Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 375248 |
|---|---|
| ensemblid | ENSG00000135976.21 |
| hgncid | 24079 |
| symbol | ANKRD36 |
| name | ankyrin repeat domain 36 |
| refseq_nuc | NM_001354587.1 |
| refseq_prot | NP_001341516.1 |
| ensembl_nuc | ENST00000420699.9 |
| ensembl_prot | ENSP00000391950.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 97113153 |
| end | 97264521 |
| strand | + |
| ver | v1.2 |
| region | chr2:97113153-97264521 |
| region5000 | chr2:97108153-97269521 |
| regionname0 | ANKRD36_chr2_97113153_97264521 |
| regionname5000 | ANKRD36_chr2_97108153_97269521 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000 | 0/0 | 0 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0001 | 0/1 | 1915 | 37 | 7 | 12 | 14 | 0 | 3 | 11 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0002 | 0/0 | 1881 | 22 | 22 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0003 | 0/0 | 1881 | 20 | 3 | 4 | 9 | 0 | 4 | 8 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0004 | 0/0 | 1881 | 11 | 3 | 6 | 0 | 2 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0005 | 0/0 | 1915 | 10 | 8 | 1 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0006 | 0/0 | 1881 | 8 | 1 | 7 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0007 | 0/0 | 1881 | 8 | 1 | 4 | 0 | 2 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0008 | 0/0 | 1903 | 8 | 0 | 0 | 8 | 0 | 0 | 7 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0009 | 0/0 | 1915 | 7 | 5 | 2 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0010 | 0/0 | 1915 | 6 | 0 | 2 | 0 | 0 | 4 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0011 | 0/0 | 1134 | 5 | 0 | 0 | 4 | 0 | 1 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0012 | 0/0 | 1915 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0013 | 0/0 | 1903 | 5 | 0 | 0 | 2 | 0 | 3 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0014 | 0/0 | 1881 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0015 | 0/0 | 1639 | 4 | 0 | 0 | 4 | 0 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0016 | 0/0 | 382 | 3 | 0 | 0 | 0 | 0 | 3 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0017 | 0/0 | 414 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0018 | 0/0 | 1881 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0019 | 0/0 | 370 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0020 | 0/0 | 1881 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0021 | 0/0 | 1881 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0022 | 0/0 | 1914 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0023 | 0/0 | 1903 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0024 | 0/0 | 1915 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0025 | 0/0 | 1881 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0026 | 0/0 | 1915 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0027 | 0/0 | 414 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0028 | 0/0 | 173 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0029 | 0/0 | 1915 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0030 | 0/0 | 1881 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0031 | 0/0 | 1639 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0032 | 0/0 | 1881 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0033 | 0/0 | 1711 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0034 | 0/0 | 1639 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0035 | 0/0 | 1847 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0036 | 0/0 | 1915 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0037 | 0/0 | 1915 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0038 | 0/0 | 1639 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0039 | 1/0 | 1915 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0040 | 0/0 | 1430 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0041 | 0/0 | 1915 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0042 | 0/0 | 1915 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0043 | 0/0 | 1881 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0044 | 0/0 | 1881 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0045 | 0/0 | 1915 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0046 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0047 | 0/0 | 1915 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0048 | 0/0 | 1914 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0049 | 0/0 | 1915 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0050 | 0/0 | 1915 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0051 | 0/0 | 1915 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0052 | 0/0 | 1903 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 5748 | 34 | 6 | 10 | 14 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0002 | 0/0 | 5646 | 22 | 22 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0003 | 0/0 | 5646 | 20 | 3 | 4 | 9 | 0 | 4 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0004 | 0/0 | 5748 | 10 | 8 | 1 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0005 | 0/0 | 5646 | 9 | 2 | 5 | 0 | 2 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0006 | 0/0 | 5748 | 8 | 0 | 0 | 8 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0007 | 0/0 | 5646 | 8 | 1 | 4 | 0 | 2 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0008 | 0/0 | 5646 | 7 | 0 | 7 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0009 | 0/0 | 5748 | 7 | 5 | 2 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0010 | 0/0 | 5748 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0011 | 0/0 | 5644 | 5 | 0 | 0 | 4 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0012 | 0/0 | 5748 | 5 | 0 | 2 | 0 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0013 | 0/0 | 5748 | 4 | 0 | 0 | 1 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0014 | 0/0 | 5646 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0015 | 0/0 | 4920 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0016 | 0/0 | 5163 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0017 | 0/0 | 5548 | 3 | 0 | 2 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0018 | 0/0 | 5646 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0019 | 0/0 | 5748 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0020 | 0/0 | 5745 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0021 | 0/0 | 5646 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0022 | 0/0 | 5646 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0023 | 0/0 | 5748 | 2 | 0 | 0 | 0 | 0 | 2 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0024 | 0/0 | 5646 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0025 | 0/0 | 5748 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0026 | 0/0 | 5748 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0027 | 0/0 | 5748 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0028 | 0/0 | 5548 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0029 | 0/0 | 5748 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0030 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0031 | 0/0 | 5393 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0032 | 0/0 | 5393 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0033 | 0/0 | 5748 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0034 | 0/0 | 5646 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0035 | 0/0 | 5136 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0036 | 0/0 | 5748 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0037 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0038 | 0/0 | 5646 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0039 | 0/0 | 5646 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0040 | 0/0 | 5748 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0041 | 0/0 | 5748 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0042 | 0/0 | 4920 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0043 | 0/0 | 5748 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0044 | 0/0 | 5748 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0045 | 0/0 | 5748 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0046 | 0/0 | 5748 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0047 | 0/0 | 5748 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0048 | 1/0 | 5748 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0049 | 0/0 | 5748 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0050 | 0/0 | 4920 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0051 | 0/0 | 4920 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0052 | 0/0 | 5646 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0053 | 0/0 | 5748 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0054 | 0/0 | 5646 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0055 | 0/0 | 5748 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0056 | 0/0 | 5646 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0057 | 0/0 | 5646 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0058 | 0/0 | 5748 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0059 | 0/0 | 5748 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0060 | 0/0 | 5748 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0061 | 0/0 | 5748 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| c0062 | 0/0 | 5544 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 787 | 127 | 28 | 35 | 39 | 2 | 21 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| t0002 | 0/0 | 787 | 42 | 29 | 3 | 9 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| t0003 | 0/0 | 787 | 16 | 0 | 0 | 13 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| t0004 | 0/0 | 787 | 9 | 3 | 3 | 0 | 2 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| t0005 | 0/0 | 787 | 7 | 6 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| t0006 | 0/0 | 588 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| t0007 | 0/0 | 787 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| t0008 | 0/0 | 787 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| t0009 | 0/0 | 787 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| t0010 | 0/0 | 787 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0009 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0016 | 0/0 | 5163 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0001c0001 | 0/1 | 5748 | 34 | 6 | 10 | 14 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0001c0036 | 0/0 | 5748 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0001c0044 | 0/0 | 5748 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0001c0046 | 0/0 | 5748 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0002c0002 | 0/0 | 5646 | 22 | 22 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0003c0003 | 0/0 | 5646 | 20 | 3 | 4 | 9 | 0 | 4 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0004c0005 | 0/0 | 5646 | 9 | 2 | 5 | 0 | 2 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0004c0024 | 0/0 | 5646 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0005c0004 | 0/0 | 5748 | 10 | 8 | 1 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0006c0008 | 0/0 | 5646 | 7 | 0 | 7 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0006c0034 | 0/0 | 5646 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0007c0007 | 0/0 | 5646 | 8 | 1 | 4 | 0 | 2 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0008c0006 | 0/0 | 5748 | 8 | 0 | 0 | 8 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0009c0009 | 0/0 | 5748 | 7 | 5 | 2 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0010c0012 | 0/0 | 5748 | 5 | 0 | 2 | 0 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0010c0059 | 0/0 | 5748 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0011c0011 | 0/0 | 5644 | 5 | 0 | 0 | 4 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0012c0010 | 0/0 | 5748 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0013c0013 | 0/0 | 5748 | 4 | 0 | 0 | 1 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0013c0025 | 0/0 | 5748 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0014c0014 | 0/0 | 5646 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0015c0015 | 0/0 | 4920 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0016c0023 | 0/0 | 5748 | 2 | 0 | 0 | 0 | 0 | 2 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0016c0053 | 0/0 | 5748 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0017c0017 | 0/0 | 5548 | 3 | 0 | 2 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0018c0018 | 0/0 | 5646 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0019c0031 | 0/0 | 5393 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0019c0032 | 0/0 | 5393 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0020c0022 | 0/0 | 5646 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0021c0021 | 0/0 | 5646 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0022c0020 | 0/0 | 5745 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0023c0019 | 0/0 | 5748 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0024c0060 | 0/0 | 5748 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0025c0057 | 0/0 | 5646 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0026c0058 | 0/0 | 5748 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0027c0028 | 0/0 | 5548 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0028c0056 | 0/0 | 5646 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0029c0055 | 0/0 | 5748 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0030c0052 | 0/0 | 5646 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0031c0051 | 0/0 | 4920 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0032c0054 | 0/0 | 5646 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0033c0035 | 0/0 | 5136 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0034c0050 | 0/0 | 4920 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0035c0062 | 0/0 | 5544 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0036c0041 | 0/0 | 5748 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0037c0040 | 0/0 | 5748 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0038c0042 | 0/0 | 4920 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0039c0048 | 1/0 | 5748 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0040c0047 | 0/0 | 5748 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0041c0045 | 0/0 | 5748 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0042c0043 | 0/0 | 5748 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0043c0039 | 0/0 | 5646 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0044c0038 | 0/0 | 5646 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0045c0049 | 0/0 | 5748 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0046c0037 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0047c0033 | 0/0 | 5748 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0048c0030 | 0/0 | 5745 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0049c0029 | 0/0 | 5748 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0050c0061 | 0/0 | 5748 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0051c0027 | 0/0 | 5748 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0052c0026 | 0/0 | 5748 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0016t0006 | 0/0 | 5750 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0001c0001t0001 | 0/1 | 6534 | 29 | 2 | 10 | 13 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0001c0001t0002 | 0/0 | 6534 | 4 | 4 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0001c0001t0007 | 0/0 | 6534 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0001c0036t0001 | 0/0 | 6534 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0001c0044t0001 | 0/0 | 6534 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0001c0046t0002 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0002c0002t0001 | 0/0 | 6432 | 19 | 19 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0002c0002t0002 | 0/0 | 6432 | 3 | 3 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0003c0003t0001 | 0/0 | 6432 | 20 | 3 | 4 | 9 | 0 | 4 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0004c0005t0004 | 0/0 | 6432 | 6 | 2 | 2 | 0 | 2 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0004c0005t0008 | 0/0 | 6432 | 2 | 0 | 2 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0004c0005t0010 | 0/0 | 6432 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0004c0024t0004 | 0/0 | 6432 | 2 | 1 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0005c0004t0002 | 0/0 | 6534 | 3 | 2 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0005c0004t0005 | 0/0 | 6534 | 7 | 6 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0006c0008t0001 | 0/0 | 6432 | 6 | 0 | 6 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0006c0008t0009 | 0/0 | 6432 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0006c0034t0001 | 0/0 | 6432 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0007c0007t0001 | 0/0 | 6432 | 8 | 1 | 4 | 0 | 2 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0008c0006t0003 | 0/0 | 6534 | 8 | 0 | 0 | 8 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0009c0009t0002 | 0/0 | 6534 | 7 | 5 | 2 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0010c0012t0001 | 0/0 | 6534 | 5 | 0 | 2 | 0 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0010c0059t0001 | 0/0 | 6534 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0011c0011t0002 | 0/0 | 6430 | 5 | 0 | 0 | 4 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0012c0010t0002 | 0/0 | 6534 | 5 | 5 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0013c0013t0003 | 0/0 | 6534 | 4 | 0 | 0 | 1 | 0 | 3 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0013c0025t0003 | 0/0 | 6534 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0014c0014t0001 | 0/0 | 6432 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0015c0015t0001 | 0/0 | 5706 | 4 | 0 | 0 | 4 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0016c0023t0001 | 0/0 | 6534 | 2 | 0 | 0 | 0 | 0 | 2 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0016c0053t0001 | 0/0 | 6534 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0017c0017t0001 | 0/0 | 6334 | 3 | 0 | 2 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0018c0018t0002 | 0/0 | 6432 | 3 | 0 | 0 | 3 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0019c0031t0007 | 0/0 | 6179 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0019c0032t0007 | 0/0 | 6179 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0020c0022t0002 | 0/0 | 6432 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0021c0021t0002 | 0/0 | 6432 | 2 | 2 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0022c0020t0001 | 0/0 | 6531 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0023c0019t0003 | 0/0 | 6534 | 2 | 0 | 0 | 2 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0024c0060t0002 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0025c0057t0001 | 0/0 | 6432 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0026c0058t0001 | 0/0 | 6534 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0027c0028t0001 | 0/0 | 6334 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0028c0056t0001 | 0/0 | 6432 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0029c0055t0002 | 0/0 | 6534 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0030c0052t0002 | 0/0 | 6432 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0031c0051t0001 | 0/0 | 5706 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0032c0054t0001 | 0/0 | 6432 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0033c0035t0001 | 0/0 | 5922 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0034c0050t0001 | 0/0 | 5706 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0035c0062t0004 | 0/0 | 6330 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0036c0041t0001 | 0/0 | 6534 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0037c0040t0002 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0038c0042t0001 | 0/0 | 5706 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0039c0048t0001 | 1/0 | 6534 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0040c0047t0001 | 0/0 | 6534 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0041c0045t0001 | 0/0 | 6534 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0042c0043t0002 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0043c0039t0001 | 0/0 | 6432 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0044c0038t0001 | 0/0 | 6432 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0045c0049t0001 | 0/0 | 6534 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0046c0037t0001 | 0/0 | 5604 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0047c0033t0002 | 0/0 | 6534 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0048c0030t0002 | 0/0 | 6531 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0049c0029t0001 | 0/0 | 6534 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0050c0061t0001 | 0/0 | 6534 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0051c0027t0001 | 0/0 | 6534 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| a0052c0026t0003 | 0/0 | 6534 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | copy fasta | chr2 | 97108153 | 97269521 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0000c0016t0006g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0000c0016t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0000c0016t0006g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0000c0016t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0081 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0001t0007g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0036t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0044t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0001c0046t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0002c0002t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0003c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0004c0005t0004g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0004c0005t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0004c0005t0004g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0004c0005t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0004c0005t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0004c0005t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0004c0005t0008g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0004c0005t0008g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0004c0005t0010g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0004c0024t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0004c0024t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0005c0004t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0005c0004t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0005c0004t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0005c0004t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0005c0004t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0005c0004t0005g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0005c0004t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0005c0004t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0005c0004t0005g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0005c0004t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0006c0008t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0006c0008t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0006c0008t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0006c0008t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0006c0008t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0006c0008t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0006c0008t0009g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0006c0034t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0007c0007t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0007c0007t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0007c0007t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0007c0007t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0007c0007t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0007c0007t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0007c0007t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0007c0007t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0008c0006t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0008c0006t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0008c0006t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0008c0006t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0008c0006t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0008c0006t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0008c0006t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0008c0006t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0009c0009t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0009c0009t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0009c0009t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0009c0009t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0009c0009t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0009c0009t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0009c0009t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0010c0012t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0010c0012t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0010c0012t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0010c0012t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0010c0012t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0010c0059t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0011c0011t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0011c0011t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0011c0011t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0011c0011t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0011c0011t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0012c0010t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0012c0010t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0012c0010t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0012c0010t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0012c0010t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0013c0013t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0013c0013t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0013c0013t0003g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0013c0013t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0013c0025t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0014c0014t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0014c0014t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0014c0014t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0014c0014t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0015c0015t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0015c0015t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0015c0015t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0015c0015t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0016c0023t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0016c0023t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0016c0053t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0017c0017t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0017c0017t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0017c0017t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0018c0018t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0018c0018t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0018c0018t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0019c0031t0007g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0019c0032t0007g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0020c0022t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0020c0022t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0021c0021t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0021c0021t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0022c0020t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0022c0020t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0023c0019t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0023c0019t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0024c0060t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0025c0057t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0026c0058t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0027c0028t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0028c0056t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0029c0055t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0030c0052t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0031c0051t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0032c0054t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0033c0035t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0034c0050t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0035c0062t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0036c0041t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0037c0040t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0038c0042t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0039c0048t0001g0009 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0040c0047t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0041c0045t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0042c0043t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0043c0039t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0044c0038t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0045c0049t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0046c0037t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0047c0033t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0048c0030t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0049c0029t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0050c0061t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0051c0027t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| a0052c0026t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0004 | c0005 | t0004 | g0016 | EUR | GBR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG00099 | hp2 | a0007 | c0007 | t0001 | g0141 | EUR | GBR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG00423 | hp1 | a0011 | c0011 | t0002 | g0047 | EAS | CHS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG00423 | hp2 | a0022 | c0020 | t0001 | g0097 | EAS | CHS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG00558 | hp1 | a0014 | c0014 | t0001 | g0150 | EAS | CHS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG00558 | hp2 | a0015 | c0015 | t0001 | g0088 | EAS | CHS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG00597 | hp1 | a0033 | c0035 | t0001 | g0136 | EAS | CHS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG00597 | hp2 | a0008 | c0006 | t0003 | g0184 | EAS | CHS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG00609 | hp1 | a0005 | c0004 | t0002 | g0002 | EAS | CHS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG00639 | hp1 | a0025 | c0057 | t0001 | g0134 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG00639 | hp2 | a0001 | c0044 | t0001 | g0001 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG00642 | hp1 | a0006 | c0008 | t0001 | g0007 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG00642 | hp2 | a0005 | c0004 | t0005 | g0204 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG00741 | hp2 | a0006 | c0008 | t0001 | g0148 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01070 | hp2 | a0017 | c0017 | t0001 | g0145 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01099 | hp1 | a0007 | c0007 | t0001 | g0139 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01099 | hp2 | a0004 | c0005 | t0004 | g0037 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01106 | hp1 | a0010 | c0012 | t0001 | g0103 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01106 | hp2 | a0007 | c0007 | t0001 | g0180 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01169 | hp2 | a0003 | c0003 | t0001 | g0133 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01175 | hp1 | a0004 | c0005 | t0008 | g0035 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01175 | hp2 | a0003 | c0003 | t0001 | g0167 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01243 | hp1 | a0029 | c0055 | t0002 | g0023 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01257 | hp2 | a0004 | c0005 | t0008 | g0041 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01261 | hp1 | a0009 | c0009 | t0002 | g0174 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01261 | hp2 | a0004 | c0024 | t0004 | g0040 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01358 | hp1 | a0007 | c0007 | t0001 | g0164 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01358 | hp2 | a0009 | c0009 | t0002 | g0178 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01361 | hp1 | a0010 | c0012 | t0001 | g0083 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01361 | hp2 | a0017 | c0017 | t0001 | g0169 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01496 | hp1 | a0003 | c0003 | t0001 | g0157 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01496 | hp2 | a0036 | c0041 | t0001 | g0113 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01515 | hp1 | a0004 | c0005 | t0004 | g0033 | EUR | IBS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01515 | hp2 | a0007 | c0007 | t0001 | g0138 | EUR | IBS | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01891 | hp1 | a0024 | c0060 | t0002 | g0024 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01934 | hp1 | a0040 | c0047 | t0001 | g0082 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01934 | hp2 | a0007 | c0007 | t0001 | g0207 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01943 | hp1 | a0001 | c0036 | t0001 | g0080 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01943 | hp2 | a0006 | c0008 | t0001 | g0147 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01975 | hp1 | a0006 | c0008 | t0001 | g0006 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01975 | hp2 | a0049 | c0029 | t0001 | g0122 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01981 | hp1 | a0004 | c0005 | t0004 | g0039 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01993 | hp1 | a0006 | c0008 | t0001 | g0005 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02004 | hp1 | a0006 | c0008 | t0001 | g0004 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02040 | hp1 | a0000 | c0016 | t0006 | g0108 | EAS | KHV | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02040 | hp2 | a0048 | c0030 | t0002 | g0003 | EAS | KHV | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02055 | hp2 | a0043 | c0039 | t0001 | g0008 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02071 | hp1 | a0013 | c0025 | t0003 | g0185 | EAS | KHV | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02083 | hp2 | a0013 | c0013 | t0003 | g0186 | EAS | KHV | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02145 | hp1 | a0030 | c0052 | t0002 | g0128 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0066 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0056 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02257 | hp2 | a0004 | c0005 | t0004 | g0032 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02258 | hp1 | a0007 | c0007 | t0001 | g0140 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02258 | hp2 | a0005 | c0004 | t0002 | g0130 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02293 | hp1 | a0028 | c0056 | t0001 | g0171 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02300 | hp1 | a0006 | c0008 | t0009 | g0146 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02451 | hp1 | a0009 | c0009 | t0002 | g0175 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02572 | hp1 | a0002 | c0002 | t0002 | g0031 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02572 | hp2 | a0020 | c0022 | t0002 | g0030 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02602 | hp1 | a0010 | c0012 | t0001 | g0075 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02602 | hp2 | a0011 | c0011 | t0002 | g0046 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02630 | hp1 | a0005 | c0004 | t0005 | g0200 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02630 | hp2 | a0037 | c0040 | t0002 | g0211 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02683 | hp1 | a0003 | c0003 | t0001 | g0168 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02698 | hp1 | a0010 | c0059 | t0001 | g0090 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02698 | hp2 | a0007 | c0007 | t0001 | g0137 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02717 | hp1 | a0012 | c0010 | t0002 | g0206 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02717 | hp2 | a0042 | c0043 | t0002 | g0210 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0183 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0052 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02738 | hp1 | a0032 | c0054 | t0001 | g0165 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0061 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02809 | hp2 | a0021 | c0021 | t0002 | g0013 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02886 | hp1 | a0004 | c0024 | t0004 | g0038 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0069 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02895 | hp1 | a0021 | c0021 | t0002 | g0012 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02895 | hp2 | a0009 | c0009 | t0002 | g0179 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02897 | hp1 | a0003 | c0003 | t0001 | g0172 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02897 | hp2 | a0009 | c0009 | t0002 | g0182 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02922 | hp1 | a0005 | c0004 | t0002 | g0129 | AFR | ESN | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02922 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | ESN | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0062 | AFR | ESN | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0053 | AFR | ESN | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03041 | hp1 | a0002 | c0002 | t0001 | g0063 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03041 | hp2 | a0020 | c0022 | t0002 | g0015 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03098 | hp1 | a0012 | c0010 | t0002 | g0027 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03098 | hp2 | a0009 | c0009 | t0002 | g0177 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03130 | hp1 | a0005 | c0004 | t0005 | g0203 | AFR | ESN | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0055 | AFR | ESN | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0054 | AFR | ESN | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03195 | hp2 | a0005 | c0004 | t0005 | g0205 | AFR | ESN | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03225 | hp1 | a0003 | c0003 | t0001 | g0135 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0132 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03486 | hp1 | a0047 | c0033 | t0002 | g0025 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0065 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0064 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03579 | hp1 | a0009 | c0009 | t0002 | g0176 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0059 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03654 | hp1 | a0027 | c0028 | t0001 | g0161 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03669 | hp1 | a0010 | c0012 | t0001 | g0092 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03669 | hp2 | a0017 | c0017 | t0001 | g0170 | SAS | PJL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03688 | hp1 | a0003 | c0003 | t0001 | g0149 | SAS | STU | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03688 | hp2 | a0026 | c0058 | t0001 | g0074 | SAS | STU | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03834 | hp1 | a0013 | c0013 | t0003 | g0187 | SAS | BEB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03834 | hp2 | a0016 | c0023 | t0001 | g0091 | SAS | BEB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03927 | hp1 | a0016 | c0023 | t0001 | g0093 | SAS | BEB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03927 | hp2 | a0035 | c0062 | t0004 | g0042 | SAS | BEB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG04115 | hp1 | a0013 | c0013 | t0003 | g0189 | SAS | STU | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG04115 | hp2 | a0016 | c0053 | t0001 | g0104 | SAS | STU | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG04204 | hp1 | a0010 | c0012 | t0001 | g0072 | SAS | STU | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG04204 | hp2 | a0013 | c0013 | t0003 | g0188 | SAS | STU | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG04228 | hp1 | a0045 | c0049 | t0001 | g0120 | SAS | STU | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG04228 | hp2 | a0003 | c0003 | t0001 | g0158 | SAS | STU | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18612 | hp1 | a0003 | c0003 | t0001 | g0159 | EAS | CHB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18612 | hp2 | a0022 | c0020 | t0001 | g0098 | EAS | CHB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18941 | hp2 | a0052 | c0026 | t0003 | g0193 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18945 | hp1 | a0011 | c0011 | t0002 | g0045 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18946 | hp1 | a0014 | c0014 | t0001 | g0155 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18946 | hp2 | a0041 | c0045 | t0001 | g0110 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18947 | hp2 | a0003 | c0003 | t0001 | g0152 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18950 | hp1 | a0003 | c0003 | t0001 | g0144 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18951 | hp1 | a0018 | c0018 | t0002 | g0044 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18951 | hp2 | a0008 | c0006 | t0003 | g0194 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18952 | hp1 | a0015 | c0015 | t0001 | g0109 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18952 | hp2 | a0003 | c0003 | t0001 | g0160 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18961 | hp1 | a0018 | c0018 | t0002 | g0043 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18961 | hp2 | a0015 | c0015 | t0001 | g0118 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18965 | hp1 | a0008 | c0006 | t0003 | g0191 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18965 | hp2 | a0000 | c0016 | t0006 | g0076 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18971 | hp1 | a0034 | c0050 | t0001 | g0087 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18971 | hp2 | a0008 | c0006 | t0003 | g0190 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18972 | hp1 | a0003 | c0003 | t0001 | g0143 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18972 | hp2 | a0001 | c0001 | t0007 | g0100 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18973 | hp1 | a0014 | c0014 | t0001 | g0156 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18973 | hp2 | a0008 | c0006 | t0003 | g0192 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18983 | hp1 | a0008 | c0006 | t0003 | g0195 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18991 | hp1 | a0003 | c0003 | t0001 | g0181 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18991 | hp2 | a0011 | c0011 | t0002 | g0049 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA18999 | hp2 | a0023 | c0019 | t0003 | g0198 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19000 | hp1 | a0003 | c0003 | t0001 | g0153 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19000 | hp2 | a0000 | c0016 | t0006 | g0119 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19002 | hp1 | a0003 | c0003 | t0001 | g0142 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19002 | hp2 | a0031 | c0051 | t0001 | g0085 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19010 | hp1 | a0003 | c0003 | t0001 | g0151 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19010 | hp2 | a0046 | c0037 | t0001 | g0099 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19030 | hp1 | a0005 | c0004 | t0005 | g0202 | AFR | LWK | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0068 | AFR | LWK | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | LWK | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19043 | hp2 | a0012 | c0010 | t0002 | g0028 | AFR | LWK | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19056 | hp2 | a0019 | c0032 | t0007 | g0127 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19068 | hp1 | a0011 | c0011 | t0002 | g0011 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19070 | hp1 | a0023 | c0019 | t0003 | g0197 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19070 | hp2 | a0050 | c0061 | t0001 | g0010 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19072 | hp1 | a0018 | c0018 | t0002 | g0048 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19072 | hp2 | a0000 | c0016 | t0006 | g0018 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19074 | hp1 | a0014 | c0014 | t0001 | g0154 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19079 | hp2 | a0019 | c0031 | t0007 | g0126 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19085 | hp1 | a0008 | c0006 | t0003 | g0196 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19085 | hp2 | a0015 | c0015 | t0001 | g0089 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19088 | hp1 | a0008 | c0006 | t0003 | g0208 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19088 | hp2 | a0038 | c0042 | t0001 | g0094 | EAS | JPT | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19240 | hp1 | a0001 | c0046 | t0002 | g0051 | AFR | YRI | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA19240 | hp2 | a0012 | c0010 | t0002 | g0026 | AFR | YRI | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | ASW | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA20129 | hp2 | a0044 | c0038 | t0001 | g0067 | AFR | ASW | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA20905 | hp1 | a0003 | c0003 | t0001 | g0166 | SAS | GIH | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| NA20905 | hp2 | a0051 | c0027 | t0001 | g0071 | SAS | GIH | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01123 | hp1 | a0003 | c0003 | t0001 | g0162 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG01123 | hp2 | a0004 | c0005 | t0010 | g0034 | AMR | CLM | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02109 | hp1 | a0006 | c0034 | t0001 | g0173 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0060 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02559 | hp1 | a0012 | c0010 | t0002 | g0029 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG02559 | hp2 | a0004 | c0005 | t0004 | g0036 | AFR | ACB | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03471 | hp1 | a0005 | c0004 | t0005 | g0201 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG03471 | hp2 | a0003 | c0003 | t0001 | g0163 | AFR | MSL | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0209 | AFR | USA | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| HG06807 | hp2 | a0005 | c0004 | t0005 | g0199 | AFR | USA | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0081 | REF | REF | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| homoSapiens_grch38 | hp1 | a0039 | c0048 | t0001 | g0009 | REF | REF | ANKRD36_chr2_97108153_97269521 | ANKRD36 | chr2 | 97108153 | 97269521 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:97113741
|
T | A | 4 | a0008a0013a0023others(1): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
start_lost | HIGH | c.2T>A | p.Met1? | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 589/6534 | 2/5748 | 1/1915 | chr2 | 97113741 | ||
| chr2:97113750
|
G | A | 4 | a0008a0013a0023others(1): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
