g0017a0001c0001t0003g0018 | 2 | NA19007.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-25+5086A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44432858 | ||||||
| chr15:44432959
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-25+5187A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44432959 | ||||||
| chr15:44433068
|
C | T | 6 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0232others(3): Show | 6 | HG02015.hp2 NA18949.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+5296C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433068 | ||||||
| chr15:44433080
|
T | A | 4 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25+5308T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433080 | ||||||
| chr15:44433195
|
G | T | 1 | a0001c0002t0005g0050 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-25+5423G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433195 | ||||||
| chr15:44433274
|
C | T | 2 | a0001c0001t0012g0065a0001c0001t0012g0066 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-25+5502C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433274 | ||||||
| chr15:44433288
|
C | T | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.-25+5516C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433288 | ||||||
| chr15:44433299
|
C | T | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.-25+5527C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433299 | ||||||
| chr15:44433329
|
A | AG | 9 | a0001c0002t0005g0031a0001c0002t0005g0039a0001c0002t0005g0044others(6): Show | 9 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+5558dupG | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44433329 | |||||
| chr15:44433330
|
G | GA | 34 | a0001c0001t0001g0078a0001c0001t0001g0132a0001c0001t0001g0219others(31): Show | 34 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(31): Show |
intron_variant | MODIFIER | c.-25+5577dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44433330 | |||||
| chr15:44433330
|
GA | G | 6 | a0001c0001t0001g0124a0001c0001t0002g0207a0001c0001t0004g0068others(3): Show | 6 | HG02071.hp1 HG02559.hp2 NA18953.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25+5577delA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44433330 | |||||
| chr15:44433331
|
A | G | 14 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(11): Show | 14 | HG02451.hp2 HG02922.hp2 HG02965.hp2 others(11): Show |
intron_variant | MODIFIER | c.-25+5559A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433331 | ||||||
| chr15:44433332
|
A | G | 1 | a0001c0002t0005g0032 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-25+5560A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433332 | ||||||
| chr15:44433352
|
A | G | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+5580A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433352 | ||||||
| chr15:44433432
|
G | A | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-25+5660G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433432 | ||||||
| chr15:44433441
|
G | A | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.-25+5669G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433441 | ||||||
| chr15:44433459
|
T | C | 1 | a0001c0001t0002g0080 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-25+5687T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433459 | ||||||
| chr15:44433459
|
T | TAC | 7 | a0001c0001t0001g0074a0001c0001t0001g0085a0001c0001t0001g0086others(4): Show | 7 | HG02155.hp1 HG03139.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.-25+5714_-25+5715d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44433459 | |||||
| chr15:44433459
|
T | TACAC | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG02280.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-25+5712_-25+5715d others(6): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44433459 | |||||
| chr15:44433459
|
TAC | T | 125 | a0001c0001t0001g0067a0001c0001t0001g0072a0001c0001t0001g0073others(122): Show | 125 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(122): Show |
intron_variant | MODIFIER | c.-25+5714_-25+5715d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44433459 | |||||
| chr15:44433459
|
TACAC | T | 6 | a0001c0001t0003g0003a0001c0001t0003g0019a0001c0001t0003g0020others(3): Show | 6 | HG00673.hp1 HG02965.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+5712_-25+5715d others(6): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44433459 | |||||
| chr15:44433459
|
TACACAC | T | 32 | a0001c0001t0003g0002a0001c0001t0003g0004a0001c0001t0003g0005others(29): Show | 32 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.-25+5710_-25+5715d others(8): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44433459 | |||||
| chr15:44433463
|
C | T | 20 | a0001c0001t0001g0205a0001c0001t0014g0225a0001c0002t0005g0031others(17): Show | 20 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.-25+5691C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433463 | ||||||
| chr15:44433465
|
C | T | 6 | a0001c0001t0003g0003a0001c0001t0003g0019a0001c0001t0003g0020others(3): Show | 6 | HG00673.hp1 HG02965.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+5693C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433465 | ||||||
| chr15:44433467
|
C | T | 18 | a0001c0001t0003g0002a0001c0001t0003g0004a0001c0001t0003g0005others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.-25+5695C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433467 | ||||||
| chr15:44433469
|
C | T | 2 | a0001c0001t0003g0014a0001c0001t0003g0015 | 2 | NA18949.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-25+5697C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433469 | ||||||
| chr15:44433496
|
C | T | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0204others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+5724C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433496 | ||||||
| chr15:44433507
|
G | A | 2 | a0001c0001t0002g0148a0001c0001t0002g0149 | 2 | HG02074.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.-25+5735G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433507 | ||||||
| chr15:44433563
|
A | G | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+5791A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433563 | ||||||
| chr15:44433585
|
T | A | 2 | a0001c0001t0004g0150a0001c0001t0004g0151 | 2 | HG00673.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.-25+5813T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433585 | ||||||
| chr15:44433619
|
A | T | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.-25+5847A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433619 | ||||||
| chr15:44433732
|
A | G | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.-25+5960A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433732 | ||||||
| chr15:44433948
|
C | T | 54 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 54 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.-25+6176C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44433948 | ||||||
| chr15:44433953
|
C | CA | 67 | a0001c0001t0001g0205a0001c0001t0003g0002a0001c0001t0003g0003others(64): Show | 67 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.-25+6195dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44433953 | |||||
| chr15:44434071
|
G | GTTAT | 10 | a0001c0001t0003g0019a0001c0003t0008g0058a0001c0003t0008g0059others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+6322_-25+6325d others(6): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44434071 | |||||
| chr15:44434071
|
G | GTTATTTA others(1): Show |
9 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(6): Show | 9 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25+6318_-25+6325d others(10): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44434071 | |||||
| chr15:44434090
|
A | T | 13 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0009others(10): Show | 13 | HG00408.hp1 HG00423.hp1 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.-25+6318A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44434090 | ||||||
| chr15:44434094
|
A | T | 30 | a0001c0001t0001g0198a0001c0001t0001g0205a0001c0001t0001g0212others(27): Show | 30 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(27): Show |
intron_variant | MODIFIER | c.-25+6322A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44434094 | ||||||
| chr15:44434140
|
G | T | 5 | a0001c0001t0001g0070a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02083.hp2 HG02135.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+6368G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44434140 | ||||||
| chr15:44434175
|
G | A | 1 | a0001c0001t0002g0148 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-25+6403G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44434175 | ||||||
| chr15:44434190
|
C | A | 62 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(59): Show | 62 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.-25+6418C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44434190 | ||||||
| chr15:44434221
|
G | A | 1 | a0003c0006t0010g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-25+6449G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44434221 | ||||||
| chr15:44434494
|
A | C | 8 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-25+6722A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44434494 | ||||||
| chr15:44434546
|
A | G | 3 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0029 | 3 | HG02572.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-25+6774A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44434546 | ||||||
| chr15:44434979
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-25+7207C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44434979 | ||||||
| chr15:44435085
|
C | T | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-25+7313C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44435085 | ||||||
| chr15:44435150
|
C | T | 2 | a0001c0001t0001g0196a0001c0001t0001g0212 | 2 | HG02895.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-25+7378C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44435150 | ||||||
| chr15:44435228
|
G | T | 17 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(14): Show | 17 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.-25+7456G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44435228 | ||||||
| chr15:44435256
|
C | CA | 32 | a0001c0001t0001g0081a0001c0001t0001g0209a0001c0001t0002g0152others(29): Show | 32 | HG01981.hp1 HG02040.hp1 HG02155.hp2 others(29): Show |
intron_variant | MODIFIER | c.-25+7505dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44435256 | |||||
| chr15:44435256
|
CA | C | 13 | a0001c0001t0001g0112a0001c0001t0003g0013a0001c0001t0003g0019others(10): Show | 13 | HG02055.hp1 HG02083.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-25+7505delA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44435256 | |||||
| chr15:44435443
|
G | A | 1 | a0001c0001t0026g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-25+7671G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44435443 | ||||||
| chr15:44435523
|
C | T | 1 | a0001c0003t0008g0063 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-25+7751C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44435523 | ||||||
| chr15:44435608
|
G | GT | 18 | a0001c0001t0001g0037a0001c0001t0001g0073a0001c0001t0001g0111others(15): Show | 18 | HG00423.hp2 HG01891.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.-25+7852dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44435608 | |||||
| chr15:44435632
|
A | C | 1 | a0001c0001t0001g0122 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-25+7860A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44435632 | ||||||
| chr15:44435651
|
A | G | 4 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25+7879A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44435651 | ||||||
| chr15:44435764
|
G | A | 1 | a0003c0006t0010g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-25+7992G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44435764 | ||||||
| chr15:44435826
|
C | T | 1 | a0003c0006t0010g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-25+8054C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44435826 | ||||||
| chr15:44435832
|
C | G | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.-25+8060C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44435832 | ||||||
| chr15:44435931
|
C | T | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.-25+8159C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44435931 | ||||||
| chr15:44435971
|
T | C | 15 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0090others(12): Show | 15 | HG00642.hp2 HG00738.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.-25+8199T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44435971 | ||||||
| chr15:44435982
|
G | A | 1 | a0001c0001t0003g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-25+8210G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44435982 | ||||||
| chr15:44436165
|
G | C | 1 | a0001c0001t0001g0115 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-25+8393G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44436165 | ||||||
| chr15:44436413
|
A | T | 1 | a0001c0001t0001g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-25+8641A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44436413 | ||||||
| chr15:44436569
|
C | T | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-25+8797C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44436569 | ||||||
| chr15:44436758
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-25+8986T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44436758 | ||||||
| chr15:44436886
|
G | C | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-25+9114G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44436886 | ||||||
| chr15:44437258
|
AT | A | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+9489delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44437258 | |||||
| chr15:44437296
|
G | C | 2 | a0001c0001t0003g0020a0001c0001t0003g0021 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-25+9524G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44437296 | ||||||
| chr15:44437427
|
A | G | 8 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-25+9655A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44437427 | ||||||
| chr15:44437611
|
C | T | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.-25+9839C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44437611 | ||||||
| chr15:44437779
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-25+10007T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44437779 | ||||||
| chr15:44437951
|
A | G | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-25+10179A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44437951 | ||||||
| chr15:44438057
|
G | C | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-25+10285G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44438057 | ||||||
| chr15:44438125
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-25+10353G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44438125 | ||||||
| chr15:44438156
|
C | T | 1 | a0001c0002t0005g0036 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-25+10384C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44438156 | ||||||
| chr15:44438263
|
C | CA | 40 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0070others(37): Show | 40 | HG00741.hp1 HG00741.hp2 HG01256.hp1 others(37): Show |
intron_variant | MODIFIER | c.-25+10506dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44438263 | |||||
| chr15:44438263
|
C | CAA | 9 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0006g0084others(6): Show | 9 | HG01167.hp2 HG01978.hp1 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+10505_-25+1050 others(6): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44438263 | |||||
| chr15:44438299
|
A | G | 4 | a0001c0001t0012g0065a0001c0001t0012g0066a0001c0001t0017g0001others(1): Show | 4 | HG01891.hp2 HG02109.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25+10527A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44438299 | ||||||
| chr15:44438486
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-25+10714A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44438486 | ||||||
| chr15:44438560
|
A | G | 1 | a0001c0001t0019g0079 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-25+10788A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44438560 | ||||||
| chr15:44438600
|
A | G | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-25+10828A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44438600 | ||||||
| chr15:44438626
|
G | C | 1 | a0001c0001t0029g0234 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-25+10854G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44438626 | ||||||
| chr15:44439121
|
A | ATAT | 14 | a0001c0001t0001g0091a0001c0001t0002g0134a0001c0001t0006g0102others(11): Show | 14 | HG01256.hp2 HG01891.hp1 HG01928.hp2 others(11): Show |
intron_variant | MODIFIER | c.-25+11369_-25+1137 others(7): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44439121 | |||||
| chr15:44439121
|
A | ATATTAT | 39 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(36): Show | 39 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.-25+11366_-25+1137 others(10): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44439121 | |||||
| chr15:44439121
|
A | ATATTATT others(2): Show |
2 | a0001c0001t0003g0009a0001c0001t0003g0019 | 2 | HG00735.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-25+11363_-25+1137 others(13): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44439121 | |||||
| chr15:44439121
|
ATAT | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0088 | 2 | HG02280.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-25+11369_-25+1137 others(7): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44439121 | |||||
| chr15:44439141
|
A | ATTG | 14 | a0001c0001t0012g0065a0001c0001t0012g0066a0001c0001t0017g0001others(11): Show | 14 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-25+11372_-25+1137 others(7): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44439141 | |||||
| chr15:44439159
|
A | T | 22 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(19): Show | 22 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.-25+11387A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44439159 | ||||||
| chr15:44439218
|
G | A | 4 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0128others(1): Show | 4 | HG03490.hp1 HG03491.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+11446G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44439218 | ||||||
| chr15:44439247
|
C | G | 1 | a0001c0001t0001g0122 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-25+11475C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44439247 | ||||||
| chr15:44439338
|
G | A | 1 | a0001c0002t0005g0036 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-25+11566G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44439338 | ||||||
| chr15:44439339
|
G | T | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-25+11567G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44439339 | ||||||
| chr15:44439404
|
C | G | 1 | a0001c0001t0026g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-25+11632C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44439404 | ||||||
| chr15:44439431
|
T | G | 1 | a0001c0001t0024g0010 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-25+11659T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44439431 | ||||||
| chr15:44439535
|
G | GT | 67 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(64): Show | 67 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.-25+11771dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44439535 | |||||
| chr15:44439546
|
G | C | 11 | a0001c0001t0001g0120a0001c0001t0001g0153a0001c0001t0001g0162others(8): Show | 11 | HG01884.hp1 HG02055.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-25+11774G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44439546 | ||||||
| chr15:44439547
|
G | A | 67 | a0001c0001t0002g0166a0001c0001t0003g0002a0001c0001t0003g0003others(64): Show | 67 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.-25+11775G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44439547 | ||||||
| chr15:44439556
|
A | G | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+11784A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44439556 | ||||||
| chr15:44439665
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-25+11893C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44439665 | ||||||
| chr15:44439892
|
G | A | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+12120G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44439892 | ||||||
| chr15:44439928
|
C | T | 2 | a0001c0001t0014g0038a0001c0001t0014g0225 | 2 | NA18955.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-25+12156C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44439928 | ||||||
| chr15:44440056
|
A | G | 1 | a0001c0001t0014g0038 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-25+12284A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44440056 | ||||||
| chr15:44440179
|
TTTTG | T | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+12419_-25+1242 others(8): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44440179 | |||||
| chr15:44440199
|
G | GT | 53 | a0001c0001t0001g0112a0001c0001t0001g0120a0001c0001t0001g0147others(50): Show | 53 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-25+12441dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44440199 | |||||
| chr15:44440199
|
G | GTT | 6 | a0001c0001t0003g0012a0001c0001t0009g0026a0001c0001t0009g0027others(3): Show | 6 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25+12440_-25+1244 others(6): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44440199 | |||||
| chr15:44440214
|
G | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0209 | 2 | HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-25+12442G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44440214 | ||||||
| chr15:44440363
|
T | G | 1 | a0003c0006t0010g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-25+12591T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44440363 | ||||||
| chr15:44440383
|
A | T | 6 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(3): Show | 6 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-25+12611A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44440383 | ||||||
| chr15:44440455
|
A | C | 54 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 54 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.-25+12683A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44440455 | ||||||
| chr15:44440659
|
A | AT | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+12897dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44440659 | |||||
| chr15:44440669
|
T | A | 1 | a0001c0001t0014g0038 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-25+12897T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44440669 | ||||||
| chr15:44440835
|
T | G | 1 | a0001c0001t0003g0004 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-25+13063T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44440835 | ||||||
| chr15:44440861
|
C | G | 62 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(59): Show | 62 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.-25+13089C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44440861 | ||||||
| chr15:44440938
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-25+13166G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44440938 | ||||||
| chr15:44440974
|
G | A | 1 | a0001c0001t0011g0054 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-25+13202G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44440974 | ||||||
| chr15:44441053
|
G | A | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.-25+13281G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44441053 | ||||||
| chr15:44441096
|
C | A | 1 | a0001c0001t0002g0149 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-25+13324C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44441096 | ||||||
| chr15:44441222
|
G | GT | 7 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0029others(4): Show | 7 | HG02572.hp1 HG02895.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.-25+13459dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44441222 | |||||
| chr15:44441241
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG01256.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-25+13469C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44441241 | ||||||
| chr15:44441244
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-25+13472C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44441244 | ||||||
| chr15:44441247
|
A | T | 2 | a0001c0001t0003g0014a0001c0001t0003g0015 | 2 | NA18949.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-25+13475A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44441247 | ||||||
| chr15:44441449
|
G | A | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02559.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-25+13677G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44441449 | ||||||
| chr15:44441472
|
C | G | 62 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(59): Show | 62 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.-25+13700C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44441472 | ||||||
| chr15:44441512
|
T | C | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-25+13740T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44441512 | ||||||
| chr15:44441647
|
C | T | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-25+13875C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44441647 | ||||||
| chr15:44441825
|
G | A | 1 | a0001c0002t0005g0050 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-25+14053G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44441825 | ||||||
| chr15:44441873
|
C | T | 1 | a0001c0001t0025g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-25+14101C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44441873 | ||||||
| chr15:44442377
|
G | C | 1 | a0001c0001t0003g0002 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-25+14605G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44442377 | ||||||
| chr15:44442446
|
C | CA | 17 | a0001c0001t0001g0157a0001c0001t0001g0205a0001c0001t0001g0230others(14): Show | 17 | HG01192.hp2 HG01891.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-25+14691dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44442446 | |||||
| chr15:44442802
|
C | T | 2 | a0002c0004t0013g0199a0002c0004t0013g0200 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-25+15030C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44442802 | ||||||
| chr15:44443044
|
G | A | 24 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(21): Show | 24 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.-25+15272G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44443044 | ||||||
| chr15:44443188
|
A | C | 1 | a0001c0001t0003g0011 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-25+15416A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44443188 | ||||||
| chr15:44443214
|
A | G | 1 | a0001c0001t0001g0072 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-25+15442A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44443214 | ||||||
| chr15:44443279
|
G | A | 1 | a0001c0001t0003g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-25+15507G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44443279 | ||||||
| chr15:44443726
|
A | T | 44 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(41): Show | 44 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.-24-15265A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44443726 | ||||||
| chr15:44443977
|
G | A | 1 | a0001c0001t0004g0168 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-24-15014G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44443977 | ||||||
| chr15:44444058
|
A | G | 1 | a0001c0001t0004g0146 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-24-14933A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44444058 | ||||||
| chr15:44444202
|
G | A | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.-24-14789G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44444202 | ||||||
| chr15:44444237
|
T | TA | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-24-14753dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444237 | |||||
| chr15:44444261
|
C | G | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-24-14730C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44444261 | ||||||
| chr15:44444302
|
T | C | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-24-14689T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44444302 | ||||||
| chr15:44444302
|
T | TAC | 33 | a0001c0001t0001g0075a0001c0001t0001g0078a0001c0001t0001g0090others(30): Show | 33 | HG00673.hp1 HG00741.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.-24-14651_-24-1465 others(6): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444302 | |||||
| chr15:44444302
|
T | TACAC | 11 | a0001c0001t0001g0082a0001c0001t0001g0088a0001c0001t0001g0218others(8): Show | 11 | HG00738.hp1 HG02280.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.-24-14653_-24-1465 others(8): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444302 | |||||
| chr15:44444302
|
T | TACACAC | 5 | a0001c0001t0001g0205a0001c0001t0001g0219a0001c0001t0012g0066others(2): Show | 5 | HG01891.hp1 HG01891.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-14655_-24-1465 others(10): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444302 | |||||
| chr15:44444302
|
T | TACACACA others(3): Show |
4 | a0001c0001t0025g0025a0001c0003t0008g0060a0001c0003t0008g0061others(1): Show | 4 | HG02109.hp1 HG02258.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-14659_-24-1465 others(14): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444302 | |||||
| chr15:44444302
|
T | TACACACA others(5): Show |
3 | a0001c0001t0012g0065a0001c0003t0008g0058a0001c0003t0008g0059 | 3 | HG02615.hp2 HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-24-14661_-24-1465 others(16): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444302 | |||||
| chr15:44444302
|
T | TACACACA others(7): Show |
1 | a0001c0003t0008g0063 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-24-14663_-24-1465 others(18): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444302 | |||||
| chr15:44444302
|
TAC | T | 29 | a0001c0001t0001g0097a0001c0001t0001g0195a0001c0001t0002g0080others(26): Show | 29 | HG00642.hp2 HG00735.hp2 HG02040.hp1 others(26): Show |
intron_variant | MODIFIER | c.-24-14651_-24-1465 others(6): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444302 | |||||
| chr15:44444302
|
TACAC | T | 4 | a0001c0001t0001g0191a0001c0001t0002g0149a0001c0001t0004g0151others(1): Show | 4 | HG00673.hp2 HG02074.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-14653_-24-1465 others(8): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444302 | |||||
| chr15:44444302
|
TACACACA others(7): Show |
T | 6 | a0001c0001t0003g0007a0001c0001t0003g0011a0001c0001t0003g0012others(3): Show | 6 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24-14663_-24-1465 others(18): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444302 | |||||
| chr15:44444302
|
TACACACA others(11): Show |
T | 1 | a0001c0001t0001g0091 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-24-14667_-24-1465 others(22): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444302 | |||||
| chr15:44444342
|
G | C | 2 | a0001c0001t0001g0070a0001c0001t0002g0137 | 2 | HG04228.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-24-14649G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44444342 | ||||||
| chr15:44444510
|
A | G | 2 | a0001c0001t0016g0188a0001c0001t0016g0189 | 2 | HG00738.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-24-14481A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44444510 | ||||||
| chr15:44444588
|
T | C | 1 | a0001c0001t0002g0217 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-24-14403T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44444588 | ||||||
| chr15:44444731
|
GT | G | 44 | a0001c0001t0001g0162a0001c0001t0003g0019a0001c0001t0003g0020others(41): Show | 44 | HG01891.hp2 HG02040.hp1 HG02055.hp1 others(41): Show |
intron_variant | MODIFIER | c.-24-14244delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444731 | |||||
| chr15:44444836
|
G | GT | 66 | a0001c0001t0001g0037a0001c0001t0001g0073a0001c0001t0001g0078others(63): Show | 66 | HG00423.hp2 HG00735.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.-24-14125dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444836 | |||||
| chr15:44444836
|
G | GTT | 10 | a0001c0001t0001g0144a0001c0001t0001g0147a0001c0001t0001g0162others(7): Show | 10 | HG01981.hp2 HG02109.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24-14126_-24-1412 others(6): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444836 | |||||
| chr15:44444836
|
G | GTTT | 6 | a0001c0001t0001g0082a0001c0001t0001g0164a0001c0001t0001g0193others(3): Show | 6 | HG00408.hp1 HG01884.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24-14127_-24-1412 others(7): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444836 | |||||
| chr15:44444836
|
G | GTTTT | 5 | a0001c0001t0001g0145a0001c0001t0001g0160a0001c0001t0009g0026others(2): Show | 5 | HG01074.hp1 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-24-14128_-24-1412 others(8): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444836 | |||||
| chr15:44444836
|
G | GTTTTTTT | 5 | a0001c0001t0003g0009a0001c0001t0003g0013a0001c0001t0003g0017others(2): Show | 5 | HG00735.hp2 HG03225.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24-14131_-24-1412 others(11): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444836 | |||||
| chr15:44444836
|
G | GTTTTTTT others(3): Show |
3 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0023 | 3 | HG03209.hp1 NA18949.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.-24-14134_-24-1412 others(14): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444836 | |||||
| chr15:44444836
|
G | GTTTTTTT others(4): Show |
2 | a0001c0001t0011g0051a0001c0001t0011g0052 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-24-14135_-24-1412 others(15): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444836 | |||||
| chr15:44444836
|
G | GTTTTTTT others(5): Show |
1 | a0001c0001t0011g0053 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-24-14136_-24-1412 others(16): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444836 | |||||
| chr15:44444836
|
G | GTTTTTTT others(6): Show |
2 | a0001c0001t0003g0003a0001c0001t0003g0018 | 2 | HG00673.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-24-14137_-24-1412 others(17): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444836 | |||||
| chr15:44444836
|
G | GTTTTTTT others(7): Show |
2 | a0001c0001t0003g0004a0001c0001t0011g0054 | 2 | HG02602.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-24-14138_-24-1412 others(18): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444836 | |||||
| chr15:44444836
|
GT | G | 6 | a0001c0001t0001g0086a0001c0001t0002g0125a0001c0002t0005g0033others(3): Show | 6 | HG01358.hp2 HG02922.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24-14125delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444836 | |||||
| chr15:44444836
|
GTTTTTTT others(3): Show |
G | 2 | a0001c0001t0003g0019a0001c0001t0009g0029 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-24-14134_-24-1412 others(14): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444836 | |||||
| chr15:44444836
|
GTTTTTTT others(6): Show |
G | 9 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(6): Show | 9 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-24-14137_-24-1412 others(17): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444836 | |||||
| chr15:44444836
|
GTTTTTTT others(7): Show |
G | 1 | a0001c0001t0012g0066 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-24-14138_-24-1412 others(18): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44444836 | |||||
| chr15:44444870
|
C | T | 1 | a0001c0001t0003g0004 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-24-14121C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44444870 | ||||||
| chr15:44444892
|
G | A | 1 | a0001c0001t0004g0150 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-24-14099G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44444892 | ||||||
| chr15:44444950
|
C | T | 2 | a0001c0001t0003g0020a0001c0001t0003g0021 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-24-14041C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44444950 | ||||||
| chr15:44445000
|
T | C | 54 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 54 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.-24-13991T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44445000 | ||||||
| chr15:44445046
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-24-13945G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44445046 | ||||||
| chr15:44445086
|
C | T | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-24-13905C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44445086 | ||||||
| chr15:44445134
|
C | A | 4 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0002g0204others(1): Show | 4 | HG01243.hp2 HG01884.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24-13857C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44445134 | ||||||
| chr15:44445248
|
C | T | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-24-13743C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44445248 | ||||||
| chr15:44445378
|
C | T | 3 | a0001c0003t0010g0055a0001c0003t0010g0057a0001c0003t0010g0064 | 3 | HG03516.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-24-13613C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44445378 | ||||||
| chr15:44445474
|
G | A | 1 | a0001c0002t0005g0041 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-24-13517G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44445474 | ||||||
| chr15:44445496
|
C | G | 3 | a0001c0003t0010g0055a0001c0003t0010g0057a0001c0003t0010g0064 | 3 | HG03516.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-24-13495C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44445496 | ||||||
| chr15:44445534
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-24-13457G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44445534 | ||||||
| chr15:44445673
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-24-13318T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44445673 | ||||||
| chr15:44445895
|
T | C | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.-24-13096T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44445895 | ||||||
| chr15:44445897
|
A | G | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-24-13094A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44445897 | ||||||
| chr15:44445898
|
A | G | 8 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-24-13093A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44445898 | ||||||
| chr15:44445900
|
C | G | 62 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(59): Show | 62 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.-24-13091C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44445900 | ||||||
| chr15:44445931
|
C | T | 42 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-24-13060C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44445931 | ||||||
| chr15:44445936
|
C | CT | 17 | a0001c0001t0001g0072a0001c0001t0001g0106a0001c0001t0001g0115others(14): Show | 17 | HG01243.hp1 HG01358.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-24-13038dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44445936 | |||||
| chr15:44445956
|
C | T | 1 | a0001c0001t0012g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-24-13035C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44445956 | ||||||
| chr15:44446006
|
G | A | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.-24-12985G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44446006 | ||||||
| chr15:44446152
|
CTGACCTC others(1): Show |
C | 2 | a0001c0001t0001g0141a0001c0001t0001g0145 | 2 | HG01074.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-24-12835_-24-1282 others(12): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44446152 | |||||
| chr15:44446157
|
C | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0147 | 2 | HG01981.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-24-12834C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44446157 | ||||||
| chr15:44446163
|
A | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0145 | 2 | HG01074.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-24-12828A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44446163 | ||||||
| chr15:44446321
|
A | G | 1 | a0001c0001t0026g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-24-12670A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44446321 | ||||||
| chr15:44446400
|
G | A | 19 | a0001c0001t0014g0225a0001c0002t0005g0031a0001c0002t0005g0032others(16): Show | 19 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-24-12591G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44446400 | ||||||
| chr15:44446446
|
G | A | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-24-12545G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44446446 | ||||||
| chr15:44446587
|
A | T | 1 | a0001c0001t0001g0122 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-24-12404A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44446587 | ||||||
| chr15:44446636
|
T | A | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.-24-12355T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44446636 | ||||||
| chr15:44446679
|
A | G | 1 | a0001c0001t0001g0099 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-24-12312A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44446679 | ||||||
| chr15:44446754
|
CT | C | 202 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0070others(199): Show | 202 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.-24-12218delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44446754 | |||||
| chr15:44446849
|
G | A | 3 | a0001c0001t0002g0126a0001c0001t0002g0213a0001c0001t0002g0214 | 3 | HG01167.hp1 HG01192.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-24-12142G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44446849 | ||||||
| chr15:44446974
|
C | T | 4 | a0001c0001t0012g0065a0001c0001t0012g0066a0001c0001t0017g0001others(1): Show | 4 | HG01891.hp2 HG02109.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-12017C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44446974 | ||||||
| chr15:44447096
|
A | G | 3 | a0001c0003t0008g0059a0001c0003t0008g0061a0001c0003t0008g0063 | 3 | HG02615.hp2 HG02630.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-24-11895A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44447096 | ||||||
| chr15:44447581
|
A | G | 1 | a0001c0002t0005g0040 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-24-11410A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44447581 | ||||||
| chr15:44447681
|
T | C | 62 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(59): Show | 62 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.-24-11310T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44447681 | ||||||
| chr15:44447822
|
C | T | 1 | a0001c0001t0024g0010 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-24-11169C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44447822 | ||||||
| chr15:44447928
|
C | T | 1 | a0001c0001t0001g0122 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-24-11063C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44447928 | ||||||
| chr15:44447952
|
C | T | 1 | a0001c0001t0003g0002 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-24-11039C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44447952 | ||||||
| chr15:44448100
|
C | A | 1 | a0003c0006t0010g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-24-10891C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44448100 | ||||||
| chr15:44448155
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.-24-10836C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44448155 | ||||||
| chr15:44448224
|
C | T | 1 | a0001c0001t0002g0180 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-24-10767C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44448224 | ||||||
| chr15:44448450
|
G | A | 67 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(64): Show | 67 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.-24-10541G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44448450 | ||||||
| chr15:44448617
|
G | A | 12 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(9): Show | 12 | HG02040.hp1 HG02155.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.-24-10374G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44448617 | ||||||
| chr15:44448661
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-24-10330A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44448661 | ||||||
| chr15:44448760
|
C | T | 1 | a0001c0001t0007g0194 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-24-10231C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44448760 | ||||||
| chr15:44448795
|
G | A | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-24-10196G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44448795 | ||||||
| chr15:44448801
|
T | C | 1 | a0001c0001t0011g0054 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-24-10190T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44448801 | ||||||
| chr15:44448921
|
T | G | 1 | a0001c0001t0001g0107 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-24-10070T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44448921 | ||||||
| chr15:44449129
|
A | G | 1 | a0001c0001t0007g0194 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-24-9862A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44449129 | ||||||
| chr15:44449372
|
T | G | 74 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0081others(71): Show | 74 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.-24-9619T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44449372 | ||||||
| chr15:44449402
|
C | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | HG00642.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-24-9589C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44449402 | ||||||
| chr15:44449442
|
C | G | 1 | a0001c0001t0001g0156 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-24-9549C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44449442 | ||||||
| chr15:44449641
|
A | G | 42 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-24-9350A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44449641 | ||||||
| chr15:44449693
|
A | G | 1 | a0001c0001t0002g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-24-9298A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44449693 | ||||||
| chr15:44449716
|
G | A | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-24-9275G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44449716 | ||||||
| chr15:44449720
|
T | C | 3 | a0001c0003t0010g0055a0001c0003t0010g0057a0001c0003t0010g0064 | 3 | HG03516.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-24-9271T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44449720 | ||||||
| chr15:44449755
|
T | C | 2 | a0001c0001t0006g0101a0001c0001t0028g0100 | 2 | NA18952.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-24-9236T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44449755 | ||||||
| chr15:44449807
|
A | G | 2 | a0001c0001t0012g0065a0001c0001t0012g0066 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-24-9184A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44449807 | ||||||
| chr15:44449945
|
T | G | 1 | a0001c0001t0014g0038 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-24-9046T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44449945 | ||||||
| chr15:44449947
|
C | T | 1 | a0001c0003t0008g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-24-9044C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44449947 | ||||||
| chr15:44449988
|
C | CA | 158 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0070others(155): Show | 158 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(155): Show |
intron_variant | MODIFIER | c.-24-8989dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44449988 | |||||
| chr15:44449988
|
CA | C | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24-8989delA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44449988 | |||||
| chr15:44450024
|
A | G | 25 | a0001c0001t0001g0096a0001c0001t0001g0122a0001c0001t0001g0143others(22): Show | 25 | HG00642.hp1 HG00738.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.-24-8967A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44450024 | ||||||
| chr15:44450440
|
A | C | 2 | a0001c0002t0005g0039a0001c0002t0005g0044 | 2 | NA18960.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-24-8551A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44450440 | ||||||
| chr15:44450572
|
TA | T | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24-8415delA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44450572 | |||||
| chr15:44450577
|
G | T | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24-8414G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44450577 | ||||||
| chr15:44450589
|
A | AT | 17 | a0001c0001t0001g0181a0001c0001t0003g0002a0001c0001t0003g0006others(14): Show | 17 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-24-8377dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44450589 | |||||
| chr15:44450589
|
AT | A | 97 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0070others(94): Show | 97 | HG00408.hp2 HG00642.hp1 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.-24-8377delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44450589 | |||||
| chr15:44450589
|
ATT | A | 6 | a0001c0001t0001g0095a0001c0001t0001g0158a0001c0001t0001g0163others(3): Show | 6 | HG01255.hp1 HG02809.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-24-8378_-24-8377d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44450589 | |||||
| chr15:44450589
|
ATTT | A | 5 | a0001c0001t0011g0051a0001c0001t0011g0052a0001c0001t0011g0053others(2): Show | 5 | HG02970.hp2 HG03098.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24-8379_-24-8377d others(5): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44450589 | |||||
| chr15:44450682
|
C | T | 1 | a0001c0001t0003g0007 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-24-8309C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44450682 | ||||||
| chr15:44450759
|
C | T | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-24-8232C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44450759 | ||||||
| chr15:44450938
|
T | C | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-24-8053T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44450938 | ||||||
| chr15:44451385
|