missense_variant | MODERATE | c.11G>A | p.Gly4Asp | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 598/6534 | 11/5748 | 4/1915 | chr2 | 97113750 | ||
| chr2:97113752
|
A | G | 4 | a0008a0013a0023others(1): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
missense_variant | MODERATE | c.13A>G | p.Lys5Glu | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 600/6534 | 13/5748 | 5/1915 | chr2 | 97113752 | ||
| chr2:97113814
|
A | T | 4 | a0008a0013a0023others(1): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
missense_variant | MODERATE | c.75A>T | p.Gln25His | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 662/6534 | 75/5748 | 25/1915 | chr2 | 97113814 | ||
| chr2:97113818
|
C | T | 4 | a0008a0013a0023others(1): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
missense_variant | MODERATE | c.79C>T | p.Pro27Ser | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 666/6534 | 79/5748 | 27/1915 | chr2 | 97113818 | ||
| chr2:97113819
|
C | A | 4 | a0008a0013a0023others(1): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
missense_variant | MODERATE | c.80C>A | p.Pro27His | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 667/6534 | 80/5748 | 27/1915 | chr2 | 97113819 | ||
| chr2:97113864
|
A | G | 4 | a0008a0018a0023others(1): Show | 14 | HG00597.hp2 NA18941.hp2 NA18951.hp1 others(11): Show |
missense_variant | MODERATE | c.125A>G | p.His42Arg | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 712/6534 | 125/5748 | 42/1915 | chr2 | 97113864 | ||
| chr2:97118138
|
T | C | 1 | a0051 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.272T>C | p.Leu91Pro | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 2/76 | 859/6534 | 272/5748 | 91/1915 | chr2 | 97118138 | ||
| chr2:97118398
|
A | G | 4 | a0010a0024a0025others(1): Show | 9 | HG00639.hp1 HG01106.hp1 HG01361.hp1 others(6): Show |
missense_variant | MODERATE | c.367A>G | p.Asn123Asp | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/76 | 954/6534 | 367/5748 | 123/1915 | chr2 | 97118398 | ||
| chr2:97118398
|
A | T | 1 | a0050 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.367A>T | p.Asn123Tyr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/76 | 954/6534 | 367/5748 | 123/1915 | chr2 | 97118398 | ||
| chr2:97118416
|
T | G | 3 | a0010a0025a0026 | 8 | HG00639.hp1 HG01106.hp1 HG01361.hp1 others(5): Show |
missense_variant | MODERATE | c.385T>G | p.Phe129Val | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/76 | 972/6534 | 385/5748 | 129/1915 | chr2 | 97118416 | ||
| chr2:97118440
|
T | C | 1 | a0027 | 1 | HG03654.hp1 | missense_variant | MODERATE | c.409T>C | p.Tyr137His | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/76 | 996/6534 | 409/5748 | 137/1915 | chr2 | 97118440 | ||
| chr2:97118443
|
G | A | 1 | a0023 | 2 | NA18999.hp2 NA19070.hp1 |
missense_variant | MODERATE | c.412G>A | p.Ala138Thr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/76 | 999/6534 | 412/5748 | 138/1915 | chr2 | 97118443 | ||
| chr2:97122920
|
C | T | 1 | a0028 | 1 | HG02293.hp1 | stop_gained | HIGH | c.520C>T | p.Arg174* | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/76 | 1107/6534 | 520/5748 | 174/1915 | chr2 | 97122920 | ||
| chr2:97124488
|
G | A | 1 | a0049 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.622G>A | p.Gly208Arg | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/76 | 1209/6534 | 622/5748 | 208/1915 | chr2 | 97124488 | ||
| chr2:97124506
|
ATTC | A | 2 | a0022a0048 | 3 | HG00423.hp2 HG02040.hp2 NA18612.hp2 |
disruptive_inframe_deletion | MODERATE | c.648_650delTCT | p.Leu217del | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/76 | 1235/6534 | 648/5748 | 216/1915 | INFO_REALIGN_3_PRIME | chr2 | 97124506 | |
| chr2:97124536
|
C | T | 1 | a0029 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.670C>T | p.Leu224Phe | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/76 | 1257/6534 | 670/5748 | 224/1915 | chr2 | 97124536 | ||
| chr2:97147001
|
TTAAACCA others(3856): Show |
T | 1 | a0019 | 1 | NA19056.hp2 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.1034+487_1102-1014 others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/76 | INFO_REALIGN_3_PRIME | chr2 | 97147001 | |||||
| chr2:97147002
|
TAAACCAT others(3855): Show |
T | 1 | a0019 | 1 | NA19079.hp2 | exon_loss_variant&splice_acceptor_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.1034+487_1102-1015 others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/76 | chr2 | 97147002 | ||||||
| chr2:97150885
|
TCTTTCCC others(8897): Show |
T | 1 | a0019 | 1 | NA19079.hp2 | exon_loss_variant | HIGH | c.1102-993_1389+1134 others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 13/76 | chr2 | 97150885 | ||||||
| chr2:97150889
|
TCCCCCTC others(8893): Show |
T | 1 | a0019 | 1 | NA19056.hp2 | exon_loss_variant | HIGH | c.1102-989_1389+1134 others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 13/76 | chr2 | 97150889 | ||||||
| chr2:97151924
|
C | T | 1 | a0016 | 3 | HG03834.hp2 HG03927.hp1 HG04115.hp2 |
stop_gained | HIGH | c.1147C>T | p.Arg383* | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 13/76 | 1734/6534 | 1147/5748 | 383/1915 | chr2 | 97151924 | ||
| chr2:97152093
|
AGTGATTC others(4367): Show |
A | 2 | a0017a0027 | 4 | HG01070.hp2 HG01361.hp2 HG03654.hp1 others(1): Show |
exon_loss_variant | HIGH | c.1162+158_1261-1637 others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/76 | INFO_REALIGN_3_PRIME | chr2 | 97152093 | |||||
| chr2:97158116
|
G | C | 2 | a0005a0048 | 11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
missense_variant | MODERATE | c.1270G>C | p.Glu424Gln | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 16/76 | 1857/6534 | 1270/5748 | 424/1915 | chr2 | 97158116 | ||
| chr2:97162132
|
G | A | 3 | a0012a0024a0047 | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
missense_variant | MODERATE | c.1423G>A | p.Ala475Thr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/76 | 2010/6534 | 1423/5748 | 475/1915 | chr2 | 97162132 | ||
| chr2:97167604
|
C | T | 1 | a0030 | 1 | HG02145.hp1 | missense_variant&splice_region_variant | MODERATE | c.1559C>T | p.Thr520Met | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 21/76 | 2146/6534 | 1559/5748 | 520/1915 | chr2 | 97167604 | ||
| chr2:97181772
|
A | G | 1 | a0020 | 2 | HG02572.hp2 HG03041.hp2 |
missense_variant | MODERATE | c.1816A>G | p.Lys606Glu | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/76 | 2403/6534 | 1816/5748 | 606/1915 | chr2 | 97181772 | ||
| chr2:97183477
|
C | T | 1 | a0031 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.1856C>T | p.Ser619Leu | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 27/76 | 2443/6534 | 1856/5748 | 619/1915 | chr2 | 97183477 | ||
| chr2:97183482
|
T | C | 12 | a0003a0006a0007others(9): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
missense_variant | MODERATE | c.1861T>C | p.Trp621Arg | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 27/76 | 2448/6534 | 1861/5748 | 621/1915 | chr2 | 97183482 | ||
| chr2:97187219
|
C | T | 4 | a0008a0013a0023others(1): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
missense_variant | MODERATE | c.2063C>T | p.Ala688Val | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 31/76 | 2650/6534 | 2063/5748 | 688/1915 | chr2 | 97187219 | ||
| chr2:97187500
|
CGAAGCTG others(11237): Show |
C | 1 | a0033 | 1 | HG00597.hp1 | exon_loss_variant | HIGH | c.2143+118_2755+104d others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/76 | INFO_REALIGN_3_PRIME | chr2 | 97187500 | |||||
| chr2:97188507
|
GGTGAGAG others(1883): Show |
G | 9 | a0003a0006a0007others(6): Show | 47 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(44): Show |
exon_loss_variant | HIGH | c.2144-494_2246-496d others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/76 | INFO_REALIGN_3_PRIME | chr2 | 97188507 | |||||
| chr2:97188626
|
CTGTGTGC others(1883): Show |
C | 1 | a0046 | 1 | NA19010.hp2 | exon_loss_variant | HIGH | c.2144-398_2246-400d others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/76 | INFO_REALIGN_3_PRIME | chr2 | 97188626 | |||||
| chr2:97189233
|
G | A | 1 | a0052 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2188G>A | p.Glu730Lys | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/76 | 2775/6534 | 2188/5748 | 730/1915 | chr2 | 97189233 | ||
| chr2:97190993
|
A | C | 1 | a0052 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2261A>C | p.Gln754Pro | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/76 | 2848/6534 | 2261/5748 | 754/1915 | chr2 | 97190993 | ||
| chr2:97191005
|
A | C | 1 | a0052 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2273A>C | p.Lys758Thr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/76 | 2860/6534 | 2273/5748 | 758/1915 | chr2 | 97191005 | ||
| chr2:97191115
|
A | G | 1 | a0052 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2281A>G | p.Thr761Ala | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/76 | 2868/6534 | 2281/5748 | 761/1915 | chr2 | 97191115 | ||
| chr2:97191116
|
C | G | 1 | a0052 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2282C>G | p.Thr761Ser | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/76 | 2869/6534 | 2282/5748 | 761/1915 | chr2 | 97191116 | ||
| chr2:97191125
|
A | C | 1 | a0052 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2291A>C | p.Lys764Thr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/76 | 2878/6534 | 2291/5748 | 764/1915 | chr2 | 97191125 | ||
| chr2:97191129
|
T | G | 1 | a0052 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2295T>G | p.Asp765Glu | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/76 | 2882/6534 | 2295/5748 | 765/1915 | chr2 | 97191129 | ||
| chr2:97191141
|
C | G | 1 | a0034 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.2307C>G | p.Asn769Lys | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/76 | 2894/6534 | 2307/5748 | 769/1915 | chr2 | 97191141 | ||
| chr2:97191149
|
C | G | 1 | a0052 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2315C>G | p.Thr772Arg | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/76 | 2902/6534 | 2315/5748 | 772/1915 | chr2 | 97191149 | ||
| chr2:97191155
|
T | A | 1 | a0052 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2321T>A | p.Ile774Lys | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/76 | 2908/6534 | 2321/5748 | 774/1915 | chr2 | 97191155 | ||
| chr2:97191175
|
G | A | 1 | a0052 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2341G>A | p.Gly781Arg | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/76 | 2928/6534 | 2341/5748 | 781/1915 | chr2 | 97191175 | ||
| chr2:97192885
|
C | A | 1 | a0052 | 1 | NA18941.hp2 | missense_variant | MODERATE | c.2375C>A | p.Thr792Lys | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/76 | 2962/6534 | 2375/5748 | 792/1915 | chr2 | 97192885 | ||
| chr2:97194734
|
C | T | 4 | a0008a0013a0023others(1): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
missense_variant | MODERATE | c.2458C>T | p.Arg820Trp | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 39/76 | 3045/6534 | 2458/5748 | 820/1915 | chr2 | 97194734 | ||
| chr2:97194750
|
T | C | 11 | a0003a0006a0007others(8): Show | 55 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(52): Show |
missense_variant | MODERATE | c.2474T>C | p.Leu825Ser | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 39/76 | 3061/6534 | 2474/5748 | 825/1915 | chr2 | 97194750 | ||
| chr2:97198471
|
G | C | 1 | a0050 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.2662G>C | p.Glu888Gln | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 43/76 | 3249/6534 | 2662/5748 | 888/1915 | chr2 | 97198471 | ||
| chr2:97198596
|
C | A | 12 | a0003a0006a0007others(9): Show | 56 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(53): Show |
missense_variant | MODERATE | c.2693C>A | p.Ala898Asp | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/76 | 3280/6534 | 2693/5748 | 898/1915 | chr2 | 97198596 | ||
| chr2:97198637
|
G | T | 12 | a0003a0006a0007others(9): Show | 56 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(53): Show |
missense_variant | MODERATE | c.2734G>T | p.Asp912Tyr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/76 | 3321/6534 | 2734/5748 | 912/1915 | chr2 | 97198637 | ||
| chr2:97200454
|
C | T | 1 | a0045 | 1 | HG04228.hp1 | missense_variant&splice_region_variant | MODERATE | c.2786C>T | p.Ala929Val | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/76 | 3373/6534 | 2786/5748 | 929/1915 | chr2 | 97200454 | ||
| chr2:97200496
|
A | G | 1 | a0033 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.2828A>G | p.Glu943Gly | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/76 | 3415/6534 | 2828/5748 | 943/1915 | chr2 | 97200496 | ||
| chr2:97204663
|
ACTGTAGG others(1865): Show |
A | 1 | a0035 | 1 | HG03927.hp2 | exon_loss_variant | HIGH | c.3061+436_3163+435d others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 51/76 | INFO_REALIGN_3_PRIME | chr2 | 97204663 | |||||
| chr2:97205943
|
C | T | 1 | a0011 | 5 | HG00423.hp1 HG02602.hp2 NA18945.hp1 others(2): Show |
missense_variant | MODERATE | c.3065C>T | p.Ser1022Phe | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 51/76 | 3652/6534 | 3065/5748 | 1022/1915 | chr2 | 97205943 | ||
| chr2:97207905
|
TTTATTAT others(1859): Show |
T | 10 | a0002a0004a0011others(7): Show | 49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
exon_loss_variant | HIGH | c.3193-14_3295-15del | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/76 | INFO_REALIGN_3_PRIME | chr2 | 97207905 | |||||
| chr2:97207985
|
T | G | 2 | a0036a0037 | 2 | HG01496.hp2 HG02630.hp2 |
missense_variant | MODERATE | c.3244T>G | p.Tyr1082Asp | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/76 | 3831/6534 | 3244/5748 | 1082/1915 | chr2 | 97207985 | ||
| chr2:97208387
|
GTTGTAAC others(29496): Show |
G | 5 | a0015a0031a0034others(2): Show | 8 | HG00558.hp2 NA18952.hp1 NA18961.hp2 others(5): Show |
exon_loss_variant | HIGH | c.3265+384_4094-3374 others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 55/76 | INFO_REALIGN_3_PRIME | chr2 | 97208387 | |||||
| chr2:97211555
|
C | A | 31 | a0002a0003a0004others(28): Show | 130 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(127): Show |
missense_variant | MODERATE | c.3377C>A | p.Pro1126Gln | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 57/76 | 3964/6534 | 3377/5748 | 1126/1915 | chr2 | 97211555 | ||
| chr2:97211555
|
C | T | 1 | a0019 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.3377C>T | p.Pro1126Leu | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 57/76 | 3964/6534 | 3377/5748 | 1126/1915 | chr2 | 97211555 | ||
| chr2:97211703
|
T | C | 9 | a0003a0006a0007others(6): Show | 44 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(41): Show |
missense_variant | MODERATE | c.3431T>C | p.Met1144Thr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/76 | 4018/6534 | 3431/5748 | 1144/1915 | chr2 | 97211703 | ||
| chr2:97211731
|
ATC | A | 1 | a0011 | 5 | HG00423.hp1 HG02602.hp2 NA18945.hp1 others(2): Show |
frameshift_variant | HIGH | c.3461_3462delCT | p.Ser1154fs | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/76 | 4048/6534 | 3461/5748 | 1154/1915 | INFO_REALIGN_3_PRIME | chr2 | 97211731 | |
| chr2:97211741
|
G | A | 1 | a0021 | 2 | HG02809.hp2 HG02895.hp1 |
missense_variant&splice_region_variant | MODERATE | c.3469G>A | p.Val1157Met | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/76 | 4056/6534 | 3469/5748 | 1157/1915 | chr2 | 97211741 | ||
| chr2:97213425
|
G | C | 39 | a0000a0001a0002others(36): Show | 173 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(170): Show |
missense_variant | MODERATE | c.3476G>C | p.Cys1159Ser | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 59/76 | 4063/6534 | 3476/5748 | 1159/1915 | chr2 | 97213425 | ||
| chr2:97217357
|
T | G | 2 | a0006a0014 | 12 | HG00558.hp1 HG00642.hp1 HG00741.hp2 others(9): Show |
missense_variant | MODERATE | c.3760T>G | p.Trp1254Gly | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/76 | 4347/6534 | 3760/5748 | 1254/1915 | chr2 | 97217357 | ||
| chr2:97241463
|
G | T | 1 | a0040 | 1 | HG01934.hp1 | stop_gained | HIGH | c.4291G>T | p.Glu1431* | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/76 | 4878/6534 | 4291/5748 | 1431/1915 | chr2 | 97241463 | ||
| chr2:97243892
|
G | T | 7 | a0008a0009a0013others(4): Show | 28 | HG00558.hp1 HG00597.hp2 HG01261.hp1 others(25): Show |
missense_variant | MODERATE | c.4354G>T | p.Val1452Leu | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/76 | 4941/6534 | 4354/5748 | 1452/1915 | chr2 | 97243892 | ||
| chr2:97245479
|
A | G | 2 | a0026a0041 | 2 | HG03688.hp2 NA18946.hp2 |
missense_variant | MODERATE | c.4814A>G | p.His1605Arg | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/76 | 5401/6534 | 4814/5748 | 1605/1915 | chr2 | 97245479 | ||
| chr2:97245828
|
TCAACTAA others(23686): Show |
T | 1 | a0000 | 4 | HG02040.hp1 NA18965.hp2 NA19000.hp2 others(1): Show |
exon_loss_variant | HIGH | c.5164_*5199del | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/76 | 5751/6534 | chr2 | 97245828 | |||||
| chr2:97246019
|
A | C | 2 | a0007a0014 | 12 | HG00099.hp2 HG00558.hp1 HG01099.hp1 others(9): Show |
missense_variant | MODERATE | c.5354A>C | p.Asn1785Thr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/76 | 5941/6534 | 5354/5748 | 1785/1915 | chr2 | 97246019 | ||
| chr2:97247504
|
G | A | 1 | a0038 | 1 | NA19088.hp2 | missense_variant | MODERATE | c.5435G>A | p.Arg1812Gln | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/76 | 6022/6534 | 5435/5748 | 1812/1915 | chr2 | 97247504 | ||
| chr2:97250158
|
T | G | 1 | a0044 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.5739T>G | p.Phe1913Leu | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/76 | 6326/6534 | 5739/5748 | 1913/1915 | chr2 | 97250158 | ||
| chr2:97264169
|
TAGCATTG others(84): Show |
T | 20 | a0001a0002a0004others(17): Show | 67 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(64): Show |
splice_acceptor_variant&splice_region_variant&3_prime_UTR_variant&intron_variant | HIGH | c.*7-65_*32delATTGAA others(85): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 76/76 | 14097 | INFO_REALIGN_3_PRIME | chr2 | 97264169 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:97113874
|
A | G | 3 | a0008c0006a0023c0019a0052c0026 | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
synonymous_variant | LOW | c.135A>G | p.Leu45Leu | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 722/6534 | 135/5748 | 45/1915 | chr2 | 97113874 | ||
| chr2:97118094
|
C | T | 3 | a0004c0005a0004c0024a0035c0062 | 12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
synonymous_variant | LOW | c.228C>T | p.Gly76Gly | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 2/76 | 815/6534 | 228/5748 | 76/1915 | chr2 | 97118094 | ||
| chr2:97127091
|
C | T | 1 | a0032c0054 | 1 | HG02738.hp1 | synonymous_variant | LOW | c.756C>T | p.Tyr252Tyr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/76 | 1343/6534 | 756/5748 | 252/1915 | chr2 | 97127091 | ||
| chr2:97142777
|
G | A | 1 | a0050c0061 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.843G>A | p.Lys281Lys | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 8/76 | 1430/6534 | 843/5748 | 281/1915 | chr2 | 97142777 | ||
| chr2:97183635
|
T | C | 1 | a0001c0036 | 1 | HG01943.hp1 | synonymous_variant | LOW | c.1920T>C | p.Gly640Gly | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/76 | 2507/6534 | 1920/5748 | 640/1915 | chr2 | 97183635 | ||
| chr2:97185332
|
A | G | 13 | a0003c0003a0006c0008a0006c0034others(10): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
synonymous_variant | LOW | c.1956A>G | p.Gln652Gln | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 29/76 | 2543/6534 | 1956/5748 | 652/1915 | chr2 | 97185332 | ||
| chr2:97189100
|
G | A | 1 | a0052c0026 | 1 | NA18941.hp2 | synonymous_variant | LOW | c.2157G>A | p.Lys719Lys | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/76 | 2744/6534 | 2157/5748 | 719/1915 | chr2 | 97189100 | ||
| chr2:97189229
|
C | T | 1 | a0052c0026 | 1 | NA18941.hp2 | synonymous_variant | LOW | c.2184C>T | p.Asp728Asp | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/76 | 2771/6534 | 2184/5748 | 728/1915 | chr2 | 97189229 | ||
| chr2:97189250
|
T | C | 1 | a0052c0026 | 1 | NA18941.hp2 | synonymous_variant | LOW | c.2205T>C | p.Asn735Asn | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/76 | 2792/6534 | 2205/5748 | 735/1915 | chr2 | 97189250 | ||
| chr2:97191141
|
C | T | 1 | a0052c0026 | 1 | NA18941.hp2 | synonymous_variant | LOW | c.2307C>T | p.Asn769Asn | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/76 | 2894/6534 | 2307/5748 | 769/1915 | chr2 | 97191141 | ||
| chr2:97198597
|
C | T | 13 | a0003c0003a0006c0008a0006c0034others(10): Show | 56 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(53): Show |
synonymous_variant | LOW | c.2694C>T | p.Ala898Ala | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/76 | 3281/6534 | 2694/5748 | 898/1915 | chr2 | 97198597 | ||
| chr2:97198639
|
T | C | 1 | a0013c0025 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.2736T>C | p.Asp912Asp | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/76 | 3323/6534 | 2736/5748 | 912/1915 | chr2 | 97198639 | ||
| chr2:97200476
|
T | A | 1 | a0047c0033 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.2808T>A | p.Ser936Ser | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/76 | 3395/6534 | 2808/5748 | 936/1915 | chr2 | 97200476 | ||
| chr2:97207827
|
A | G | 1 | a0004c0024 | 2 | HG01261.hp2 HG02886.hp1 |
synonymous_variant | LOW | c.3180A>G | p.Pro1060Pro | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 53/76 | 3767/6534 | 3180/5748 | 1060/1915 | chr2 | 97207827 | ||
| chr2:97217350
|
A | G | 3 | a0006c0008a0006c0034a0014c0014 | 12 | HG00558.hp1 HG00642.hp1 HG00741.hp2 others(9): Show |
synonymous_variant | LOW | c.3753A>G | p.Thr1251Thr | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/76 | 4340/6534 | 3753/5748 | 1251/1915 | chr2 | 97217350 | ||
| chr2:97243924
|
A | C | 6 | a0006c0034a0010c0059a0016c0053others(3): Show | 6 | HG02109.hp1 HG02630.hp2 HG02698.hp1 others(3): Show |
synonymous_variant | LOW | c.4386A>C | p.Ile1462Ile | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/76 | 4973/6534 | 4386/5748 | 1462/1915 | chr2 | 97243924 | ||
| chr2:97243990
|
A | G | 2 | a0001c0046a0051c0027 | 2 | NA19240.hp1 NA20905.hp2 |
synonymous_variant | LOW | c.4452A>G | p.Ala1484Ala | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/76 | 5039/6534 | 4452/5748 | 1484/1915 | chr2 | 97243990 | ||
| chr2:97245738
|
A | G | 1 | a0050c0061 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.5073A>G | p.Gln1691Gln | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/76 | 5660/6534 | 5073/5748 | 1691/1915 | chr2 | 97245738 | ||
| chr2:97245820
|
A | C | 1 | a0001c0044 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.5155A>C | p.Arg1719Arg | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/76 | 5742/6534 | 5155/5748 | 1719/1915 | chr2 | 97245820 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:97113158
|
A | G | 1 | a0004c0005t0010 | 1 | HG01123.hp2 | 5_prime_UTR_variant | MODIFIER | c.-582A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 582 | chr2 | 97113158 | |||||
| chr2:97113180
|
A | G | 1 | a0006c0008t0009 | 1 | HG02300.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-560A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | chr2 | 97113180 | ||||||
| chr2:97113428
|
G | A | 1 | a0005c0004t0005 | 7 | HG00642.hp2 HG02630.hp1 HG03130.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-312G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 312 | chr2 | 97113428 | |||||
| chr2:97113454
|
C | G | 5 | a0004c0005t0004a0004c0005t0008a0004c0005t0010others(2): Show | 12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-286C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 286 | chr2 | 97113454 | |||||
| chr2:97113631
|
T | C | 5 | a0008c0006t0003a0013c0013t0003a0013c0025t0003others(2): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-109T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 109 | chr2 | 97113631 | |||||
| chr2:97113645
|
G | C | 5 | a0008c0006t0003a0013c0013t0003a0013c0025t0003others(2): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-95G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 95 | chr2 | 97113645 | |||||
| chr2:97113660
|
T | C | 5 | a0008c0006t0003a0013c0013t0003a0013c0025t0003others(2): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-80T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 80 | chr2 | 97113660 | |||||
| chr2:97113661
|
C | T | 5 | a0008c0006t0003a0013c0013t0003a0013c0025t0003others(2): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-79C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | chr2 | 97113661 | ||||||
| chr2:97113735
|
C | A | 5 | a0008c0006t0003a0013c0013t0003a0013c0025t0003others(2): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
5_prime_UTR_variant | MODIFIER | c.-5C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/76 | 5 | chr2 | 97113735 | |||||
| chr2:97264463
|
C | G | 3 | a0001c0001t0007a0019c0031t0007a0019c0032t0007 | 3 | NA18972.hp2 NA19056.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*141C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 76/76 | 14296 | chr2 | 97264463 | |||||
| chr2:97264497
|
G | A | 27 | a0001c0001t0002a0001c0046t0002a0002c0002t0002others(24): Show | 75 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*175G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 76/76 | 14330 | chr2 | 97264497 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:97114099
|
G | C | 2 | a0005c0004t0002g0002a0048c0030t0002g0003 | 2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.197+163G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97114099 | ||||||
| chr2:97114296
|
G | T | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.197+360G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97114296 | ||||||
| chr2:97114436
|
C | G | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.197+500C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97114436 | ||||||
| chr2:97114508
|
A | G | 1 | a0002c0002t0002g0209 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.197+572A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97114508 | ||||||
| chr2:97114758
|
A | C | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.197+822A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97114758 | ||||||
| chr2:97114902
|
C | A | 4 | a0006c0008t0001g0004a0006c0008t0001g0005a0006c0008t0001g0006others(1): Show | 4 | HG00642.hp1 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.197+966C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97114902 | ||||||
| chr2:97114908
|
C | T | 1 | a0008c0006t0003g0208 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.197+972C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97114908 | ||||||
| chr2:97115334
|
A | T | 1 | a0007c0007t0001g0207 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.197+1398A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97115334 | ||||||
| chr2:97115374
|
A | G | 1 | a0012c0010t0002g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.197+1438A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97115374 | ||||||
| chr2:97115460
|
A | G | 7 | a0005c0004t0005g0199a0005c0004t0005g0200a0005c0004t0005g0201others(4): Show | 7 | HG00642.hp2 HG02630.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.197+1524A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97115460 | ||||||
| chr2:97115561
|
G | A | 1 | a0043c0039t0001g0008 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.197+1625G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97115561 | ||||||
| chr2:97115571
|
C | G | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.197+1635C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97115571 | ||||||
| chr2:97115654
|
T | TC | 211 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.197+1719dupC | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | INFO_REALIGN_3_PRIME | chr2 | 97115654 | |||||
| chr2:97115740
|
T | G | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.197+1804T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97115740 | ||||||
| chr2:97115756
|
C | G | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.197+1820C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97115756 | ||||||
| chr2:97115863
|
A | G | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.197+1927A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97115863 | ||||||
| chr2:97115944
|
A | G | 1 | a0002c0002t0001g0183 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.197+2008A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97115944 | ||||||
| chr2:97116155
|
G | A | 1 | a0011c0011t0002g0011 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.198-1909G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97116155 | ||||||
| chr2:97116270
|
G | T | 72 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(69): Show | 72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.198-1794G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97116270 | ||||||
| chr2:97116450
|
A | G | 1 | a0002c0002t0002g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.198-1614A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97116450 | ||||||
| chr2:97116926
|
G | C | 3 | a0001c0001t0001g0014a0021c0021t0002g0012a0021c0021t0002g0013 | 3 | HG02293.hp2 HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.198-1138G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97116926 | ||||||
| chr2:97117047
|
CT | C | 61 | a0000c0016t0006g0018a0001c0001t0001g0019a0002c0002t0001g0017others(58): Show | 61 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.198-1001delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | INFO_REALIGN_3_PRIME | chr2 | 97117047 | |||||
| chr2:97117258
|
T | G | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.198-806T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97117258 | ||||||
| chr2:97117259
|
T | A | 211 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.198-805T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97117259 | ||||||
| chr2:97117651
|
T | C | 4 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.198-413T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97117651 | ||||||
| chr2:97117671
|
GTAATATC | G | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.198-389_198-383del others(7): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | INFO_REALIGN_3_PRIME | chr2 | 97117671 | |||||
| chr2:97117895
|
G | C | 1 | a0003c0003t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.198-169G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97117895 | ||||||
| chr2:97117912
|
C | T | 1 | a0007c0007t0001g0180 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.198-152C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97117912 | ||||||
| chr2:97117920
|
T | C | 48 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(45): Show | 48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.198-144T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97117920 | ||||||
| chr2:97117953
|
ATGT | A | 3 | a0020c0022t0002g0015a0020c0022t0002g0030a0024c0060t0002g0024 | 3 | HG01891.hp1 HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.198-107_198-105del others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | INFO_REALIGN_3_PRIME | chr2 | 97117953 | |||||
| chr2:97118007
|
G | A | 1 | a0024c0060t0002g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.198-57G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 1/75 | chr2 | 97118007 | ||||||
| chr2:97118182
|
T | C | 2 | a0002c0002t0002g0031a0025c0057t0001g0134 | 2 | HG00639.hp1 HG02572.hp1 |
splice_region_variant&intron_variant | LOW | c.312+4T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 2/75 | chr2 | 97118182 | ||||||
| chr2:97118328
|
G | A | 3 | a0006c0008t0001g0004a0006c0008t0001g0005a0006c0008t0001g0006 | 3 | HG01975.hp1 HG01993.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.313-16G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 2/75 | chr2 | 97118328 | ||||||
| chr2:97118558
|
C | A | 71 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(68): Show | 71 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.486+41C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97118558 | ||||||
| chr2:97118947
|
A | AC | 80 | a0001c0001t0001g0131a0001c0001t0002g0020a0001c0001t0002g0021others(77): Show | 80 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.486+430_486+431ins others(1): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97118947 | ||||||
| chr2:97118959
|
G | A | 1 | a0033c0035t0001g0136 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.486+442G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97118959 | ||||||
| chr2:97118975
|
T | C | 26 | a0004c0005t0004g0016a0004c0005t0004g0032a0004c0005t0004g0033others(23): Show | 26 | HG00099.hp1 HG00099.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.486+458T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97118975 | ||||||
| chr2:97119059
|
A | C | 1 | a0029c0055t0002g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.486+542A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97119059 | ||||||
| chr2:97119231
|
G | A | 1 | a0007c0007t0001g0137 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.486+714G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97119231 | ||||||
| chr2:97119294
|
A | G | 1 | a0030c0052t0002g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.486+777A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97119294 | ||||||
| chr2:97119688
|
G | A | 147 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.486+1171G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97119688 | ||||||
| chr2:97119695
|
C | A | 1 | a0009c0009t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.486+1178C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97119695 | ||||||
| chr2:97119814
|
C | CACA | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.486+1314_486+1316d others(5): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | INFO_REALIGN_3_PRIME | chr2 | 97119814 | |||||
| chr2:97119816
|
C | A | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.486+1299C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97119816 | ||||||
| chr2:97119817
|
A | C | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.486+1300A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97119817 | ||||||
| chr2:97120024
|
G | C | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.486+1507G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120024 | ||||||
| chr2:97120142
|
CTT | C | 6 | a0009c0009t0002g0175a0009c0009t0002g0176a0009c0009t0002g0177others(3): Show | 6 | HG01358.hp2 HG02451.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.486+1628_486+1629d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | INFO_REALIGN_3_PRIME | chr2 | 97120142 | |||||
| chr2:97120462
|
C | A | 5 | a0003c0003t0001g0142a0003c0003t0001g0143a0003c0003t0001g0144others(2): Show | 5 | HG00597.hp1 HG01261.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+1945C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120462 | ||||||
| chr2:97120470
|
T | TA | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.486+1960dupA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | INFO_REALIGN_3_PRIME | chr2 | 97120470 | |||||
| chr2:97120544
|
T | C | 1 | a0009c0009t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.486+2027T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120544 | ||||||
| chr2:97120648
|
G | A | 1 | a0017c0017t0001g0145 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.486+2131G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120648 | ||||||
| chr2:97120664
|
T | C | 1 | a0009c0009t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.486+2147T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120664 | ||||||
| chr2:97120735
|
T | C | 1 | a0009c0009t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-2152T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120735 | ||||||
| chr2:97120736
|
G | T | 1 | a0009c0009t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-2151G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120736 | ||||||
| chr2:97120748
|
T | C | 1 | a0009c0009t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-2139T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120748 | ||||||
| chr2:97120827
|
T | C | 2 | a0005c0004t0005g0199a0009c0009t0002g0174 | 2 | HG01261.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.487-2060T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120827 | ||||||
| chr2:97120887
|
G | A | 1 | a0009c0009t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-2000G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120887 | ||||||
| chr2:97120917
|
C | T | 13 | a0002c0002t0001g0017a0002c0002t0001g0060a0002c0002t0001g0061others(10): Show | 13 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.487-1970C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120917 | ||||||
| chr2:97120939
|
G | A | 121 | a0002c0002t0001g0017a0002c0002t0001g0060a0002c0002t0001g0061others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.487-1948G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97120939 | ||||||
| chr2:97121014
|
C | G | 2 | a0019c0031t0007g0126a0019c0032t0007g0127 | 2 | NA19056.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.487-1873C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121014 | ||||||
| chr2:97121103
|
T | C | 1 | a0009c0009t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-1784T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121103 | ||||||
| chr2:97121217
|
A | G | 1 | a0002c0002t0002g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.487-1670A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121217 | ||||||
| chr2:97121282
|
G | A | 1 | a0009c0009t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-1605G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121282 | ||||||
| chr2:97121333
|
A | G | 1 | a0030c0052t0002g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.487-1554A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121333 | ||||||
| chr2:97121422
|
C | T | 6 | a0005c0004t0005g0199a0005c0004t0005g0201a0005c0004t0005g0202others(3): Show | 6 | HG00642.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.487-1465C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121422 | ||||||
| chr2:97121503
|
G | A | 1 | a0008c0006t0003g0184 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.487-1384G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121503 | ||||||
| chr2:97121513
|
T | G | 1 | a0009c0009t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-1374T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121513 | ||||||
| chr2:97121532
|
C | T | 1 | a0002c0002t0002g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.487-1355C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121532 | ||||||
| chr2:97121595
|
A | G | 1 | a0009c0009t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-1292A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121595 | ||||||
| chr2:97121604
|
C | T | 6 | a0005c0004t0005g0199a0005c0004t0005g0201a0005c0004t0005g0202others(3): Show | 6 | HG00642.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.487-1283C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121604 | ||||||
| chr2:97121624
|
C | T | 1 | a0009c0009t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-1263C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121624 | ||||||
| chr2:97121644
|
C | T | 1 | a0009c0009t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-1243C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121644 | ||||||
| chr2:97121665
|
A | T | 1 | a0009c0009t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-1222A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121665 | ||||||
| chr2:97121685
|
C | T | 1 | a0009c0009t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-1202C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121685 | ||||||
| chr2:97121786
|
A | T | 1 | a0009c0009t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.487-1101A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121786 | ||||||
| chr2:97121797
|
T | G | 2 | a0009c0009t0002g0174a0020c0022t0002g0015 | 2 | HG01261.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.487-1090T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121797 | ||||||
| chr2:97121821
|
G | A | 55 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(52): Show | 55 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(52): Show |
intron_variant | MODIFIER | c.487-1066G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97121821 | ||||||
| chr2:97122147
|
T | C | 74 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(71): Show | 74 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.487-740T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97122147 | ||||||
| chr2:97122155
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.487-732C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97122155 | ||||||
| chr2:97122182
|
A | T | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.487-705A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97122182 | ||||||
| chr2:97122223
|
C | T | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.487-664C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97122223 | ||||||
| chr2:97122373
|
G | T | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.487-514G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97122373 | ||||||
| chr2:97122454
|
G | A | 28 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.487-433G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97122454 | ||||||
| chr2:97122676
|
A | G | 1 | a0043c0039t0001g0008 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.487-211A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 3/75 | chr2 | 97122676 | ||||||
| chr2:97123283
|
T | G | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.593+290T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123283 | ||||||
| chr2:97123292
|
G | A | 2 | a0008c0006t0003g0190a0008c0006t0003g0191 | 2 | NA18965.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.593+299G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123292 | ||||||
| chr2:97123420
|
G | A | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.593+427G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123420 | ||||||
| chr2:97123435
|
A | G | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.593+442A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123435 | ||||||
| chr2:97123449
|
T | TACTTC | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.593+457_593+458ins others(5): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123449 | |||||
| chr2:97123478
|
G | A | 1 | a0003c0003t0001g0181 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.593+485G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123478 | ||||||
| chr2:97123491
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.593+498C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123491 | ||||||
| chr2:97123538
|
ATTG | A | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.593+546_593+548del others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123538 | ||||||
| chr2:97123613
|
T | TTA | 30 | a0000c0016t0006g0119a0001c0001t0001g0014a0001c0001t0001g0114others(27): Show | 30 | HG00099.hp1 HG00609.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.593+643_593+644dup others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123613 | |||||
| chr2:97123613
|
T | TTATA | 7 | a0001c0001t0001g0121a0001c0001t0001g0123a0001c0046t0002g0051others(4): Show | 7 | HG01975.hp2 HG02083.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.593+641_593+644dup others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123613 | |||||
| chr2:97123613
|
T | TTATATA | 8 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(5): Show | 8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.593+639_593+644dup others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123613 | |||||
| chr2:97123613
|
T | TTATATAT others(3): Show |
1 | a0037c0040t0002g0211 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.593+635_593+644dup others(10): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123613 | |||||
| chr2:97123613
|
TTA | T | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.593+643_593+644del others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123613 | |||||
| chr2:97123613
|
TTATATAT others(5): Show |
T | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.593+633_593+644del others(12): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123613 | |||||
| chr2:97123664
|
A | G | 1 | a0012c0010t0002g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.593+671A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123664 | ||||||
| chr2:97123798
|
T | C | 1 | a0001c0001t0001g0070 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.594-662T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123798 | ||||||
| chr2:97123839
|
TA | T | 49 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(46): Show | 49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.594-619delA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123839 | |||||
| chr2:97123893
|
T | A | 1 | a0001c0046t0002g0051 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.594-567T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123893 | ||||||
| chr2:97123957
|
T | TTA | 22 | a0001c0001t0001g0112a0001c0001t0001g0124a0004c0005t0008g0041others(19): Show | 22 | HG00642.hp1 HG00741.hp2 HG01257.hp2 others(19): Show |
intron_variant | MODIFIER | c.594-486_594-485dup others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123957 | |||||
| chr2:97123957
|
T | TTATA | 26 | a0003c0003t0001g0142a0003c0003t0001g0143a0003c0003t0001g0144others(23): Show | 26 | HG00558.hp1 HG00597.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.594-488_594-485dup others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123957 | |||||
| chr2:97123957
|
T | TTATATA | 20 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0162others(17): Show | 20 | HG00639.hp1 HG01099.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.594-490_594-485dup others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123957 | |||||
| chr2:97123957
|
T | TTATATAT others(1): Show |
3 | a0003c0003t0001g0172a0006c0034t0001g0173a0017c0017t0001g0145 | 3 | HG01070.hp2 HG02109.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.594-492_594-485dup others(8): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123957 | |||||
| chr2:97123957
|
T | TTATATAT others(3): Show |
1 | a0007c0007t0001g0141 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.594-494_594-485dup others(10): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123957 | |||||
| chr2:97123957
|
TTA | T | 2 | a0002c0002t0002g0209a0029c0055t0002g0023 | 2 | HG01243.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.594-486_594-485del others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | INFO_REALIGN_3_PRIME | chr2 | 97123957 | |||||
| chr2:97123978
|
G | A | 1 | a0037c0040t0002g0211 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.594-482G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97123978 | ||||||
| chr2:97124041
|
T | G | 8 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(5): Show | 8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.594-419T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97124041 | ||||||
| chr2:97124146
|
A | C | 2 | a0005c0004t0002g0129a0005c0004t0002g0130 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.594-314A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97124146 | ||||||
| chr2:97124402
|