C | T | 1 | a0001c0001t0003g0017 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-24-7606C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44451385 | ||||||
| chr15:44451637
|
T | G | 1 | a0001c0001t0009g0026 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-24-7354T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44451637 | ||||||
| chr15:44451744
|
G | A | 1 | a0001c0001t0014g0038 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-24-7247G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44451744 | ||||||
| chr15:44451779
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-24-7212A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44451779 | ||||||
| chr15:44451820
|
C | G | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.-24-7171C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44451820 | ||||||
| chr15:44451859
|
A | T | 1 | a0001c0001t0001g0097 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-24-7132A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44451859 | ||||||
| chr15:44452411
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.-24-6580C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44452411 | ||||||
| chr15:44453026
|
A | G | 42 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.-24-5965A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44453026 | ||||||
| chr15:44453534
|
T | C | 1 | a0001c0001t0001g0218 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-24-5457T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44453534 | ||||||
| chr15:44453575
|
T | TC | 19 | a0001c0001t0001g0092a0001c0001t0001g0098a0001c0001t0001g0115others(16): Show | 19 | HG00597.hp2 HG00642.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.-24-5409dupC | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44453575 | |||||
| chr15:44453589
|
C | T | 8 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.-24-5402C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44453589 | ||||||
| chr15:44453734
|
G | A | 4 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-24-5257G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44453734 | ||||||
| chr15:44454288
|
G | A | 4 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-4703G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44454288 | ||||||
| chr15:44454328
|
C | A | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-24-4663C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44454328 | ||||||
| chr15:44454558
|
A | G | 1 | a0001c0001t0014g0038 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-24-4433A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44454558 | ||||||
| chr15:44454770
|
A | T | 122 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0070others(119): Show | 122 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.-24-4221A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44454770 | ||||||
| chr15:44454773
|
C | T | 122 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0070others(119): Show | 122 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.-24-4218C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44454773 | ||||||
| chr15:44454775
|
C | T | 2 | a0001c0001t0016g0188a0001c0001t0016g0189 | 2 | HG00738.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-24-4216C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44454775 | ||||||
| chr15:44454859
|
G | A | 10 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(7): Show | 10 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-24-4132G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44454859 | ||||||
| chr15:44455034
|
C | T | 13 | a0001c0001t0001g0132a0001c0001t0001g0141a0001c0001t0001g0145others(10): Show | 13 | HG01074.hp1 HG02015.hp2 HG02300.hp1 others(10): Show |
intron_variant | MODIFIER | c.-24-3957C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44455034 | ||||||
| chr15:44455147
|
G | T | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-24-3844G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44455147 | ||||||
| chr15:44455186
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-24-3805A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44455186 | ||||||
| chr15:44455385
|
C | T | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24-3606C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44455385 | ||||||
| chr15:44455481
|
G | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0193 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-24-3510G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44455481 | ||||||
| chr15:44455494
|
G | A | 1 | a0003c0006t0010g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-24-3497G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44455494 | ||||||
| chr15:44455511
|
G | A | 2 | a0001c0001t0016g0188a0001c0001t0016g0189 | 2 | HG00738.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-24-3480G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44455511 | ||||||
| chr15:44455599
|
A | G | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-24-3392A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44455599 | ||||||
| chr15:44455699
|
T | C | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24-3292T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44455699 | ||||||
| chr15:44455774
|
G | C | 54 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 54 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.-24-3217G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44455774 | ||||||
| chr15:44455839
|
A | AT | 20 | a0001c0001t0001g0073a0001c0001t0001g0078a0001c0001t0001g0088others(17): Show | 20 | HG00597.hp2 HG00642.hp2 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.-24-3122dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44455839 | |||||
| chr15:44455839
|
A | ATT | 5 | a0001c0001t0001g0176a0001c0001t0001g0227a0001c0001t0009g0027others(2): Show | 5 | HG01081.hp2 HG02055.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24-3123_-24-3122d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44455839 | |||||
| chr15:44455839
|
AT | A | 80 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0091others(77): Show | 80 | HG00408.hp2 HG00735.hp1 HG00738.hp2 others(77): Show |
intron_variant | MODIFIER | c.-24-3122delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44455839 | |||||
| chr15:44455839
|
ATT | A | 32 | a0001c0001t0001g0196a0001c0001t0002g0180a0001c0001t0002g0183others(29): Show | 32 | HG00423.hp2 HG02040.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.-24-3123_-24-3122d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44455839 | |||||
| chr15:44455839
|
ATTT | A | 24 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(21): Show | 24 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.-24-3124_-24-3122d others(5): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44455839 | |||||
| chr15:44455875
|
G | T | 1 | a0001c0001t0001g0193 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-24-3116G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44455875 | ||||||
| chr15:44455882
|
C | T | 1 | a0001c0001t0009g0026 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-24-3109C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44455882 | ||||||
| chr15:44455952
|
G | A | 1 | a0001c0001t0004g0139 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-24-3039G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44455952 | ||||||
| chr15:44456072
|
G | A | 24 | a0001c0001t0001g0122a0001c0001t0001g0143a0001c0001t0001g0154others(21): Show | 24 | HG00642.hp1 HG00738.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-24-2919G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456072 | ||||||
| chr15:44456129
|
C | T | 1 | a0001c0001t0003g0003 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-24-2862C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456129 | ||||||
| chr15:44456140
|
G | A | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24-2851G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456140 | ||||||
| chr15:44456180
|
C | T | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | HG01081.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-24-2811C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456180 | ||||||
| chr15:44456221
|
C | T | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24-2770C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456221 | ||||||
| chr15:44456428
|
T | G | 1 | a0001c0001t0001g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-24-2563T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456428 | ||||||
| chr15:44456471
|
A | T | 4 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0001g0164others(1): Show | 4 | HG01884.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-2520A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456471 | ||||||
| chr15:44456664
|
A | C | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-24-2327A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456664 | ||||||
| chr15:44456698
|
G | T | 1 | a0001c0001t0001g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-24-2293G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456698 | ||||||
| chr15:44456707
|
A | AT | 19 | a0001c0001t0002g0126a0001c0001t0003g0002a0001c0001t0003g0003others(16): Show | 19 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.-24-2276dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44456707 | |||||
| chr15:44456853
|
C | CT | 6 | a0001c0001t0001g0154a0001c0001t0001g0174a0001c0001t0001g0175others(3): Show | 6 | HG00642.hp1 HG02572.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24-2126dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44456853 | |||||
| chr15:44456866
|
C | T | 1 | a0001c0003t0008g0058 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-24-2125C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456866 | ||||||
| chr15:44456878
|
G | T | 63 | a0001c0001t0002g0184a0001c0001t0003g0002a0001c0001t0003g0003others(60): Show | 63 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.-24-2113G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456878 | ||||||
| chr15:44456881
|
T | C | 11 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(8): Show | 11 | HG00423.hp1 HG00673.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.-24-2110T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456881 | ||||||
| chr15:44456881
|
T | G | 32 | a0001c0001t0003g0019a0001c0001t0003g0020a0001c0001t0003g0021others(29): Show | 32 | HG01891.hp1 HG02040.hp1 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.-24-2110T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456881 | ||||||
| chr15:44456881
|
T | TC | 4 | a0001c0001t0003g0007a0001c0001t0003g0011a0001c0001t0003g0012others(1): Show | 4 | HG00408.hp1 HG00597.hp1 NA18992.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-2110_-24-2109i others(3): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456881 | ||||||
| chr15:44456881
|
T | TG | 5 | a0001c0001t0003g0002a0001c0001t0011g0051a0001c0001t0011g0052others(2): Show | 5 | HG02970.hp2 HG03098.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24-2110_-24-2109i others(3): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456881 | ||||||
| chr15:44456881
|
T | TTG | 9 | a0001c0003t0008g0059a0001c0003t0008g0060a0001c0003t0008g0061others(6): Show | 9 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-24-2109_-24-2108i others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44456881 | |||||
| chr15:44456882
|
T | C | 1 | a0001c0001t0003g0013 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-24-2109T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456882 | ||||||
| chr15:44456888
|
C | G | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.-24-2103C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456888 | ||||||
| chr15:44456940
|
G | A | 4 | a0001c0001t0012g0065a0001c0001t0012g0066a0001c0001t0017g0001others(1): Show | 4 | HG01891.hp2 HG02109.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-2051G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456940 | ||||||
| chr15:44456955
|
C | T | 1 | a0001c0002t0005g0045 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-24-2036C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44456955 | ||||||
| chr15:44457024
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-24-1967G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44457024 | ||||||
| chr15:44457325
|
C | G | 1 | a0001c0001t0002g0216 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-24-1666C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44457325 | ||||||
| chr15:44457344
|
C | T | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-24-1647C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44457344 | ||||||
| chr15:44457401
|
C | T | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.-24-1590C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44457401 | ||||||
| chr15:44457452
|
T | G | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-24-1539T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44457452 | ||||||
| chr15:44457525
|
A | C | 1 | a0001c0001t0025g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-24-1466A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44457525 | ||||||
| chr15:44457555
|
CTTTGTTA others(12): Show |
C | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-24-1433_-24-1415d others(21): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44457555 | |||||
| chr15:44457599
|
T | TG | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.-24-1384dupG | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr15 | 44457599 | |||||
| chr15:44457656
|
A | T | 1 | a0001c0002t0005g0041 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-24-1335A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44457656 | ||||||
| chr15:44457672
|
T | C | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.-24-1319T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44457672 | ||||||
| chr15:44457704
|
C | T | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-24-1287C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44457704 | ||||||
| chr15:44457768
|
C | G | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.-24-1223C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44457768 | ||||||
| chr15:44457984
|
C | G | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-24-1007C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44457984 | ||||||
| chr15:44458093
|
C | T | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.-24-898C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44458093 | ||||||
| chr15:44458136
|
G | A | 1 | a0001c0001t0020g0167 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-24-855G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44458136 | ||||||
| chr15:44458246
|
C | T | 1 | a0001c0002t0005g0050 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-24-745C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44458246 | ||||||
| chr15:44458321
|
G | A | 1 | a0001c0001t0014g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-24-670G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44458321 | ||||||
| chr15:44458400
|
A | G | 19 | a0001c0001t0014g0225a0001c0002t0005g0031a0001c0002t0005g0032others(16): Show | 19 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.-24-591A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44458400 | ||||||
| chr15:44458492
|
A | G | 1 | a0001c0001t0002g0152 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-24-499A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44458492 | ||||||
| chr15:44458655
|
C | T | 1 | a0001c0001t0003g0002 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-24-336C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44458655 | ||||||
| chr15:44458695
|
A | G | 1 | a0001c0001t0026g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-24-296A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 1/12 | chr15 | 44458695 | ||||||
| chr15:44459266
|
G | A | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.186+66G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44459266 | ||||||
| chr15:44459276
|
C | G | 1 | a0001c0001t0003g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.186+76C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44459276 | ||||||
| chr15:44459309
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.186+109C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44459309 | ||||||
| chr15:44459310
|
G | A | 8 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.186+110G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44459310 | ||||||
| chr15:44459312
|
G | C | 1 | a0001c0001t0003g0002 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.186+112G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44459312 | ||||||
| chr15:44459354
|
C | T | 1 | a0001c0001t0003g0002 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.186+154C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44459354 | ||||||
| chr15:44459465
|
C | T | 1 | a0001c0001t0022g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.186+265C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44459465 | ||||||
| chr15:44459494
|
C | T | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.186+294C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44459494 | ||||||
| chr15:44459637
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.186+437A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44459637 | ||||||
| chr15:44459693
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.186+493G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44459693 | ||||||
| chr15:44459752
|
T | G | 1 | a0001c0001t0001g0074 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.186+552T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44459752 | ||||||
| chr15:44459832
|
A | T | 1 | a0001c0001t0004g0192 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.186+632A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44459832 | ||||||
| chr15:44459840
|
C | G | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.186+640C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44459840 | ||||||
| chr15:44460045
|
A | G | 18 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(15): Show | 18 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.186+845A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44460045 | ||||||
| chr15:44460180
|
C | T | 8 | a0001c0002t0005g0039a0001c0002t0005g0044a0001c0002t0005g0045others(5): Show | 8 | HG02040.hp1 HG02155.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.186+980C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44460180 | ||||||
| chr15:44460225
|
C | G | 1 | a0001c0001t0012g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.186+1025C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44460225 | ||||||
| chr15:44460305
|
T | C | 1 | a0001c0001t0001g0124 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.186+1105T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44460305 | ||||||
| chr15:44460333
|
C | T | 1 | a0001c0001t0012g0065 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.186+1133C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44460333 | ||||||
| chr15:44460359
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.186+1159C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44460359 | ||||||
| chr15:44460360
|
G | A | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.186+1160G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44460360 | ||||||
| chr15:44460389
|
T | C | 1 | a0001c0001t0002g0148 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.186+1189T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44460389 | ||||||
| chr15:44460397
|
C | T | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.186+1197C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44460397 | ||||||
| chr15:44460506
|
T | G | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.186+1306T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44460506 | ||||||
| chr15:44460507
|
A | G | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.186+1307A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44460507 | ||||||
| chr15:44460711
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0004g0123 | 2 | NA18944.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.186+1511G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44460711 | ||||||
| chr15:44460971
|
C | CT | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.186+1775dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44460971 | |||||
| chr15:44460980
|
T | G | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.186+1780T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44460980 | ||||||
| chr15:44461064
|
A | G | 1 | a0001c0001t0022g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.186+1864A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44461064 | ||||||
| chr15:44461461
|
T | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0081 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.186+2261T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44461461 | ||||||
| chr15:44461511
|
C | A | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.186+2311C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44461511 | ||||||
| chr15:44461573
|
CT | C | 15 | a0001c0001t0001g0067a0001c0001t0001g0091a0001c0001t0001g0105others(12): Show | 15 | HG00408.hp2 HG00423.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.186+2397delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44461573 | |||||
| chr15:44461573
|
CTT | C | 27 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(24): Show | 27 | HG00408.hp1 HG00597.hp1 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.186+2396_186+2397d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44461573 | |||||
| chr15:44461573
|
CTTT | C | 22 | a0001c0001t0003g0012a0001c0001t0003g0013a0001c0001t0003g0018others(19): Show | 22 | HG02040.hp1 HG02055.hp1 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.186+2395_186+2397d others(5): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44461573 | |||||
| chr15:44461573
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.186+2386_186+2397d others(14): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44461573 | |||||
| chr15:44461623
|
G | A | 4 | a0001c0001t0012g0065a0001c0001t0012g0066a0001c0001t0017g0001others(1): Show | 4 | HG01891.hp2 HG02109.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.186+2423G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44461623 | ||||||
| chr15:44461817
|
G | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0081 | 2 | HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.186+2617G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44461817 | ||||||
| chr15:44461880
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.186+2680A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44461880 | ||||||
| chr15:44462006
|
A | G | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.186+2806A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44462006 | ||||||
| chr15:44462036
|
A | G | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.186+2836A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44462036 | ||||||
| chr15:44462219
|
G | A | 6 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0232others(3): Show | 6 | HG02015.hp2 NA18949.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.186+3019G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44462219 | ||||||
| chr15:44462358
|
T | C | 8 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.186+3158T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44462358 | ||||||
| chr15:44462475
|
A | T | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.186+3275A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44462475 | ||||||
| chr15:44462616
|
C | G | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.186+3416C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44462616 | ||||||
| chr15:44462637
|
G | A | 1 | a0004c0007t0002g0076 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.186+3437G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44462637 | ||||||
| chr15:44462661
|
G | A | 1 | a0001c0001t0007g0129 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.186+3461G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44462661 | ||||||
| chr15:44462700
|
C | CT | 23 | a0001c0001t0001g0090a0001c0001t0001g0118a0001c0001t0001g0130others(20): Show | 23 | HG00741.hp1 HG00741.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.186+3524dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44462700 | |||||
| chr15:44462700
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0017g0001a0001c0002t0005g0045 | 2 | HG02109.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.186+3513_186+3524d others(14): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44462700 | |||||
| chr15:44462700
|
C | CTTTTTTT others(6): Show |
8 | a0001c0001t0018g0030a0001c0002t0005g0039a0001c0002t0005g0046others(5): Show | 8 | HG02040.hp1 HG02155.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.186+3512_186+3524d others(15): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44462700 | |||||
| chr15:44462700
|
C | CTTTTTTT others(7): Show |
7 | a0001c0002t0005g0044a0001c0003t0008g0058a0001c0003t0008g0061others(4): Show | 7 | HG02630.hp2 HG02886.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.186+3511_186+3524d others(16): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44462700 | |||||
| chr15:44462700
|
C | CTTTTTTT others(8): Show |
1 | a0001c0003t0008g0060 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.186+3510_186+3524d others(17): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44462700 | |||||
| chr15:44462700
|
C | CTTTTTTT others(9): Show |
1 | a0001c0003t0010g0064 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.186+3509_186+3524d others(18): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44462700 | |||||
| chr15:44462700
|
CT | C | 30 | a0001c0001t0001g0082a0001c0001t0001g0091a0001c0001t0001g0103others(27): Show | 30 | HG01074.hp1 HG01074.hp2 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.186+3524delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44462700 | |||||
| chr15:44462700
|
CTTTTTTT others(2): Show |
C | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.186+3516_186+3524d others(11): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44462700 | |||||
| chr15:44462737
|
T | A | 1 | a0001c0001t0004g0168 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.186+3537T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44462737 | ||||||
| chr15:44462753
|
G | C | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.186+3553G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44462753 | ||||||
| chr15:44462849
|
G | A | 1 | a0004c0007t0002g0076 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.186+3649G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44462849 | ||||||
| chr15:44462865
|
C | A | 1 | a0001c0001t0003g0002 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.186+3665C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44462865 | ||||||
| chr15:44463130
|
T | C | 1 | a0003c0006t0010g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.186+3930T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44463130 | ||||||
| chr15:44463303
|
G | A | 1 | a0001c0002t0005g0035 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.186+4103G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44463303 | ||||||
| chr15:44463383
|
C | T | 1 | a0001c0001t0002g0137 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.186+4183C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44463383 | ||||||
| chr15:44463483
|
A | C | 42 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.186+4283A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44463483 | ||||||
| chr15:44463522
|
A | T | 1 | a0001c0001t0014g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.186+4322A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44463522 | ||||||
| chr15:44463571
|
A | G | 1 | a0001c0001t0024g0010 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.186+4371A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44463571 | ||||||
| chr15:44463614
|
C | G | 1 | a0001c0001t0014g0038 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.186+4414C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44463614 | ||||||
| chr15:44463620
|
A | G | 1 | a0001c0001t0002g0134 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.186+4420A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44463620 | ||||||
| chr15:44463787
|
C | T | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.186+4587C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44463787 | ||||||
| chr15:44464070
|
C | T | 42 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.186+4870C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44464070 | ||||||
| chr15:44464128
|
G | C | 1 | a0001c0001t0001g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.186+4928G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44464128 | ||||||
| chr15:44464188
|
T | C | 2 | a0001c0001t0006g0102a0001c0001t0006g0113 | 2 | HG01167.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.186+4988T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44464188 | ||||||
| chr15:44464436
|
G | A | 1 | a0001c0001t0022g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.186+5236G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44464436 | ||||||
| chr15:44464508
|
A | C | 1 | a0001c0001t0002g0087 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.186+5308A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44464508 | ||||||
| chr15:44464520
|
G | A | 44 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(41): Show | 44 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.186+5320G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44464520 | ||||||
| chr15:44464589
|
T | G | 1 | a0001c0001t0006g0135 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.186+5389T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44464589 | ||||||
| chr15:44464680
|
T | C | 5 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(2): Show | 5 | HG02559.hp1 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.186+5480T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44464680 | ||||||
| chr15:44464730
|
A | G | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.186+5530A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44464730 | ||||||
| chr15:44464754
|
T | G | 1 | a0001c0001t0004g0150 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.186+5554T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44464754 | ||||||
| chr15:44464815
|
C | G | 1 | a0001c0001t0014g0038 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.186+5615C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44464815 | ||||||
| chr15:44464859
|
C | A | 1 | a0001c0002t0005g0050 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.186+5659C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44464859 | ||||||
| chr15:44464958
|
GGCCTCCC others(1224): Show |
G | 1 | a0001c0001t0002g0179 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.186+5796_186+7026d others(2): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44464958 | |||||
| chr15:44464983
|
G | A | 3 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0159 | 3 | HG02559.hp1 HG02976.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.186+5783G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44464983 | ||||||
| chr15:44464985
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.186+5785C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44464985 | ||||||
| chr15:44465295
|
A | C | 2 | a0001c0003t0008g0060a0001c0003t0008g0062 | 2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.186+6095A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44465295 | ||||||
| chr15:44465712
|
C | CT | 21 | a0001c0001t0001g0067a0001c0001t0001g0073a0001c0001t0001g0074others(18): Show | 21 | HG00597.hp2 HG01255.hp2 HG01981.hp2 others(18): Show |
intron_variant | MODIFIER | c.186+6532dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44465712 | |||||
| chr15:44465712
|
CT | C | 14 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(11): Show | 14 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.186+6532delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44465712 | |||||
| chr15:44465712
|
CTT | C | 40 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(37): Show | 40 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.186+6531_186+6532d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44465712 | |||||
| chr15:44465853
|
A | T | 1 | a0001c0001t0014g0038 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.186+6653A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44465853 | ||||||
| chr15:44465940
|
CT | C | 37 | a0001c0001t0001g0074a0001c0001t0003g0020a0001c0001t0003g0021others(34): Show | 37 | HG01891.hp1 HG02040.hp1 HG02109.hp1 others(34): Show |
intron_variant | MODIFIER | c.186+6753delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44465940 | |||||
| chr15:44466019
|
C | G | 1 | a0001c0001t0001g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.186+6819C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44466019 | ||||||
| chr15:44466047
|
G | A | 1 | a0001c0001t0007g0185 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.186+6847G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44466047 | ||||||
| chr15:44466138
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.186+6938T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44466138 | ||||||
| chr15:44466227
|
G | A | 24 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(21): Show | 24 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.186+7027G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44466227 | ||||||
| chr15:44466687
|
A | G | 3 | a0001c0003t0010g0055a0001c0003t0010g0057a0001c0003t0010g0064 | 3 | HG03516.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.186+7487A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44466687 | ||||||
| chr15:44466708
|
G | A | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.186+7508G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44466708 | ||||||
| chr15:44466720
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG01256.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.186+7520G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44466720 | ||||||
| chr15:44466754
|
A | G | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.186+7554A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44466754 | ||||||
| chr15:44466776
|
C | CA | 59 | a0001c0001t0001g0072a0001c0001t0001g0110a0001c0001t0001g0111others(56): Show | 59 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.186+7589dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44466776 | |||||
| chr15:44466776
|
CA | C | 24 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(21): Show | 24 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.186+7589delA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44466776 | |||||
| chr15:44466803
|
G | A | 8 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.186+7603G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44466803 | ||||||
| chr15:44466807
|
C | T | 16 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(13): Show | 16 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.186+7607C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44466807 | ||||||
| chr15:44466940
|
A | AAAAAC | 42 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.186+7757_186+7761d others(7): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44466940 | |||||
| chr15:44467058
|
T | C | 2 | a0001c0001t0003g0017a0001c0001t0003g0018 | 2 | NA19007.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.186+7858T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44467058 | ||||||
| chr15:44467125
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0147 | 2 | HG01981.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.186+7925G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44467125 | ||||||
| chr15:44467191
|
C | A | 1 | a0001c0003t0010g0064 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.186+7991C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44467191 | ||||||
| chr15:44467806
|
C | T | 20 | a0001c0001t0014g0038a0001c0001t0014g0225a0001c0002t0005g0031others(17): Show | 20 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.186+8606C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44467806 | ||||||
| chr15:44467875
|
C | G | 2 | a0001c0001t0001g0093a0001c0001t0023g0083 | 2 | HG03491.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.186+8675C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44467875 | ||||||
| chr15:44467963
|
T | A | 1 | a0001c0001t0002g0149 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.186+8763T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44467963 | ||||||
| chr15:44467974
|
G | A | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.186+8774G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44467974 | ||||||
| chr15:44468075
|
G | A | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.186+8875G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44468075 | ||||||
| chr15:44468109
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.186+8909C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44468109 | ||||||
| chr15:44468162
|
G | A | 4 | a0001c0001t0011g0051a0001c0001t0011g0052a0001c0001t0011g0053others(1): Show | 4 | HG02970.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.186+8962G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44468162 | ||||||
| chr15:44468291
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.186+9091G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44468291 | ||||||
| chr15:44468312
|
ACAT | A | 2 | a0001c0001t0012g0065a0001c0001t0012g0066 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.186+9116_186+9118d others(5): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44468312 | |||||
| chr15:44468324
|
G | T | 20 | a0001c0001t0014g0038a0001c0001t0014g0225a0001c0002t0005g0031others(17): Show | 20 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.186+9124G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44468324 | ||||||
| chr15:44468340
|
T | TTAATACT others(3): Show |
2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG01256.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.186+9143_186+9152d others(12): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44468340 | |||||
| chr15:44468615
|
G | T | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.186+9415G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44468615 | ||||||
| chr15:44468674
|
C | G | 1 | a0001c0001t0003g0003 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.186+9474C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44468674 | ||||||
| chr15:44468886
|
C | T | 5 | a0001c0001t0004g0068a0001c0001t0004g0069a0001c0001t0004g0116others(2): Show | 5 | HG02027.hp1 NA18965.hp2 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.186+9686C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44468886 | ||||||
| chr15:44469047
|
C | T | 2 | a0001c0001t0012g0065a0001c0001t0012g0066 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.186+9847C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44469047 | ||||||
| chr15:44469129
|
G | A | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.186+9929G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44469129 | ||||||
| chr15:44469226
|
A | G | 1 | a0001c0001t0002g0127 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.186+10026A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44469226 | ||||||
| chr15:44469330
|
A | AT | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.186+10131dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44469330 | |||||
| chr15:44469610
|
G | T | 19 | a0001c0001t0014g0225a0001c0002t0005g0031a0001c0002t0005g0032others(16): Show | 19 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.186+10410G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44469610 | ||||||
| chr15:44469955
|
G | A | 2 | a0001c0001t0003g0017a0001c0001t0003g0018 | 2 | NA19007.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.186+10755G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44469955 | ||||||
| chr15:44470053
|
A | C | 1 | a0001c0001t0001g0109 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.186+10853A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44470053 | ||||||
| chr15:44470097
|
C | CA | 48 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0001g0086others(45): Show | 48 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.186+10921dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44470097 | |||||
| chr15:44470097
|
CA | C | 37 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(34): Show | 37 | HG01891.hp1 HG01891.hp2 HG02040.hp1 others(34): Show |
intron_variant | MODIFIER | c.186+10921delA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44470097 | |||||
| chr15:44470097
|
CAAA | C | 7 | a0001c0001t0001g0155a0001c0001t0001g0156a0001c0001t0001g0157others(4): Show | 7 | HG02559.hp1 HG02572.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.186+10919_186+1092 others(7): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44470097 | |||||
| chr15:44470138
|
A | G | 2 | a0001c0001t0003g0013a0001c0001t0003g0016 | 2 | NA18953.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.186+10938A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44470138 | ||||||
| chr15:44470142
|
A | G | 4 | a0001c0001t0011g0051a0001c0001t0011g0052a0001c0001t0011g0053others(1): Show | 4 | HG02970.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.186+10942A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44470142 | ||||||
| chr15:44470225
|
A | AC | 62 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(59): Show | 62 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.186+11025_186+1102 others(5): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44470225 | ||||||
| chr15:44470283
|
ACTTGTT | A | 4 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(1): Show | 4 | HG00642.hp1 HG02572.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.186+11090_186+1109 others(10): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44470283 | |||||
| chr15:44470427
|
G | A | 19 | a0001c0001t0014g0225a0001c0002t0005g0031a0001c0002t0005g0032others(16): Show | 19 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.186+11227G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44470427 | ||||||
| chr15:44470614
|
AT | A | 3 | a0001c0001t0001g0072a0001c0001t0002g0148a0001c0001t0004g0231 | 3 | HG02148.hp2 NA18977.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.186+11419delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44470614 | |||||
| chr15:44470614
|
ATT | A | 53 | a0001c0001t0001g0110a0001c0001t0001g0115a0001c0001t0001g0141others(50): Show | 53 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.186+11418_186+1141 others(6): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44470614 | |||||
| chr15:44470867
|
C | T | 1 | a0001c0002t0005g0050 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.186+11667C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44470867 | ||||||
| chr15:44470934
|
T | C | 1 | a0001c0001t0002g0134 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.186+11734T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44470934 | ||||||
| chr15:44471055
|
A | G | 1 | a0003c0006t0010g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.186+11855A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44471055 | ||||||
| chr15:44471079
|
A | G | 2 | a0001c0001t0015g0104a0001c0001t0015g0224 | 2 | NA18986.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.186+11879A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44471079 | ||||||
| chr15:44471132
|
C | T | 2 | a0001c0001t0001g0164a0001c0001t0001g0193 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.186+11932C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44471132 | ||||||
| chr15:44471270
|
A | C | 1 | a0001c0001t0001g0218 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.186+12070A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44471270 | ||||||
| chr15:44471400
|
A | G | 62 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(59): Show | 62 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.186+12200A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44471400 | ||||||
| chr15:44471904
|
A | G | 1 | a0001c0001t0001g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.187-12320A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44471904 | ||||||
| chr15:44471939
|
C | T | 1 | a0001c0001t0006g0084 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.187-12285C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44471939 | ||||||
| chr15:44471971
|
T | TA | 7 | a0001c0002t0005g0044a0001c0002t0005g0045a0001c0002t0005g0046others(4): Show | 7 | HG02040.hp1 HG02155.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.187-12240dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44471971 | |||||
| chr15:44471971
|
TA | T | 7 | a0001c0001t0001g0075a0001c0001t0001g0109a0001c0001t0003g0016others(4): Show | 7 | HG02165.hp2 HG02965.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.187-12240delA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44471971 | |||||
| chr15:44472063
|
G | T | 1 | a0001c0001t0003g0017 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.187-12161G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44472063 | ||||||
| chr15:44472298
|
T | G | 2 | a0001c0001t0001g0099a0001c0001t0006g0094 | 2 | HG02293.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.187-11926T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44472298 | ||||||
| chr15:44472350
|
G | T | 18 | a0001c0002t0005g0031a0001c0002t0005g0032a0001c0002t0005g0033others(15): Show | 18 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.187-11874G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44472350 | ||||||
| chr15:44472404
|
C | T | 42 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.187-11820C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44472404 | ||||||
| chr15:44472526
|
T | C | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.187-11698T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44472526 | ||||||
| chr15:44472543
|
G | GT | 6 | a0001c0001t0001g0120a0001c0001t0001g0128a0001c0001t0003g0006others(3): Show | 6 | HG01891.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.187-11668dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44472543 | |||||
| chr15:44472612
|
C | T | 1 | a0001c0001t0002g0217 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.187-11612C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44472612 | ||||||
| chr15:44472874
|
C | T | 1 | a0001c0001t0001g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.187-11350C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44472874 | ||||||
| chr15:44472940
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.187-11284C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44472940 | ||||||
| chr15:44472952
|
C | T | 4 | a0001c0001t0001g0154a0001c0001t0001g0174a0001c0001t0001g0175others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.187-11272C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44472952 | ||||||
| chr15:44472955
|
C | G | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.187-11269C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44472955 | ||||||
| chr15:44473238
|
G | A | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.187-10986G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44473238 | ||||||
| chr15:44473332
|
A | G | 3 | a0001c0003t0010g0055a0001c0003t0010g0057a0001c0003t0010g0064 | 3 | HG03516.hp2 HG06807.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.187-10892A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44473332 | ||||||
| chr15:44473441
|
G | A | 1 | a0001c0001t0004g0190 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.187-10783G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44473441 | ||||||
| chr15:44473514
|
C | A | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.187-10710C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44473514 | ||||||
| chr15:44473707
|
A | G | 18 | a0001c0002t0005g0031a0001c0002t0005g0032a0001c0002t0005g0033others(15): Show | 18 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.187-10517A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44473707 | ||||||
| chr15:44473743
|
C | G | 4 | a0001c0001t0012g0065a0001c0001t0012g0066a0001c0001t0017g0001others(1): Show | 4 | HG01891.hp2 HG02109.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.187-10481C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44473743 | ||||||
| chr15:44473904
|
C | G | 8 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.187-10320C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44473904 | ||||||
| chr15:44473991
|
G | A | 1 | a0001c0002t0005g0035 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.187-10233G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44473991 | ||||||
| chr15:44474221
|
C | T | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.187-10003C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44474221 | ||||||
| chr15:44474268
|
A | G | 2 | a0001c0001t0012g0065a0001c0001t0012g0066 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.187-9956A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44474268 | ||||||
| chr15:44474364
|
G | A | 19 | a0001c0001t0014g0225a0001c0002t0005g0031a0001c0002t0005g0032others(16): Show | 19 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.187-9860G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44474364 | ||||||
| chr15:44474396
|
C | T | 2 | a0001c0001t0012g0065a0001c0001t0012g0066 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.187-9828C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44474396 | ||||||
| chr15:44474412
|
C | T | 2 | a0001c0002t0005g0039a0001c0002t0005g0044 | 2 | NA18960.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.187-9812C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44474412 | ||||||
| chr15:44474418
|
A | C | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.187-9806A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44474418 | ||||||
| chr15:44474635
|
C | A | 2 | a0001c0001t0015g0104a0001c0001t0015g0224 | 2 | NA18986.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.187-9589C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44474635 | ||||||
| chr15:44474713
|
G | C | 1 | a0001c0001t0002g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.187-9511G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44474713 | ||||||
| chr15:44474717
|
A | G | 1 | a0001c0001t0002g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.187-9507A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44474717 | ||||||
| chr15:44474821
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.187-9403A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44474821 | ||||||