T | C | 1 | a0051c0027t0001g0071 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.594-58T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 4/75 | chr2 | 97124402 | ||||||
| chr2:97125069
|
A | G | 1 | a0001c0046t0002g0051 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.731+472A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125069 | ||||||
| chr2:97125140
|
T | C | 1 | a0013c0025t0003g0185 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.731+543T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125140 | ||||||
| chr2:97125221
|
C | G | 1 | a0030c0052t0002g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.731+624C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125221 | ||||||
| chr2:97125232
|
C | A | 2 | a0005c0004t0002g0129a0005c0004t0002g0130 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.731+635C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125232 | ||||||
| chr2:97125272
|
G | GT | 13 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(10): Show | 13 | HG00423.hp1 HG02572.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.731+683dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | INFO_REALIGN_3_PRIME | chr2 | 97125272 | |||||
| chr2:97125318
|
T | A | 1 | a0033c0035t0001g0136 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.731+721T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125318 | ||||||
| chr2:97125364
|
A | G | 4 | a0002c0002t0002g0031a0002c0002t0002g0132a0021c0021t0002g0012others(1): Show | 4 | HG02572.hp1 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.731+767A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125364 | ||||||
| chr2:97125414
|
T | G | 211 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(208): Show | 211 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.731+817T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125414 | ||||||
| chr2:97125588
|
C | G | 1 | a0028c0056t0001g0171 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.731+991C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125588 | ||||||
| chr2:97125711
|
A | G | 1 | a0028c0056t0001g0171 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.731+1114A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125711 | ||||||
| chr2:97125783
|
T | C | 2 | a0005c0004t0002g0129a0005c0004t0002g0130 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.731+1186T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125783 | ||||||
| chr2:97125859
|
T | C | 1 | a0029c0055t0002g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.732-1208T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97125859 | ||||||
| chr2:97126492
|
C | G | 1 | a0023c0019t0003g0198 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.732-575C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97126492 | ||||||
| chr2:97126649
|
A | G | 2 | a0011c0011t0002g0011a0011c0011t0002g0049 | 2 | NA18991.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.732-418A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 5/75 | chr2 | 97126649 | ||||||
| chr2:97127587
|
G | A | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.799+453G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97127587 | ||||||
| chr2:97127692
|
C | T | 5 | a0013c0013t0003g0186a0013c0013t0003g0187a0013c0013t0003g0188others(2): Show | 5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.799+558C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97127692 | ||||||
| chr2:97127878
|
T | A | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.799+744T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97127878 | ||||||
| chr2:97127913
|
A | G | 2 | a0001c0001t0001g0111a0041c0045t0001g0110 | 2 | NA18946.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.799+779A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97127913 | ||||||
| chr2:97128104
|
G | A | 1 | a0010c0012t0001g0072 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.799+970G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128104 | ||||||
| chr2:97128158
|
T | C | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.799+1024T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128158 | ||||||
| chr2:97128162
|
A | C | 72 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(69): Show | 72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.799+1028A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128162 | ||||||
| chr2:97128261
|
T | G | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.799+1127T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128261 | ||||||
| chr2:97128269
|
T | A | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.799+1135T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128269 | ||||||
| chr2:97128285
|
C | T | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.799+1151C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128285 | ||||||
| chr2:97128300
|
A | T | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.799+1166A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128300 | ||||||
| chr2:97128308
|
C | T | 2 | a0011c0011t0002g0011a0011c0011t0002g0049 | 2 | NA18991.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.799+1174C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128308 | ||||||
| chr2:97128441
|
C | A | 1 | a0013c0025t0003g0185 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.799+1307C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128441 | ||||||
| chr2:97128538
|
A | G | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022 | 3 | HG01891.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.799+1404A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128538 | ||||||
| chr2:97128597
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.799+1463T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128597 | ||||||
| chr2:97128656
|
T | A | 1 | a0030c0052t0002g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.799+1522T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128656 | ||||||
| chr2:97128953
|
C | T | 2 | a0009c0009t0002g0179a0009c0009t0002g0182 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.799+1819C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97128953 | ||||||
| chr2:97129156
|
C | T | 1 | a0001c0001t0002g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.799+2022C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97129156 | ||||||
| chr2:97129532
|
G | A | 11 | a0005c0004t0002g0002a0005c0004t0002g0129a0005c0004t0002g0130others(8): Show | 11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.799+2398G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97129532 | ||||||
| chr2:97129921
|
T | C | 1 | a0002c0002t0001g0060 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.799+2787T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97129921 | ||||||
| chr2:97129947
|
A | G | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.799+2813A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97129947 | ||||||
| chr2:97129964
|
C | G | 76 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(73): Show | 76 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.799+2830C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97129964 | ||||||
| chr2:97130162
|
A | C | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.799+3028A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97130162 | ||||||
| chr2:97130207
|
C | A | 2 | a0017c0017t0001g0145a0027c0028t0001g0161 | 2 | HG01070.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.799+3073C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97130207 | ||||||
| chr2:97130242
|
T | C | 2 | a0010c0012t0001g0075a0026c0058t0001g0074 | 2 | HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.799+3108T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97130242 | ||||||
| chr2:97130332
|
A | G | 1 | a0009c0009t0002g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.799+3198A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97130332 | ||||||
| chr2:97130434
|
C | T | 1 | a0025c0057t0001g0134 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.799+3300C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97130434 | ||||||
| chr2:97130459
|
G | C | 1 | a0002c0002t0002g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.799+3325G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97130459 | ||||||
| chr2:97130588
|
G | GA | 8 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(5): Show | 8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.799+3465dupA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97130588 | |||||
| chr2:97130645
|
TA | T | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.799+3513delA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97130645 | |||||
| chr2:97130858
|
T | C | 1 | a0013c0013t0003g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.799+3724T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97130858 | ||||||
| chr2:97130898
|
C | G | 1 | a0001c0001t0001g0019 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.799+3764C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97130898 | ||||||
| chr2:97130948
|
G | GT | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.799+3815dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97130948 | |||||
| chr2:97131194
|
A | AT | 9 | a0005c0004t0002g0129a0005c0004t0002g0130a0005c0004t0005g0199others(6): Show | 9 | HG00642.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.799+4073dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97131194 | |||||
| chr2:97131488
|
C | T | 49 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(46): Show | 49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.799+4354C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97131488 | ||||||
| chr2:97131749
|
G | A | 74 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(71): Show | 74 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.799+4615G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97131749 | ||||||
| chr2:97131820
|
T | C | 1 | a0000c0016t0006g0076 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.799+4686T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97131820 | ||||||
| chr2:97131884
|
A | G | 1 | a0001c0001t0001g0070 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.799+4750A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97131884 | ||||||
| chr2:97131892
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.799+4758G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97131892 | ||||||
| chr2:97131897
|
C | T | 1 | a0001c0001t0001g0070 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.799+4763C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97131897 | ||||||
| chr2:97131930
|
G | A | 8 | a0007c0007t0001g0137a0007c0007t0001g0138a0007c0007t0001g0139others(5): Show | 8 | HG00099.hp2 HG01099.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.799+4796G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97131930 | ||||||
| chr2:97131943
|
T | C | 28 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.799+4809T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97131943 | ||||||
| chr2:97131974
|
C | A | 9 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(6): Show | 9 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.799+4840C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97131974 | ||||||
| chr2:97132029
|
G | T | 1 | a0023c0019t0003g0198 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.799+4895G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97132029 | ||||||
| chr2:97132048
|
G | C | 2 | a0002c0002t0001g0052a0005c0004t0005g0200 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.799+4914G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97132048 | ||||||
| chr2:97132069
|
T | C | 10 | a0002c0002t0001g0060a0002c0002t0001g0061a0002c0002t0001g0062others(7): Show | 10 | HG00558.hp1 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.799+4935T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97132069 | ||||||
| chr2:97132305
|
A | G | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.799+5171A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97132305 | ||||||
| chr2:97132326
|
G | A | 2 | a0005c0004t0002g0002a0048c0030t0002g0003 | 2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.799+5192G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97132326 | ||||||
| chr2:97132532
|
C | T | 72 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(69): Show | 72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.799+5398C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97132532 | ||||||
| chr2:97132703
|
A | T | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.799+5569A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97132703 | ||||||
| chr2:97133169
|
C | T | 1 | a0008c0006t0003g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.799+6035C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97133169 | ||||||
| chr2:97133254
|
T | TAACATAG others(337): Show |
1 | a0003c0003t0001g0153 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.799+6132_799+6133i others(346): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97133254 | |||||
| chr2:97133254
|
T | TAACATAG others(338): Show |
1 | a0003c0003t0001g0152 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.799+6132_799+6133i others(347): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97133254 | |||||
| chr2:97133254
|
T | TAACATAG others(342): Show |
1 | a0003c0003t0001g0151 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.799+6132_799+6133i others(351): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97133254 | |||||
| chr2:97133254
|
T | TAACATAG others(334): Show |
4 | a0014c0014t0001g0150a0014c0014t0001g0154a0014c0014t0001g0155others(1): Show | 4 | HG00558.hp1 NA18946.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.799+6132_799+6133i others(343): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97133254 | |||||
| chr2:97133548
|
A | G | 49 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(46): Show | 49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.799+6414A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97133548 | ||||||
| chr2:97133623
|
G | A | 4 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.799+6489G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97133623 | ||||||
| chr2:97133927
|
A | G | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.799+6793A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97133927 | ||||||
| chr2:97134230
|
G | A | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.799+7096G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97134230 | ||||||
| chr2:97134510
|
A | G | 1 | a0015c0015t0001g0109 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.799+7376A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97134510 | ||||||
| chr2:97134517
|
G | A | 1 | a0015c0015t0001g0109 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.799+7383G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97134517 | ||||||
| chr2:97135140
|
T | C | 1 | a0014c0014t0001g0154 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.800-7500T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135140 | ||||||
| chr2:97135323
|
T | C | 1 | a0018c0018t0002g0043 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.800-7317T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135323 | ||||||
| chr2:97135417
|
A | G | 2 | a0020c0022t0002g0015a0020c0022t0002g0030 | 2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.800-7223A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135417 | ||||||
| chr2:97135478
|
A | G | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.800-7162A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135478 | ||||||
| chr2:97135537
|
G | A | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.800-7103G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135537 | ||||||
| chr2:97135606
|
A | G | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.800-7034A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135606 | ||||||
| chr2:97135631
|
C | T | 145 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.800-7009C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135631 | ||||||
| chr2:97135699
|
G | A | 1 | a0008c0006t0003g0184 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.800-6941G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135699 | ||||||
| chr2:97135794
|
C | G | 1 | a0001c0001t0001g0070 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.800-6846C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135794 | ||||||
| chr2:97135926
|
G | A | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.800-6714G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97135926 | ||||||
| chr2:97136203
|
A | ATCCAGGT others(7): Show |
1 | a0044c0038t0001g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.800-6428_800-6427i others(16): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97136203 | |||||
| chr2:97136582
|
G | A | 147 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.800-6058G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97136582 | ||||||
| chr2:97136602
|
C | A | 1 | a0001c0001t0002g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.800-6038C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97136602 | ||||||
| chr2:97136688
|
C | T | 1 | a0009c0009t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.800-5952C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97136688 | ||||||
| chr2:97137191
|
G | T | 1 | a0003c0003t0001g0153 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.800-5449G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97137191 | ||||||
| chr2:97137592
|
TACAC | T | 74 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(71): Show | 74 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.800-5035_800-5032d others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97137592 | |||||
| chr2:97137594
|
C | T | 5 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(2): Show | 5 | HG02040.hp1 NA18950.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.800-5046C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97137594 | ||||||
| chr2:97137607
|
A | G | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.800-5033A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97137607 | ||||||
| chr2:97137745
|
T | G | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.800-4895T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97137745 | ||||||
| chr2:97137953
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.800-4687C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97137953 | ||||||
| chr2:97138101
|
CA | C | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.800-4538delA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97138101 | ||||||
| chr2:97138122
|
CG | C | 5 | a0004c0005t0004g0037a0004c0005t0004g0039a0004c0024t0004g0038others(2): Show | 5 | HG01099.hp2 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.800-4516delG | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97138122 | |||||
| chr2:97138195
|
C | A | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.800-4445C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97138195 | ||||||
| chr2:97138394
|
C | T | 1 | a0010c0012t0001g0075 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.800-4246C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97138394 | ||||||
| chr2:97138685
|
A | T | 6 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.800-3955A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97138685 | ||||||
| chr2:97138880
|
G | A | 1 | a0002c0002t0001g0183 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.800-3760G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97138880 | ||||||
| chr2:97139548
|
T | G | 1 | a0013c0025t0003g0185 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.800-3092T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97139548 | ||||||
| chr2:97139575
|
G | A | 1 | a0013c0025t0003g0185 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.800-3065G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97139575 | ||||||
| chr2:97139591
|
G | A | 1 | a0003c0003t0001g0149 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.800-3049G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97139591 | ||||||
| chr2:97139735
|
T | C | 1 | a0003c0003t0001g0153 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.800-2905T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97139735 | ||||||
| chr2:97139865
|
C | T | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.800-2775C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97139865 | ||||||
| chr2:97139938
|
T | C | 1 | a0029c0055t0002g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.800-2702T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97139938 | ||||||
| chr2:97140055
|
C | T | 1 | a0043c0039t0001g0008 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.800-2585C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97140055 | ||||||
| chr2:97140118
|
C | G | 1 | a0002c0002t0001g0069 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.800-2522C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97140118 | ||||||
| chr2:97140273
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.800-2367G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97140273 | ||||||
| chr2:97140281
|
G | A | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.800-2359G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97140281 | ||||||
| chr2:97140679
|
C | T | 2 | a0018c0018t0002g0043a0018c0018t0002g0048 | 2 | NA18961.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.800-1961C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97140679 | ||||||
| chr2:97140693
|
A | G | 1 | a0002c0002t0002g0132 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.800-1947A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97140693 | ||||||
| chr2:97140705
|
C | A | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.800-1935C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97140705 | ||||||
| chr2:97140813
|
G | T | 2 | a0009c0009t0002g0174a0009c0009t0002g0178 | 2 | HG01261.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.800-1827G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97140813 | ||||||
| chr2:97141228
|
C | CAT | 17 | a0005c0004t0005g0200a0008c0006t0003g0184a0008c0006t0003g0190others(14): Show | 17 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.800-1399_800-1398d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97141228 | |||||
| chr2:97141279
|
AAAG | A | 49 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(46): Show | 49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.800-1357_800-1355d others(5): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97141279 | |||||
| chr2:97141380
|
AAG | A | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.800-1256_800-1255d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | INFO_REALIGN_3_PRIME | chr2 | 97141380 | |||||
| chr2:97141465
|
T | A | 1 | a0044c0038t0001g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.800-1175T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97141465 | ||||||
| chr2:97141665
|
C | G | 2 | a0019c0031t0007g0126a0019c0032t0007g0127 | 2 | NA19056.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.800-975C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97141665 | ||||||
| chr2:97141667
|
A | G | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.800-973A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97141667 | ||||||
| chr2:97141789
|
T | A | 1 | a0005c0004t0002g0002 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.800-851T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97141789 | ||||||
| chr2:97141885
|
A | G | 21 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(18): Show | 21 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.800-755A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97141885 | ||||||
| chr2:97142080
|
T | C | 1 | a0024c0060t0002g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.800-560T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97142080 | ||||||
| chr2:97142098
|
A | G | 2 | a0005c0004t0002g0002a0048c0030t0002g0003 | 2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.800-542A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97142098 | ||||||
| chr2:97142307
|
C | G | 3 | a0023c0019t0003g0198a0037c0040t0002g0211a0042c0043t0002g0210 | 3 | HG02630.hp2 HG02717.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.800-333C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97142307 | ||||||
| chr2:97142310
|
G | A | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.800-330G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97142310 | ||||||
| chr2:97142461
|
G | A | 147 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.800-179G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 6/75 | chr2 | 97142461 | ||||||
| chr2:97142943
|
C | G | 2 | a0009c0009t0002g0179a0009c0009t0002g0182 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.901+108C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 8/75 | chr2 | 97142943 | ||||||
| chr2:97143088
|
C | T | 1 | a0007c0007t0001g0140 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.901+253C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 8/75 | chr2 | 97143088 | ||||||
| chr2:97143258
|
C | A | 2 | a0003c0003t0001g0133a0003c0003t0001g0162 | 2 | HG01123.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.901+423C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 8/75 | chr2 | 97143258 | ||||||
| chr2:97143446
|
A | C | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.901+611A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 8/75 | chr2 | 97143446 | ||||||
| chr2:97143587
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.901+752A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 8/75 | chr2 | 97143587 | ||||||
| chr2:97144159
|
T | A | 1 | a0001c0001t0001g0081 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.902-359T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 8/75 | chr2 | 97144159 | ||||||
| chr2:97144287
|
T | C | 1 | a0024c0060t0002g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.902-231T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 8/75 | chr2 | 97144287 | ||||||
| chr2:97144773
|
A | T | 8 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(5): Show | 8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1003+61A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | chr2 | 97144773 | ||||||
| chr2:97144805
|
G | A | 5 | a0013c0013t0003g0186a0013c0013t0003g0187a0013c0013t0003g0188others(2): Show | 5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1003+93G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | chr2 | 97144805 | ||||||
| chr2:97144860
|
G | T | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1003+148G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | chr2 | 97144860 | ||||||
| chr2:97145061
|
T | C | 49 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(46): Show | 49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.1003+349T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | chr2 | 97145061 | ||||||
| chr2:97145649
|
C | T | 3 | a0001c0001t0001g0073a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG00609.hp2 NA18941.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.1004-837C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | chr2 | 97145649 | ||||||
| chr2:97145741
|
G | T | 1 | a0002c0002t0001g0059 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1004-745G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | chr2 | 97145741 | ||||||
| chr2:97145805
|
C | G | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1004-681C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | chr2 | 97145805 | ||||||
| chr2:97145854
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1004-632A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | chr2 | 97145854 | ||||||
| chr2:97146246
|
T | C | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1004-240T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | chr2 | 97146246 | ||||||
| chr2:97146273
|
A | AT | 122 | a0002c0002t0001g0017a0002c0002t0001g0060a0002c0002t0001g0061others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1004-200dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 10/75 | INFO_REALIGN_3_PRIME | chr2 | 97146273 | |||||
| chr2:97146702
|
G | A | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.1034+186G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97146702 | ||||||
| chr2:97146767
|
G | C | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1034+251G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97146767 | ||||||
| chr2:97146852
|
G | A | 2 | a0021c0021t0002g0012a0021c0021t0002g0013 | 2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1034+336G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97146852 | ||||||
| chr2:97146939
|
A | G | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1034+423A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97146939 | ||||||
| chr2:97146976
|
G | A | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1034+460G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97146976 | ||||||
| chr2:97147267
|
G | T | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1034+751G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97147267 | ||||||
| chr2:97147411
|
C | T | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1034+895C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97147411 | ||||||
| chr2:97147470
|
C | T | 2 | a0023c0019t0003g0197a0023c0019t0003g0198 | 2 | NA18999.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1034+954C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97147470 | ||||||
| chr2:97147546
|
A | G | 48 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(45): Show | 48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1034+1030A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97147546 | ||||||
| chr2:97147640
|
A | G | 1 | a0001c0036t0001g0080 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1034+1124A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97147640 | ||||||
| chr2:97147682
|
C | G | 1 | a0001c0001t0002g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1034+1166C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97147682 | ||||||
| chr2:97148032
|
G | C | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1035-1263G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97148032 | ||||||
| chr2:97148567
|
T | C | 8 | a0011c0011t0002g0011a0011c0011t0002g0045a0011c0011t0002g0046others(5): Show | 8 | HG00423.hp1 HG02602.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.1035-728T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97148567 | ||||||
| chr2:97148730
|
CA | C | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1035-564delA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97148730 | ||||||
| chr2:97148783
|
A | G | 11 | a0005c0004t0002g0002a0005c0004t0002g0129a0005c0004t0002g0130others(8): Show | 11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.1035-512A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97148783 | ||||||
| chr2:97148813
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1035-482C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97148813 | ||||||
| chr2:97148871
|
C | G | 1 | a0002c0002t0001g0066 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1035-424C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97148871 | ||||||
| chr2:97148871
|
C | T | 1 | a0001c0001t0002g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1035-424C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97148871 | ||||||
| chr2:97148962
|
C | G | 1 | a0008c0006t0003g0196 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1035-333C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97148962 | ||||||
| chr2:97149192
|
T | G | 1 | a0001c0001t0001g0077 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1035-103T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97149192 | ||||||
| chr2:97149198
|
A | AT | 5 | a0004c0005t0004g0037a0004c0005t0004g0039a0004c0024t0004g0038others(2): Show | 5 | HG01099.hp2 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1035-90dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | INFO_REALIGN_3_PRIME | chr2 | 97149198 | |||||
| chr2:97149207
|
G | T | 1 | a0030c0052t0002g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1035-88G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97149207 | ||||||
| chr2:97149210
|
T | G | 5 | a0004c0005t0004g0037a0004c0005t0004g0039a0004c0024t0004g0038others(2): Show | 5 | HG01099.hp2 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1035-85T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97149210 | ||||||
| chr2:97149215
|
A | C | 5 | a0004c0005t0004g0037a0004c0005t0004g0039a0004c0024t0004g0038others(2): Show | 5 | HG01099.hp2 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1035-80A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97149215 | ||||||
| chr2:97149217
|
A | G | 5 | a0004c0005t0004g0037a0004c0005t0004g0039a0004c0024t0004g0038others(2): Show | 5 | HG01099.hp2 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1035-78A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97149217 | ||||||
| chr2:97149219
|
G | A | 79 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(76): Show | 79 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(76): Show |
intron_variant | MODIFIER | c.1035-76G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 11/75 | chr2 | 97149219 | ||||||
| chr2:97149382
|
A | G | 1 | a0010c0012t0001g0103 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1101+21A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97149382 | ||||||
| chr2:97149582
|
G | GA | 28 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.1101+229dupA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | INFO_REALIGN_3_PRIME | chr2 | 97149582 | |||||
| chr2:97149850
|
T | C | 1 | a0009c0009t0002g0174 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1101+489T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97149850 | ||||||
| chr2:97150500
|
C | A | 1 | a0009c0009t0002g0178 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1101+1139C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97150500 | ||||||
| chr2:97150572
|
G | A | 8 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(5): Show | 8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1101+1211G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97150572 | ||||||
| chr2:97150706
|
A | T | 9 | a0002c0002t0001g0060a0002c0002t0001g0061a0002c0002t0001g0062others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1102-1173A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97150706 | ||||||
| chr2:97150776
|
T | C | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1102-1103T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97150776 | ||||||
| chr2:97150869
|
A | T | 2 | a0019c0031t0007g0126a0019c0032t0007g0127 | 2 | NA19056.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1102-1010A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97150869 | ||||||
| chr2:97150872
|
G | T | 2 | a0019c0031t0007g0126a0019c0032t0007g0127 | 2 | NA19056.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1102-1007G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97150872 | ||||||
| chr2:97150886
|
C | T | 1 | a0019c0032t0007g0127 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1102-993C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97150886 | ||||||
| chr2:97150893
|
C | T | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1102-986C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97150893 | ||||||
| chr2:97151083
|
C | G | 11 | a0005c0004t0002g0002a0005c0004t0002g0129a0005c0004t0002g0130others(8): Show | 11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.1102-796C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97151083 | ||||||
| chr2:97151084
|
G | T | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1102-795G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97151084 | ||||||
| chr2:97151167
|
T | C | 1 | a0007c0007t0001g0207 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1102-712T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97151167 | ||||||
| chr2:97151285
|
C | T | 1 | a0002c0002t0001g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1102-594C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97151285 | ||||||
| chr2:97151455
|
A | G | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.1102-424A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97151455 | ||||||
| chr2:97151654
|
A | G | 1 | a0004c0005t0004g0036 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1102-225A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97151654 | ||||||
| chr2:97151693
|
T | C | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1102-186T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | chr2 | 97151693 | ||||||
| chr2:97151827
|
C | CT | 209 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(206): Show | 209 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.1102-51dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 12/75 | INFO_REALIGN_3_PRIME | chr2 | 97151827 | |||||
| chr2:97152065
|
TCACTG | T | 4 | a0017c0017t0001g0145a0017c0017t0001g0169a0017c0017t0001g0170others(1): Show | 4 | HG01070.hp2 HG01361.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1162+129_1162+133d others(7): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 13/75 | INFO_REALIGN_3_PRIME | chr2 | 97152065 | |||||
| chr2:97152236
|
C | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1163-268C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 13/75 | chr2 | 97152236 | ||||||
| chr2:97152239
|
T | C | 1 | a0015c0015t0001g0109 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1163-265T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 13/75 | chr2 | 97152239 | ||||||
| chr2:97152394
|
C | T | 1 | a0020c0022t0002g0015 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1163-110C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 13/75 | chr2 | 97152394 | ||||||
| chr2:97152611
|
A | G | 52 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(49): Show | 52 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1193+77A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97152611 | ||||||
| chr2:97153107
|
C | T | 1 | a0002c0002t0002g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1193+573C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97153107 | ||||||
| chr2:97153117
|
T | A | 1 | a0002c0002t0002g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1193+583T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97153117 | ||||||
| chr2:97153261
|
T | G | 1 | a0010c0012t0001g0103 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1193+727T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97153261 | ||||||
| chr2:97153973
|
A | C | 2 | a0001c0001t0002g0050a0001c0046t0002g0051 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1194-702A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97153973 | ||||||
| chr2:97154154
|
C | G | 1 | a0002c0002t0002g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1194-521C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97154154 | ||||||
| chr2:97154300
|
A | G | 2 | a0020c0022t0002g0015a0020c0022t0002g0030 | 2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1194-375A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97154300 | ||||||
| chr2:97154539
|
T | C | 2 | a0002c0002t0001g0061a0040c0047t0001g0082 | 2 | HG01934.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1194-136T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97154539 | ||||||
| chr2:97154653
|
G | T | 3 | a0001c0001t0001g0019a0003c0003t0001g0159a0003c0003t0001g0160 | 3 | NA18612.hp1 NA18950.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1194-22G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97154653 | ||||||
| chr2:97154655
|
A | C | 3 | a0001c0001t0001g0019a0003c0003t0001g0159a0003c0003t0001g0160 | 3 | NA18612.hp1 NA18950.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.1194-20A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 14/75 | chr2 | 97154655 | ||||||
| chr2:97154925
|
T | TG | 4 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1260+185dupG | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | INFO_REALIGN_3_PRIME | chr2 | 97154925 | |||||
| chr2:97155015
|
T | C | 52 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(49): Show | 52 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1260+274T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97155015 | ||||||
| chr2:97155027
|
C | T | 1 | a0004c0005t0008g0035 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1260+286C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97155027 | ||||||
| chr2:97155083
|
A | C | 52 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(49): Show | 52 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1260+342A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97155083 | ||||||
| chr2:97155761
|
A | G | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1260+1020A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97155761 | ||||||
| chr2:97155765
|
C | T | 52 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(49): Show | 52 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1260+1024C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97155765 | ||||||
| chr2:97155837
|
G | T | 1 | a0002c0002t0001g0069 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1260+1096G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97155837 | ||||||
| chr2:97155933
|
A | G | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1260+1192A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97155933 | ||||||
| chr2:97155955
|
A | T | 1 | a0001c0001t0001g0081 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1260+1214A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97155955 | ||||||
| chr2:97156026
|
T | C | 3 | a0002c0002t0001g0062a0002c0002t0001g0063a0002c0002t0001g0064 | 3 | HG02976.hp1 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1260+1285T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156026 | ||||||
| chr2:97156100
|
G | C | 9 | a0005c0004t0002g0129a0005c0004t0002g0130a0005c0004t0005g0199others(6): Show | 9 | HG00642.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1260+1359G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156100 | ||||||
| chr2:97156398
|
G | A | 8 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(5): Show | 8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1260+1657G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156398 | ||||||
| chr2:97156489
|
C | T | 48 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(45): Show | 48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1261-1618C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156489 | ||||||
| chr2:97156605
|
T | C | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1261-1502T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156605 | ||||||
| chr2:97156673
|
A | G | 1 | a0001c0001t0001g0081 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1261-1434A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156673 | ||||||
| chr2:97156674
|
T | TA | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1261-1430dupA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | INFO_REALIGN_3_PRIME | chr2 | 97156674 | |||||
| chr2:97156726
|
G | A | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1261-1381G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156726 | ||||||
| chr2:97156750
|
T | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0105 | 2 | HG00609.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1261-1357T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156750 | ||||||
| chr2:97156826
|
C | T | 74 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(71): Show | 74 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1261-1281C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156826 | ||||||
| chr2:97156827
|
A | C | 74 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(71): Show | 74 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1261-1280A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156827 | ||||||
| chr2:97156853
|
C | G | 9 | a0002c0002t0001g0060a0002c0002t0001g0061a0002c0002t0001g0062others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1261-1254C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156853 | ||||||
| chr2:97156982
|
C | T | 1 | a0003c0003t0001g0168 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1261-1125C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97156982 | ||||||
| chr2:97157130
|
CCT | C | 7 | a0005c0004t0005g0199a0005c0004t0005g0200a0005c0004t0005g0201others(4): Show | 7 | HG00642.hp2 HG02630.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1261-958_1261-957d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | INFO_REALIGN_3_PRIME | chr2 | 97157130 | |||||
| chr2:97157131
|
C | CTCTCTCT others(1): Show |
56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1261-969_1261-968i others(10): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | INFO_REALIGN_3_PRIME | chr2 | 97157131 | |||||
| chr2:97157143
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1261-964C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97157143 | ||||||
| chr2:97157275
|
A | G | 147 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1261-832A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97157275 | ||||||
| chr2:97157500
|
A | G | 147 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1261-607A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97157500 | ||||||
| chr2:97157592
|
C | T | 1 | a0007c0007t0001g0137 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1261-515C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97157592 | ||||||
| chr2:97157821
|
T | G | 2 | a0020c0022t0002g0015a0020c0022t0002g0030 | 2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1261-286T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97157821 | ||||||
| chr2:97157846
|
A | G | 1 | a0003c0003t0001g0167 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1261-261A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 15/75 | chr2 | 97157846 | ||||||
| chr2:97158215
|
TTTTCTTT others(7): Show |
T | 2 | a0001c0001t0002g0050a0001c0046t0002g0051 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1321+55_1321+68del others(14): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 16/75 | INFO_REALIGN_3_PRIME | chr2 | 97158215 | |||||
| chr2:97158234
|
T | C | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1321+67T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 16/75 | chr2 | 97158234 | ||||||
| chr2:97158306
|
C | T | 13 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(10): Show | 13 | HG00423.hp1 HG02572.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.1321+139C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 16/75 | chr2 | 97158306 | ||||||
| chr2:97158308
|
A | G | 1 | a0002c0002t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1321+141A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 16/75 | chr2 | 97158308 | ||||||
| chr2:97158773
|
A | G | 1 | a0004c0005t0010g0034 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1389+118A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97158773 | ||||||
| chr2:97158824
|
G | A | 3 | a0018c0018t0002g0043a0018c0018t0002g0044a0018c0018t0002g0048 | 3 | NA18951.hp1 NA18961.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1389+169G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97158824 | ||||||
| chr2:97158959
|