| chr15:44475112
|
C | T | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.187-9112C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44475112 | ||||||
| chr15:44475561
|
C | T | 1 | a0001c0001t0001g0218 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.187-8663C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44475561 | ||||||
| chr15:44475638
|
CA | C | 178 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0070others(175): Show | 178 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(175): Show |
intron_variant | MODIFIER | c.187-8570delA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44475638 | |||||
| chr15:44475638
|
CAA | C | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.187-8571_187-8570d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44475638 | |||||
| chr15:44475754
|
T | C | 4 | a0001c0001t0011g0051a0001c0001t0011g0052a0001c0001t0011g0053others(1): Show | 4 | HG02970.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.187-8470T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44475754 | ||||||
| chr15:44475806
|
G | A | 2 | a0001c0001t0001g0197a0004c0007t0002g0076 | 2 | NA19001.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.187-8418G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44475806 | ||||||
| chr15:44475810
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.187-8414C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44475810 | ||||||
| chr15:44476013
|
G | C | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.187-8211G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44476013 | ||||||
| chr15:44476071
|
A | AT | 46 | a0001c0001t0001g0164a0001c0001t0001g0193a0001c0001t0003g0002others(43): Show | 46 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(43): Show |
intron_variant | MODIFIER | c.187-8144dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44476071 | |||||
| chr15:44476093
|
A | G | 1 | a0001c0002t0005g0035 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.187-8131A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44476093 | ||||||
| chr15:44476213
|
C | T | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.187-8011C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44476213 | ||||||
| chr15:44476214
|
G | A | 1 | a0001c0001t0026g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.187-8010G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44476214 | ||||||
| chr15:44476237
|
T | G | 6 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0029others(3): Show | 6 | HG02572.hp1 HG02895.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.187-7987T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44476237 | ||||||
| chr15:44476269
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.187-7955T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44476269 | ||||||
| chr15:44476308
|
C | T | 5 | a0001c0001t0001g0070a0001c0001t0001g0109a0001c0001t0001g0110others(2): Show | 5 | HG02083.hp2 HG02135.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.187-7916C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44476308 | ||||||
| chr15:44476628
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.187-7596C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44476628 | ||||||
| chr15:44476760
|
T | C | 1 | a0001c0001t0014g0038 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.187-7464T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44476760 | ||||||
| chr15:44476932
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.187-7292C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44476932 | ||||||
| chr15:44476981
|
T | C | 1 | a0001c0001t0022g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.187-7243T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44476981 | ||||||
| chr15:44477017
|
A | G | 25 | a0001c0001t0001g0096a0001c0001t0001g0122a0001c0001t0001g0128others(22): Show | 25 | HG00642.hp1 HG00738.hp2 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.187-7207A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44477017 | ||||||
| chr15:44477086
|
A | G | 44 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(41): Show | 44 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.187-7138A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44477086 | ||||||
| chr15:44477476
|
A | G | 1 | a0001c0001t0002g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.187-6748A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44477476 | ||||||
| chr15:44477532
|
C | CT | 4 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.187-6687dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44477532 | |||||
| chr15:44477537
|
T | TA | 6 | a0001c0001t0004g0168a0001c0001t0012g0065a0001c0001t0012g0066others(3): Show | 6 | HG00408.hp2 HG01891.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.187-6675dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44477537 | |||||
| chr15:44477538
|
A | T | 2 | a0001c0001t0003g0013a0001c0001t0003g0016 | 2 | NA18953.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.187-6686A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44477538 | ||||||
| chr15:44477634
|
C | T | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.187-6590C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44477634 | ||||||
| chr15:44477635
|
A | G | 44 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(41): Show | 44 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.187-6589A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44477635 | ||||||
| chr15:44477707
|
G | A | 42 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.187-6517G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44477707 | ||||||
| chr15:44477857
|
A | C | 1 | a0001c0001t0006g0135 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.187-6367A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44477857 | ||||||
| chr15:44478021
|
A | G | 2 | a0001c0002t0005g0039a0001c0002t0005g0044 | 2 | NA18960.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.187-6203A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44478021 | ||||||
| chr15:44478125
|
AGC | A | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.187-6098_187-6097d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44478125 | ||||||
| chr15:44478184
|
T | C | 44 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(41): Show | 44 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.187-6040T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44478184 | ||||||
| chr15:44478342
|
C | T | 4 | a0001c0001t0012g0065a0001c0001t0012g0066a0001c0001t0017g0001others(1): Show | 4 | HG01891.hp2 HG02109.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.187-5882C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44478342 | ||||||
| chr15:44478379
|
G | A | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.187-5845G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44478379 | ||||||
| chr15:44478417
|
A | C | 4 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.187-5807A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44478417 | ||||||
| chr15:44478443
|
ACT | A | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.187-5778_187-5777d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44478443 | |||||
| chr15:44478452
|
CA | C | 57 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0081others(54): Show | 57 | HG00423.hp2 HG00597.hp2 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.187-5741delA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44478452 | |||||
| chr15:44478452
|
CAA | C | 62 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0088others(59): Show | 62 | HG00741.hp1 HG01071.hp1 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.187-5742_187-5741d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44478452 | |||||
| chr15:44478452
|
CAAA | C | 32 | a0001c0001t0001g0082a0001c0001t0001g0122a0001c0001t0001g0128others(29): Show | 32 | HG00642.hp1 HG00738.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.187-5743_187-5741d others(5): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44478452 | |||||
| chr15:44478452
|
CAAAA | C | 9 | a0001c0001t0001g0196a0001c0001t0003g0005a0001c0001t0003g0011others(6): Show | 9 | HG00408.hp1 HG01891.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.187-5744_187-5741d others(6): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44478452 | |||||
| chr15:44478452
|
CAAAAA | C | 23 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(20): Show | 23 | HG00423.hp1 HG00597.hp1 HG00673.hp1 others(20): Show |
intron_variant | MODIFIER | c.187-5745_187-5741d others(7): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44478452 | |||||
| chr15:44478452
|
CAAAAAAA others(3): Show |
C | 24 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(21): Show | 24 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.187-5750_187-5741d others(12): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44478452 | |||||
| chr15:44478684
|
A | G | 2 | a0001c0001t0002g0221a0001c0001t0002g0223 | 2 | HG01192.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.187-5540A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44478684 | ||||||
| chr15:44478807
|
C | A | 1 | a0001c0001t0001g0096 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.187-5417C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44478807 | ||||||
| chr15:44478812
|
T | C | 2 | a0001c0001t0012g0065a0001c0001t0012g0066 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.187-5412T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44478812 | ||||||
| chr15:44478843
|
G | A | 5 | a0001c0001t0001g0154a0001c0001t0001g0174a0001c0001t0001g0175others(2): Show | 5 | HG00642.hp1 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.187-5381G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44478843 | ||||||
| chr15:44479062
|
A | T | 1 | a0001c0001t0001g0220 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.187-5162A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44479062 | ||||||
| chr15:44479065
|
A | C | 2 | a0001c0001t0003g0017a0001c0001t0003g0018 | 2 | NA19007.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.187-5159A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44479065 | ||||||
| chr15:44479077
|
C | A | 4 | a0001c0001t0001g0219a0001c0001t0004g0068a0001c0001t0004g0069others(1): Show | 4 | HG03225.hp2 NA18965.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.187-5147C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44479077 | ||||||
| chr15:44479077
|
C | CA | 20 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(17): Show | 20 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(17): Show |
intron_variant | MODIFIER | c.187-5134dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44479077 | |||||
| chr15:44479077
|
CA | C | 12 | a0001c0001t0012g0065a0001c0001t0012g0066a0001c0003t0008g0058others(9): Show | 12 | HG01891.hp2 HG02258.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.187-5134delA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44479077 | |||||
| chr15:44479081
|
A | C | 2 | a0001c0001t0001g0191a0001c0001t0004g0150 | 2 | HG02071.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.187-5143A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44479081 | ||||||
| chr15:44479227
|
G | A | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.187-4997G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44479227 | ||||||
| chr15:44479407
|
C | CT | 66 | a0001c0001t0001g0074a0001c0001t0001g0078a0001c0001t0001g0081others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.187-4795dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44479407 | |||||
| chr15:44479407
|
C | CTT | 18 | a0001c0001t0001g0106a0001c0001t0001g0228a0001c0001t0003g0018others(15): Show | 18 | HG01358.hp1 HG01891.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.187-4796_187-4795d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44479407 | |||||
| chr15:44479407
|
CT | C | 7 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0163others(4): Show | 7 | HG02922.hp1 HG03490.hp1 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.187-4795delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44479407 | |||||
| chr15:44479438
|
A | T | 5 | a0001c0001t0001g0099a0001c0001t0002g0087a0001c0001t0006g0094others(2): Show | 5 | HG01167.hp2 HG01928.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.187-4786A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44479438 | ||||||
| chr15:44479468
|
A | G | 8 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.187-4756A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44479468 | ||||||
| chr15:44479471
|
G | A | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.187-4753G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44479471 | ||||||
| chr15:44479762
|
A | G | 6 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(3): Show | 6 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.187-4462A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44479762 | ||||||
| chr15:44479817
|
G | A | 3 | a0001c0001t0003g0013a0001c0001t0003g0016a0001c0001t0007g0206 | 3 | NA18953.hp1 NA18953.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.187-4407G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44479817 | ||||||
| chr15:44479856
|
CTA | C | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.187-4365_187-4364d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44479856 | |||||
| chr15:44480116
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.187-4108C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44480116 | ||||||
| chr15:44480187
|
C | A | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.187-4037C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44480187 | ||||||
| chr15:44480267
|
G | C | 12 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(9): Show | 12 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.187-3957G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44480267 | ||||||
| chr15:44480308
|
T | G | 1 | a0001c0001t0001g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.187-3916T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44480308 | ||||||
| chr15:44480393
|
G | A | 18 | a0001c0002t0005g0031a0001c0002t0005g0032a0001c0002t0005g0033others(15): Show | 18 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.187-3831G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44480393 | ||||||
| chr15:44480727
|
G | C | 1 | a0001c0001t0022g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.187-3497G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44480727 | ||||||
| chr15:44481068
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.187-3156G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44481068 | ||||||
| chr15:44481201
|
A | G | 1 | a0001c0001t0002g0221 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.187-3023A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44481201 | ||||||
| chr15:44481289
|
G | A | 24 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(21): Show | 24 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.187-2935G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44481289 | ||||||
| chr15:44481331
|
G | A | 1 | a0001c0001t0028g0100 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.187-2893G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44481331 | ||||||
| chr15:44481388
|
T | C | 1 | a0001c0001t0022g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.187-2836T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44481388 | ||||||
| chr15:44481461
|
C | A | 2 | a0002c0004t0013g0199a0002c0004t0013g0200 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.187-2763C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44481461 | ||||||
| chr15:44481625
|
G | A | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.187-2599G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44481625 | ||||||
| chr15:44481661
|
C | T | 2 | a0001c0001t0002g0125a0001c0001t0002g0127 | 2 | HG01358.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.187-2563C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44481661 | ||||||
| chr15:44481924
|
A | G | 24 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(21): Show | 24 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.187-2300A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44481924 | ||||||
| chr15:44482004
|
C | T | 3 | a0001c0001t0002g0179a0001c0001t0002g0221a0001c0001t0002g0223 | 3 | HG01071.hp2 HG01192.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.187-2220C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44482004 | ||||||
| chr15:44482019
|
C | T | 8 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.187-2205C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44482019 | ||||||
| chr15:44482080
|
G | A | 16 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(13): Show | 16 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.187-2144G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44482080 | ||||||
| chr15:44482083
|
G | T | 16 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(13): Show | 16 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.187-2141G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44482083 | ||||||
| chr15:44482145
|
T | G | 11 | a0001c0001t0001g0067a0001c0001t0001g0073a0001c0001t0001g0117others(8): Show | 11 | HG00741.hp2 HG02040.hp2 HG02074.hp1 others(8): Show |
intron_variant | MODIFIER | c.187-2079T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44482145 | ||||||
| chr15:44482195
|
G | T | 1 | a0001c0001t0002g0223 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.187-2029G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44482195 | ||||||
| chr15:44482252
|
G | A | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.187-1972G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44482252 | ||||||
| chr15:44482342
|
G | A | 1 | a0001c0002t0005g0036 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.187-1882G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44482342 | ||||||
| chr15:44482523
|
GTAT | G | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.187-1696_187-1694d others(5): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44482523 | |||||
| chr15:44482994
|
C | CAT | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.187-1230_187-1229i others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44482994 | ||||||
| chr15:44482995
|
T | A | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.187-1229T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44482995 | ||||||
| chr15:44483000
|
C | T | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.187-1224C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44483000 | ||||||
| chr15:44483119
|
C | T | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.187-1105C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44483119 | ||||||
| chr15:44483152
|
G | A | 1 | a0001c0001t0026g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.187-1072G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44483152 | ||||||
| chr15:44483190
|
C | T | 1 | a0003c0006t0010g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.187-1034C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44483190 | ||||||
| chr15:44483283
|
G | A | 1 | a0001c0001t0002g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.187-941G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44483283 | ||||||
| chr15:44483376
|
A | T | 1 | a0001c0001t0007g0071 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.187-848A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44483376 | ||||||
| chr15:44483431
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.187-793G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44483431 | ||||||
| chr15:44483538
|
CA | C | 5 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(2): Show | 5 | HG02109.hp2 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.187-673delA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr15 | 44483538 | |||||
| chr15:44483719
|
A | G | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.187-505A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44483719 | ||||||
| chr15:44483877
|
T | G | 44 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(41): Show | 44 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.187-347T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44483877 | ||||||
| chr15:44484091
|
A | G | 1 | a0001c0001t0014g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.187-133A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 2/12 | chr15 | 44484091 | ||||||
| chr15:44484508
|
G | A | 3 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0029 | 3 | HG02572.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.325+146G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 3/12 | chr15 | 44484508 | ||||||
| chr15:44484908
|
G | A | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.325+546G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 3/12 | chr15 | 44484908 | ||||||
| chr15:44485290
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.325+928C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 3/12 | chr15 | 44485290 | ||||||
| chr15:44485477
|
T | G | 5 | a0001c0001t0001g0110a0001c0001t0004g0068a0001c0001t0004g0069others(2): Show | 5 | HG02027.hp1 HG02165.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.326-1074T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 3/12 | chr15 | 44485477 | ||||||
| chr15:44485488
|
T | C | 2 | a0001c0001t0012g0065a0001c0001t0012g0066 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.326-1063T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 3/12 | chr15 | 44485488 | ||||||
| chr15:44485708
|
A | C | 42 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.326-843A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 3/12 | chr15 | 44485708 | ||||||
| chr15:44485744
|
A | G | 13 | a0001c0001t0001g0078a0001c0001t0001g0091a0001c0001t0001g0095others(10): Show | 13 | HG00642.hp2 HG00738.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.326-807A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 3/12 | chr15 | 44485744 | ||||||
| chr15:44486040
|
G | A | 1 | a0001c0001t0003g0022 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.326-511G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 3/12 | chr15 | 44486040 | ||||||
| chr15:44486121
|
C | T | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.326-430C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 3/12 | chr15 | 44486121 | ||||||
| chr15:44486441
|
C | T | 1 | a0001c0001t0001g0226 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.326-110C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 3/12 | chr15 | 44486441 | ||||||
| chr15:44486738
|
T | A | 182 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0081others(179): Show | 182 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.475+38T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44486738 | ||||||
| chr15:44486739
|
A | T | 2 | a0001c0001t0015g0104a0001c0001t0015g0224 | 2 | NA18986.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.475+39A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44486739 | ||||||
| chr15:44486758
|
G | GT | 14 | a0001c0001t0001g0070a0001c0001t0001g0120a0001c0001t0001g0124others(11): Show | 14 | HG00741.hp1 HG02055.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.475+76dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 44486758 | |||||
| chr15:44486764
|
T | G | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG01256.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.475+64T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44486764 | ||||||
| chr15:44486787
|
A | T | 6 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(3): Show | 6 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.475+87A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44486787 | ||||||
| chr15:44486912
|
T | A | 1 | a0001c0001t0004g0123 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.475+212T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44486912 | ||||||
| chr15:44487019
|
C | T | 1 | a0001c0002t0005g0050 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.475+319C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44487019 | ||||||
| chr15:44487142
|
C | T | 1 | a0001c0001t0006g0102 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.475+442C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44487142 | ||||||
| chr15:44487178
|
G | A | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.475+478G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44487178 | ||||||
| chr15:44487211
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.475+511C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44487211 | ||||||
| chr15:44487315
|
C | T | 3 | a0001c0001t0002g0179a0001c0001t0002g0221a0001c0001t0002g0223 | 3 | HG01071.hp2 HG01192.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.475+615C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44487315 | ||||||
| chr15:44487419
|
T | C | 24 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(21): Show | 24 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.475+719T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44487419 | ||||||
| chr15:44487421
|
A | T | 24 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(21): Show | 24 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.475+721A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44487421 | ||||||
| chr15:44487596
|
T | C | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.475+896T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44487596 | ||||||