T | C | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1389+304T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97158959 | ||||||
| chr2:97159112
|
A | G | 1 | a0002c0002t0002g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1389+457A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97159112 | ||||||
| chr2:97159154
|
T | G | 1 | a0001c0001t0001g0131 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1389+499T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97159154 | ||||||
| chr2:97159213
|
C | T | 7 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1389+558C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97159213 | ||||||
| chr2:97159257
|
G | A | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1389+602G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97159257 | ||||||
| chr2:97159292
|
A | G | 2 | a0003c0003t0001g0167a0025c0057t0001g0134 | 2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1389+637A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97159292 | ||||||
| chr2:97159476
|
T | A | 11 | a0005c0004t0002g0002a0005c0004t0002g0129a0005c0004t0002g0130others(8): Show | 11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.1389+821T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97159476 | ||||||
| chr2:97159624
|
G | T | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1389+969G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97159624 | ||||||
| chr2:97159913
|
C | T | 1 | a0014c0014t0001g0156 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1389+1258C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97159913 | ||||||
| chr2:97159955
|
T | A | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+1300T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97159955 | ||||||
| chr2:97160262
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1389+1607A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97160262 | ||||||
| chr2:97160366
|
C | T | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1389+1711C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97160366 | ||||||
| chr2:97160402
|
G | A | 2 | a0001c0001t0001g0070a0011c0011t0002g0045 | 2 | NA18945.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1390-1697G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97160402 | ||||||
| chr2:97160576
|
G | A | 3 | a0003c0003t0001g0163a0003c0003t0001g0172a0006c0034t0001g0173 | 3 | HG02109.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1390-1523G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97160576 | ||||||
| chr2:97160694
|
G | A | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1390-1405G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97160694 | ||||||
| chr2:97160722
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1390-1377T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97160722 | ||||||
| chr2:97160959
|
T | A | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1390-1140T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97160959 | ||||||
| chr2:97160969
|
G | A | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1390-1130G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97160969 | ||||||
| chr2:97161004
|
A | G | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1390-1095A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97161004 | ||||||
| chr2:97161036
|
G | C | 1 | a0003c0003t0001g0181 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1390-1063G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97161036 | ||||||
| chr2:97161115
|
T | G | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1390-984T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97161115 | ||||||
| chr2:97161231
|
T | C | 122 | a0002c0002t0001g0017a0002c0002t0001g0060a0002c0002t0001g0061others(119): Show | 122 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1390-868T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97161231 | ||||||
| chr2:97161690
|
G | A | 1 | a0004c0005t0004g0037 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1390-409G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97161690 | ||||||
| chr2:97161732
|
T | C | 48 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(45): Show | 48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1390-367T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97161732 | ||||||
| chr2:97161852
|
C | A | 1 | a0001c0001t0002g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1390-247C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97161852 | ||||||
| chr2:97162044
|
CTGAT | C | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1390-51_1390-48del others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | INFO_REALIGN_3_PRIME | chr2 | 97162044 | |||||
| chr2:97162053
|
T | C | 49 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(46): Show | 49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.1390-46T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | chr2 | 97162053 | ||||||
| chr2:97162081
|
C | CT | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
splice_region_variant&intron_variant | LOW | c.1390-6dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 17/75 | INFO_REALIGN_3_PRIME | chr2 | 97162081 | |||||
| chr2:97162145
|
G | A | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1429+7G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162145 | ||||||
| chr2:97162158
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1429+20T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162158 | ||||||
| chr2:97162354
|
T | G | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1429+216T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162354 | ||||||
| chr2:97162460
|
A | C | 1 | a0001c0001t0001g0077 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1429+322A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162460 | ||||||
| chr2:97162516
|
G | C | 3 | a0001c0001t0001g0084a0010c0012t0001g0083a0040c0047t0001g0082 | 3 | HG01169.hp1 HG01361.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.1429+378G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162516 | ||||||
| chr2:97162556
|
G | T | 1 | a0001c0001t0007g0100 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1429+418G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162556 | ||||||
| chr2:97162699
|
G | A | 1 | a0041c0045t0001g0110 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1429+561G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162699 | ||||||
| chr2:97162876
|
G | T | 1 | a0029c0055t0002g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1429+738G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162876 | ||||||
| chr2:97162917
|
C | A | 8 | a0011c0011t0002g0011a0011c0011t0002g0045a0011c0011t0002g0046others(5): Show | 8 | HG00423.hp1 HG02602.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.1429+779C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162917 | ||||||
| chr2:97162947
|
A | G | 1 | a0004c0005t0004g0016 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1429+809A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97162947 | ||||||
| chr2:97163049
|
T | C | 74 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(71): Show | 74 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1429+911T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163049 | ||||||
| chr2:97163127
|
C | T | 47 | a0003c0003t0001g0133a0003c0003t0001g0142a0003c0003t0001g0143others(44): Show | 47 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.1429+989C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163127 | ||||||
| chr2:97163192
|
A | G | 133 | a0002c0002t0001g0017a0002c0002t0001g0060a0002c0002t0001g0061others(130): Show | 133 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.1429+1054A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163192 | ||||||
| chr2:97163589
|
T | C | 1 | a0031c0051t0001g0085 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1430-694T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163589 | ||||||
| chr2:97163711
|
T | G | 1 | a0001c0001t0002g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1430-572T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163711 | ||||||
| chr2:97163721
|
G | T | 1 | a0001c0001t0002g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1430-562G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163721 | ||||||
| chr2:97163751
|
A | G | 1 | a0000c0016t0006g0119 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1430-532A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163751 | ||||||
| chr2:97163847
|
T | C | 1 | a0007c0007t0001g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1430-436T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163847 | ||||||
| chr2:97163876
|
C | T | 2 | a0020c0022t0002g0015a0020c0022t0002g0030 | 2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1430-407C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163876 | ||||||
| chr2:97163877
|
G | A | 21 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(18): Show | 21 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.1430-406G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163877 | ||||||
| chr2:97163912
|
C | T | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1430-371C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97163912 | ||||||
| chr2:97164125
|
T | A | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1430-158T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 18/75 | chr2 | 97164125 | ||||||
| chr2:97164616
|
A | G | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1531+147A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97164616 | ||||||
| chr2:97164863
|
C | T | 1 | a0016c0053t0001g0104 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1531+394C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97164863 | ||||||
| chr2:97164878
|
G | A | 1 | a0002c0002t0001g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1531+409G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97164878 | ||||||
| chr2:97165029
|
C | T | 48 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(45): Show | 48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1531+560C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97165029 | ||||||
| chr2:97165117
|
A | G | 1 | a0003c0003t0001g0158 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1531+648A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97165117 | ||||||
| chr2:97165143
|
A | G | 1 | a0002c0002t0001g0064 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1531+674A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97165143 | ||||||
| chr2:97165657
|
G | T | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1531+1188G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97165657 | ||||||
| chr2:97165720
|
A | G | 6 | a0005c0004t0005g0199a0005c0004t0005g0201a0005c0004t0005g0202others(3): Show | 6 | HG00642.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1531+1251A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97165720 | ||||||
| chr2:97165876
|
T | G | 2 | a0020c0022t0002g0015a0020c0022t0002g0030 | 2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1531+1407T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97165876 | ||||||
| chr2:97166049
|
GT | G | 74 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(71): Show | 74 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1532-1526delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | INFO_REALIGN_3_PRIME | chr2 | 97166049 | |||||
| chr2:97166168
|
G | T | 3 | a0015c0015t0001g0109a0015c0015t0001g0118a0046c0037t0001g0099 | 3 | NA18952.hp1 NA18961.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1532-1409G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97166168 | ||||||
| chr2:97166354
|
A | G | 6 | a0005c0004t0005g0199a0005c0004t0005g0201a0005c0004t0005g0202others(3): Show | 6 | HG00642.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1532-1223A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97166354 | ||||||
| chr2:97166990
|
C | T | 1 | a0001c0001t0002g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1532-587C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97166990 | ||||||
| chr2:97167141
|
A | G | 2 | a0005c0004t0002g0002a0048c0030t0002g0003 | 2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1532-436A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97167141 | ||||||
| chr2:97167500
|
T | G | 9 | a0005c0004t0002g0129a0005c0004t0002g0130a0005c0004t0005g0199others(6): Show | 9 | HG00642.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1532-77T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97167500 | ||||||
| chr2:97167536
|
G | A | 2 | a0002c0002t0001g0017a0002c0002t0001g0068 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1532-41G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 20/75 | chr2 | 97167536 | ||||||
| chr2:97167779
|
A | G | 1 | a0002c0002t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1633+12A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97167779 | ||||||
| chr2:97168028
|
A | G | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1633+261A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97168028 | ||||||
| chr2:97168033
|
A | C | 1 | a0029c0055t0002g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1633+266A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97168033 | ||||||
| chr2:97168140
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1633+373C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97168140 | ||||||
| chr2:97168335
|
C | G | 1 | a0020c0022t0002g0030 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1633+568C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97168335 | ||||||
| chr2:97168336
|
G | A | 1 | a0005c0004t0005g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1633+569G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97168336 | ||||||
| chr2:97168373
|
C | T | 3 | a0001c0001t0001g0096a0022c0020t0001g0097a0022c0020t0001g0098 | 3 | HG00423.hp2 NA18612.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.1633+606C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97168373 | ||||||
| chr2:97168631
|
C | T | 48 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(45): Show | 48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1633+864C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97168631 | ||||||
| chr2:97168632
|
G | A | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1633+865G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97168632 | ||||||
| chr2:97168883
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1633+1116G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97168883 | ||||||
| chr2:97169403
|
G | C | 1 | a0005c0004t0005g0202 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1633+1636G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97169403 | ||||||
| chr2:97169497
|
T | C | 11 | a0005c0004t0002g0002a0005c0004t0002g0129a0005c0004t0002g0130others(8): Show | 11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.1633+1730T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97169497 | ||||||
| chr2:97169652
|
G | A | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.1633+1885G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97169652 | ||||||
| chr2:97169743
|
C | A | 48 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(45): Show | 48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1633+1976C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97169743 | ||||||
| chr2:97170005
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1633+2238C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97170005 | ||||||
| chr2:97170034
|
G | C | 1 | a0010c0012t0001g0083 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1633+2267G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97170034 | ||||||
| chr2:97170134
|
G | A | 1 | a0017c0017t0001g0169 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1633+2367G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97170134 | ||||||
| chr2:97170396
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1633+2629C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97170396 | ||||||
| chr2:97170733
|
A | G | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1633+2966A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97170733 | ||||||
| chr2:97170886
|
C | T | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1633+3119C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97170886 | ||||||
| chr2:97170896
|
G | A | 4 | a0017c0017t0001g0145a0017c0017t0001g0169a0017c0017t0001g0170others(1): Show | 4 | HG01070.hp2 HG01361.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1633+3129G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97170896 | ||||||
| chr2:97170962
|
A | C | 5 | a0013c0013t0003g0186a0013c0013t0003g0187a0013c0013t0003g0188others(2): Show | 5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1633+3195A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97170962 | ||||||
| chr2:97171029
|
GTCATTAA others(7120): Show |
G | 1 | a0019c0031t0007g0126 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1633+3376_1634-146 others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | INFO_REALIGN_3_PRIME | chr2 | 97171029 | |||||
| chr2:97171264
|
C | T | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1633+3497C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97171264 | ||||||
| chr2:97171399
|
A | T | 1 | a0002c0002t0001g0069 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1633+3632A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97171399 | ||||||
| chr2:97171544
|
A | C | 3 | a0015c0015t0001g0109a0015c0015t0001g0118a0046c0037t0001g0099 | 3 | NA18952.hp1 NA18961.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1633+3777A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97171544 | ||||||
| chr2:97171549
|
G | T | 3 | a0015c0015t0001g0109a0015c0015t0001g0118a0046c0037t0001g0099 | 3 | NA18952.hp1 NA18961.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1633+3782G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97171549 | ||||||
| chr2:97171557
|
G | C | 10 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(7): Show | 10 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1633+3790G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97171557 | ||||||
| chr2:97171563
|
A | G | 1 | a0013c0013t0003g0189 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1633+3796A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97171563 | ||||||
| chr2:97171728
|
A | C | 2 | a0021c0021t0002g0012a0021c0021t0002g0013 | 2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1633+3961A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97171728 | ||||||
| chr2:97172132
|
T | A | 147 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1633+4365T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172132 | ||||||
| chr2:97172174
|
C | T | 74 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(71): Show | 74 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.1633+4407C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172174 | ||||||
| chr2:97172337
|
A | C | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1633+4570A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172337 | ||||||
| chr2:97172395
|
C | A | 1 | a0001c0001t0001g0079 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1633+4628C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172395 | ||||||
| chr2:97172496
|
T | G | 44 | a0003c0003t0001g0133a0003c0003t0001g0142a0003c0003t0001g0143others(41): Show | 44 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1633+4729T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172496 | ||||||
| chr2:97172696
|
A | G | 1 | a0003c0003t0001g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1633+4929A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172696 | ||||||
| chr2:97172740
|
C | T | 1 | a0015c0015t0001g0109 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1633+4973C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172740 | ||||||
| chr2:97172831
|
A | ATG | 72 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(69): Show | 72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1633+5090_1633+509 others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | INFO_REALIGN_3_PRIME | chr2 | 97172831 | |||||
| chr2:97172831
|
A | ATGTG | 15 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(12): Show | 15 | HG00423.hp1 HG01123.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1633+5088_1633+509 others(8): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | INFO_REALIGN_3_PRIME | chr2 | 97172831 | |||||
| chr2:97172831
|
ATGTG | A | 2 | a0005c0004t0002g0002a0048c0030t0002g0003 | 2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1633+5088_1633+509 others(8): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | INFO_REALIGN_3_PRIME | chr2 | 97172831 | |||||
| chr2:97172859
|
A | G | 2 | a0001c0001t0002g0022a0037c0040t0002g0211 | 2 | HG02630.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1633+5092A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172859 | ||||||
| chr2:97172859
|
ATG | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1633+5100_1633+510 others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | INFO_REALIGN_3_PRIME | chr2 | 97172859 | |||||
| chr2:97172861
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1633+5094G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172861 | ||||||
| chr2:97172908
|
C | A | 10 | a0001c0001t0001g0125a0002c0002t0001g0052a0002c0002t0001g0053others(7): Show | 10 | HG02257.hp1 HG02451.hp2 HG02698.hp2 others(7): Show |
intron_variant | MODIFIER | c.1633+5141C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97172908 | ||||||
| chr2:97173407
|
T | G | 5 | a0013c0013t0003g0186a0013c0013t0003g0187a0013c0013t0003g0188others(2): Show | 5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.1633+5640T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97173407 | ||||||
| chr2:97173630
|
C | T | 1 | a0002c0002t0001g0069 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1633+5863C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97173630 | ||||||
| chr2:97173721
|
G | A | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1633+5954G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97173721 | ||||||
| chr2:97173876
|
G | T | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1634-5862G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97173876 | ||||||
| chr2:97174203
|
A | T | 8 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(5): Show | 8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1634-5535A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174203 | ||||||
| chr2:97174204
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1634-5534G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174204 | ||||||
| chr2:97174206
|
C | T | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.1634-5532C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174206 | ||||||
| chr2:97174529
|
G | A | 1 | a0004c0005t0004g0036 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1634-5209G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174529 | ||||||
| chr2:97174951
|
C | G | 1 | a0038c0042t0001g0094 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1634-4787C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174951 | ||||||
| chr2:97174964
|
C | A | 1 | a0002c0002t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4774C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174964 | ||||||
| chr2:97174965
|
A | C | 1 | a0002c0002t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4773A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174965 | ||||||
| chr2:97174966
|
G | A | 2 | a0002c0002t0001g0061a0003c0003t0001g0149 | 2 | HG02809.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1634-4772G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174966 | ||||||
| chr2:97174967
|
G | A | 13 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(10): Show | 13 | HG00423.hp1 HG02572.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.1634-4771G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174967 | ||||||
| chr2:97174967
|
G | C | 1 | a0002c0002t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4771G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174967 | ||||||
| chr2:97174968
|
G | A | 1 | a0002c0002t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4770G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174968 | ||||||
| chr2:97174969
|
A | C | 1 | a0002c0002t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4769A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174969 | ||||||
| chr2:97174971
|
G | C | 1 | a0002c0002t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4767G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174971 | ||||||
| chr2:97174972
|
A | T | 1 | a0002c0002t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4766A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97174972 | ||||||
| chr2:97175003
|
T | G | 7 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(4): Show | 7 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1634-4735T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175003 | ||||||
| chr2:97175007
|
G | A | 1 | a0048c0030t0002g0003 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1634-4731G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175007 | ||||||
| chr2:97175019
|
T | C | 1 | a0008c0006t0003g0192 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1634-4719T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175019 | ||||||
| chr2:97175094
|
T | G | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1634-4644T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175094 | ||||||
| chr2:97175159
|
T | C | 1 | a0002c0002t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4579T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175159 | ||||||
| chr2:97175160
|
T | A | 1 | a0002c0002t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4578T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175160 | ||||||
| chr2:97175162
|
C | A | 1 | a0002c0002t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4576C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175162 | ||||||
| chr2:97175167
|
T | A | 1 | a0002c0002t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4571T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175167 | ||||||
| chr2:97175169
|
T | C | 29 | a0002c0002t0001g0061a0002c0002t0002g0031a0002c0002t0002g0132others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.1634-4569T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175169 | ||||||
| chr2:97175170
|
T | A | 1 | a0002c0002t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4568T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175170 | ||||||
| chr2:97175171
|
C | G | 1 | a0002c0002t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4567C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175171 | ||||||
| chr2:97175172
|
T | A | 1 | a0002c0002t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4566T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175172 | ||||||
| chr2:97175173
|
A | T | 1 | a0002c0002t0001g0061 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1634-4565A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175173 | ||||||
| chr2:97175198
|
A | G | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1634-4540A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175198 | ||||||
| chr2:97175354
|
G | A | 6 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(3): Show | 6 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634-4384G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175354 | ||||||
| chr2:97175360
|
T | C | 1 | a0014c0014t0001g0155 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1634-4378T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175360 | ||||||
| chr2:97175411
|
C | T | 4 | a0017c0017t0001g0145a0017c0017t0001g0169a0017c0017t0001g0170others(1): Show | 4 | HG01070.hp2 HG01361.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1634-4327C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175411 | ||||||
| chr2:97175467
|
G | A | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1634-4271G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175467 | ||||||
| chr2:97175535
|
C | G | 1 | a0003c0003t0001g0162 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1634-4203C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175535 | ||||||
| chr2:97175547
|
C | G | 1 | a0008c0006t0003g0192 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1634-4191C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175547 | ||||||
| chr2:97175603
|
G | C | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1634-4135G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175603 | ||||||
| chr2:97175759
|
C | T | 132 | a0001c0001t0002g0020a0001c0001t0002g0021a0002c0002t0001g0017others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1634-3979C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175759 | ||||||
| chr2:97175986
|
G | C | 2 | a0021c0021t0002g0012a0021c0021t0002g0013 | 2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1634-3752G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175986 | ||||||
| chr2:97175990
|
T | C | 2 | a0021c0021t0002g0012a0021c0021t0002g0013 | 2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1634-3748T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175990 | ||||||
| chr2:97175992
|
G | C | 2 | a0021c0021t0002g0012a0021c0021t0002g0013 | 2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1634-3746G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97175992 | ||||||
| chr2:97176002
|
A | C | 2 | a0021c0021t0002g0012a0021c0021t0002g0013 | 2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1634-3736A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176002 | ||||||
| chr2:97176008
|
G | C | 2 | a0021c0021t0002g0012a0021c0021t0002g0013 | 2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1634-3730G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176008 | ||||||
| chr2:97176147
|
G | C | 1 | a0007c0007t0001g0138 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1634-3591G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176147 | ||||||
| chr2:97176185
|
C | T | 1 | a0042c0043t0002g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1634-3553C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176185 | ||||||
| chr2:97176308
|
C | T | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1634-3430C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176308 | ||||||
| chr2:97176315
|
G | T | 1 | a0042c0043t0002g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1634-3423G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176315 | ||||||
| chr2:97176399
|
G | C | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1634-3339G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176399 | ||||||
| chr2:97176453
|
CT | C | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1634-3277delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | INFO_REALIGN_3_PRIME | chr2 | 97176453 | |||||
| chr2:97176580
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1634-3158A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176580 | ||||||
| chr2:97176669
|
C | T | 57 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(54): Show | 57 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.1634-3069C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176669 | ||||||
| chr2:97176787
|
C | T | 48 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(45): Show | 48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1634-2951C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176787 | ||||||
| chr2:97176840
|
G | T | 6 | a0005c0004t0005g0199a0005c0004t0005g0201a0005c0004t0005g0202others(3): Show | 6 | HG00642.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634-2898G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176840 | ||||||
| chr2:97176856
|
A | G | 6 | a0005c0004t0005g0199a0005c0004t0005g0201a0005c0004t0005g0202others(3): Show | 6 | HG00642.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1634-2882A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97176856 | ||||||
| chr2:97177172
|
A | G | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022 | 3 | HG01891.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1634-2566A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97177172 | ||||||
| chr2:97177369
|
A | C | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1634-2369A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97177369 | ||||||
| chr2:97177432
|
A | G | 1 | a0024c0060t0002g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1634-2306A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97177432 | ||||||
| chr2:97177436
|
G | T | 2 | a0003c0003t0001g0151a0003c0003t0001g0152 | 2 | NA18947.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1634-2302G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97177436 | ||||||
| chr2:97177502
|
G | A | 1 | a0002c0002t0001g0066 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1634-2236G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97177502 | ||||||
| chr2:97177730
|
G | C | 1 | a0030c0052t0002g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1634-2008G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97177730 | ||||||
| chr2:97177926
|
C | T | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1634-1812C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97177926 | ||||||
| chr2:97178370
|
C | T | 3 | a0002c0002t0001g0061a0002c0002t0001g0063a0002c0002t0001g0064 | 3 | HG02809.hp1 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1634-1368C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178370 | ||||||
| chr2:97178379
|
G | A | 7 | a0001c0001t0001g0070a0001c0001t0001g0084a0001c0001t0001g0086others(4): Show | 7 | HG01169.hp1 HG01361.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.1634-1359G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178379 | ||||||
| chr2:97178490
|
A | C | 1 | a0004c0005t0008g0035 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1634-1248A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178490 | ||||||
| chr2:97178571
|
C | T | 3 | a0003c0003t0001g0159a0003c0003t0001g0160a0003c0003t0001g0181 | 3 | NA18612.hp1 NA18952.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1634-1167C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178571 | ||||||
| chr2:97178654
|
A | T | 48 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(45): Show | 48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1634-1084A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178654 | ||||||
| chr2:97178674
|
T | G | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1634-1064T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178674 | ||||||
| chr2:97178676
|
T | G | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1634-1062T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178676 | ||||||
| chr2:97178692
|
G | C | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1634-1046G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178692 | ||||||
| chr2:97178704
|
G | A | 1 | a0041c0045t0001g0110 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1634-1034G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178704 | ||||||
| chr2:97178804
|
T | G | 48 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(45): Show | 48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1634-934T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178804 | ||||||
| chr2:97178805
|
G | GT | 48 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(45): Show | 48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1634-932dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | INFO_REALIGN_3_PRIME | chr2 | 97178805 | |||||
| chr2:97178843
|
T | G | 1 | a0020c0022t0002g0015 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1634-895T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178843 | ||||||
| chr2:97178847
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1634-891A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97178847 | ||||||
| chr2:97179249
|
C | G | 8 | a0011c0011t0002g0011a0011c0011t0002g0045a0011c0011t0002g0046others(5): Show | 8 | HG00423.hp1 HG02602.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.1634-489C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97179249 | ||||||
| chr2:97179363
|
C | T | 49 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(46): Show | 49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.1634-375C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97179363 | ||||||
| chr2:97179498
|
T | C | 2 | a0003c0003t0001g0159a0003c0003t0001g0160 | 2 | NA18612.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1634-240T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97179498 | ||||||
| chr2:97179635
|
C | T | 13 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(10): Show | 13 | HG00423.hp1 HG02572.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.1634-103C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97179635 | ||||||
| chr2:97179678
|
T | C | 1 | a0036c0041t0001g0113 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1634-60T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97179678 | ||||||
| chr2:97179736
|
A | G | 1 | a0003c0003t0001g0153 | 1 | NA19000.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.1634-2A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 22/75 | chr2 | 97179736 | ||||||
| chr2:97179792
|
G | A | 1 | a0006c0008t0009g0146 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1662+26G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 23/75 | chr2 | 97179792 | ||||||
| chr2:97179844
|
C | T | 1 | a0001c0046t0002g0051 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1663-17C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 23/75 | chr2 | 97179844 | ||||||
| chr2:97180054
|
T | G | 8 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(5): Show | 8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1735+121T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180054 | ||||||
| chr2:97180204
|
A | G | 2 | a0005c0004t0002g0002a0048c0030t0002g0003 | 2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.1735+271A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180204 | ||||||
| chr2:97180266
|
A | C | 1 | a0029c0055t0002g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1735+333A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180266 | ||||||
| chr2:97180284
|
C | T | 44 | a0003c0003t0001g0133a0003c0003t0001g0142a0003c0003t0001g0143others(41): Show | 44 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1735+351C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180284 | ||||||
| chr2:97180383
|
C | T | 1 | a0003c0003t0001g0166 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1735+450C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180383 | ||||||
| chr2:97180517
|
T | C | 1 | a0001c0001t0001g0081 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1735+584T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180517 | ||||||
| chr2:97180547
|
G | A | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022 | 3 | HG01891.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1735+614G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180547 | ||||||
| chr2:97180592
|
CT | C | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1735+660delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180592 | ||||||
| chr2:97180691
|
G | A | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1735+758G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180691 | ||||||
| chr2:97180715
|
G | A | 1 | a0047c0033t0002g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1735+782G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180715 | ||||||
| chr2:97180837
|
A | G | 1 | a0043c0039t0001g0008 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1736-761A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180837 | ||||||
| chr2:97180888
|
T | C | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1736-710T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97180888 | ||||||
| chr2:97181105
|
T | C | 2 | a0005c0004t0002g0129a0005c0004t0002g0130 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1736-493T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97181105 | ||||||
| chr2:97181113
|
T | C | 147 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1736-485T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97181113 | ||||||
| chr2:97181202
|
A | T | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1736-396A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 24/75 | chr2 | 97181202 | ||||||
| chr2:97181821
|
A | G | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1837+28A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97181821 | ||||||
| chr2:97181836
|
A | G | 2 | a0003c0003t0001g0172a0006c0034t0001g0173 | 2 | HG02109.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1837+43A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97181836 | ||||||
| chr2:97181869
|
A | G | 48 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(45): Show | 48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.1837+76A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97181869 | ||||||
| chr2:97181869
|
A | T | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1837+76A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97181869 | ||||||
| chr2:97181952
|
C | T | 1 | a0002c0002t0001g0057 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1837+159C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97181952 | ||||||
| chr2:97182192
|
C | T | 4 | a0017c0017t0001g0145a0017c0017t0001g0169a0017c0017t0001g0170others(1): Show | 4 | HG01070.hp2 HG01361.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1837+399C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97182192 | ||||||
| chr2:97182268
|
T | TAAG | 72 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(69): Show | 72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1837+476_1837+478d others(5): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | INFO_REALIGN_3_PRIME | chr2 | 97182268 | |||||
| chr2:97182327
|
T | C | 72 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(69): Show | 72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1837+534T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97182327 | ||||||
| chr2:97182407
|
A | C | 1 | a0029c0055t0002g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1837+614A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97182407 | ||||||
| chr2:97182552
|
A | G | 72 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(69): Show | 72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.1837+759A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97182552 | ||||||
| chr2:97182578
|
A | G | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1837+785A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97182578 | ||||||
| chr2:97182858
|
A | G | 1 | a0047c0033t0002g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1838-601A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97182858 | ||||||
| chr2:97182951
|
C | T | 1 | a0003c0003t0001g0144 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1838-508C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97182951 | ||||||
| chr2:97183087
|
A | G | 1 | a0002c0002t0001g0068 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1838-372A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97183087 | ||||||
| chr2:97183399
|
T | C | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1838-60T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97183399 | ||||||
| chr2:97183401
|
T | C | 1 | a0006c0008t0001g0147 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1838-58T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 26/75 | chr2 | 97183401 | ||||||
| chr2:97183555
|
G | C | 1 | a0020c0022t0002g0030 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1867-27G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 27/75 | chr2 | 97183555 | ||||||
| chr2:97183726
|
C | T | 1 | a0029c0055t0002g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1939+72C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97183726 | ||||||
| chr2:97183827
|
A | G | 1 | a0001c0001t0001g0019 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1939+173A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97183827 | ||||||
| chr2:97183880
|
A | G | 7 | a0007c0007t0001g0137a0007c0007t0001g0138a0007c0007t0001g0139others(4): Show | 7 | HG00099.hp2 HG01099.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1939+226A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97183880 | ||||||
| chr2:97183932
|
T | G | 145 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(142): Show | 145 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.1939+278T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97183932 | ||||||
| chr2:97184138
|
G | T | 5 | a0008c0006t0003g0192a0008c0006t0003g0194a0008c0006t0003g0195others(2): Show | 5 | NA18941.hp2 NA18951.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.1939+484G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97184138 | ||||||
| chr2:97184218
|
G | A | 44 | a0003c0003t0001g0133a0003c0003t0001g0142a0003c0003t0001g0143others(41): Show | 44 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.1939+564G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97184218 | ||||||
| chr2:97184331
|
C | T | 1 | a0002c0002t0001g0183 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1939+677C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97184331 | ||||||
| chr2:97184686
|
A | T | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022 | 3 | HG01891.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1940-630A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97184686 | ||||||
| chr2:97184693
|
G | T | 1 | a0029c0055t0002g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1940-623G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97184693 | ||||||
| chr2:97184738
|
A | G | 2 | a0001c0001t0001g0095a0001c0001t0001g0123 | 2 | NA18999.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.1940-578A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97184738 | ||||||
| chr2:97184808
|
A | G | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.1940-508A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97184808 | ||||||
| chr2:97184940
|
C | T | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.1940-376C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97184940 | ||||||
| chr2:97185021
|
G | A | 2 | a0003c0003t0001g0159a0003c0003t0001g0160 | 2 | NA18612.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1940-295G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97185021 | ||||||
| chr2:97185073
|
T | A | 1 | a0046c0037t0001g0099 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1940-243T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 28/75 | chr2 | 97185073 | ||||||
| chr2:97185576
|
A | G | 1 | a0004c0005t0004g0036 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2041+66A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97185576 | ||||||
| chr2:97185594
|
C | T | 1 | a0027c0028t0001g0161 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2041+84C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97185594 | ||||||
| chr2:97185683
|
C | A | 1 | a0005c0004t0005g0200 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2041+173C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97185683 | ||||||
| chr2:97185692
|
G | A | 1 | a0005c0004t0005g0200 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2041+182G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97185692 | ||||||
| chr2:97185846
|
A | C | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2041+336A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97185846 | ||||||
| chr2:97185927
|
T | C | 1 | a0007c0007t0001g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2041+417T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97185927 | ||||||
| chr2:97186091
|
A | T | 1 | a0001c0001t0001g0077 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2041+581A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97186091 | ||||||
| chr2:97186099
|
A | C | 8 | a0011c0011t0002g0011a0011c0011t0002g0045a0011c0011t0002g0046others(5): Show | 8 | HG00423.hp1 HG02602.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.2041+589A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97186099 | ||||||
| chr2:97186155
|
G | A | 1 | a0043c0039t0001g0008 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2041+645G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97186155 | ||||||
| chr2:97186244
|
G | A | 147 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.2041+734G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97186244 | ||||||
| chr2:97186445
|
A | G | 4 | a0004c0005t0004g0016a0004c0005t0004g0033a0004c0005t0008g0035others(1): Show | 4 | HG00099.hp1 HG01175.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.2042-753A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97186445 | ||||||
| chr2:97186532
|
G | T | 72 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(69): Show | 72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.2042-666G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97186532 | ||||||
| chr2:97186647
|
A | C | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2042-551A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97186647 | ||||||
| chr2:97186800
|
C | T | 2 | a0021c0021t0002g0012a0021c0021t0002g0013 | 2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2042-398C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97186800 | ||||||
| chr2:97186835
|
T | C | 1 | a0045c0049t0001g0120 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2042-363T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97186835 | ||||||
| chr2:97187011
|
G | A | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2042-187G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 30/75 | chr2 | 97187011 | ||||||
| chr2:97187307
|
T | C | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2071-22T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 31/75 | chr2 | 97187307 | ||||||
| chr2:97187465
|
T | G | 1 | a0002c0002t0002g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2143+64T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97187465 | ||||||
| chr2:97187490
|
G | C | 1 | a0004c0005t0004g0036 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2143+89G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97187490 | ||||||
| chr2:97187546
|
A | G | 1 | a0045c0049t0001g0120 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2143+145A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97187546 | ||||||
| chr2:97187586
|
A | ATGATCTT others(1881): Show |
5 | a0013c0013t0003g0186a0013c0013t0003g0187a0013c0013t0003g0188others(2): Show | 5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.2144-637_2144-636i others(1890): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | INFO_REALIGN_3_PRIME | chr2 | 97187586 | |||||
| chr2:97187728
|
G | C | 1 | a0034c0050t0001g0087 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2143+327G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97187728 | ||||||
| chr2:97187851
|
A | G | 1 | a0029c0055t0002g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2143+450A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97187851 | ||||||
| chr2:97187861
|
C | T | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2143+460C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97187861 | ||||||
| chr2:97187896
|
A | C | 47 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(44): Show | 47 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.2143+495A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97187896 | ||||||
| chr2:97188207
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2143+806T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188207 | ||||||
| chr2:97188214
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2143+813C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188214 | ||||||
| chr2:97188215
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2143+814T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188215 | ||||||
| chr2:97188235
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2143+834T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188235 | ||||||
| chr2:97188276
|
C | A | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.2144-811C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188276 | ||||||
| chr2:97188287
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-800A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188287 | ||||||
| chr2:97188346
|
G | T | 3 | a0018c0018t0002g0043a0018c0018t0002g0044a0018c0018t0002g0048 | 3 | NA18951.hp1 NA18961.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.2144-741G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188346 | ||||||
| chr2:97188381
|
G | T | 1 | a0041c0045t0001g0110 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2144-706G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188381 | ||||||
| chr2:97188419
|
G | C | 2 | a0001c0001t0001g0131a0052c0026t0003g0193 | 2 | HG02071.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.2144-668G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188419 | ||||||
| chr2:97188439
|
T | G | 1 | a0012c0010t0002g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2144-648T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188439 | ||||||
| chr2:97188447
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-640T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188447 | ||||||
| chr2:97188451
|
C | T | 16 | a0004c0024t0004g0040a0008c0006t0003g0184a0008c0006t0003g0190others(13): Show | 16 | HG00597.hp2 HG01261.hp2 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.2144-636C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188451 | ||||||
| chr2:97188455
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-632A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188455 | ||||||
| chr2:97188458
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-629C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188458 | ||||||
| chr2:97188478
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-609T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188478 | ||||||
| chr2:97188498
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-589C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188498 | ||||||
| chr2:97188507
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-580G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188507 | ||||||
| chr2:97188593
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-494T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188593 | ||||||
| chr2:97188599
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-488A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188599 | ||||||
| chr2:97188603
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-484G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188603 | ||||||
| chr2:97188609
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-478C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188609 | ||||||
| chr2:97188614
|
T | G | 8 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(5): Show | 8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2144-473T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188614 | ||||||
| chr2:97188619
|
G | A | 9 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(6): Show | 9 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2144-468G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188619 | ||||||
| chr2:97188626
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-461C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188626 | ||||||
| chr2:97188644
|
A | G | 1 | a0002c0002t0001g0064 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2144-443A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188644 | ||||||
| chr2:97188689
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-398G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188689 | ||||||
| chr2:97188761
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-326A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188761 | ||||||
| chr2:97188809
|
G | A | 1 | a0047c0033t0002g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2144-278G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188809 | ||||||
| chr2:97188853
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-234A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188853 | ||||||
| chr2:97188855
|
A | G | 6 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2144-232A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188855 | ||||||
| chr2:97188861
|
C | T | 9 | a0005c0004t0002g0129a0005c0004t0002g0130a0005c0004t0005g0199others(6): Show | 9 | HG00642.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2144-226C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188861 | ||||||
| chr2:97188872
|
A | G | 6 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2144-215A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188872 | ||||||
| chr2:97188882
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-205T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97188882 | ||||||
| chr2:97189047
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-40A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97189047 | ||||||
| chr2:97189052
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2144-35C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 32/75 | chr2 | 97189052 | ||||||
| chr2:97189130
|
G | A | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2172+15G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/75 | chr2 | 97189130 | ||||||
| chr2:97189135
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2172+20C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/75 | chr2 | 97189135 | ||||||
| chr2:97189151
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2172+36T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/75 | chr2 | 97189151 | ||||||
| chr2:97189168
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2173-50C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/75 | chr2 | 97189168 | ||||||
| chr2:97189196
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2173-22T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/75 | chr2 | 97189196 | ||||||
| chr2:97189215
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | splice_region_variant&intron_variant | LOW | c.2173-3A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 33/75 | chr2 | 97189215 | ||||||
| chr2:97189300
|
C | T | 2 | a0001c0001t0002g0050a0001c0046t0002g0051 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2245+10C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189300 | ||||||
| chr2:97189305
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+15C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189305 | ||||||
| chr2:97189311
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+21C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189311 | ||||||
| chr2:97189320
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+30G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189320 | ||||||
| chr2:97189325
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+35A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189325 | ||||||
| chr2:97189334
|
G | T | 4 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(1): Show | 4 | HG02040.hp1 NA18965.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245+44G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189334 | ||||||
| chr2:97189336
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+46A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189336 | ||||||
| chr2:97189342
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+52C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189342 | ||||||
| chr2:97189349
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+59A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189349 | ||||||
| chr2:97189350
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+60C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189350 | ||||||
| chr2:97189353
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+63C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189353 | ||||||
| chr2:97189358
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+68A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189358 | ||||||
| chr2:97189360
|
ATCAGCGG others(4): Show |
A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+72_2245+82del others(11): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | INFO_REALIGN_3_PRIME | chr2 | 97189360 | |||||
| chr2:97189373
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+83G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189373 | ||||||
| chr2:97189376
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+86T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189376 | ||||||
| chr2:97189377
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+87G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189377 | ||||||
| chr2:97189378
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+88G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189378 | ||||||
| chr2:97189387
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+97C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189387 | ||||||
| chr2:97189389
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+99T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189389 | ||||||
| chr2:97189392
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+102T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189392 | ||||||
| chr2:97189402
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+112C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189402 | ||||||
| chr2:97189404
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+114G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189404 | ||||||
| chr2:97189412
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+122A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189412 | ||||||
| chr2:97189414
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+124G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189414 | ||||||
| chr2:97189422
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+132G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189422 | ||||||
| chr2:97189433
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+143T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189433 | ||||||
| chr2:97189435
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+145A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189435 | ||||||
| chr2:97189439
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+149A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189439 | ||||||
| chr2:97189443
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+153C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189443 | ||||||
| chr2:97189451
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+161C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189451 | ||||||
| chr2:97189453
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+163C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189453 | ||||||
| chr2:97189455
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+165A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189455 | ||||||
| chr2:97189466
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+176C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189466 | ||||||
| chr2:97189467
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+177T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189467 | ||||||
| chr2:97189474
|
G | A | 4 | a0001c0001t0001g0112a0001c0001t0001g0124a0002c0002t0001g0061others(1): Show | 4 | HG02683.hp2 HG02809.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245+184G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189474 | ||||||
| chr2:97189491
|
A | C | 8 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(5): Show | 8 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2245+201A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189491 | ||||||
| chr2:97189511
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+221G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189511 | ||||||
| chr2:97189517
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+227G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189517 | ||||||
| chr2:97189527
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+237T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189527 | ||||||
| chr2:97189529
|
C | T | 24 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(21): Show | 24 | HG00597.hp2 HG01261.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.2245+239C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189529 | ||||||
| chr2:97189538
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+248A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189538 | ||||||
| chr2:97189539
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+249G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189539 | ||||||
| chr2:97189543
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+253C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189543 | ||||||
| chr2:97189548
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+258C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189548 | ||||||
| chr2:97189548
|
C | T | 49 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(46): Show | 49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.2245+258C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189548 | ||||||
| chr2:97189574
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+284G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189574 | ||||||
| chr2:97189586
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+296T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189586 | ||||||
| chr2:97189598
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+308G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189598 | ||||||
| chr2:97189603
|
A | G | 2 | a0005c0004t0002g0129a0005c0004t0002g0130 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2245+313A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189603 | ||||||
| chr2:97189604
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+314C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189604 | ||||||
| chr2:97189617
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+327A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189617 | ||||||
| chr2:97189640
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+350C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189640 | ||||||
| chr2:97189645
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+355G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189645 | ||||||
| chr2:97189655
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+365A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189655 | ||||||
| chr2:97189666
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+376G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189666 | ||||||
| chr2:97189669
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+379A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189669 | ||||||
| chr2:97189677
|
G | A | 162 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(159): Show | 162 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.2245+387G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189677 | ||||||
| chr2:97189685
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+395A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189685 | ||||||
| chr2:97189711
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+421C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189711 | ||||||
| chr2:97189711
|
C | T | 1 | a0005c0004t0005g0201 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2245+421C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189711 | ||||||
| chr2:97189716
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+426A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189716 | ||||||
| chr2:97189720
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+430A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189720 | ||||||
| chr2:97189731
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+441G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189731 | ||||||
| chr2:97189732
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+442A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189732 | ||||||
| chr2:97189759
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+469T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189759 | ||||||
| chr2:97189767
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+477C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189767 | ||||||
| chr2:97189770
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+480A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189770 | ||||||
| chr2:97189779
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+489A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189779 | ||||||
| chr2:97189792
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+502T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189792 | ||||||
| chr2:97189806
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+516A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189806 | ||||||
| chr2:97189814
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+524C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189814 | ||||||
| chr2:97189816
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+526G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189816 | ||||||
| chr2:97189826
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+536T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189826 | ||||||
| chr2:97189845
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+555C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189845 | ||||||
| chr2:97189847
|
T | C | 1 | a0043c0039t0001g0008 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2245+557T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189847 | ||||||
| chr2:97189861
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+571G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189861 | ||||||
| chr2:97189863
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+573G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189863 | ||||||
| chr2:97189865
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+575C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189865 | ||||||
| chr2:97189871
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+581A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189871 | ||||||
| chr2:97189890
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+600T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189890 | ||||||
| chr2:97189892
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+602C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189892 | ||||||
| chr2:97189898
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+608T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189898 | ||||||
| chr2:97189908
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+618C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189908 | ||||||
| chr2:97189909
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+619A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189909 | ||||||
| chr2:97189929
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+639G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189929 | ||||||
| chr2:97189930
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+640G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189930 | ||||||
| chr2:97189936
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+646G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189936 | ||||||
| chr2:97189944
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+654A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189944 | ||||||
| chr2:97189957
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+667T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189957 | ||||||
| chr2:97189965
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+675C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189965 | ||||||
| chr2:97189966
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+676T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189966 | ||||||
| chr2:97189997
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+707C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97189997 | ||||||
| chr2:97190002
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+712C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190002 | ||||||
| chr2:97190008
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+718A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190008 | ||||||
| chr2:97190017
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+727T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190017 | ||||||
| chr2:97190018
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+728A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190018 | ||||||
| chr2:97190021
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+731G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190021 | ||||||
| chr2:97190035
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+745C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190035 | ||||||
| chr2:97190084
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+794C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190084 | ||||||
| chr2:97190096
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+806A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190096 | ||||||
| chr2:97190104
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+814C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190104 | ||||||
| chr2:97190121
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2245+831G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190121 | ||||||
| chr2:97190125
|
G | A | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2245+835G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190125 | ||||||
| chr2:97190138
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-840C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190138 | ||||||
| chr2:97190152
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-826A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190152 | ||||||
| chr2:97190160
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-818T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190160 | ||||||
| chr2:97190164
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-814C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190164 | ||||||
| chr2:97190166
|
C | A | 24 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(21): Show | 24 | HG00597.hp2 HG01261.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.2246-812C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190166 | ||||||
| chr2:97190170
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-808A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190170 | ||||||
| chr2:97190172
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-806A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190172 | ||||||
| chr2:97190175
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-803G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190175 | ||||||
| chr2:97190177
|
A | C | 25 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(22): Show | 25 | HG00597.hp2 HG01261.hp1 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.2246-801A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190177 | ||||||
| chr2:97190188
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-790A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190188 | ||||||
| chr2:97190195
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-783C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190195 | ||||||
| chr2:97190197
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-781G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190197 | ||||||
| chr2:97190211
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-767A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190211 | ||||||
| chr2:97190218
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-760G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190218 | ||||||
| chr2:97190220
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-758T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190220 | ||||||
| chr2:97190235
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-743T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190235 | ||||||
| chr2:97190250
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-728T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190250 | ||||||
| chr2:97190266
|
A | G | 5 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(2): Show | 5 | HG02559.hp1 HG02717.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2246-712A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190266 | ||||||
| chr2:97190294
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-684A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190294 | ||||||
| chr2:97190299
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-679G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190299 | ||||||
| chr2:97190299
|
G | GAT | 2 | a0005c0004t0002g0002a0048c0030t0002g0003 | 2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.2246-674_2246-673d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | INFO_REALIGN_3_PRIME | chr2 | 97190299 | |||||
| chr2:97190309
|
C | G | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2246-669C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190309 | ||||||
| chr2:97190312
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-666T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190312 | ||||||
| chr2:97190321
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-657C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190321 | ||||||
| chr2:97190324
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-654C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190324 | ||||||
| chr2:97190341
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-637C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190341 | ||||||
| chr2:97190345
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-633G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190345 | ||||||
| chr2:97190348
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-630A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190348 | ||||||
| chr2:97190374
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-604G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190374 | ||||||
| chr2:97190388
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-590A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190388 | ||||||
| chr2:97190437
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-541C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190437 | ||||||
| chr2:97190438
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-540A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190438 | ||||||
| chr2:97190468
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-510T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190468 | ||||||
| chr2:97190471
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-507A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190471 | ||||||
| chr2:97190483
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-495C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190483 | ||||||
| chr2:97190492
|
C | A | 1 | a0026c0058t0001g0074 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2246-486C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190492 | ||||||
| chr2:97190493
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-485T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190493 | ||||||
| chr2:97190499
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-479G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190499 | ||||||
| chr2:97190504
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-474T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190504 | ||||||
| chr2:97190511
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-467G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190511 | ||||||
| chr2:97190512
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-466G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190512 | ||||||
| chr2:97190524
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-454C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190524 | ||||||
| chr2:97190549
|
GA | G | 12 | a0004c0005t0004g0016a0004c0005t0004g0032a0004c0005t0004g0033others(9): Show | 12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.2246-428delA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190549 | ||||||
| chr2:97190561
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-417T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190561 | ||||||
| chr2:97190572
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-406C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190572 | ||||||
| chr2:97190579
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-399A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190579 | ||||||
| chr2:97190596
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-382C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190596 | ||||||
| chr2:97190597
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-381C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190597 | ||||||
| chr2:97190642
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-336G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190642 | ||||||
| chr2:97190650
|
C | G | 2 | a0001c0001t0001g0086a0052c0026t0003g0193 | 2 | NA18941.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.2246-328C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190650 | ||||||
| chr2:97190651
|
G | A | 1 | a0004c0024t0004g0038 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2246-327G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190651 | ||||||
| chr2:97190662
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-316G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190662 | ||||||
| chr2:97190690
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-288T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190690 | ||||||
| chr2:97190698
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-280C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190698 | ||||||
| chr2:97190706
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-272C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190706 | ||||||
| chr2:97190707
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-271C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190707 | ||||||
| chr2:97190724
|
G | A | 48 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(45): Show | 48 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.2246-254G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190724 | ||||||
| chr2:97190729
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-249T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190729 | ||||||
| chr2:97190741
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-237C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190741 | ||||||
| chr2:97190743
|
A | G | 15 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(12): Show | 15 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.2246-235A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190743 | ||||||
| chr2:97190752
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-226G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190752 | ||||||
| chr2:97190756
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-222C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190756 | ||||||
| chr2:97190772
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-206C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190772 | ||||||
| chr2:97190777
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-201A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190777 | ||||||
| chr2:97190780
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-198A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190780 | ||||||
| chr2:97190810
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-168A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190810 | ||||||
| chr2:97190811
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-167C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190811 | ||||||
| chr2:97190828
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-150T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190828 | ||||||
| chr2:97190833
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-145C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190833 | ||||||
| chr2:97190840
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-138A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190840 | ||||||
| chr2:97190844
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-134G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190844 | ||||||
| chr2:97190845
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-133A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190845 | ||||||
| chr2:97190846
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-132C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190846 | ||||||
| chr2:97190857
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-121A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190857 | ||||||
| chr2:97190863
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-115G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190863 | ||||||
| chr2:97190871
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-107A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190871 | ||||||
| chr2:97190875
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-103G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190875 | ||||||
| chr2:97190885
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-93A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190885 | ||||||
| chr2:97190888
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-90G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190888 | ||||||
| chr2:97190890
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-88T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190890 | ||||||
| chr2:97190892
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-86C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190892 | ||||||
| chr2:97190895
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-83C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190895 | ||||||
| chr2:97190897
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-81G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190897 | ||||||
| chr2:97190901
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-77G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190901 | ||||||
| chr2:97190903
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-75T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190903 | ||||||
| chr2:97190910
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-68G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190910 | ||||||
| chr2:97190911
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-67T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190911 | ||||||
| chr2:97190912
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-66G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190912 | ||||||
| chr2:97190932
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-46A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190932 | ||||||
| chr2:97190937
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-41G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190937 | ||||||
| chr2:97190938
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-40T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190938 | ||||||
| chr2:97190942
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2246-36T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 34/75 | chr2 | 97190942 | ||||||
| chr2:97191012
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | splice_region_variant&intron_variant | LOW | c.2274+6T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191012 | ||||||
| chr2:97191017
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2274+11T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191017 | ||||||
| chr2:97191035
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2274+29C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191035 | ||||||
| chr2:97191036
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2274+30T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191036 | ||||||
| chr2:97191040
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2274+34A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191040 | ||||||
| chr2:97191044
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2274+38C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191044 | ||||||
| chr2:97191048
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2274+42A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191048 | ||||||
| chr2:97191059
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2275-50T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191059 | ||||||
| chr2:97191087
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2275-22C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191087 | ||||||
| chr2:97191090
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2275-19T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191090 | ||||||
| chr2:97191091
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2275-18C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 35/75 | chr2 | 97191091 | ||||||
| chr2:97191196
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+15G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191196 | ||||||
| chr2:97191198
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+17C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191198 | ||||||
| chr2:97191200
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+19T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191200 | ||||||
| chr2:97191207
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+26T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191207 | ||||||
| chr2:97191233
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+52T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191233 | ||||||
| chr2:97191241
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+60T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191241 | ||||||
| chr2:97191249
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+68G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191249 | ||||||
| chr2:97191253
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+72T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191253 | ||||||
| chr2:97191254
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+73G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191254 | ||||||
| chr2:97191257
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+76C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191257 | ||||||
| chr2:97191258
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+77T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191258 | ||||||
| chr2:97191265
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+84C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191265 | ||||||
| chr2:97191268
|
C | T | 1 | a0013c0013t0003g0186 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2347+87C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191268 | ||||||
| chr2:97191269
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+88G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191269 | ||||||
| chr2:97191282
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+101A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191282 | ||||||
| chr2:97191284
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+103C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191284 | ||||||
| chr2:97191292
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+111T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191292 | ||||||
| chr2:97191294
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+113T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191294 | ||||||
| chr2:97191298
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+117G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191298 | ||||||
| chr2:97191305
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+124T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191305 | ||||||
| chr2:97191312
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+131G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191312 | ||||||
| chr2:97191313
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+132C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191313 | ||||||
| chr2:97191315
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+134G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191315 | ||||||
| chr2:97191325
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+144G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191325 | ||||||
| chr2:97191333
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+152G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191333 | ||||||
| chr2:97191348
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+167T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191348 | ||||||
| chr2:97191363
|
G | A | 3 | a0003c0003t0001g0159a0003c0003t0001g0160a0052c0026t0003g0193 | 3 | NA18612.hp1 NA18941.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.2347+182G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191363 | ||||||
| chr2:97191365
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+184A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191365 | ||||||
| chr2:97191391
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+210C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191391 | ||||||
| chr2:97191397
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+216T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191397 | ||||||
| chr2:97191423
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+242G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191423 | ||||||
| chr2:97191428
|
C | A | 15 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(12): Show | 15 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.2347+247C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191428 | ||||||
| chr2:97191430
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+249T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191430 | ||||||
| chr2:97191442
|
G | C | 43 | a0003c0003t0001g0133a0003c0003t0001g0142a0003c0003t0001g0143others(40): Show | 43 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.2347+261G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191442 | ||||||
| chr2:97191449
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+268G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191449 | ||||||
| chr2:97191466
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+285C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191466 | ||||||
| chr2:97191470