| chr15:44487607
|
C | T | 1 | a0001c0001t0003g0009 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.475+907C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44487607 | ||||||
| chr15:44487628
|
G | C | 8 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.475+928G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44487628 | ||||||
| chr15:44487725
|
A | G | 4 | a0001c0001t0001g0143a0001c0001t0001g0170a0001c0001t0001g0178others(1): Show | 4 | HG01255.hp2 HG02970.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.475+1025A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44487725 | ||||||
| chr15:44487838
|
G | A | 6 | a0001c0001t0001g0072a0001c0001t0001g0107a0001c0001t0001g0230others(3): Show | 6 | HG02015.hp2 NA18949.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.475+1138G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44487838 | ||||||
| chr15:44487874
|
A | G | 42 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.475+1174A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44487874 | ||||||
| chr15:44487914
|
G | A | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.475+1214G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44487914 | ||||||
| chr15:44488088
|
T | C | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.475+1388T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44488088 | ||||||
| chr15:44488109
|
C | CA | 22 | a0001c0001t0004g0123a0001c0001t0009g0026a0001c0001t0009g0027others(19): Show | 22 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.475+1425dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr15 | 44488109 | |||||
| chr15:44488111
|
A | G | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.475+1411A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44488111 | ||||||
| chr15:44488163
|
G | C | 4 | a0001c0001t0004g0068a0001c0001t0004g0069a0001c0001t0004g0116others(1): Show | 4 | HG02027.hp1 NA18965.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.475+1463G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44488163 | ||||||
| chr15:44488559
|
T | C | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.475+1859T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44488559 | ||||||
| chr15:44488671
|
T | C | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.475+1971T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44488671 | ||||||
| chr15:44488777
|
C | T | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.476-2007C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44488777 | ||||||
| chr15:44488778
|
C | T | 4 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.476-2006C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44488778 | ||||||
| chr15:44488871
|
T | G | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.476-1913T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44488871 | ||||||
| chr15:44489119
|
A | C | 54 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 54 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.476-1665A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44489119 | ||||||
| chr15:44489143
|
C | G | 5 | a0001c0001t0001g0154a0001c0001t0001g0174a0001c0001t0001g0175others(2): Show | 5 | HG00642.hp1 HG02572.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.476-1641C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44489143 | ||||||
| chr15:44489594
|
G | T | 28 | a0001c0001t0001g0072a0001c0001t0001g0103a0001c0001t0001g0107others(25): Show | 28 | HG01074.hp1 HG01981.hp2 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.476-1190G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44489594 | ||||||
| chr15:44489748
|
G | A | 4 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.476-1036G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44489748 | ||||||
| chr15:44490123
|
C | A | 2 | a0001c0001t0002g0173a0001c0001t0002g0180 | 2 | NA18960.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.476-661C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44490123 | ||||||
| chr15:44490210
|
C | T | 1 | a0001c0001t0002g0173 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.476-574C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44490210 | ||||||
| chr15:44490319
|
G | T | 1 | a0001c0001t0001g0082 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.476-465G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44490319 | ||||||
| chr15:44490657
|
A | G | 18 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(15): Show | 18 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.476-127A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 4/12 | chr15 | 44490657 | ||||||
| chr15:44491062
|
A | G | 8 | a0001c0002t0005g0039a0001c0002t0005g0044a0001c0002t0005g0045others(5): Show | 8 | HG02040.hp1 HG02155.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.691+63A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44491062 | ||||||
| chr15:44491147
|
G | C | 18 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(15): Show | 18 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.691+148G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44491147 | ||||||
| chr15:44491279
|
A | G | 1 | a0001c0001t0004g0150 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.691+280A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44491279 | ||||||
| chr15:44491312
|
G | T | 1 | a0001c0001t0002g0217 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.691+313G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44491312 | ||||||
| chr15:44491502
|
T | G | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.691+503T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44491502 | ||||||
| chr15:44491630
|
G | A | 3 | a0001c0001t0001g0132a0001c0001t0001g0182a0001c0001t0001g0198 | 3 | NA18975.hp2 NA19007.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.691+631G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44491630 | ||||||
| chr15:44492243
|
G | A | 2 | a0001c0001t0003g0020a0001c0001t0003g0021 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.691+1244G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44492243 | ||||||
| chr15:44492346
|
A | G | 2 | a0001c0001t0001g0174a0001c0001t0001g0176 | 2 | HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.691+1347A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44492346 | ||||||
| chr15:44492458
|
T | C | 7 | a0001c0001t0001g0067a0001c0001t0001g0073a0001c0001t0001g0117others(4): Show | 7 | HG02040.hp2 HG02074.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.691+1459T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44492458 | ||||||
| chr15:44492881
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.691+1882A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44492881 | ||||||
| chr15:44493008
|
G | A | 3 | a0001c0001t0004g0190a0001c0001t0025g0025a0001c0001t0026g0024 | 3 | HG01891.hp1 HG02109.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.691+2009G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44493008 | ||||||
| chr15:44493084
|
C | CT | 8 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.691+2095dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr15 | 44493084 | |||||
| chr15:44493101
|
G | C | 12 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(9): Show | 12 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.691+2102G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44493101 | ||||||
| chr15:44493267
|
G | C | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.691+2268G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44493267 | ||||||
| chr15:44493326
|
C | A | 4 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.691+2327C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44493326 | ||||||
| chr15:44493471
|
A | G | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.691+2472A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44493471 | ||||||
| chr15:44493601
|
C | G | 3 | a0001c0002t0005g0031a0001c0002t0005g0032a0001c0002t0005g0034 | 3 | HG02257.hp1 HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.691+2602C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44493601 | ||||||
| chr15:44493657
|
G | A | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.691+2658G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44493657 | ||||||
| chr15:44494087
|
T | C | 1 | a0001c0001t0023g0083 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.692-2293T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44494087 | ||||||
| chr15:44494095
|
T | G | 1 | a0001c0001t0003g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.692-2285T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44494095 | ||||||
| chr15:44494210
|
C | T | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.692-2170C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44494210 | ||||||
| chr15:44494274
|
G | C | 1 | a0001c0001t0001g0088 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.692-2106G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44494274 | ||||||
| chr15:44494371
|
C | T | 1 | a0003c0006t0010g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.692-2009C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44494371 | ||||||
| chr15:44494444
|
C | T | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.692-1936C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44494444 | ||||||
| chr15:44494454
|
A | T | 12 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(9): Show | 12 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.692-1926A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44494454 | ||||||
| chr15:44494563
|
G | A | 1 | a0001c0001t0022g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.692-1817G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44494563 | ||||||
| chr15:44494669
|
C | G | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.692-1711C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44494669 | ||||||
| chr15:44494780
|
G | A | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.692-1600G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44494780 | ||||||
| chr15:44494832
|
C | T | 1 | a0001c0001t0007g0131 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.692-1548C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44494832 | ||||||
| chr15:44494846
|
G | A | 2 | a0001c0001t0012g0065a0001c0001t0012g0066 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.692-1534G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44494846 | ||||||
| chr15:44494952
|
A | C | 1 | a0001c0001t0014g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.692-1428A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44494952 | ||||||
| chr15:44495036
|
A | G | 4 | a0001c0001t0012g0065a0001c0001t0012g0066a0001c0001t0017g0001others(1): Show | 4 | HG01891.hp2 HG02109.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.692-1344A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44495036 | ||||||
| chr15:44495044
|
T | C | 1 | a0001c0002t0005g0033 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.692-1336T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44495044 | ||||||
| chr15:44495152
|
T | C | 2 | a0001c0001t0003g0020a0001c0001t0003g0021 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.692-1228T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44495152 | ||||||
| chr15:44495354
|
C | T | 2 | a0001c0001t0001g0226a0001c0001t0001g0227 | 2 | HG01081.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.692-1026C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44495354 | ||||||
| chr15:44495364
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.692-1016T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44495364 | ||||||
| chr15:44495506
|
G | A | 1 | a0001c0001t0014g0038 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.692-874G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44495506 | ||||||
| chr15:44495548
|
C | CA | 8 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(5): Show | 8 | HG01891.hp2 HG02109.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.692-817dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr15 | 44495548 | |||||
| chr15:44495600
|
T | C | 1 | a0001c0001t0020g0167 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.692-780T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44495600 | ||||||
| chr15:44495624
|
C | T | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.692-756C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44495624 | ||||||
| chr15:44495671
|
C | T | 2 | a0001c0001t0012g0065a0001c0001t0012g0066 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.692-709C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44495671 | ||||||
| chr15:44495709
|
G | A | 8 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.692-671G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44495709 | ||||||
| chr15:44495773
|
A | G | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.692-607A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44495773 | ||||||
| chr15:44495842
|
G | C | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.692-538G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44495842 | ||||||
| chr15:44495932
|
C | CA | 9 | a0001c0001t0001g0197a0001c0001t0009g0026a0001c0001t0009g0027others(6): Show | 9 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.692-438dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr15 | 44495932 | |||||
| chr15:44495993
|
G | A | 1 | a0001c0001t0002g0126 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.692-387G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44495993 | ||||||
| chr15:44496027
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.692-353C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44496027 | ||||||
| chr15:44496090
|
A | G | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.692-290A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44496090 | ||||||
| chr15:44496226
|
G | A | 43 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(40): Show | 43 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.692-154G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44496226 | ||||||
| chr15:44496282
|
A | C | 1 | a0001c0001t0001g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.692-98A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44496282 | ||||||
| chr15:44496373
|
T | C | 1 | a0001c0001t0002g0125 | 1 | HG01358.hp2 | splice_region_variant&intron_variant | LOW | c.692-7T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 5/12 | chr15 | 44496373 | ||||||
| chr15:44496507
|
G | A | 54 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 54 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.770+49G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 6/12 | chr15 | 44496507 | ||||||
| chr15:44497276
|
T | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0147 | 2 | HG01981.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.882+138T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44497276 | ||||||
| chr15:44497385
|
A | G | 6 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(3): Show | 6 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.882+247A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44497385 | ||||||
| chr15:44497490
|
C | T | 1 | a0001c0001t0004g0139 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.882+352C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44497490 | ||||||
| chr15:44497491
|
G | A | 1 | a0001c0001t0022g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.882+353G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44497491 | ||||||
| chr15:44497526
|
C | T | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+388C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44497526 | ||||||
| chr15:44497772
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0145 | 2 | HG01074.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.882+634C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44497772 | ||||||
| chr15:44497806
|
G | A | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.882+668G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44497806 | ||||||
| chr15:44497818
|
A | G | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.882+680A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44497818 | ||||||
| chr15:44497998
|
GA | G | 42 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.882+869delA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr15 | 44497998 | |||||
| chr15:44498139
|
T | C | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.882+1001T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44498139 | ||||||
| chr15:44498431
|
C | A | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.882+1293C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44498431 | ||||||
| chr15:44498465
|
A | C | 1 | a0001c0001t0024g0010 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.883-1262A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44498465 | ||||||
| chr15:44498478
|
C | T | 1 | a0001c0001t0014g0038 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.883-1249C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44498478 | ||||||
| chr15:44498487
|
G | A | 4 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0205others(1): Show | 4 | HG03490.hp1 HG03491.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-1240G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44498487 | ||||||
| chr15:44498513
|
G | A | 1 | a0001c0001t0026g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.883-1214G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44498513 | ||||||
| chr15:44498637
|
C | T | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.883-1090C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44498637 | ||||||
| chr15:44498678
|
T | TA | 2 | a0001c0001t0002g0080a0001c0001t0002g0204 | 2 | HG01243.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.883-1048dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr15 | 44498678 | |||||
| chr15:44498758
|
G | A | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.883-969G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44498758 | ||||||
| chr15:44498883
|
G | A | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.883-844G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44498883 | ||||||
| chr15:44498968
|
A | G | 1 | a0001c0002t0005g0042 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.883-759A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44498968 | ||||||
| chr15:44499150
|
C | G | 4 | a0001c0001t0011g0051a0001c0001t0011g0052a0001c0001t0011g0053others(1): Show | 4 | HG02970.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-577C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44499150 | ||||||
| chr15:44499259
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.883-468G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44499259 | ||||||
| chr15:44499311
|
A | G | 4 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.883-416A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44499311 | ||||||
| chr15:44499464
|
A | T | 1 | a0001c0001t0001g0226 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.883-263A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44499464 | ||||||
| chr15:44499498
|
A | G | 4 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-229A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44499498 | ||||||
| chr15:44499649
|
T | G | 2 | a0001c0002t0005g0033a0001c0002t0005g0036 | 2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.883-78T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44499649 | ||||||
| chr15:44499656
|
T | G | 4 | a0001c0001t0011g0051a0001c0001t0011g0052a0001c0001t0011g0053others(1): Show | 4 | HG02970.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.883-71T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 7/12 | chr15 | 44499656 | ||||||
| chr15:44500500
|
C | G | 1 | a0001c0001t0003g0004 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.969+687C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44500500 | ||||||
| chr15:44500545
|
A | G | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.969+732A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44500545 | ||||||
| chr15:44500739
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.969+926C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44500739 | ||||||
| chr15:44500800
|
A | T | 18 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(15): Show | 18 | HG02055.hp1 HG02258.hp2 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.969+987A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44500800 | ||||||
| chr15:44500850
|
C | T | 1 | a0003c0006t0010g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.969+1037C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44500850 | ||||||
| chr15:44500951
|
A | G | 9 | a0001c0001t0001g0115a0001c0001t0001g0143a0001c0001t0001g0160others(6): Show | 9 | HG01243.hp1 HG01255.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.969+1138A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44500951 | ||||||
| chr15:44501020
|
G | A | 1 | a0001c0001t0002g0166 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.969+1207G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44501020 | ||||||
| chr15:44501195
|
G | A | 44 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(41): Show | 44 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.969+1382G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44501195 | ||||||
| chr15:44501414
|
C | T | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.969+1601C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44501414 | ||||||
| chr15:44501460
|
T | C | 4 | a0001c0001t0011g0051a0001c0001t0011g0052a0001c0001t0011g0053others(1): Show | 4 | HG02970.hp2 HG03098.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.969+1647T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44501460 | ||||||
| chr15:44501727
|
G | T | 1 | a0001c0003t0008g0058 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.969+1914G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44501727 | ||||||
| chr15:44501799
|
A | G | 1 | a0001c0001t0001g0111 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.969+1986A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44501799 | ||||||
| chr15:44502104
|
T | C | 1 | a0001c0001t0006g0138 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.969+2291T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44502104 | ||||||
| chr15:44502132
|
C | CTT | 7 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0127others(4): Show | 7 | HG00735.hp1 HG01167.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.969+2320_969+2321d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44502132 | |||||
| chr15:44502174
|
AAATT | A | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.969+2364_969+2367d others(6): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44502174 | |||||
| chr15:44502294
|
A | C | 1 | a0001c0001t0001g0122 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.969+2481A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44502294 | ||||||
| chr15:44502362
|
G | A | 1 | a0001c0001t0001g0208 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.969+2549G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44502362 | ||||||
| chr15:44502465
|
G | A | 1 | a0001c0001t0003g0023 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.969+2652G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44502465 | ||||||
| chr15:44502683
|
G | A | 1 | a0001c0001t0002g0125 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.969+2870G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44502683 | ||||||
| chr15:44502971
|
G | A | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.969+3158G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44502971 | ||||||
| chr15:44503115
|
T | G | 44 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(41): Show | 44 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.969+3302T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44503115 | ||||||
| chr15:44503143
|
T | A | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.969+3330T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44503143 | ||||||
| chr15:44503177
|
A | G | 1 | a0001c0001t0026g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.969+3364A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44503177 | ||||||
| chr15:44503199
|
G | T | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.969+3386G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44503199 | ||||||
| chr15:44503200
|
G | C | 1 | a0001c0001t0002g0126 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.969+3387G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44503200 | ||||||
| chr15:44503252
|
T | C | 1 | a0001c0001t0025g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.969+3439T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44503252 | ||||||
| chr15:44503975
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.969+4162T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44503975 | ||||||
| chr15:44504085
|
C | T | 8 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.969+4272C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44504085 | ||||||
| chr15:44504209
|
G | T | 6 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(3): Show | 6 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.969+4396G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44504209 | ||||||
| chr15:44504337
|
G | A | 1 | a0001c0001t0003g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.969+4524G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44504337 | ||||||