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+289A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191470 | ||||||
| chr2:97191523
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+342A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191523 | ||||||
| chr2:97191526
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+345G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191526 | ||||||
| chr2:97191541
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+360T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191541 | ||||||
| chr2:97191544
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+363A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191544 | ||||||
| chr2:97191547
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+366C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191547 | ||||||
| chr2:97191565
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+384T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191565 | ||||||
| chr2:97191590
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+409G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191590 | ||||||
| chr2:97191592
|
G | A | 5 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(2): Show | 5 | HG02559.hp1 HG02717.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.2347+411G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191592 | ||||||
| chr2:97191594
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+413C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191594 | ||||||
| chr2:97191598
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+417C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191598 | ||||||
| chr2:97191598
|
C | T | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2347+417C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191598 | ||||||
| chr2:97191599
|
G | A | 3 | a0003c0003t0001g0133a0003c0003t0001g0162a0003c0003t0001g0166 | 3 | HG01123.hp1 HG01169.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2347+418G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191599 | ||||||
| chr2:97191609
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+428C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191609 | ||||||
| chr2:97191610
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+429C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191610 | ||||||
| chr2:97191628
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+447C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191628 | ||||||
| chr2:97191631
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+450G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191631 | ||||||
| chr2:97191673
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+492C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191673 | ||||||
| chr2:97191679
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+498T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191679 | ||||||
| chr2:97191681
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+500T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191681 | ||||||
| chr2:97191690
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+509G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191690 | ||||||
| chr2:97191695
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+514T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191695 | ||||||
| chr2:97191697
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+516C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191697 | ||||||
| chr2:97191698
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+517C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191698 | ||||||
| chr2:97191725
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+544A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191725 | ||||||
| chr2:97191735
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+554G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191735 | ||||||
| chr2:97191738
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+557A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191738 | ||||||
| chr2:97191739
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+558T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191739 | ||||||
| chr2:97191744
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+563T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191744 | ||||||
| chr2:97191750
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+569A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191750 | ||||||
| chr2:97191751
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+570A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191751 | ||||||
| chr2:97191752
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+571C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191752 | ||||||
| chr2:97191765
|
G | A | 3 | a0001c0001t0001g0111a0041c0045t0001g0110a0052c0026t0003g0193 | 3 | NA18941.hp2 NA18946.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.2347+584G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191765 | ||||||
| chr2:97191771
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+590A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191771 | ||||||
| chr2:97191773
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+592A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191773 | ||||||
| chr2:97191779
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+598A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191779 | ||||||
| chr2:97191781
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+600A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191781 | ||||||
| chr2:97191789
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+608T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191789 | ||||||
| chr2:97191790
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+609G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191790 | ||||||
| chr2:97191798
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+617A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191798 | ||||||
| chr2:97191810
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+629C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191810 | ||||||
| chr2:97191819
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+638C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191819 | ||||||
| chr2:97191820
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+639A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191820 | ||||||
| chr2:97191823
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+642C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191823 | ||||||
| chr2:97191826
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+645C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191826 | ||||||
| chr2:97191839
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+658G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191839 | ||||||
| chr2:97191847
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+666G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191847 | ||||||
| chr2:97191848
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+667C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191848 | ||||||
| chr2:97191866
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+685C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191866 | ||||||
| chr2:97191899
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+718C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191899 | ||||||
| chr2:97191900
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+719C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191900 | ||||||
| chr2:97191917
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+736T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191917 | ||||||
| chr2:97191958
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+777A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191958 | ||||||
| chr2:97191962
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+781A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191962 | ||||||
| chr2:97191965
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+784T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191965 | ||||||
| chr2:97191968
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+787T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191968 | ||||||
| chr2:97191983
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+802G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191983 | ||||||
| chr2:97191987
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+806A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97191987 | ||||||
| chr2:97192001
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2347+820A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192001 | ||||||
| chr2:97192020
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-838T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192020 | ||||||
| chr2:97192042
|
T | C | 10 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(7): Show | 10 | HG00597.hp2 NA18951.hp2 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2348-816T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192042 | ||||||
| chr2:97192055
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-803T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192055 | ||||||
| chr2:97192070
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-788G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192070 | ||||||
| chr2:97192090
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-768A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192090 | ||||||
| chr2:97192099
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-759T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192099 | ||||||
| chr2:97192102
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-756A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192102 | ||||||
| chr2:97192106
|
T | A | 1 | a0001c0001t0002g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2348-752T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192106 | ||||||
| chr2:97192117
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-741A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192117 | ||||||
| chr2:97192139
|
A | G | 1 | a0027c0028t0001g0161 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2348-719A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192139 | ||||||
| chr2:97192149
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-709A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192149 | ||||||
| chr2:97192192
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-666G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192192 | ||||||
| chr2:97192196
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-662T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192196 | ||||||
| chr2:97192204
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-654G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192204 | ||||||
| chr2:97192207
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-651G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192207 | ||||||
| chr2:97192221
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-637A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192221 | ||||||
| chr2:97192222
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-636G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192222 | ||||||
| chr2:97192227
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-631G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192227 | ||||||
| chr2:97192241
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-617T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192241 | ||||||
| chr2:97192317
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-541T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192317 | ||||||
| chr2:97192318
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-540G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192318 | ||||||
| chr2:97192320
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-538A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192320 | ||||||
| chr2:97192348
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-510A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192348 | ||||||
| chr2:97192351
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-507C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192351 | ||||||
| chr2:97192372
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-486C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192372 | ||||||
| chr2:97192398
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-460G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192398 | ||||||
| chr2:97192402
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-456G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192402 | ||||||
| chr2:97192403
|
C | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-455C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192403 | ||||||
| chr2:97192404
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-454T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192404 | ||||||
| chr2:97192441
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-417C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192441 | ||||||
| chr2:97192442
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-416G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192442 | ||||||
| chr2:97192445
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-413T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192445 | ||||||
| chr2:97192489
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-369C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192489 | ||||||
| chr2:97192522
|
C | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-336C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192522 | ||||||
| chr2:97192542
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-316T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192542 | ||||||
| chr2:97192562
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-296C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192562 | ||||||
| chr2:97192571
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-287G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192571 | ||||||
| chr2:97192575
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-283C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192575 | ||||||
| chr2:97192579
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-279T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192579 | ||||||
| chr2:97192583
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-275A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192583 | ||||||
| chr2:97192588
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-270G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192588 | ||||||
| chr2:97192604
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-254C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192604 | ||||||
| chr2:97192605
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-253A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192605 | ||||||
| chr2:97192610
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-248G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192610 | ||||||
| chr2:97192658
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-200G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192658 | ||||||
| chr2:97192673
|
G | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-185G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192673 | ||||||
| chr2:97192691
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-167T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192691 | ||||||
| chr2:97192709
|
C | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-149C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192709 | ||||||
| chr2:97192726
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-132T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192726 | ||||||
| chr2:97192727
|
A | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-131A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192727 | ||||||
| chr2:97192731
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-127G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192731 | ||||||
| chr2:97192769
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-89A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192769 | ||||||
| chr2:97192782
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-76A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192782 | ||||||
| chr2:97192784
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-74A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192784 | ||||||
| chr2:97192791
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-67T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192791 | ||||||
| chr2:97192812
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-46T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192812 | ||||||
| chr2:97192816
|
A | G | 1 | a0048c0030t0002g0003 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2348-42A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192816 | ||||||
| chr2:97192819
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-39G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192819 | ||||||
| chr2:97192822
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-36A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192822 | ||||||
| chr2:97192835
|
T | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-23T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192835 | ||||||
| chr2:97192839
|
T | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2348-19T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192839 | ||||||
| chr2:97192851
|
T | G | 1 | a0002c0002t0001g0064 | 1 | HG03540.hp1 | splice_region_variant&intron_variant | LOW | c.2348-7T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 36/75 | chr2 | 97192851 | ||||||
| chr2:97192891
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | splice_region_variant&intron_variant | LOW | c.2376+5T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/75 | chr2 | 97192891 | ||||||
| chr2:97192895
|
A | G | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2376+9A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/75 | chr2 | 97192895 | ||||||
| chr2:97192897
|
A | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2376+11A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/75 | chr2 | 97192897 | ||||||
| chr2:97192912
|
G | T | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2376+26G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/75 | chr2 | 97192912 | ||||||
| chr2:97192915
|
T | C | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2376+29T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/75 | chr2 | 97192915 | ||||||
| chr2:97192916
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2376+30G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/75 | chr2 | 97192916 | ||||||
| chr2:97192916
|
G | GAGTTAAT others(1864): Show |
5 | a0013c0013t0003g0186a0013c0013t0003g0187a0013c0013t0003g0188others(2): Show | 5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.2376+36_2376+37ins others(1871): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/75 | INFO_REALIGN_3_PRIME | chr2 | 97192916 | |||||
| chr2:97192916
|
G | GAGTTAAT others(1864): Show |
10 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(7): Show | 10 | HG00597.hp2 NA18951.hp2 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2376+36_2376+37ins others(1871): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/75 | INFO_REALIGN_3_PRIME | chr2 | 97192916 | |||||
| chr2:97192966
|
T | A | 1 | a0003c0003t0001g0133 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2377-15T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 37/75 | chr2 | 97192966 | ||||||
| chr2:97193311
|
C | T | 55 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(52): Show | 55 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.2449+258C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193311 | ||||||
| chr2:97193330
|
A | G | 146 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(143): Show | 146 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(143): Show |
intron_variant | MODIFIER | c.2449+277A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193330 | ||||||
| chr2:97193407
|
G | T | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2449+354G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193407 | ||||||
| chr2:97193446
|
C | T | 21 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(18): Show | 21 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.2449+393C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193446 | ||||||
| chr2:97193490
|
T | A | 71 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(68): Show | 71 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2449+437T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193490 | ||||||
| chr2:97193491
|
A | G | 111 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(108): Show | 111 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(108): Show |
intron_variant | MODIFIER | c.2449+438A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193491 | ||||||
| chr2:97193537
|
A | G | 71 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(68): Show | 71 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2449+484A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193537 | ||||||
| chr2:97193560
|
G | A | 4 | a0007c0007t0001g0138a0007c0007t0001g0139a0007c0007t0001g0180others(1): Show | 4 | HG01099.hp1 HG01106.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.2449+507G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193560 | ||||||
| chr2:97193613
|
T | G | 1 | a0002c0002t0001g0060 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2449+560T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193613 | ||||||
| chr2:97193639
|
A | G | 23 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(20): Show | 23 | HG00597.hp2 HG01261.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.2449+586A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193639 | ||||||
| chr2:97193839
|
A | C | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2449+786A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193839 | ||||||
| chr2:97193859
|
C | T | 2 | a0001c0001t0001g0070a0019c0031t0007g0126 | 2 | NA19079.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.2449+806C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193859 | ||||||
| chr2:97193942
|
T | C | 2 | a0003c0003t0001g0151a0003c0003t0001g0152 | 2 | NA18947.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.2450-784T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193942 | ||||||
| chr2:97193950
|
A | C | 1 | a0008c0006t0003g0196 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.2450-776A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97193950 | ||||||
| chr2:97194217
|
C | G | 1 | a0003c0003t0001g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2450-509C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97194217 | ||||||
| chr2:97194306
|
A | G | 71 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(68): Show | 71 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2450-420A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97194306 | ||||||
| chr2:97194341
|
T | A | 1 | a0003c0003t0001g0159 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2450-385T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97194341 | ||||||
| chr2:97194386
|
C | T | 1 | a0001c0001t0002g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2450-340C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97194386 | ||||||
| chr2:97194486
|
C | T | 129 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(126): Show | 129 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.2450-240C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97194486 | ||||||
| chr2:97194627
|
C | A | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.2450-99C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 38/75 | chr2 | 97194627 | ||||||
| chr2:97194792
|
G | A | 29 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.2478+38G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 39/75 | chr2 | 97194792 | ||||||
| chr2:97194956
|
A | C | 1 | a0001c0001t0001g0125 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2551+39A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97194956 | ||||||
| chr2:97195044
|
C | G | 1 | a0002c0002t0002g0031 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2551+127C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195044 | ||||||
| chr2:97195109
|
C | T | 1 | a0032c0054t0001g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2551+192C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195109 | ||||||
| chr2:97195110
|
G | A | 8 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(5): Show | 8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2551+193G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195110 | ||||||
| chr2:97195234
|
G | A | 71 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(68): Show | 71 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2551+317G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195234 | ||||||
| chr2:97195260
|
G | A | 2 | a0015c0015t0001g0088a0015c0015t0001g0089 | 2 | HG00558.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.2551+343G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195260 | ||||||
| chr2:97195268
|
G | A | 1 | a0048c0030t0002g0003 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2551+351G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195268 | ||||||
| chr2:97195300
|
A | T | 1 | a0048c0030t0002g0003 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2551+383A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195300 | ||||||
| chr2:97195308
|
A | G | 1 | a0048c0030t0002g0003 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2551+391A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195308 | ||||||
| chr2:97195334
|
G | A | 1 | a0048c0030t0002g0003 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2551+417G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195334 | ||||||
| chr2:97195389
|
T | G | 1 | a0048c0030t0002g0003 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2551+472T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195389 | ||||||
| chr2:97195603
|
A | C | 49 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(46): Show | 49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.2551+686A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195603 | ||||||
| chr2:97195712
|
T | A | 1 | a0003c0003t0001g0181 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2551+795T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195712 | ||||||
| chr2:97195777
|
T | G | 2 | a0021c0021t0002g0012a0021c0021t0002g0013 | 2 | HG02809.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2552-816T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195777 | ||||||
| chr2:97195808
|
T | A | 1 | a0004c0005t0004g0033 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2552-785T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195808 | ||||||
| chr2:97195870
|
A | G | 5 | a0013c0013t0003g0186a0013c0013t0003g0187a0013c0013t0003g0188others(2): Show | 5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.2552-723A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195870 | ||||||
| chr2:97195899
|
C | T | 147 | a0001c0001t0001g0095a0001c0001t0002g0020a0001c0001t0002g0021others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.2552-694C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195899 | ||||||
| chr2:97195935
|
C | T | 21 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(18): Show | 21 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.2552-658C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97195935 | ||||||
| chr2:97196193
|
G | T | 4 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.2552-400G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97196193 | ||||||
| chr2:97196241
|
G | T | 2 | a0002c0002t0001g0069a0043c0039t0001g0008 | 2 | HG02055.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2552-352G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97196241 | ||||||
| chr2:97196292
|
A | G | 1 | a0012c0010t0002g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2552-301A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97196292 | ||||||
| chr2:97196323
|
G | GC | 71 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(68): Show | 71 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2552-270_2552-269i others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97196323 | ||||||
| chr2:97196375
|
G | A | 1 | a0010c0059t0001g0090 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2552-218G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97196375 | ||||||
| chr2:97196481
|
G | A | 1 | a0003c0003t0001g0181 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.2552-112G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97196481 | ||||||
| chr2:97196523
|
T | A | 140 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(137): Show | 140 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.2552-70T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 40/75 | chr2 | 97196523 | ||||||
| chr2:97196659
|
G | A | 55 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(52): Show | 55 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.2580+38G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 41/75 | chr2 | 97196659 | ||||||
| chr2:97196677
|
A | T | 8 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(5): Show | 8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2581-39A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 41/75 | chr2 | 97196677 | ||||||
| chr2:97196900
|
G | T | 9 | a0002c0002t0001g0060a0002c0002t0001g0061a0002c0002t0001g0062others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.2653+112G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97196900 | ||||||
| chr2:97196919
|
C | T | 55 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(52): Show | 55 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.2653+131C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97196919 | ||||||
| chr2:97196990
|
A | C | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2653+202A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97196990 | ||||||
| chr2:97196994
|
T | G | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2653+206T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97196994 | ||||||
| chr2:97197133
|
C | T | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2653+345C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197133 | ||||||
| chr2:97197134
|
C | G | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.2653+346C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197134 | ||||||
| chr2:97197179
|
C | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.2653+391C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197179 | ||||||
| chr2:97197189
|
C | A | 2 | a0005c0004t0002g0129a0005c0004t0002g0130 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2653+401C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197189 | ||||||
| chr2:97197191
|
G | C | 49 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(46): Show | 49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.2653+403G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197191 | ||||||
| chr2:97197200
|
C | G | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2653+412C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197200 | ||||||
| chr2:97197283
|
G | A | 1 | a0016c0023t0001g0091 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2653+495G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197283 | ||||||
| chr2:97197501
|
A | G | 1 | a0004c0005t0004g0037 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2653+713A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197501 | ||||||
| chr2:97197588
|
G | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0105 | 2 | HG00609.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.2653+800G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197588 | ||||||
| chr2:97197751
|
C | A | 1 | a0005c0004t0005g0203 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2654-712C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197751 | ||||||
| chr2:97197788
|
G | T | 71 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(68): Show | 71 | HG00099.hp2 HG00558.hp1 HG00597.hp2 others(68): Show |
intron_variant | MODIFIER | c.2654-675G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197788 | ||||||
| chr2:97197794
|
A | G | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.2654-669A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197794 | ||||||
| chr2:97197881
|
C | A | 1 | a0020c0022t0002g0015 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2654-582C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97197881 | ||||||
| chr2:97198123
|
A | C | 2 | a0003c0003t0001g0172a0006c0034t0001g0173 | 2 | HG02109.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2654-340A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97198123 | ||||||
| chr2:97198142
|
T | G | 1 | a0018c0018t0002g0044 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2654-321T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97198142 | ||||||
| chr2:97198285
|
T | C | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2654-178T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97198285 | ||||||
| chr2:97198331
|
A | T | 1 | a0002c0002t0002g0209 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2654-132A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97198331 | ||||||
| chr2:97198332
|
C | A | 1 | a0002c0002t0002g0209 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2654-131C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 42/75 | chr2 | 97198332 | ||||||
| chr2:97198536
|
C | T | 6 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2682+45C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 43/75 | chr2 | 97198536 | ||||||
| chr2:97198551
|
T | C | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.2683-35T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 43/75 | chr2 | 97198551 | ||||||
| chr2:97198578
|
C | G | 1 | a0047c0033t0002g0025 | 1 | HG03486.hp1 | splice_region_variant&intron_variant | LOW | c.2683-8C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 43/75 | chr2 | 97198578 | ||||||
| chr2:97198839
|
G | A | 1 | a0047c0033t0002g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2755+181G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97198839 | ||||||
| chr2:97198916
|
C | T | 57 | a0001c0001t0002g0022a0003c0003t0001g0133a0003c0003t0001g0135others(54): Show | 57 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.2755+258C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97198916 | ||||||
| chr2:97198926
|
C | T | 2 | a0002c0002t0001g0069a0043c0039t0001g0008 | 2 | HG02055.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2755+268C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97198926 | ||||||
| chr2:97199063
|
A | G | 1 | a0010c0059t0001g0090 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2755+405A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199063 | ||||||
| chr2:97199112
|
T | C | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.2755+454T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199112 | ||||||
| chr2:97199192
|
C | T | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.2755+534C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199192 | ||||||
| chr2:97199235
|
A | C | 3 | a0005c0004t0002g0002a0048c0030t0002g0003a0050c0061t0001g0010 | 3 | HG00609.hp1 HG02040.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.2755+577A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199235 | ||||||
| chr2:97199304
|
C | A | 17 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(14): Show | 17 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.2755+646C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199304 | ||||||
| chr2:97199307
|
A | T | 15 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(12): Show | 15 | HG00423.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2755+649A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199307 | ||||||
| chr2:97199323
|
G | T | 1 | a0016c0023t0001g0093 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2755+665G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199323 | ||||||
| chr2:97199324
|
G | T | 1 | a0016c0023t0001g0093 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2755+666G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199324 | ||||||
| chr2:97199329
|
C | A | 1 | a0016c0023t0001g0093 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2755+671C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199329 | ||||||
| chr2:97199398
|
T | A | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022 | 3 | HG01891.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.2755+740T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199398 | ||||||
| chr2:97199404
|
G | A | 1 | a0047c0033t0002g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2755+746G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199404 | ||||||
| chr2:97199420
|
G | C | 12 | a0004c0005t0004g0016a0004c0005t0004g0032a0004c0005t0004g0033others(9): Show | 12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.2755+762G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199420 | ||||||
| chr2:97199466
|
G | A | 1 | a0047c0033t0002g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2755+808G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199466 | ||||||
| chr2:97199719
|
C | G | 6 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2756-615C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199719 | ||||||
| chr2:97199788
|
G | A | 1 | a0047c0033t0002g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2756-546G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199788 | ||||||
| chr2:97199825
|
G | C | 1 | a0041c0045t0001g0110 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2756-509G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199825 | ||||||
| chr2:97199887
|
G | T | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2756-447G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199887 | ||||||
| chr2:97199963
|
G | T | 5 | a0013c0013t0003g0186a0013c0013t0003g0187a0013c0013t0003g0188others(2): Show | 5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.2756-371G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97199963 | ||||||
| chr2:97200092
|
A | G | 48 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(45): Show | 48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2756-242A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97200092 | ||||||
| chr2:97200277
|
A | G | 1 | a0005c0004t0002g0130 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2756-57A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 44/75 | chr2 | 97200277 | ||||||
| chr2:97200584
|
C | T | 2 | a0012c0010t0002g0026a0012c0010t0002g0028 | 2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2857+59C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97200584 | ||||||
| chr2:97200633
|
A | G | 17 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(14): Show | 17 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.2857+108A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97200633 | ||||||
| chr2:97200699
|
C | A | 1 | a0043c0039t0001g0008 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2857+174C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97200699 | ||||||
| chr2:97200705
|
T | C | 12 | a0004c0005t0004g0016a0004c0005t0004g0032a0004c0005t0004g0033others(9): Show | 12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.2857+180T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97200705 | ||||||
| chr2:97200717
|
C | T | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2857+192C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97200717 | ||||||
| chr2:97200946
|
C | A | 8 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(5): Show | 8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2857+421C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97200946 | ||||||
| chr2:97200997
|
G | T | 7 | a0007c0007t0001g0137a0007c0007t0001g0138a0007c0007t0001g0139others(4): Show | 7 | HG00099.hp2 HG01099.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.2857+472G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97200997 | ||||||
| chr2:97201031
|
T | G | 9 | a0001c0001t0001g0114a0009c0009t0002g0174a0009c0009t0002g0175others(6): Show | 9 | HG01261.hp1 HG01358.hp2 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.2857+506T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201031 | ||||||
| chr2:97201125
|
T | C | 1 | a0004c0005t0004g0037 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.2857+600T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201125 | ||||||
| chr2:97201167
|
A | G | 1 | a0033c0035t0001g0136 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2857+642A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201167 | ||||||
| chr2:97201191
|
A | G | 17 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(14): Show | 17 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.2857+666A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201191 | ||||||
| chr2:97201192
|
C | T | 75 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(72): Show | 75 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.2857+667C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201192 | ||||||
| chr2:97201343
|
T | A | 1 | a0047c0033t0002g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2857+818T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201343 | ||||||
| chr2:97201447
|
A | T | 1 | a0012c0010t0002g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2858-755A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201447 | ||||||
| chr2:97201685
|
G | A | 7 | a0005c0004t0005g0199a0005c0004t0005g0200a0005c0004t0005g0201others(4): Show | 7 | HG00642.hp2 HG02630.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.2858-517G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201685 | ||||||
| chr2:97201697
|
G | T | 1 | a0043c0039t0001g0008 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2858-505G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201697 | ||||||
| chr2:97201733
|
A | G | 2 | a0007c0007t0001g0138a0047c0033t0002g0025 | 2 | HG01515.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2858-469A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201733 | ||||||
| chr2:97201751
|
C | T | 3 | a0010c0012t0001g0075a0010c0012t0001g0103a0026c0058t0001g0074 | 3 | HG01106.hp1 HG02602.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.2858-451C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201751 | ||||||
| chr2:97201765
|
A | G | 1 | a0047c0033t0002g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2858-437A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201765 | ||||||
| chr2:97201829
|
A | G | 2 | a0013c0013t0003g0188a0013c0013t0003g0189 | 2 | HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2858-373A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201829 | ||||||
| chr2:97201889
|
A | C | 10 | a0002c0002t0001g0060a0002c0002t0001g0061a0002c0002t0001g0062others(7): Show | 10 | HG01106.hp2 HG02109.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2858-313A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97201889 | ||||||
| chr2:97202053
|
C | T | 5 | a0013c0013t0003g0186a0013c0013t0003g0187a0013c0013t0003g0188others(2): Show | 5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.2858-149C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97202053 | ||||||
| chr2:97202093
|
T | C | 1 | a0009c0009t0002g0176 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2858-109T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97202093 | ||||||
| chr2:97202118
|
A | C | 1 | a0005c0004t0002g0129 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2858-84A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97202118 | ||||||
| chr2:97202133
|
G | C | 75 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(72): Show | 75 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.2858-69G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 46/75 | chr2 | 97202133 | ||||||
| chr2:97202237
|
A | G | 1 | a0003c0003t0001g0149 | 1 | HG03688.hp1 | splice_region_variant&intron_variant | LOW | c.2886+7A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 47/75 | chr2 | 97202237 | ||||||
| chr2:97202425
|
C | G | 1 | a0037c0040t0002g0211 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2959+32C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97202425 | ||||||
| chr2:97202433
|
G | A | 1 | a0008c0006t0003g0208 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2959+40G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97202433 | ||||||
| chr2:97202476
|
C | T | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2959+83C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97202476 | ||||||
| chr2:97202503
|
A | G | 6 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2959+110A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97202503 | ||||||
| chr2:97202576
|
T | C | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.2959+183T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97202576 | ||||||
| chr2:97202774
|
C | G | 8 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0002g0050others(5): Show | 8 | HG01106.hp1 HG02055.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2959+381C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97202774 | ||||||
| chr2:97202946
|
G | C | 1 | a0003c0003t0001g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2959+553G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97202946 | ||||||
| chr2:97203006
|
C | G | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.2959+613C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203006 | ||||||
| chr2:97203100
|
T | G | 2 | a0006c0008t0009g0146a0047c0033t0002g0025 | 2 | HG02300.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2959+707T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203100 | ||||||
| chr2:97203165
|
C | A | 1 | a0012c0010t0002g0026 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2959+772C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203165 | ||||||
| chr2:97203168
|
A | T | 3 | a0003c0003t0001g0163a0003c0003t0001g0172a0006c0034t0001g0173 | 3 | HG02109.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2959+775A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203168 | ||||||
| chr2:97203189
|
T | C | 48 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(45): Show | 48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.2959+796T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203189 | ||||||
| chr2:97203319
|
C | T | 72 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(69): Show | 72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.2960-749C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203319 | ||||||
| chr2:97203416
|
C | G | 2 | a0001c0001t0002g0050a0001c0046t0002g0051 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2960-652C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203416 | ||||||
| chr2:97203445
|
C | A | 1 | a0010c0012t0001g0075 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2960-623C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203445 | ||||||
| chr2:97203468
|
C | G | 1 | a0005c0004t0002g0130 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2960-600C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203468 | ||||||
| chr2:97203489
|
G | T | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.2960-579G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203489 | ||||||
| chr2:97203682
|
T | G | 1 | a0038c0042t0001g0094 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2960-386T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203682 | ||||||
| chr2:97203692
|
T | C | 9 | a0001c0046t0002g0051a0002c0002t0001g0052a0002c0002t0001g0053others(6): Show | 9 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.2960-376T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203692 | ||||||
| chr2:97203740
|
G | C | 1 | a0001c0046t0002g0051 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2960-328G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203740 | ||||||
| chr2:97203742
|
C | G | 1 | a0001c0046t0002g0051 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2960-326C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203742 | ||||||
| chr2:97203742
|
C | T | 1 | a0012c0010t0002g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2960-326C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203742 | ||||||
| chr2:97203743
|
G | A | 1 | a0001c0001t0002g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2960-325G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203743 | ||||||
| chr2:97203802
|
A | G | 147 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.2960-266A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203802 | ||||||
| chr2:97203871
|
A | T | 2 | a0005c0004t0002g0129a0005c0004t0002g0130 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.2960-197A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203871 | ||||||
| chr2:97203930
|
C | G | 1 | a0022c0020t0001g0098 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2960-138C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 48/75 | chr2 | 97203930 | ||||||
| chr2:97204117
|
A | G | 2 | a0008c0006t0003g0190a0008c0006t0003g0191 | 2 | NA18965.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.2988+21A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 49/75 | chr2 | 97204117 | ||||||
| chr2:97204141
|
C | A | 1 | a0001c0001t0001g0073 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2988+45C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 49/75 | chr2 | 97204141 | ||||||
| chr2:97204153
|
C | CT | 13 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(10): Show | 13 | HG00423.hp1 HG02572.hp1 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.2989-35dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 49/75 | INFO_REALIGN_3_PRIME | chr2 | 97204153 | |||||
| chr2:97204185
|
A | G | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | splice_region_variant&intron_variant | LOW | c.2989-6A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 49/75 | chr2 | 97204185 | ||||||
| chr2:97204303
|
A | T | 1 | a0029c0055t0002g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3061+40A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204303 | ||||||
| chr2:97204314
|
G | A | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.3061+51G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204314 | ||||||
| chr2:97204335
|
A | T | 47 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(44): Show | 47 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.3061+72A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204335 | ||||||
| chr2:97204344
|
C | T | 1 | a0003c0003t0001g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3061+81C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204344 | ||||||
| chr2:97204444
|
A | G | 1 | a0014c0014t0001g0155 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.3061+181A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204444 | ||||||
| chr2:97204492
|
T | G | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.3061+229T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204492 | ||||||
| chr2:97204495
|
A | G | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.3061+232A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204495 | ||||||
| chr2:97204497
|
A | G | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.3061+234A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204497 | ||||||
| chr2:97204510
|
A | G | 72 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(69): Show | 72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.3061+247A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204510 | ||||||
| chr2:97204517
|
G | A | 2 | a0001c0001t0002g0050a0001c0046t0002g0051 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3061+254G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204517 | ||||||
| chr2:97204568
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3061+305G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204568 | ||||||
| chr2:97204576
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3061+313G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204576 | ||||||
| chr2:97204579
|
G | A | 1 | a0001c0001t0002g0022 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3061+316G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204579 | ||||||
| chr2:97204580
|
A | G | 73 | a0001c0001t0002g0022a0003c0003t0001g0133a0003c0003t0001g0135others(70): Show | 73 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.3061+317A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204580 | ||||||
| chr2:97204602
|
A | T | 72 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(69): Show | 72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.3061+339A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204602 | ||||||
| chr2:97204656
|
C | G | 3 | a0018c0018t0002g0043a0018c0018t0002g0044a0018c0018t0002g0048 | 3 | NA18951.hp1 NA18961.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.3061+393C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204656 | ||||||
| chr2:97204675
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3061+412C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204675 | ||||||
| chr2:97204890
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0125 | 2 | HG03654.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.3061+627G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204890 | ||||||
| chr2:97204898
|
A | G | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3061+635A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204898 | ||||||
| chr2:97204948
|
C | T | 1 | a0004c0005t0004g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3061+685C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97204948 | ||||||
| chr2:97205076
|
T | C | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3061+813T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97205076 | ||||||
| chr2:97205109
|
T | C | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3062-831T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97205109 | ||||||
| chr2:97205224
|
G | A | 48 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(45): Show | 48 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.3062-716G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97205224 | ||||||
| chr2:97205304
|
G | A | 21 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(18): Show | 21 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.3062-636G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97205304 | ||||||
| chr2:97205577
|
G | A | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.3062-363G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97205577 | ||||||
| chr2:97205614
|
T | A | 1 | a0001c0001t0001g0019 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3062-326T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97205614 | ||||||
| chr2:97205705
|
G | A | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.3062-235G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97205705 | ||||||
| chr2:97205889
|
A | G | 27 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(24): Show | 27 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.3062-51A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 50/75 | chr2 | 97205889 | ||||||
| chr2:97205998
|
G | A | 1 | a0001c0001t0002g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3090+30G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 51/75 | chr2 | 97205998 | ||||||
| chr2:97206169
|
G | A | 11 | a0004c0005t0004g0016a0004c0005t0004g0032a0004c0005t0004g0033others(8): Show | 11 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.3163+34G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97206169 | ||||||
| chr2:97206182
|
A | G | 1 | a0005c0004t0002g0002 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3163+47A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97206182 | ||||||
| chr2:97206209
|
C | T | 1 | a0043c0039t0001g0008 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3163+74C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97206209 | ||||||
| chr2:97206271
|
C | A | 13 | a0002c0002t0001g0017a0002c0002t0001g0068a0005c0004t0002g0002others(10): Show | 13 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.3163+136C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97206271 | ||||||
| chr2:97206341
|
G | A | 1 | a0003c0003t0001g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3163+206G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97206341 | ||||||
| chr2:97206359
|
A | G | 1 | a0008c0006t0003g0196 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.3163+224A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97206359 | ||||||
| chr2:97206411
|
T | G | 56 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(53): Show | 56 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.3163+276T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97206411 | ||||||
| chr2:97206708
|
C | G | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3163+573C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97206708 | ||||||
| chr2:97207009
|
C | G | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3164-802C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207009 | ||||||
| chr2:97207070
|
G | A | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3164-741G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207070 | ||||||
| chr2:97207086
|
G | T | 1 | a0002c0002t0001g0066 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3164-725G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207086 | ||||||
| chr2:97207305
|
A | T | 11 | a0005c0004t0002g0002a0005c0004t0002g0129a0005c0004t0002g0130others(8): Show | 11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.3164-506A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207305 | ||||||
| chr2:97207324
|
T | A | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3164-487T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207324 | ||||||
| chr2:97207422
|
T | C | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3164-389T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207422 | ||||||
| chr2:97207425
|
T | A | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3164-386T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207425 | ||||||
| chr2:97207425
|
T | G | 1 | a0002c0002t0001g0069 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3164-386T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207425 | ||||||
| chr2:97207430
|
C | G | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3164-381C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207430 | ||||||
| chr2:97207431
|
C | T | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3164-380C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207431 | ||||||
| chr2:97207454
|
A | C | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3164-357A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207454 | ||||||
| chr2:97207482
|
C | G | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3164-329C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207482 | ||||||
| chr2:97207484
|
G | C | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3164-327G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207484 | ||||||
| chr2:97207584
|
A | G | 11 | a0005c0004t0002g0002a0005c0004t0002g0129a0005c0004t0002g0130others(8): Show | 11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.3164-227A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207584 | ||||||
| chr2:97207650
|
G | A | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.3164-161G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207650 | ||||||
| chr2:97207656
|
C | T | 48 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(45): Show | 48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.3164-155C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207656 | ||||||
| chr2:97207705
|
G | A | 1 | a0001c0001t0007g0100 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.3164-106G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207705 | ||||||
| chr2:97207752
|
G | A | 7 | a0003c0003t0001g0151a0003c0003t0001g0152a0003c0003t0001g0153others(4): Show | 7 | HG00558.hp1 NA18946.hp1 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.3164-59G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207752 | ||||||
| chr2:97207778
|
C | T | 72 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(69): Show | 72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.3164-33C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 52/75 | chr2 | 97207778 | ||||||
| chr2:97207893
|
A | T | 48 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(45): Show | 48 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.3193-41A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 53/75 | chr2 | 97207893 | ||||||
| chr2:97208087
|
C | A | 3 | a0013c0013t0003g0187a0013c0013t0003g0188a0013c0013t0003g0189 | 3 | HG03834.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.3265+81C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208087 | ||||||
| chr2:97208172
|
T | C | 1 | a0007c0007t0001g0180 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.3265+166T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208172 | ||||||
| chr2:97208187
|
G | A | 1 | a0005c0004t0002g0002 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3265+181G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208187 | ||||||
| chr2:97208262
|
T | C | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3265+256T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208262 | ||||||
| chr2:97208316
|
G | A | 2 | a0005c0004t0002g0002a0048c0030t0002g0003 | 2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.3265+310G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208316 | ||||||
| chr2:97208357
|
C | A | 8 | a0015c0015t0001g0088a0015c0015t0001g0089a0015c0015t0001g0109others(5): Show | 8 | HG00558.hp2 NA18952.hp1 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.3265+351C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208357 | ||||||
| chr2:97208359
|
C | T | 8 | a0015c0015t0001g0088a0015c0015t0001g0089a0015c0015t0001g0109others(5): Show | 8 | HG00558.hp2 NA18952.hp1 NA18961.hp2 others(5): Show |
intron_variant | MODIFIER | c.3265+353C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208359 | ||||||
| chr2:97208361
|
T | C | 1 | a0001c0001t0002g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3265+355T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208361 | ||||||
| chr2:97208471
|
G | A | 2 | a0005c0004t0005g0204a0005c0004t0005g0205 | 2 | HG00642.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.3265+465G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208471 | ||||||
| chr2:97208520
|
G | T | 3 | a0001c0001t0001g0073a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG00609.hp2 NA18941.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.3265+514G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208520 | ||||||
| chr2:97208588
|
A | G | 72 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(69): Show | 72 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.3265+582A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208588 | ||||||
| chr2:97208613
|
A | C | 1 | a0033c0035t0001g0136 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3265+607A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208613 | ||||||
| chr2:97208621
|
G | A | 1 | a0033c0035t0001g0136 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.3265+615G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208621 | ||||||
| chr2:97208952
|
C | G | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022 | 3 | HG01891.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3266-729C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97208952 | ||||||
| chr2:97209139
|
A | T | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3266-542A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97209139 | ||||||
| chr2:97209161
|
T | C | 1 | a0006c0008t0001g0004 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3266-520T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97209161 | ||||||
| chr2:97209182
|
A | G | 1 | a0047c0033t0002g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3266-499A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97209182 | ||||||
| chr2:97209207
|
A | T | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.3266-474A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97209207 | ||||||
| chr2:97209249
|
T | G | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.3266-432T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97209249 | ||||||
| chr2:97209290
|
C | G | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3266-391C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97209290 | ||||||
| chr2:97209452
|
G | A | 2 | a0005c0004t0002g0129a0005c0004t0002g0130 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3266-229G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97209452 | ||||||
| chr2:97209472
|
T | A | 1 | a0024c0060t0002g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3266-209T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97209472 | ||||||
| chr2:97209550
|
C | CA | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3266-128dupA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | INFO_REALIGN_3_PRIME | chr2 | 97209550 | |||||
| chr2:97209586
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.3266-95C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 54/75 | chr2 | 97209586 | ||||||
| chr2:97210159
|
T | C | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3367+287T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97210159 | ||||||
| chr2:97210160
|
A | C | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3367+288A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97210160 | ||||||
| chr2:97210273
|
G | C | 147 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.3367+401G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97210273 | ||||||
| chr2:97210359
|
A | T | 1 | a0003c0003t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3367+487A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97210359 | ||||||
| chr2:97210509
|
A | T | 1 | a0043c0039t0001g0008 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3367+637A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97210509 | ||||||
| chr2:97210543
|
G | C | 1 | a0001c0001t0001g0121 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3367+671G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97210543 | ||||||
| chr2:97210757
|
A | G | 7 | a0007c0007t0001g0137a0007c0007t0001g0138a0007c0007t0001g0139others(4): Show | 7 | HG00099.hp2 HG01099.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.3368-789A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97210757 | ||||||
| chr2:97210887
|
C | A | 1 | a0047c0033t0002g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3368-659C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97210887 | ||||||
| chr2:97211062
|
G | A | 61 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(58): Show | 61 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.3368-484G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97211062 | ||||||
| chr2:97211143
|
A | G | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3368-403A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97211143 | ||||||
| chr2:97211266
|
C | T | 68 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(65): Show | 68 | HG00099.hp2 HG00597.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.3368-280C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97211266 | ||||||
| chr2:97211311
|
G | C | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3368-235G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97211311 | ||||||
| chr2:97211403
|
G | A | 1 | a0028c0056t0001g0171 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3368-143G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 56/75 | chr2 | 97211403 | ||||||
| chr2:97211613
|
T | C | 2 | a0005c0004t0002g0129a0005c0004t0002g0130 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3396+39T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 57/75 | chr2 | 97211613 | ||||||
| chr2:97211662
|
T | C | 130 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(127): Show | 130 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(127): Show |
splice_region_variant&intron_variant | LOW | c.3397-7T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 57/75 | chr2 | 97211662 | ||||||
| chr2:97211765
|
A | G | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3469+24A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/75 | chr2 | 97211765 | ||||||
| chr2:97211942
|
T | C | 1 | a0047c0033t0002g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3469+201T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/75 | chr2 | 97211942 | ||||||
| chr2:97212200
|
G | A | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3469+459G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/75 | chr2 | 97212200 | ||||||
| chr2:97212228
|
G | A | 1 | a0024c0060t0002g0024 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3469+487G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/75 | chr2 | 97212228 | ||||||
| chr2:97212296
|
A | T | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3469+555A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/75 | chr2 | 97212296 | ||||||
| chr2:97212341
|
C | A | 1 | a0003c0003t0001g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3469+600C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/75 | chr2 | 97212341 | ||||||
| chr2:97212458
|
A | T | 73 | a0003c0003t0001g0133a0003c0003t0001g0135a0003c0003t0001g0142others(70): Show | 73 | HG00099.hp2 HG00558.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.3469+717A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/75 | chr2 | 97212458 | ||||||
| chr2:97213032
|
C | G | 1 | a0013c0025t0003g0185 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3470-387C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 58/75 | chr2 | 97213032 | ||||||
| chr2:97213960
|
C | T | 2 | a0002c0002t0001g0017a0002c0002t0001g0068 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3571+346C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97213960 | ||||||
| chr2:97214015
|
C | T | 17 | a0005c0004t0005g0200a0008c0006t0003g0184a0008c0006t0003g0190others(14): Show | 17 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.3571+401C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97214015 | ||||||
| chr2:97214290
|
A | G | 147 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.3571+676A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97214290 | ||||||
| chr2:97214300
|
TAA | T | 203 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.3571+688_3571+689d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | INFO_REALIGN_3_PRIME | chr2 | 97214300 | |||||
| chr2:97214307
|
G | A | 1 | a0037c0040t0002g0211 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3571+693G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97214307 | ||||||
| chr2:97214322
|
GTTTT | G | 147 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(144): Show | 147 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.3571+711_3571+714d others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | INFO_REALIGN_3_PRIME | chr2 | 97214322 | |||||
| chr2:97214815
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3572-486C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97214815 | ||||||
| chr2:97214848
|
C | T | 1 | a0020c0022t0002g0030 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3572-453C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97214848 | ||||||
| chr2:97214849
|
CT | C | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3572-450delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | INFO_REALIGN_3_PRIME | chr2 | 97214849 | |||||
| chr2:97215094
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3572-207T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97215094 | ||||||
| chr2:97215101
|
T | C | 11 | a0005c0004t0002g0002a0005c0004t0002g0129a0005c0004t0002g0130others(8): Show | 11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.3572-200T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97215101 | ||||||
| chr2:97215137
|
A | T | 1 | a0001c0001t0001g0121 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3572-164A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97215137 | ||||||
| chr2:97215156
|
C | G | 1 | a0003c0003t0001g0151 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.3572-145C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 60/75 | chr2 | 97215156 | ||||||
| chr2:97215341
|
C | G | 1 | a0010c0012t0001g0092 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3600+12C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 61/75 | chr2 | 97215341 | ||||||
| chr2:97215530
|
G | A | 68 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(65): Show | 68 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.3673+33G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97215530 | ||||||
| chr2:97215558
|
T | G | 1 | a0020c0022t0002g0030 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.3673+61T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97215558 | ||||||
| chr2:97215806
|
G | A | 1 | a0008c0006t0003g0191 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.3673+309G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97215806 | ||||||
| chr2:97215807
|
G | T | 1 | a0001c0046t0002g0051 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3673+310G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97215807 | ||||||
| chr2:97215817
|
A | C | 1 | a0002c0002t0001g0066 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3673+320A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97215817 | ||||||
| chr2:97215875
|
A | C | 12 | a0004c0005t0004g0016a0004c0005t0004g0032a0004c0005t0004g0033others(9): Show | 12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.3673+378A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97215875 | ||||||
| chr2:97216210
|
A | T | 1 | a0030c0052t0002g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3673+713A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97216210 | ||||||
| chr2:97216678
|
A | G | 1 | a0016c0023t0001g0091 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3674-499A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97216678 | ||||||
| chr2:97216887
|
G | A | 1 | a0001c0001t0001g0070 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.3674-290G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97216887 | ||||||
| chr2:97216911
|
G | A | 147 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.3674-266G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97216911 | ||||||
| chr2:97216924
|
C | T | 2 | a0003c0003t0001g0160a0003c0003t0001g0181 | 2 | NA18952.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.3674-253C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97216924 | ||||||
| chr2:97217137
|
A | G | 1 | a0006c0008t0001g0004 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3674-40A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 62/75 | chr2 | 97217137 | ||||||
| chr2:97217234
|
T | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3702+29T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 63/75 | chr2 | 97217234 | ||||||
| chr2:97217833
|
C | T | 1 | a0002c0002t0001g0056 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3775+461C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97217833 | ||||||
| chr2:97217837
|
A | G | 12 | a0006c0008t0001g0004a0006c0008t0001g0005a0006c0008t0001g0006others(9): Show | 12 | HG00558.hp1 HG00642.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.3775+465A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97217837 | ||||||
| chr2:97217863
|
G | C | 1 | a0001c0001t0001g0101 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.3775+491G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97217863 | ||||||
| chr2:97217868
|
A | G | 12 | a0006c0008t0001g0004a0006c0008t0001g0005a0006c0008t0001g0006others(9): Show | 12 | HG00558.hp1 HG00642.hp1 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.3775+496A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97217868 | ||||||
| chr2:97218090
|
C | G | 1 | a0002c0002t0001g0069 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3775+718C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97218090 | ||||||
| chr2:97218168
|
A | G | 1 | a0002c0002t0001g0065 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3775+796A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97218168 | ||||||
| chr2:97218322
|
T | C | 168 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(165): Show | 168 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.3776-728T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97218322 | ||||||
| chr2:97218516
|
T | C | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3776-534T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97218516 | ||||||
| chr2:97218855
|
G | GT | 154 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(151): Show | 154 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.3776-191dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | INFO_REALIGN_3_PRIME | chr2 | 97218855 | |||||
| chr2:97218855
|
G | GTTTTTGA others(53002): Show |
1 | a0001c0001t0001g0095 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.3776-191_3776-190i others(53011): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | INFO_REALIGN_3_PRIME | chr2 | 97218855 | |||||
| chr2:97218880
|
C | G | 16 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(13): Show | 16 | HG00423.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.3776-170C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97218880 | ||||||
| chr2:97219026
|
T | C | 131 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(128): Show | 131 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.3776-24T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 64/75 | chr2 | 97219026 | ||||||
| chr2:97219451
|
T | TTTTTTTG others(10): Show |
2 | a0002c0002t0001g0017a0002c0002t0001g0068 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3877+234_3877+250d others(19): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97219451 | |||||
| chr2:97219596
|
C | G | 19 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(16): Show | 19 | HG02109.hp2 HG02145.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.3877+350C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97219596 | ||||||
| chr2:97219742
|
A | G | 9 | a0002c0002t0001g0060a0002c0002t0001g0061a0002c0002t0001g0062others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3877+496A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97219742 | ||||||
| chr2:97219834
|
A | G | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3877+588A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97219834 | ||||||
| chr2:97219851
|
T | A | 8 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(5): Show | 8 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.3877+605T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97219851 | ||||||
| chr2:97219867
|
C | T | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3877+621C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97219867 | ||||||
| chr2:97219880
|
T | G | 3 | a0003c0003t0001g0163a0003c0003t0001g0172a0006c0034t0001g0173 | 3 | HG02109.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3877+634T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97219880 | ||||||
| chr2:97219962
|
T | G | 1 | a0030c0052t0002g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3877+716T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97219962 | ||||||
| chr2:97220051
|
C | CTG | 3 | a0003c0003t0001g0151a0003c0003t0001g0152a0003c0003t0001g0157 | 3 | HG01496.hp1 NA18947.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.3877+839_3877+840d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220051 | |||||
| chr2:97220051
|
CTG | C | 2 | a0006c0008t0001g0005a0007c0007t0001g0207 | 2 | HG01934.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.3877+839_3877+840d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220051 | |||||
| chr2:97220051
|
CTGTG | C | 4 | a0003c0003t0001g0181a0006c0008t0001g0004a0006c0008t0001g0006others(1): Show | 4 | HG00642.hp1 HG01975.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.3877+837_3877+840d others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220051 | |||||
| chr2:97220051
|
CTGTGTG | C | 8 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(5): Show | 8 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.3877+835_3877+840d others(8): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220051 | |||||
| chr2:97220051
|
CTGTGTGT others(1): Show |
C | 5 | a0001c0046t0002g0051a0003c0003t0001g0135a0013c0025t0003g0185others(2): Show | 5 | HG02071.hp1 HG03225.hp1 NA19074.hp1 others(2): Show |
intron_variant | MODIFIER | c.3877+833_3877+840d others(10): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220051 | |||||
| chr2:97220051
|
CTGTGTGT others(3): Show |
C | 143 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(140): Show | 143 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.3877+831_3877+840d others(12): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220051 | |||||
| chr2:97220051
|
CTGTGTGT others(5): Show |
C | 8 | a0008c0006t0003g0184a0009c0009t0002g0174a0009c0009t0002g0175others(5): Show | 8 | HG00597.hp2 HG01261.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.3877+829_3877+840d others(14): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220051 | |||||
| chr2:97220085
|
G | T | 2 | a0014c0014t0001g0155a0032c0054t0001g0165 | 2 | HG02738.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.3877+839G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220085 | ||||||
| chr2:97220086
|
T | C | 1 | a0032c0054t0001g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3877+840T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220086 | ||||||
| chr2:97220106
|
T | C | 1 | a0022c0020t0001g0098 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3877+860T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220106 | ||||||
| chr2:97220189
|
T | C | 1 | a0032c0054t0001g0165 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3877+943T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220189 | ||||||
| chr2:97220241
|
A | G | 6 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0002g0020others(3): Show | 6 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.3877+995A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220241 | ||||||
| chr2:97220248
|
C | A | 6 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0002g0020others(3): Show | 6 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.3877+1002C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220248 | ||||||
| chr2:97220269
|
G | C | 2 | a0001c0001t0001g0079a0024c0060t0002g0024 | 2 | HG01891.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.3877+1023G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220269 | ||||||
| chr2:97220277
|
G | GTAC | 50 | a0001c0001t0001g0079a0002c0002t0001g0069a0002c0002t0002g0031others(47): Show | 50 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.3877+1031_3877+103 others(7): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220277 | ||||||
| chr2:97220278
|
G | A | 50 | a0001c0001t0001g0079a0002c0002t0001g0069a0002c0002t0002g0031others(47): Show | 50 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.3877+1032G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220278 | ||||||
| chr2:97220289
|
G | T | 20 | a0005c0004t0002g0002a0005c0004t0002g0129a0005c0004t0002g0130others(17): Show | 20 | HG00609.hp1 HG00642.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.3877+1043G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220289 | ||||||
| chr2:97220312
|
G | T | 5 | a0010c0012t0001g0072a0010c0012t0001g0075a0010c0012t0001g0092others(2): Show | 5 | HG01106.hp1 HG02602.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.3877+1066G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220312 | ||||||
| chr2:97220375
|
A | T | 58 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(55): Show | 58 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.3877+1129A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220375 | ||||||
| chr2:97220452
|
T | G | 2 | a0041c0045t0001g0110a0050c0061t0001g0010 | 2 | NA18946.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.3877+1206T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220452 | ||||||
| chr2:97220476
|
T | C | 76 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(73): Show | 76 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.3877+1230T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220476 | ||||||
| chr2:97220490
|
A | G | 1 | a0017c0017t0001g0170 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3877+1244A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220490 | ||||||
| chr2:97220558
|
G | A | 68 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(65): Show | 68 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.3877+1312G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220558 | ||||||
| chr2:97220691
|
T | C | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3877+1445T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220691 | ||||||
| chr2:97220719
|
G | A | 1 | a0003c0003t0001g0152 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.3877+1473G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220719 | ||||||
| chr2:97220729
|
C | CT | 120 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0070others(117): Show | 120 | HG00099.hp1 HG00423.hp1 HG00558.hp1 others(117): Show |
intron_variant | MODIFIER | c.3877+1501dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220729 | |||||
| chr2:97220729
|
CT | C | 10 | a0003c0003t0001g0160a0009c0009t0002g0174a0009c0009t0002g0175others(7): Show | 10 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.3877+1501delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220729 | |||||
| chr2:97220729
|
CTT | C | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3877+1500_3877+150 others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220729 | |||||
| chr2:97220761
|
C | CTT | 63 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(60): Show | 63 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.3877+1526_3877+152 others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220761 | |||||
| chr2:97220761
|
C | CTTT | 63 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(60): Show | 63 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.3877+1525_3877+152 others(7): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97220761 | |||||
| chr2:97220774
|
A | T | 67 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(64): Show | 67 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.3877+1528A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220774 | ||||||
| chr2:97220775
|
A | T | 26 | a0002c0002t0002g0031a0002c0002t0002g0132a0004c0005t0004g0016others(23): Show | 26 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.3877+1529A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220775 | ||||||
| chr2:97220776
|
T | A | 69 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(66): Show | 69 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.3877+1530T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220776 | ||||||
| chr2:97220776
|
T | TA | 15 | a0004c0005t0004g0016a0004c0005t0004g0032a0004c0005t0004g0033others(12): Show | 15 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.3877+1530_3877+153 others(5): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220776 | ||||||
| chr2:97220777
|
T | A | 27 | a0002c0002t0002g0031a0002c0002t0002g0132a0004c0005t0004g0016others(24): Show | 27 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.3877+1531T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220777 | ||||||
| chr2:97220789
|
T | A | 62 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(59): Show | 62 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.3877+1543T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220789 | ||||||
| chr2:97220866
|
C | T | 1 | a0004c0005t0004g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3877+1620C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220866 | ||||||
| chr2:97220934
|
G | C | 62 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(59): Show | 62 | HG00423.hp2 HG00558.hp1 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.3877+1688G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220934 | ||||||
| chr2:97220937
|
C | G | 1 | a0010c0012t0001g0075 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3877+1691C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220937 | ||||||
| chr2:97220942
|
C | A | 1 | a0010c0012t0001g0075 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3877+1696C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220942 | ||||||
| chr2:97220962
|
A | G | 1 | a0001c0001t0001g0019 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3877+1716A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220962 | ||||||
| chr2:97220985
|
A | T | 1 | a0001c0001t0001g0019 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3877+1739A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97220985 | ||||||
| chr2:97221024
|
A | G | 203 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(200): Show | 203 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(200): Show |
intron_variant | MODIFIER | c.3877+1778A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221024 | ||||||
| chr2:97221142
|
A | G | 69 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(66): Show | 69 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.3877+1896A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221142 | ||||||
| chr2:97221170
|
T | G | 8 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(5): Show | 8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.3877+1924T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221170 | ||||||
| chr2:97221259
|
G | T | 1 | a0001c0001t0002g0021 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3877+2013G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221259 | ||||||
| chr2:97221433
|
G | A | 1 | a0003c0003t0001g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3877+2187G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221433 | ||||||
| chr2:97221605
|
A | G | 7 | a0001c0001t0001g0106a0004c0005t0004g0016a0004c0005t0004g0033others(4): Show | 7 | HG00099.hp1 HG01123.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.3877+2359A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221605 | ||||||
| chr2:97221653
|
G | A | 11 | a0005c0004t0002g0002a0005c0004t0002g0129a0005c0004t0002g0130others(8): Show | 11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.3877+2407G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221653 | ||||||
| chr2:97221707
|
A | T | 1 | a0002c0002t0001g0069 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3877+2461A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221707 | ||||||
| chr2:97221740
|
C | T | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3877+2494C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221740 | ||||||
| chr2:97221772
|
CT | C | 9 | a0002c0002t0001g0060a0002c0002t0001g0061a0002c0002t0001g0062others(6): Show | 9 | HG02109.hp2 HG02145.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.3877+2529delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97221772 | |||||
| chr2:97221806
|
G | T | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3877+2560G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221806 | ||||||
| chr2:97221883
|
G | A | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.3877+2637G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221883 | ||||||
| chr2:97221945
|
TG | T | 7 | a0007c0007t0001g0137a0007c0007t0001g0138a0007c0007t0001g0139others(4): Show | 7 | HG00099.hp2 HG01099.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.3877+2700delG | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97221945 | ||||||
| chr2:97222088
|
T | A | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3878-2718T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222088 | ||||||
| chr2:97222159
|
C | A | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3878-2647C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222159 | ||||||
| chr2:97222178
|
G | A | 1 | a0003c0003t0001g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3878-2628G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222178 | ||||||
| chr2:97222250
|
T | G | 70 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(67): Show | 70 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.3878-2556T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222250 | ||||||
| chr2:97222310
|
G | A | 12 | a0004c0005t0004g0016a0004c0005t0004g0032a0004c0005t0004g0033others(9): Show | 12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.3878-2496G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222310 | ||||||
| chr2:97222415
|
G | A | 158 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(155): Show | 158 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.3878-2391G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222415 | ||||||
| chr2:97222499
|
G | C | 69 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(66): Show | 69 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.3878-2307G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222499 | ||||||
| chr2:97222543
|
C | T | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3878-2263C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222543 | ||||||
| chr2:97222591
|
C | G | 11 | a0005c0004t0002g0002a0005c0004t0002g0129a0005c0004t0002g0130others(8): Show | 11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.3878-2215C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222591 | ||||||
| chr2:97222691
|
A | G | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3878-2115A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222691 | ||||||
| chr2:97222872
|
T | A | 2 | a0020c0022t0002g0015a0020c0022t0002g0030 | 2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.3878-1934T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222872 | ||||||
| chr2:97222883
|
C | T | 1 | a0003c0003t0001g0167 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3878-1923C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222883 | ||||||
| chr2:97222913
|
A | G | 2 | a0001c0001t0002g0050a0001c0046t0002g0051 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.3878-1893A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222913 | ||||||
| chr2:97222958
|
A | G | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022 | 3 | HG01891.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.3878-1848A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222958 | ||||||