| chr15:44504708
|
C | CAA | 43 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(40): Show | 43 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.969+4906_969+4907d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44504708 | |||||
| chr15:44504738
|
G | A | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.969+4925G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44504738 | ||||||
| chr15:44505233
|
A | C | 2 | a0001c0001t0002g0148a0001c0001t0002g0149 | 2 | HG02074.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.969+5420A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44505233 | ||||||
| chr15:44505358
|
G | A | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.969+5545G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44505358 | ||||||
| chr15:44505377
|
C | T | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.969+5564C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44505377 | ||||||
| chr15:44505476
|
C | G | 66 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(63): Show | 66 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.969+5663C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44505476 | ||||||
| chr15:44505735
|
C | CA | 6 | a0001c0001t0001g0233a0001c0001t0002g0221a0001c0001t0003g0006others(3): Show | 6 | HG00423.hp2 HG02572.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.969+5937dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44505735 | |||||
| chr15:44505805
|
T | C | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.969+5992T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44505805 | ||||||
| chr15:44505805
|
TAGA | T | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.969+5995_969+5997d others(5): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44505805 | |||||
| chr15:44505815
|
G | A | 1 | a0001c0001t0003g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.969+6002G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44505815 | ||||||
| chr15:44505873
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.969+6060T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44505873 | ||||||
| chr15:44505950
|
T | C | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.969+6137T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44505950 | ||||||
| chr15:44506025
|
C | CT | 14 | a0001c0001t0001g0091a0001c0001t0001g0124a0001c0001t0001g0208others(11): Show | 14 | HG00423.hp2 HG00597.hp2 HG01256.hp2 others(11): Show |
intron_variant | MODIFIER | c.969+6234dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506025 | |||||
| chr15:44506025
|
C | CTT | 7 | a0001c0001t0002g0216a0001c0001t0009g0026a0001c0001t0009g0028others(4): Show | 7 | HG00735.hp1 HG02055.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.969+6233_969+6234d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506025 | |||||
| chr15:44506025
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.969+6219_969+6234d others(18): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506025 | |||||
| chr15:44506025
|
C | CTTTTTTT others(10): Show |
5 | a0001c0001t0003g0005a0001c0001t0003g0020a0001c0001t0003g0021others(2): Show | 5 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.969+6218_969+6234d others(19): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506025 | |||||
| chr15:44506025
|
C | CTTTTTTT others(11): Show |
3 | a0001c0001t0003g0012a0001c0001t0003g0018a0001c0001t0003g0019 | 3 | NA18992.hp2 NA19085.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.969+6217_969+6234d others(20): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506025 | |||||
| chr15:44506025
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0030g0008 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.969+6216_969+6234d others(21): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506025 | |||||
| chr15:44506025
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0003g0003 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.969+6215_969+6234d others(22): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506025 | |||||
| chr15:44506025
|
C | CTTTTTTT others(14): Show |
2 | a0001c0001t0003g0004a0001c0001t0024g0010 | 2 | HG00423.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.969+6214_969+6234d others(23): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506025 | |||||
| chr15:44506025
|
C | CTTTTTTT others(17): Show |
4 | a0001c0001t0003g0006a0001c0001t0003g0013a0001c0001t0012g0065others(1): Show | 4 | HG01891.hp2 HG03130.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.969+6234_969+6235i others(26): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506025 | |||||
| chr15:44506025
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0003g0016 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.969+6234_969+6235i others(27): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506025 | |||||
| chr15:44506025
|
C | CTTTTTTT others(19): Show |
3 | a0001c0001t0003g0009a0001c0001t0003g0014a0001c0001t0003g0017 | 3 | HG00735.hp2 NA18952.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.969+6234_969+6235i others(28): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506025 | |||||
| chr15:44506025
|
C | CTTTTTTT others(23): Show |
1 | a0001c0001t0003g0015 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.969+6234_969+6235i others(32): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506025 | |||||
| chr15:44506025
|
C | CTTTTTTT others(32): Show |
1 | a0001c0001t0003g0002 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.969+6234_969+6235i others(41): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506025 | |||||
| chr15:44506025
|
C | CTTTTTTT others(34): Show |
1 | a0001c0001t0003g0007 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.969+6234_969+6235i others(43): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506025 | |||||
| chr15:44506025
|
CT | C | 21 | a0001c0001t0002g0184a0001c0001t0014g0038a0001c0001t0014g0225others(18): Show | 21 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.969+6234delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506025 | |||||
| chr15:44506025
|
CTTTTTT | C | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.969+6229_969+6234d others(8): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506025 | |||||
| chr15:44506091
|
G | T | 1 | a0001c0001t0002g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.969+6278G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506091 | ||||||
| chr15:44506103
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | HG01256.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.969+6290C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506103 | ||||||
| chr15:44506109
|
A | G | 1 | a0001c0001t0026g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.969+6296A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506109 | ||||||
| chr15:44506122
|
C | T | 1 | a0001c0001t0006g0101 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.969+6309C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506122 | ||||||
| chr15:44506142
|
G | A | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.969+6329G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506142 | ||||||
| chr15:44506190
|
C | T | 2 | a0001c0001t0016g0188a0001c0001t0016g0189 | 2 | HG00738.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.969+6377C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506190 | ||||||
| chr15:44506246
|
T | A | 4 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.969+6433T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506246 | ||||||
| chr15:44506274
|
C | T | 4 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.969+6461C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506274 | ||||||
| chr15:44506336
|
CCCATTGG others(49): Show |
C | 1 | a0001c0002t0005g0044 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.969+6524_969+6579d others(58): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506336 | ||||||
| chr15:44506412
|
C | CT | 26 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0120others(23): Show | 26 | HG01243.hp1 HG01884.hp2 HG01981.hp1 others(23): Show |
intron_variant | MODIFIER | c.969+6620dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506412 | |||||
| chr15:44506412
|
C | CTTTTTTT | 10 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0007others(7): Show | 10 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(7): Show |
intron_variant | MODIFIER | c.969+6614_969+6620d others(9): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506412 | |||||
| chr15:44506412
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0003g0020a0001c0001t0003g0022a0001c0001t0030g0008 | 3 | HG02965.hp2 NA19055.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.969+6611_969+6620d others(12): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506412 | |||||
| chr15:44506412
|
C | CTTTTTTT others(4): Show |
2 | a0001c0001t0003g0021a0001c0001t0003g0023 | 2 | HG03209.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.969+6610_969+6620d others(13): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506412 | |||||
| chr15:44506412
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0003g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.969+6607_969+6620d others(16): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506412 | |||||
| chr15:44506412
|
C | CTTTTTTT others(44): Show |
1 | a0001c0002t0005g0044 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.969+6613_969+6614i others(53): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506412 | |||||
| chr15:44506412
|
C | CTTTTTTT others(10): Show |
1 | a0001c0002t0005g0045 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.969+6604_969+6620d others(19): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506412 | |||||
| chr15:44506412
|
C | CTTTTTTT others(11): Show |
1 | a0001c0001t0003g0002 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.969+6603_969+6620d others(20): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506412 | |||||
| chr15:44506412
|
C | CTTTTTTT others(13): Show |
2 | a0001c0002t0005g0046a0001c0002t0005g0048 | 2 | NA18965.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.969+6601_969+6620d others(22): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506412 | |||||
| chr15:44506412
|
C | CTTTTTTT others(15): Show |
1 | a0001c0002t0005g0050 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.969+6620_969+6621i others(24): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506412 | |||||
| chr15:44506412
|
C | CTTTTTTT others(22): Show |
1 | a0001c0002t0005g0047 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.969+6620_969+6621i others(31): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506412 | |||||
| chr15:44506412
|
C | CTTTTTTT others(24): Show |
1 | a0001c0002t0005g0039 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.969+6620_969+6621i others(33): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506412 | |||||
| chr15:44506412
|
C | CTTTTTTT others(25): Show |
1 | a0001c0001t0014g0038 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.969+6620_969+6621i others(34): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506412 | |||||
| chr15:44506412
|
C | CTTTTTTT others(29): Show |
1 | a0001c0002t0005g0049 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.969+6620_969+6621i others(38): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506412 | |||||
| chr15:44506412
|
CT | C | 18 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0001g0088others(15): Show | 18 | HG00642.hp1 HG01243.hp2 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.969+6620delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44506412 | |||||
| chr15:44506448
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.969+6635G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506448 | ||||||
| chr15:44506481
|
A | G | 58 | a0001c0001t0002g0080a0001c0001t0002g0125a0001c0001t0002g0126others(55): Show | 58 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.969+6668A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506481 | ||||||
| chr15:44506494
|
A | G | 1 | a0001c0001t0004g0146 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.969+6681A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506494 | ||||||
| chr15:44506552
|
T | C | 1 | a0001c0002t0005g0050 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.969+6739T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506552 | ||||||
| chr15:44506577
|
G | A | 4 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(1): Show | 4 | HG02055.hp1 HG02572.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.969+6764G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506577 | ||||||
| chr15:44506603
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0145 | 2 | HG01074.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.969+6790C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506603 | ||||||
| chr15:44506769
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.969+6956C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506769 | ||||||
| chr15:44506805
|
C | T | 4 | a0001c0001t0002g0180a0001c0003t0008g0059a0001c0003t0008g0061others(1): Show | 4 | HG02615.hp2 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.969+6992C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506805 | ||||||
| chr15:44506831
|
A | G | 1 | a0001c0001t0006g0084 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.969+7018A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506831 | ||||||
| chr15:44506835
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.969+7022T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506835 | ||||||
| chr15:44506868
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0145 | 2 | HG01074.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.969+7055G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506868 | ||||||
| chr15:44506928
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.969+7115G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506928 | ||||||
| chr15:44506982
|
C | T | 42 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(39): Show | 42 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.969+7169C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506982 | ||||||
| chr15:44506983
|
G | A | 1 | a0001c0001t0001g0165 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.969+7170G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44506983 | ||||||
| chr15:44507058
|
C | T | 113 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0081others(110): Show | 113 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.969+7245C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44507058 | ||||||
| chr15:44507441
|
A | C | 3 | a0001c0002t0005g0040a0001c0002t0005g0041a0001c0002t0005g0043 | 3 | NA18971.hp1 NA18986.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.970-7157A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44507441 | ||||||
| chr15:44507465
|
T | G | 2 | a0001c0001t0004g0150a0001c0001t0004g0151 | 2 | HG00673.hp2 HG02071.hp2 |
intron_variant | MODIFIER | c.970-7133T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44507465 | ||||||
| chr15:44507557
|
G | C | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.970-7041G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44507557 | ||||||
| chr15:44507762
|
G | T | 24 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(21): Show | 24 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.970-6836G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44507762 | ||||||
| chr15:44507952
|
C | CTGTATTT others(23): Show |
1 | a0001c0002t0005g0044 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.970-6645_970-6616d others(32): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44507952 | |||||
| chr15:44508246
|
C | A | 1 | a0003c0006t0010g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.970-6352C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44508246 | ||||||
| chr15:44508508
|
CAG | C | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.970-6088_970-6087d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44508508 | |||||
| chr15:44508579
|
A | G | 1 | a0001c0001t0001g0232 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.970-6019A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44508579 | ||||||
| chr15:44508806
|
C | G | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.970-5792C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44508806 | ||||||
| chr15:44508812
|
G | A | 171 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0070others(168): Show | 171 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(168): Show |
intron_variant | MODIFIER | c.970-5786G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44508812 | ||||||
| chr15:44509053
|
T | C | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.970-5545T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44509053 | ||||||
| chr15:44509190
|
T | A | 1 | a0001c0002t0005g0044 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.970-5408T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44509190 | ||||||
| chr15:44509402
|
C | T | 215 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0070others(212): Show | 215 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(212): Show |
intron_variant | MODIFIER | c.970-5196C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44509402 | ||||||
| chr15:44509407
|
A | G | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.970-5191A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44509407 | ||||||
| chr15:44509638
|
T | C | 1 | a0001c0001t0003g0005 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.970-4960T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44509638 | ||||||
| chr15:44509650
|
TG | T | 18 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(15): Show | 18 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(15): Show |
intron_variant | MODIFIER | c.970-4947delG | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44509650 | ||||||
| chr15:44509699
|
G | C | 54 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(51): Show | 54 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.970-4899G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44509699 | ||||||
| chr15:44509886
|
A | G | 4 | a0001c0001t0001g0154a0001c0001t0001g0174a0001c0001t0001g0175others(1): Show | 4 | HG02572.hp2 HG02717.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.970-4712A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44509886 | ||||||
| chr15:44509928
|
A | AAT | 10 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(7): Show | 10 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.970-4655_970-4654d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44509928 | |||||
| chr15:44510097
|
G | A | 1 | a0001c0001t0001g0117 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.970-4501G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44510097 | ||||||
| chr15:44510235
|
C | T | 2 | a0001c0001t0002g0148a0001c0001t0002g0149 | 2 | HG02074.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.970-4363C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44510235 | ||||||
| chr15:44510698
|
T | A | 1 | a0001c0001t0001g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.970-3900T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44510698 | ||||||
| chr15:44510869
|
G | A | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.970-3729G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44510869 | ||||||
| chr15:44510964
|
C | T | 4 | a0001c0001t0001g0115a0001c0001t0001g0202a0001c0001t0001g0203others(1): Show | 4 | HG01243.hp1 HG01884.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.970-3634C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44510964 | ||||||
| chr15:44511097
|
C | A | 1 | a0001c0001t0001g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.970-3501C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44511097 | ||||||
| chr15:44511348
|
T | C | 16 | a0001c0001t0003g0003a0001c0001t0003g0004a0001c0001t0003g0005others(13): Show | 16 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.970-3250T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44511348 | ||||||
| chr15:44511474
|
C | T | 65 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(62): Show | 65 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.970-3124C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44511474 | ||||||
| chr15:44511619
|
C | A | 1 | a0001c0001t0001g0170 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.970-2979C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44511619 | ||||||
| chr15:44511720
|
G | T | 18 | a0001c0002t0005g0031a0001c0002t0005g0032a0001c0002t0005g0033others(15): Show | 18 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.970-2878G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44511720 | ||||||
| chr15:44511810
|
G | A | 3 | a0001c0001t0002g0215a0001c0001t0012g0065a0001c0001t0012g0066 | 3 | HG01891.hp2 HG02486.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.970-2788G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44511810 | ||||||
| chr15:44511867
|
C | CA | 69 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0075others(66): Show | 69 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.970-2706dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44511867 | |||||
| chr15:44511867
|
C | CAA | 8 | a0001c0001t0001g0181a0001c0001t0001g0198a0001c0001t0001g0208others(5): Show | 8 | HG02015.hp2 HG02970.hp1 HG03704.hp1 others(5): Show |
intron_variant | MODIFIER | c.970-2707_970-2706d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44511867 | |||||
| chr15:44511867
|
CA | C | 21 | a0001c0001t0002g0087a0001c0001t0006g0138a0001c0001t0009g0026others(18): Show | 21 | HG01891.hp2 HG02055.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.970-2706delA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44511867 | |||||
| chr15:44511867
|
CAA | C | 9 | a0001c0001t0017g0001a0001c0001t0025g0025a0001c0001t0026g0024others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.970-2707_970-2706d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44511867 | |||||
| chr15:44511885
|
A | G | 14 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(11): Show | 14 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.970-2713A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44511885 | ||||||
| chr15:44511911
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0001g0176 | 2 | HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.970-2687C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44511911 | ||||||
| chr15:44512041
|
A | T | 2 | a0001c0001t0002g0080a0001c0001t0002g0204 | 2 | HG01243.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.970-2557A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44512041 | ||||||
| chr15:44512067
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.970-2531T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44512067 | ||||||
| chr15:44512713
|
C | T | 17 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(14): Show | 17 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.970-1885C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44512713 | ||||||
| chr15:44512818
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.970-1780C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44512818 | ||||||
| chr15:44512974
|
G | A | 65 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(62): Show | 65 | HG00408.hp1 HG00597.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.970-1624G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44512974 | ||||||
| chr15:44513071
|
C | CA | 9 | a0001c0001t0001g0122a0001c0001t0001g0147a0001c0001t0003g0019others(6): Show | 9 | HG01891.hp2 HG02965.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.970-1512dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr15 | 44513071 | |||||
| chr15:44513084
|
A | C | 1 | a0001c0001t0003g0005 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.970-1514A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44513084 | ||||||
| chr15:44513490
|
A | G | 19 | a0001c0001t0018g0030a0001c0002t0005g0031a0001c0002t0005g0032others(16): Show | 19 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.970-1108A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44513490 | ||||||
| chr15:44513537
|
T | G | 6 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(3): Show | 6 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.970-1061T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44513537 | ||||||
| chr15:44513563
|
G | T | 3 | a0001c0002t0005g0031a0001c0002t0005g0032a0001c0002t0005g0034 | 3 | HG02257.hp1 HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.970-1035G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44513563 | ||||||
| chr15:44513583
|
T | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0195 | 2 | NA18944.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.970-1015T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44513583 | ||||||
| chr15:44513597
|
T | C | 3 | a0001c0001t0012g0065a0001c0001t0012g0066a0001c0001t0017g0001 | 3 | HG01891.hp2 HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.970-1001T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44513597 | ||||||
| chr15:44513613
|
C | G | 1 | a0001c0001t0002g0137 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.970-985C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44513613 | ||||||
| chr15:44514059
|
T | C | 17 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(14): Show | 17 | HG00408.hp1 HG00597.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.970-539T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44514059 | ||||||
| chr15:44514306
|
C | G | 7 | a0001c0001t0001g0103a0001c0001t0001g0120a0001c0001t0001g0153others(4): Show | 7 | HG02055.hp2 HG02257.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.970-292C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44514306 | ||||||
| chr15:44514405
|
C | T | 1 | a0001c0001t0002g0213 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.970-193C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44514405 | ||||||
| chr15:44514450
|
T | C | 14 | a0001c0001t0001g0072a0001c0001t0001g0107a0001c0001t0001g0132others(11): Show | 14 | HG01074.hp1 HG02015.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.970-148T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 8/12 | chr15 | 44514450 | ||||||
| chr15:44514969
|
T | A | 6 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(3): Show | 6 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1112+125T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44514969 | ||||||
| chr15:44515107
|
G | A | 65 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(62): Show | 65 | HG00408.hp1 HG00597.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.1112+263G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44515107 | ||||||
| chr15:44515113
|
T | TG | 30 | a0001c0001t0025g0025a0001c0001t0026g0024a0001c0002t0005g0031others(27): Show | 30 | HG01891.hp1 HG02040.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.1112+276dupG | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 44515113 | |||||
| chr15:44515324
|
G | A | 1 | a0001c0001t0026g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1112+480G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44515324 | ||||||
| chr15:44515419
|
C | T | 2 | a0001c0002t0005g0046a0001c0002t0005g0048 | 2 | NA18965.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1112+575C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44515419 | ||||||
| chr15:44515573
|
A | G | 8 | a0001c0002t0005g0039a0001c0002t0005g0044a0001c0002t0005g0045others(5): Show | 8 | HG02040.hp1 HG02155.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.1112+729A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44515573 | ||||||
| chr15:44515608
|
C | T | 2 | a0001c0001t0004g0123a0001c0001t0004g0151 | 2 | HG00673.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.1112+764C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44515608 | ||||||
| chr15:44515717
|
A | G | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1112+873A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44515717 | ||||||
| chr15:44515785
|
A | C | 36 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(33): Show | 36 | HG01891.hp2 HG02040.hp1 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.1112+941A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44515785 | ||||||
| chr15:44515878
|
A | T | 1 | a0001c0001t0001g0182 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1112+1034A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44515878 | ||||||
| chr15:44515880
|
A | G | 3 | a0001c0001t0002g0179a0001c0001t0002g0213a0001c0001t0002g0221 | 3 | HG01071.hp2 HG01192.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1112+1036A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44515880 | ||||||
| chr15:44515930
|
T | C | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1112+1086T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44515930 | ||||||
| chr15:44515931
|
C | T | 17 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(14): Show | 17 | HG00408.hp1 HG00597.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.1112+1087C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44515931 | ||||||
| chr15:44515986
|
C | CT | 33 | a0001c0001t0001g0164a0001c0001t0001g0193a0001c0001t0001g0202others(30): Show | 33 | HG01884.hp1 HG01891.hp2 HG02040.hp1 others(30): Show |
intron_variant | MODIFIER | c.1112+1157dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 44515986 | |||||
| chr15:44516251
|
A | C | 22 | a0001c0001t0012g0065a0001c0001t0012g0066a0001c0001t0017g0001others(19): Show | 22 | HG01891.hp2 HG02040.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1112+1407A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44516251 | ||||||
| chr15:44516252
|
G | A | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1112+1408G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44516252 | ||||||
| chr15:44516718
|
A | C | 3 | a0001c0001t0001g0132a0001c0001t0001g0182a0001c0001t0001g0198 | 3 | NA18975.hp2 NA19007.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1112+1874A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44516718 | ||||||
| chr15:44516793
|
T | G | 3 | a0001c0001t0002g0214a0001c0001t0002g0223a0001c0005t0001g0161 | 3 | HG01167.hp1 HG01192.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1112+1949T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44516793 | ||||||
| chr15:44516864
|
C | CAG | 184 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0074others(181): Show | 184 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(181): Show |
intron_variant | MODIFIER | c.1112+2021_1112+202 others(6): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 44516864 | |||||
| chr15:44516879
|
A | G | 38 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(35): Show | 38 | HG01891.hp1 HG01891.hp2 HG02040.hp1 others(35): Show |
intron_variant | MODIFIER | c.1112+2035A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44516879 | ||||||
| chr15:44516943
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1112+2099G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44516943 | ||||||
| chr15:44516965
|
G | T | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1112+2121G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44516965 | ||||||
| chr15:44517337
|
C | T | 4 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113-1832C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44517337 | ||||||
| chr15:44517384
|
C | G | 3 | a0001c0001t0002g0214a0001c0001t0002g0223a0001c0005t0001g0161 | 3 | HG01167.hp1 HG01192.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1113-1785C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44517384 | ||||||
| chr15:44517397
|
A | G | 4 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(1): Show | 4 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1113-1772A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44517397 | ||||||
| chr15:44517446
|
C | T | 2 | a0001c0001t0007g0077a0001c0001t0007g0129 | 2 | HG02165.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.1113-1723C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44517446 | ||||||
| chr15:44517450
|
A | T | 3 | a0001c0001t0001g0067a0001c0001t0001g0073a0001c0001t0001g0195 | 3 | NA18944.hp2 NA19063.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1113-1719A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44517450 | ||||||
| chr15:44517754
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1113-1415C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44517754 | ||||||
| chr15:44518069
|
T | G | 1 | a0001c0001t0004g0133 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1113-1100T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44518069 | ||||||
| chr15:44518085
|
A | C | 2 | a0001c0001t0004g0210a0001c0001t0004g0211 | 2 | NA18998.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1113-1084A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44518085 | ||||||
| chr15:44518138
|
C | T | 65 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(62): Show | 65 | HG00408.hp1 HG00597.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.1113-1031C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44518138 | ||||||
| chr15:44518192
|
T | C | 1 | a0003c0006t0010g0056 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1113-977T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44518192 | ||||||
| chr15:44518280
|
A | G | 1 | a0001c0001t0018g0030 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1113-889A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44518280 | ||||||
| chr15:44518292
|
A | T | 65 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(62): Show | 65 | HG00408.hp1 HG00597.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.1113-877A>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44518292 | ||||||
| chr15:44518566
|
C | CA | 30 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(27): Show | 30 | HG01891.hp2 HG02040.hp1 HG02055.hp1 others(27): Show |
intron_variant | MODIFIER | c.1113-595dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr15 | 44518566 | |||||
| chr15:44518818
|
G | A | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1113-351G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44518818 | ||||||
| chr15:44518892
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1113-277G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44518892 | ||||||
| chr15:44518941
|
A | C | 11 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(8): Show | 11 | HG00642.hp1 HG02559.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1113-228A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44518941 | ||||||
| chr15:44518953
|
G | A | 1 | a0001c0002t0005g0036 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1113-216G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44518953 | ||||||
| chr15:44519147
|
T | C | 1 | a0001c0001t0003g0019 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1113-22T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 10/12 | chr15 | 44519147 | ||||||
| chr15:44519560
|
T | C | 1 | a0001c0001t0022g0114 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1239+265T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | chr15 | 44519560 | ||||||
| chr15:44519623
|
CT | C | 6 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0060others(3): Show | 6 | HG02258.hp2 HG02615.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1239+330delT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 44519623 | |||||
| chr15:44519729
|
G | A | 232 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0070others(229): Show | 232 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(229): Show |
intron_variant | MODIFIER | c.1239+434G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | chr15 | 44519729 | ||||||
| chr15:44519764
|
G | GT | 9 | a0001c0001t0001g0106a0001c0001t0002g0125a0001c0001t0003g0020others(6): Show | 9 | HG01358.hp1 HG01358.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.1239+478dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 44519764 | |||||
| chr15:44519822
|
T | G | 24 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(21): Show | 24 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1239+527T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | chr15 | 44519822 | ||||||
| chr15:44519836
|
G | A | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1239+541G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | chr15 | 44519836 | ||||||
| chr15:44519841
|
C | T | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1239+546C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | chr15 | 44519841 | ||||||
| chr15:44519900
|
G | A | 1 | a0001c0001t0004g0151 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1239+605G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | chr15 | 44519900 | ||||||
| chr15:44519962
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1239+667C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | chr15 | 44519962 | ||||||
| chr15:44520051
|
G | C | 1 | a0001c0001t0004g0146 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1239+756G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | chr15 | 44520051 | ||||||
| chr15:44520080
|
C | CATCCT | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1239+786_1239+790d others(7): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 44520080 | |||||
| chr15:44520129
|
TTTC | T | 4 | a0001c0003t0008g0058a0001c0003t0008g0059a0001c0003t0008g0061others(1): Show | 4 | HG02615.hp2 HG02630.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239+837_1239+839d others(5): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 44520129 | |||||
| chr15:44520154
|
C | CT | 10 | a0001c0001t0001g0092a0001c0001t0001g0106a0001c0001t0002g0125others(7): Show | 10 | HG00735.hp1 HG01167.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.1239+872dupT | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 44520154 | |||||
| chr15:44520172
|
C | T | 1 | a0001c0001t0017g0001 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1239+877C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | chr15 | 44520172 | ||||||
| chr15:44520222
|
C | T | 17 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(14): Show | 17 | HG00408.hp1 HG00597.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.1239+927C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | chr15 | 44520222 | ||||||
| chr15:44520241
|
C | T | 6 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(3): Show | 6 | HG02965.hp2 HG03209.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1239+946C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | chr15 | 44520241 | ||||||
| chr15:44520294
|
G | A | 1 | a0001c0001t0025g0025 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1239+999G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | chr15 | 44520294 | ||||||
| chr15:44520496
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1240-815G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | chr15 | 44520496 | ||||||
| chr15:44520547
|
T | C | 18 | a0001c0002t0005g0031a0001c0002t0005g0032a0001c0002t0005g0033others(15): Show | 18 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.1240-764T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | chr15 | 44520547 | ||||||
| chr15:44520709
|
C | A | 1 | a0001c0001t0002g0180 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1240-602C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | chr15 | 44520709 | ||||||
| chr15:44520930
|
A | G | 1 | a0001c0001t0002g0187 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1240-381A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | chr15 | 44520930 | ||||||
| chr15:44521076
|
T | G | 24 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(21): Show | 24 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1240-235T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | chr15 | 44521076 | ||||||
| chr15:44521168
|
CAAAGA | C | 20 | a0001c0001t0004g0068a0001c0001t0004g0069a0001c0001t0004g0116others(17): Show | 20 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.1240-138_1240-134d others(7): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr15 | 44521168 | |||||
| chr15:44521413
|
G | A | 29 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(26): Show | 29 | HG01891.hp1 HG01891.hp2 HG02040.hp1 others(26): Show |
splice_region_variant&intron_variant | LOW | c.1335+7G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44521413 | ||||||
| chr15:44521503
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1335+97T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44521503 | ||||||
| chr15:44521660
|
C | T | 1 | a0001c0001t0014g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1335+254C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44521660 | ||||||
| chr15:44521689
|
A | G | 3 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0029 | 3 | HG02572.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1335+283A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44521689 | ||||||
| chr15:44521795
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1335+389G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44521795 | ||||||
| chr15:44521811
|
G | T | 24 | a0001c0001t0003g0020a0001c0001t0003g0021a0001c0001t0003g0022others(21): Show | 24 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1335+405G>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44521811 | ||||||
| chr15:44521937
|
C | CA | 113 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0072others(110): Show | 113 | HG00408.hp2 HG00673.hp2 HG00735.hp1 others(110): Show |
intron_variant | MODIFIER | c.1335+557dupA | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 44521937 | |||||
| chr15:44521937
|
C | CAA | 72 | a0001c0001t0001g0037a0001c0001t0001g0074a0001c0001t0001g0081others(69): Show | 72 | HG00423.hp1 HG00423.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1335+556_1335+557d others(4): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 44521937 | |||||
| chr15:44521937
|
C | CAAA | 18 | a0001c0001t0001g0088a0001c0001t0001g0164a0001c0001t0001g0212others(15): Show | 18 | HG00408.hp1 HG00673.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.1335+555_1335+557d others(5): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 44521937 | |||||
| chr15:44521937
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0009g0026 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1335+547_1335+557d others(13): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 44521937 | |||||
| chr15:44521937
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0009g0029 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1335+545_1335+557d others(15): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 44521937 | |||||
| chr15:44521937
|
C | CAAAAAAA others(9): Show |
3 | a0001c0001t0011g0051a0001c0001t0011g0052a0001c0001t0011g0054 | 3 | HG02970.hp2 HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1335+542_1335+557d others(18): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 44521937 | |||||
| chr15:44521937
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0011g0053 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1335+541_1335+557d others(19): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 44521937 | |||||
| chr15:44521937
|
C | CAAAAAAA others(26): Show |
1 | a0001c0001t0009g0028 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1335+557_1335+558i others(35): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 44521937 | |||||
| chr15:44521964
|
C | A | 1 | a0001c0001t0009g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1335+558C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44521964 | ||||||
| chr15:44521964
|
C | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0145 | 2 | HG01074.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1335+558C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44521964 | ||||||
| chr15:44521966
|
T | A | 1 | a0001c0001t0009g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1335+560T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44521966 | ||||||
| chr15:44521967
|
G | A | 1 | a0001c0001t0009g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1335+561G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44521967 | ||||||
| chr15:44521969
|
T | A | 2 | a0001c0001t0001g0130a0001c0001t0009g0027 | 2 | HG00741.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1335+563T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44521969 | ||||||
| chr15:44521970
|
G | C | 2 | a0001c0001t0001g0130a0001c0001t0009g0027 | 2 | HG00741.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1335+564G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44521970 | ||||||
| chr15:44522141
|
C | A | 1 | a0001c0001t0001g0153 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1335+735C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44522141 | ||||||
| chr15:44522232
|
C | G | 1 | a0001c0001t0014g0038 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1335+826C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44522232 | ||||||
| chr15:44522314
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1335+908G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44522314 | ||||||
| chr15:44522475
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1335+1069G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44522475 | ||||||
| chr15:44522507
|
C | T | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1335+1101C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44522507 | ||||||
| chr15:44522608
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1335+1202C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44522608 | ||||||
| chr15:44522962
|
A | G | 228 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0070others(225): Show | 228 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.1336-1147A>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44522962 | ||||||
| chr15:44523048
|
G | A | 2 | a0001c0001t0002g0213a0001c0001t0002g0221 | 2 | HG01192.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.1336-1061G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44523048 | ||||||
| chr15:44523331
|
G | C | 1 | a0001c0003t0008g0063 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1336-778G>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44523331 | ||||||
| chr15:44523332
|
A | C | 1 | a0001c0003t0008g0063 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1336-777A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44523332 | ||||||
| chr15:44523334
|
T | G | 1 | a0001c0003t0008g0063 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1336-775T>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44523334 | ||||||
| chr15:44523382
|
T | A | 168 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0070others(165): Show | 168 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.1336-727T>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44523382 | ||||||
| chr15:44523386
|
C | G | 1 | a0001c0001t0001g0119 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1336-723C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44523386 | ||||||
| chr15:44523388
|
C | CTACA | 21 | a0001c0001t0001g0103a0001c0001t0001g0120a0001c0001t0001g0153others(18): Show | 21 | HG00673.hp1 HG00673.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1336-666_1336-663d others(6): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 44523388 | |||||
| chr15:44523388
|
C | CTACATAC others(1): Show |
5 | a0001c0001t0002g0080a0001c0001t0002g0136a0001c0001t0002g0187others(2): Show | 5 | HG00423.hp1 HG00741.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.1336-670_1336-663d others(10): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 44523388 | |||||
| chr15:44523388
|
CTACA | C | 90 | a0001c0001t0001g0070a0001c0001t0001g0072a0001c0001t0001g0075others(87): Show | 90 | HG00597.hp2 HG00642.hp1 HG00735.hp1 others(87): Show |
intron_variant | MODIFIER | c.1336-666_1336-663d others(6): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 44523388 | |||||
| chr15:44523388
|
CTACATAC others(1): Show |
C | 28 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0001g0086others(25): Show | 28 | HG00423.hp2 HG00642.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1336-670_1336-663d others(10): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 44523388 | |||||
| chr15:44523388
|
CTACATAC others(5): Show |
C | 30 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0073others(27): Show | 30 | HG00408.hp1 HG00597.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1336-674_1336-663d others(14): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 44523388 | |||||
| chr15:44523388
|
CTACATAC others(9): Show |
C | 2 | a0001c0001t0016g0188a0001c0001t0016g0189 | 2 | HG00738.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1336-678_1336-663d others(18): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 44523388 | |||||
| chr15:44523388
|
CTACATAC others(17): Show |
C | 1 | a0001c0001t0002g0166 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1336-686_1336-663d others(26): Show |
CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr15 | 44523388 | |||||
| chr15:44523396
|
A | C | 1 | a0001c0001t0001g0091 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1336-713A>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44523396 | ||||||
| chr15:44523615
|
C | G | 4 | a0001c0001t0001g0074a0001c0001t0001g0081a0001c0001t0001g0164others(1): Show | 4 | HG01884.hp1 HG02486.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1336-494C>G | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44523615 | ||||||
| chr15:44523619
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1336-490C>T | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44523619 | ||||||
| chr15:44523725
|
T | C | 65 | a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0004others(62): Show | 65 | HG00408.hp1 HG00597.hp1 HG00673.hp1 others(62): Show |
intron_variant | MODIFIER | c.1336-384T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44523725 | ||||||
| chr15:44523726
|
T | C | 2 | a0001c0001t0025g0025a0001c0001t0026g0024 | 2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1336-383T>C | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44523726 | ||||||
| chr15:44523772
|
G | A | 1 | a0001c0001t0014g0038 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1336-337G>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44523772 | ||||||
| chr15:44523813
|
C | A | 12 | a0001c0001t0009g0026a0001c0001t0009g0027a0001c0001t0009g0028others(9): Show | 12 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1336-296C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44523813 | ||||||
| chr15:44524026
|
C | A | 1 | a0001c0001t0001g0228 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1336-83C>A | CTDSPL2 | ENSG00000137770.14 | transcript | ENST00000260327.9 | protein_coding | 12/12 | chr15 | 44524026 |