| chr2:97222997
|
C | T | 2 | a0002c0002t0001g0017a0002c0002t0001g0068 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3878-1809C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97222997 | ||||||
| chr2:97223098
|
C | CT | 93 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(90): Show | 93 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.3878-1688dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97223098 | |||||
| chr2:97223098
|
C | CTT | 22 | a0001c0001t0001g0101a0001c0001t0001g0107a0001c0001t0007g0100others(19): Show | 22 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.3878-1689_3878-168 others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97223098 | |||||
| chr2:97223098
|
CT | C | 10 | a0008c0006t0003g0190a0008c0006t0003g0191a0008c0006t0003g0192others(7): Show | 10 | NA18941.hp2 NA18951.hp2 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.3878-1688delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97223098 | |||||
| chr2:97223098
|
CTT | C | 5 | a0013c0013t0003g0186a0013c0013t0003g0187a0013c0013t0003g0188others(2): Show | 5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.3878-1689_3878-168 others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97223098 | |||||
| chr2:97223123
|
C | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1683C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223123 | ||||||
| chr2:97223124
|
A | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1682A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223124 | ||||||
| chr2:97223131
|
T | C | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1675T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223131 | ||||||
| chr2:97223155
|
T | C | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1651T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223155 | ||||||
| chr2:97223176
|
C | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1630C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223176 | ||||||
| chr2:97223186
|
C | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1620C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223186 | ||||||
| chr2:97223222
|
C | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1584C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223222 | ||||||
| chr2:97223235
|
A | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1571A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223235 | ||||||
| chr2:97223261
|
C | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1545C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223261 | ||||||
| chr2:97223262
|
A | G | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1544A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223262 | ||||||
| chr2:97223320
|
T | C | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1486T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223320 | ||||||
| chr2:97223337
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1469G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223337 | ||||||
| chr2:97223344
|
T | C | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1462T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223344 | ||||||
| chr2:97223345
|
T | C | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1461T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223345 | ||||||
| chr2:97223346
|
G | A | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1460G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223346 | ||||||
| chr2:97223359
|
A | G | 1 | a0006c0034t0001g0173 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3878-1447A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223359 | ||||||
| chr2:97223539
|
T | C | 129 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(126): Show | 129 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.3878-1267T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223539 | ||||||
| chr2:97223637
|
T | C | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1169T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223637 | ||||||
| chr2:97223665
|
C | T | 2 | a0001c0001t0002g0020a0001c0001t0002g0021 | 2 | HG01891.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.3878-1141C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223665 | ||||||
| chr2:97223689
|
A | C | 11 | a0005c0004t0002g0002a0005c0004t0002g0129a0005c0004t0002g0130others(8): Show | 11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.3878-1117A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97223689 | ||||||
| chr2:97224066
|
T | C | 2 | a0003c0003t0001g0168a0032c0054t0001g0165 | 2 | HG02683.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.3878-740T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224066 | ||||||
| chr2:97224179
|
T | G | 131 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(128): Show | 131 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.3878-627T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224179 | ||||||
| chr2:97224263
|
G | T | 1 | a0002c0002t0001g0057 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3878-543G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224263 | ||||||
| chr2:97224431
|
G | A | 62 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(59): Show | 62 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.3878-375G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224431 | ||||||
| chr2:97224436
|
G | GT | 12 | a0004c0005t0004g0016a0004c0005t0004g0032a0004c0005t0004g0033others(9): Show | 12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.3878-363dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97224436 | |||||
| chr2:97224444
|
G | GT | 9 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0192others(6): Show | 9 | HG00597.hp2 HG04115.hp1 NA18941.hp2 others(6): Show |
intron_variant | MODIFIER | c.3878-355dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97224444 | |||||
| chr2:97224444
|
G | T | 12 | a0004c0005t0004g0016a0004c0005t0004g0032a0004c0005t0004g0033others(9): Show | 12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.3878-362G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224444 | ||||||
| chr2:97224452
|
G | GT | 61 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(58): Show | 61 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.3878-341dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97224452 | |||||
| chr2:97224452
|
G | T | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3878-354G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224452 | ||||||
| chr2:97224453
|
T | G | 1 | a0013c0025t0003g0185 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3878-353T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224453 | ||||||
| chr2:97224456
|
T | G | 3 | a0004c0005t0004g0037a0004c0005t0004g0039a0035c0062t0004g0042 | 3 | HG01099.hp2 HG01981.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.3878-350T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224456 | ||||||
| chr2:97224606
|
C | T | 1 | a0001c0046t0002g0051 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3878-200C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224606 | ||||||
| chr2:97224730
|
G | A | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3878-76G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | chr2 | 97224730 | ||||||
| chr2:97224796
|
A | AT | 147 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
splice_acceptor_variant&intron_variant | HIGH | c.3878-3dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 66/75 | INFO_REALIGN_3_PRIME | chr2 | 97224796 | |||||
| chr2:97225227
|
C | T | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.3951+348C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97225227 | ||||||
| chr2:97225266
|
G | C | 21 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(18): Show | 21 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.3951+387G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97225266 | ||||||
| chr2:97225484
|
T | C | 3 | a0018c0018t0002g0043a0018c0018t0002g0044a0018c0018t0002g0048 | 3 | NA18951.hp1 NA18961.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.3951+605T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97225484 | ||||||
| chr2:97225699
|
C | T | 1 | a0003c0003t0001g0149 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3951+820C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97225699 | ||||||
| chr2:97225803
|
G | C | 1 | a0001c0001t0001g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3951+924G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97225803 | ||||||
| chr2:97225990
|
G | T | 1 | a0001c0001t0001g0123 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3951+1111G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97225990 | ||||||
| chr2:97226002
|
T | C | 160 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(157): Show | 160 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.3951+1123T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226002 | ||||||
| chr2:97226066
|
A | C | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3951+1187A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226066 | ||||||
| chr2:97226073
|
C | G | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3951+1194C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226073 | ||||||
| chr2:97226075
|
G | A | 3 | a0001c0001t0001g0070a0019c0032t0007g0127a0026c0058t0001g0074 | 3 | HG03688.hp2 NA19056.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3951+1196G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226075 | ||||||
| chr2:97226086
|
T | C | 144 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(141): Show | 144 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(141): Show |
intron_variant | MODIFIER | c.3951+1207T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226086 | ||||||
| chr2:97226087
|
G | A | 1 | a0035c0062t0004g0042 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.3951+1208G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226087 | ||||||
| chr2:97226157
|
G | A | 2 | a0002c0002t0002g0209a0003c0003t0001g0135 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.3951+1278G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226157 | ||||||
| chr2:97226257
|
C | G | 162 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(159): Show | 162 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.3951+1378C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226257 | ||||||
| chr2:97226442
|
C | G | 156 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(153): Show | 156 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.3951+1563C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226442 | ||||||
| chr2:97226445
|
G | A | 156 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(153): Show | 156 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.3951+1566G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226445 | ||||||
| chr2:97226550
|
G | A | 157 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(154): Show | 157 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.3951+1671G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226550 | ||||||
| chr2:97226561
|
C | T | 94 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(91): Show | 94 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.3951+1682C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226561 | ||||||
| chr2:97226562
|
C | G | 94 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(91): Show | 94 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.3951+1683C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226562 | ||||||
| chr2:97226566
|
G | T | 94 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(91): Show | 94 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.3951+1687G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226566 | ||||||
| chr2:97226635
|
T | C | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3951+1756T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226635 | ||||||
| chr2:97226828
|
G | T | 156 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(153): Show | 156 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.3951+1949G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226828 | ||||||
| chr2:97226839
|
C | T | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3951+1960C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226839 | ||||||
| chr2:97226894
|
G | A | 1 | a0003c0003t0001g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3951+2015G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226894 | ||||||
| chr2:97226923
|
A | C | 5 | a0013c0013t0003g0186a0013c0013t0003g0187a0013c0013t0003g0188others(2): Show | 5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.3951+2044A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226923 | ||||||
| chr2:97226943
|
C | T | 2 | a0003c0003t0001g0159a0003c0003t0001g0160 | 2 | NA18612.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.3951+2064C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226943 | ||||||
| chr2:97226958
|
T | G | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3951+2079T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226958 | ||||||
| chr2:97226979
|
G | A | 1 | a0009c0009t0002g0175 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3951+2100G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97226979 | ||||||
| chr2:97227106
|
C | T | 1 | a0001c0001t0001g0111 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.3951+2227C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97227106 | ||||||
| chr2:97227185
|
T | G | 4 | a0003c0003t0001g0159a0007c0007t0001g0138a0007c0007t0001g0139others(1): Show | 4 | HG01099.hp1 HG01515.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.3951+2306T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97227185 | ||||||
| chr2:97227254
|
A | G | 2 | a0002c0002t0001g0017a0002c0002t0001g0068 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3951+2375A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97227254 | ||||||
| chr2:97227345
|
G | C | 1 | a0019c0031t0007g0126 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3951+2466G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97227345 | ||||||
| chr2:97227379
|
T | C | 1 | a0001c0001t0001g0121 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3951+2500T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97227379 | ||||||
| chr2:97227615
|
A | C | 2 | a0002c0002t0001g0017a0002c0002t0001g0068 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3951+2736A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97227615 | ||||||
| chr2:97227950
|
G | A | 12 | a0004c0005t0004g0016a0004c0005t0004g0032a0004c0005t0004g0033others(9): Show | 12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.3951+3071G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97227950 | ||||||
| chr2:97228023
|
C | T | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3951+3144C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228023 | ||||||
| chr2:97228196
|
G | A | 28 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.3951+3317G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228196 | ||||||
| chr2:97228238
|
A | G | 3 | a0001c0001t0001g0073a0001c0001t0001g0105a0001c0001t0001g0106 | 3 | HG00609.hp2 NA18941.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.3951+3359A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228238 | ||||||
| chr2:97228265
|
C | T | 12 | a0004c0005t0004g0016a0004c0005t0004g0032a0004c0005t0004g0033others(9): Show | 12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.3951+3386C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228265 | ||||||
| chr2:97228368
|
T | G | 163 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(160): Show | 163 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.3951+3489T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228368 | ||||||
| chr2:97228391
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3951+3512G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228391 | ||||||
| chr2:97228473
|
G | A | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3951+3594G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228473 | ||||||
| chr2:97228586
|
G | A | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3951+3707G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228586 | ||||||
| chr2:97228635
|
C | T | 1 | a0002c0002t0001g0069 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3951+3756C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228635 | ||||||
| chr2:97228638
|
C | T | 4 | a0003c0003t0001g0159a0007c0007t0001g0138a0007c0007t0001g0139others(1): Show | 4 | HG01099.hp1 HG01515.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.3951+3759C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228638 | ||||||
| chr2:97228646
|
T | C | 49 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(46): Show | 49 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(46): Show |
intron_variant | MODIFIER | c.3951+3767T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228646 | ||||||
| chr2:97228743
|
G | T | 1 | a0002c0002t0001g0066 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3951+3864G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228743 | ||||||
| chr2:97228792
|
C | G | 2 | a0002c0002t0001g0017a0002c0002t0001g0068 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.3951+3913C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228792 | ||||||
| chr2:97228849
|
T | C | 3 | a0003c0003t0001g0163a0003c0003t0001g0172a0006c0034t0001g0173 | 3 | HG02109.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3951+3970T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228849 | ||||||
| chr2:97228862
|
A | G | 4 | a0003c0003t0001g0159a0007c0007t0001g0138a0007c0007t0001g0139others(1): Show | 4 | HG01099.hp1 HG01515.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.3951+3983A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97228862 | ||||||
| chr2:97229068
|
A | G | 8 | a0011c0011t0002g0011a0011c0011t0002g0045a0011c0011t0002g0046others(5): Show | 8 | HG00423.hp1 HG02602.hp2 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.3951+4189A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97229068 | ||||||
| chr2:97229089
|
G | A | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3951+4210G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97229089 | ||||||
| chr2:97229375
|
T | C | 6 | a0005c0004t0005g0199a0005c0004t0005g0201a0005c0004t0005g0202others(3): Show | 6 | HG00642.hp2 HG03130.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.3952-4355T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97229375 | ||||||
| chr2:97229538
|
C | T | 1 | a0002c0002t0001g0068 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3952-4192C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97229538 | ||||||
| chr2:97229547
|
G | A | 5 | a0004c0005t0004g0037a0004c0005t0004g0039a0004c0024t0004g0038others(2): Show | 5 | HG01099.hp2 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.3952-4183G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97229547 | ||||||
| chr2:97229713
|
A | G | 11 | a0003c0003t0001g0135a0009c0009t0002g0174a0009c0009t0002g0175others(8): Show | 11 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.3952-4017A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97229713 | ||||||
| chr2:97229772
|
G | A | 21 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(18): Show | 21 | HG02055.hp2 HG02109.hp2 HG02145.hp2 others(18): Show |
intron_variant | MODIFIER | c.3952-3958G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97229772 | ||||||
| chr2:97230239
|
C | T | 145 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(142): Show | 145 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.3952-3491C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97230239 | ||||||
| chr2:97230473
|
C | T | 5 | a0003c0003t0001g0159a0006c0034t0001g0173a0007c0007t0001g0138others(2): Show | 5 | HG01099.hp1 HG01515.hp2 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.3952-3257C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97230473 | ||||||
| chr2:97230563
|
A | T | 147 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.3952-3167A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97230563 | ||||||
| chr2:97230621
|
A | C | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.3952-3109A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97230621 | ||||||
| chr2:97230712
|
G | A | 4 | a0014c0014t0001g0150a0014c0014t0001g0154a0014c0014t0001g0155others(1): Show | 4 | HG00558.hp1 NA18946.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.3952-3018G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97230712 | ||||||
| chr2:97230713
|
C | T | 4 | a0014c0014t0001g0150a0014c0014t0001g0154a0014c0014t0001g0155others(1): Show | 4 | HG00558.hp1 NA18946.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.3952-3017C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97230713 | ||||||
| chr2:97230803
|
A | G | 2 | a0001c0001t0001g0070a0019c0032t0007g0127 | 2 | NA19056.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3952-2927A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97230803 | ||||||
| chr2:97230950
|
A | T | 147 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.3952-2780A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97230950 | ||||||
| chr2:97231061
|
CT | C | 2 | a0001c0001t0001g0070a0019c0032t0007g0127 | 2 | NA19056.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.3952-2668delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231061 | ||||||
| chr2:97231137
|
G | T | 1 | a0010c0012t0001g0092 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3952-2593G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231137 | ||||||
| chr2:97231240
|
C | G | 1 | a0003c0003t0001g0181 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.3952-2490C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231240 | ||||||
| chr2:97231245
|
G | A | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3952-2485G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231245 | ||||||
| chr2:97231402
|
A | G | 1 | a0002c0002t0001g0069 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.3952-2328A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231402 | ||||||
| chr2:97231423
|
C | T | 1 | a0005c0004t0005g0200 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3952-2307C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231423 | ||||||
| chr2:97231546
|
C | T | 5 | a0013c0013t0003g0186a0013c0013t0003g0187a0013c0013t0003g0188others(2): Show | 5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.3952-2184C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231546 | ||||||
| chr2:97231622
|
A | G | 1 | a0002c0002t0001g0066 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3952-2108A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231622 | ||||||
| chr2:97231647
|
A | C | 1 | a0013c0025t0003g0185 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3952-2083A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231647 | ||||||
| chr2:97231724
|
C | T | 1 | a0004c0005t0004g0037 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3952-2006C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231724 | ||||||
| chr2:97231864
|
A | G | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.3952-1866A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231864 | ||||||
| chr2:97231871
|
G | A | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.3952-1859G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231871 | ||||||
| chr2:97231948
|
G | A | 2 | a0002c0002t0001g0069a0043c0039t0001g0008 | 2 | HG02055.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.3952-1782G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231948 | ||||||
| chr2:97231963
|
A | G | 1 | a0001c0046t0002g0051 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3952-1767A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97231963 | ||||||
| chr2:97232024
|
A | T | 1 | a0005c0004t0005g0200 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3952-1706A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232024 | ||||||
| chr2:97232036
|
T | C | 131 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(128): Show | 131 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.3952-1694T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232036 | ||||||
| chr2:97232280
|
G | A | 159 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(156): Show | 159 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.3952-1450G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232280 | ||||||
| chr2:97232385
|
G | C | 160 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(157): Show | 160 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.3952-1345G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232385 | ||||||
| chr2:97232410
|
A | T | 87 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(84): Show | 87 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.3952-1320A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232410 | ||||||
| chr2:97232412
|
A | G | 1 | a0048c0030t0002g0003 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.3952-1318A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232412 | ||||||
| chr2:97232418
|
A | G | 1 | a0004c0005t0010g0034 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.3952-1312A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232418 | ||||||
| chr2:97232457
|
A | C | 1 | a0030c0052t0002g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3952-1273A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232457 | ||||||
| chr2:97232501
|
T | A | 1 | a0001c0001t0001g0077 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3952-1229T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232501 | ||||||
| chr2:97232559
|
G | A | 4 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.3952-1171G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232559 | ||||||
| chr2:97232596
|
T | C | 1 | a0043c0039t0001g0008 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3952-1134T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232596 | ||||||
| chr2:97232645
|
T | A | 1 | a0001c0001t0001g0077 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.3952-1085T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232645 | ||||||
| chr2:97232684
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0123 | 2 | NA18999.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.3952-1046C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232684 | ||||||
| chr2:97232810
|
T | C | 2 | a0005c0004t0002g0129a0005c0004t0002g0130 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3952-920T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232810 | ||||||
| chr2:97232875
|
T | C | 5 | a0013c0013t0003g0186a0013c0013t0003g0187a0013c0013t0003g0188others(2): Show | 5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.3952-855T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232875 | ||||||
| chr2:97232927
|
C | T | 139 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(136): Show | 139 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.3952-803C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97232927 | ||||||
| chr2:97233009
|
TA | T | 159 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(156): Show | 159 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.3952-706delA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | INFO_REALIGN_3_PRIME | chr2 | 97233009 | |||||
| chr2:97233011
|
A | T | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.3952-719A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97233011 | ||||||
| chr2:97233087
|
G | A | 1 | a0002c0002t0002g0209 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3952-643G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97233087 | ||||||
| chr2:97233094
|
G | T | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.3952-636G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97233094 | ||||||
| chr2:97233249
|
G | C | 5 | a0013c0013t0003g0186a0013c0013t0003g0187a0013c0013t0003g0188others(2): Show | 5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.3952-481G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97233249 | ||||||
| chr2:97233560
|
T | C | 1 | a0007c0007t0001g0138 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.3952-170T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 67/75 | chr2 | 97233560 | ||||||
| chr2:97233932
|
T | C | 1 | a0029c0055t0002g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4093+61T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97233932 | ||||||
| chr2:97234350
|
A | T | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4093+479A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97234350 | ||||||
| chr2:97234492
|
T | C | 164 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(161): Show | 164 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.4093+621T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97234492 | ||||||
| chr2:97234813
|
T | C | 12 | a0004c0005t0004g0016a0004c0005t0004g0032a0004c0005t0004g0033others(9): Show | 12 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.4093+942T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97234813 | ||||||
| chr2:97234898
|
T | A | 1 | a0043c0039t0001g0008 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4093+1027T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97234898 | ||||||
| chr2:97234972
|
T | TA | 2 | a0023c0019t0003g0197a0023c0019t0003g0198 | 2 | NA18999.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.4093+1101_4093+110 others(5): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97234972 | ||||||
| chr2:97234973
|
C | A | 2 | a0023c0019t0003g0197a0023c0019t0003g0198 | 2 | NA18999.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.4093+1102C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97234973 | ||||||
| chr2:97235015
|
C | T | 1 | a0002c0002t0002g0209 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4093+1144C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235015 | ||||||
| chr2:97235016
|
A | G | 166 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(163): Show | 166 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(163): Show |
intron_variant | MODIFIER | c.4093+1145A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235016 | ||||||
| chr2:97235106
|
G | T | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4093+1235G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235106 | ||||||
| chr2:97235168
|
C | T | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4093+1297C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235168 | ||||||
| chr2:97235240
|
A | G | 1 | a0001c0001t0001g0123 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.4093+1369A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235240 | ||||||
| chr2:97235253
|
C | T | 1 | a0012c0010t0002g0028 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.4093+1382C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235253 | ||||||
| chr2:97235373
|
A | G | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4093+1502A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235373 | ||||||
| chr2:97235418
|
G | T | 165 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(162): Show | 165 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.4093+1547G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235418 | ||||||
| chr2:97235436
|
C | T | 1 | a0030c0052t0002g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.4093+1565C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235436 | ||||||
| chr2:97235518
|
A | G | 86 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(83): Show | 86 | HG00423.hp2 HG00597.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.4093+1647A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97235518 | ||||||
| chr2:97236163
|
T | C | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.4093+2292T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97236163 | ||||||
| chr2:97236339
|
T | C | 1 | a0003c0003t0001g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4093+2468T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97236339 | ||||||
| chr2:97236534
|
T | C | 1 | a0010c0059t0001g0090 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4093+2663T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97236534 | ||||||
| chr2:97236887
|
C | T | 1 | a0003c0003t0001g0135 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4093+3016C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97236887 | ||||||
| chr2:97236973
|
C | T | 7 | a0007c0007t0001g0138a0007c0007t0001g0139a0007c0007t0001g0207others(4): Show | 7 | HG00558.hp1 HG01099.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.4093+3102C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97236973 | ||||||
| chr2:97237215
|
A | G | 2 | a0001c0046t0002g0051a0050c0061t0001g0010 | 2 | NA19070.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.4093+3344A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97237215 | ||||||
| chr2:97237273
|
C | T | 12 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(9): Show | 12 | HG00423.hp1 HG02572.hp1 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.4093+3402C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97237273 | ||||||
| chr2:97237276
|
G | C | 56 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(53): Show | 56 | HG00423.hp2 HG00609.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.4093+3405G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97237276 | ||||||
| chr2:97237358
|
T | C | 1 | a0018c0018t0002g0044 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.4093+3487T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97237358 | ||||||
| chr2:97237427
|
T | C | 7 | a0001c0046t0002g0051a0013c0013t0003g0186a0013c0013t0003g0187others(4): Show | 7 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.4093+3556T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97237427 | ||||||
| chr2:97237531
|
C | T | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4093+3660C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97237531 | ||||||
| chr2:97237761
|
G | A | 126 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(123): Show | 126 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.4094-3505G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97237761 | ||||||
| chr2:97237801
|
T | C | 2 | a0002c0002t0001g0058a0044c0038t0001g0067 | 2 | NA20129.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4094-3465T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97237801 | ||||||
| chr2:97237903
|
A | G | 10 | a0001c0046t0002g0051a0015c0015t0001g0088a0015c0015t0001g0089others(7): Show | 10 | HG00558.hp2 NA18952.hp1 NA18961.hp2 others(7): Show |
intron_variant | MODIFIER | c.4094-3363A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97237903 | ||||||
| chr2:97238131
|
A | G | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.4094-3135A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97238131 | ||||||
| chr2:97238349
|
G | A | 1 | a0029c0055t0002g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4094-2917G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97238349 | ||||||
| chr2:97238479
|
G | A | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4094-2787G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97238479 | ||||||
| chr2:97238527
|
C | T | 72 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(69): Show | 72 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.4094-2739C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97238527 | ||||||
| chr2:97238951
|
C | A | 133 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(130): Show | 133 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.4094-2315C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97238951 | ||||||
| chr2:97239014
|
A | G | 2 | a0002c0002t0001g0065a0002c0002t0001g0183 | 2 | HG02723.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.4094-2252A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97239014 | ||||||
| chr2:97239170
|
A | C | 5 | a0013c0013t0003g0186a0013c0013t0003g0187a0013c0013t0003g0188others(2): Show | 5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.4094-2096A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97239170 | ||||||
| chr2:97239239
|
G | A | 1 | a0005c0004t0005g0204 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.4094-2027G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97239239 | ||||||
| chr2:97239295
|
C | T | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4094-1971C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97239295 | ||||||
| chr2:97239339
|
G | GT | 9 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(6): Show | 9 | HG01261.hp1 HG01358.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.4094-1914dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97239339 | |||||
| chr2:97239339
|
GT | G | 132 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(129): Show | 132 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.4094-1914delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97239339 | |||||
| chr2:97239339
|
GTT | G | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.4094-1915_4094-191 others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97239339 | |||||
| chr2:97239715
|
C | T | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4094-1551C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97239715 | ||||||
| chr2:97239771
|
T | C | 1 | a0001c0046t0002g0051 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4094-1495T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97239771 | ||||||
| chr2:97239951
|
A | G | 1 | a0009c0009t0002g0177 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4094-1315A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97239951 | ||||||
| chr2:97240109
|
G | GT | 138 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(135): Show | 138 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.4094-1150dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240109 | |||||
| chr2:97240117
|
A | T | 5 | a0001c0001t0001g0111a0004c0005t0010g0034a0008c0006t0003g0190others(2): Show | 5 | HG01123.hp2 HG01496.hp2 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.4094-1149A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97240117 | ||||||
| chr2:97240273
|
G | A | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4094-993G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97240273 | ||||||
| chr2:97240348
|
T | G | 4 | a0002c0002t0001g0183a0003c0003t0001g0168a0016c0053t0001g0104others(1): Show | 4 | HG02683.hp1 HG02723.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.4094-918T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97240348 | ||||||
| chr2:97240467
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4094-799G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97240467 | ||||||
| chr2:97240541
|
C | T | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4094-725C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97240541 | ||||||
| chr2:97240732
|
G | T | 159 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(156): Show | 159 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.4094-534G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97240732 | ||||||
| chr2:97240912
|
A | G | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.4094-354A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97240912 | ||||||
| chr2:97240982
|
G | GT | 14 | a0003c0003t0001g0142a0003c0003t0001g0158a0006c0008t0001g0005others(11): Show | 14 | HG00099.hp2 HG00597.hp1 HG00639.hp1 others(11): Show |
intron_variant | MODIFIER | c.4094-248dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | |||||
| chr2:97240982
|
G | GTT | 5 | a0003c0003t0001g0135a0003c0003t0001g0143a0003c0003t0001g0159others(2): Show | 5 | HG01175.hp2 HG01358.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.4094-249_4094-248d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | |||||
| chr2:97240982
|
GT | G | 5 | a0003c0003t0001g0157a0003c0003t0001g0172a0006c0008t0001g0148others(2): Show | 5 | HG00741.hp2 HG01070.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.4094-248delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | |||||
| chr2:97240982
|
GTTTTTT | G | 28 | a0000c0016t0006g0119a0001c0001t0001g0019a0001c0001t0001g0070others(25): Show | 28 | HG00423.hp2 HG00558.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.4094-253_4094-248d others(8): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | |||||
| chr2:97240982
|
GTTTTTTT | G | 93 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(90): Show | 93 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.4094-254_4094-248d others(9): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | |||||
| chr2:97240982
|
GTTTTTTT others(1): Show |
G | 16 | a0002c0002t0001g0058a0002c0002t0001g0060a0002c0002t0001g0061others(13): Show | 16 | HG00558.hp2 HG01243.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.4094-255_4094-248d others(10): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | |||||
| chr2:97240982
|
GTTTTTTT others(4): Show |
G | 1 | a0013c0013t0003g0189 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4094-258_4094-248d others(13): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | |||||
| chr2:97240982
|
GTTTTTTT others(5): Show |
G | 4 | a0008c0006t0003g0191a0013c0013t0003g0187a0013c0013t0003g0188others(1): Show | 4 | HG03834.hp1 HG04204.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.4094-259_4094-248d others(14): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | |||||
| chr2:97240982
|
GTTTTTTT others(6): Show |
G | 10 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0192others(7): Show | 10 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.4094-260_4094-248d others(15): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | |||||
| chr2:97240982
|
GTTTTTTT others(7): Show |
G | 3 | a0002c0002t0001g0183a0003c0003t0001g0168a0032c0054t0001g0165 | 3 | HG02683.hp1 HG02723.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.4094-261_4094-248d others(16): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | |||||
| chr2:97240982
|
GTTTTTTT others(10): Show |
G | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.4094-264_4094-248d others(19): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | INFO_REALIGN_3_PRIME | chr2 | 97240982 | |||||
| chr2:97240999
|
T | G | 9 | a0005c0004t0002g0129a0005c0004t0002g0130a0005c0004t0005g0199others(6): Show | 9 | HG00642.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.4094-267T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97240999 | ||||||
| chr2:97241086
|
A | G | 1 | a0003c0003t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4094-180A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97241086 | ||||||
| chr2:97241173
|
G | A | 2 | a0001c0001t0001g0112a0001c0001t0001g0124 | 2 | HG02683.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.4094-93G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97241173 | ||||||
| chr2:97241244
|
C | G | 3 | a0002c0002t0001g0183a0005c0004t0002g0129a0005c0004t0002g0130 | 3 | HG02258.hp2 HG02723.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4094-22C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 68/75 | chr2 | 97241244 | ||||||
| chr2:97241501
|
A | G | 138 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(135): Show | 138 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.4307+22A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97241501 | ||||||
| chr2:97241507
|
G | C | 1 | a0020c0022t0002g0030 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4307+28G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97241507 | ||||||
| chr2:97241556
|
C | T | 63 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(60): Show | 63 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.4307+77C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97241556 | ||||||
| chr2:97241604
|
T | C | 1 | a0004c0005t0010g0034 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.4307+125T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97241604 | ||||||
| chr2:97241794
|
A | G | 1 | a0003c0003t0001g0167 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4307+315A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97241794 | ||||||
| chr2:97241933
|
T | G | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.4307+454T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97241933 | ||||||
| chr2:97242014
|
G | A | 1 | a0007c0007t0001g0140 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4307+535G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242014 | ||||||
| chr2:97242031
|
C | A | 1 | a0003c0003t0001g0157 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4307+552C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242031 | ||||||
| chr2:97242076
|
G | A | 6 | a0001c0001t0001g0073a0001c0001t0001g0096a0001c0001t0001g0105others(3): Show | 6 | HG00423.hp2 HG00609.hp2 NA18612.hp2 others(3): Show |
intron_variant | MODIFIER | c.4307+597G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242076 | ||||||
| chr2:97242145
|
G | T | 1 | a0005c0004t0002g0129 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4307+666G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242145 | ||||||
| chr2:97242205
|
G | A | 3 | a0002c0002t0001g0183a0004c0005t0004g0039a0035c0062t0004g0042 | 3 | HG01981.hp1 HG02723.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.4307+726G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242205 | ||||||
| chr2:97242288
|
C | CA | 136 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(133): Show | 136 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.4307+826dupA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | INFO_REALIGN_3_PRIME | chr2 | 97242288 | |||||
| chr2:97242288
|
C | CAA | 5 | a0002c0002t0001g0183a0012c0010t0002g0026a0021c0021t0002g0012others(2): Show | 5 | HG02055.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4307+825_4307+826d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | INFO_REALIGN_3_PRIME | chr2 | 97242288 | |||||
| chr2:97242306
|
T | A | 7 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4307+827T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242306 | ||||||
| chr2:97242339
|
G | A | 1 | a0002c0002t0001g0183 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4307+860G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242339 | ||||||
| chr2:97242445
|
G | A | 1 | a0015c0015t0001g0109 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.4307+966G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242445 | ||||||
| chr2:97242524
|
T | G | 5 | a0007c0007t0001g0164a0014c0014t0001g0150a0014c0014t0001g0154others(2): Show | 5 | HG00558.hp1 HG01358.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.4307+1045T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242524 | ||||||
| chr2:97242551
|
A | G | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.4307+1072A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242551 | ||||||
| chr2:97242555
|
G | T | 168 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(165): Show | 168 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.4307+1076G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242555 | ||||||
| chr2:97242580
|
C | A | 1 | a0002c0002t0001g0183 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.4307+1101C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242580 | ||||||
| chr2:97242770
|
T | C | 1 | a0004c0005t0004g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4308-1076T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97242770 | ||||||
| chr2:97243012
|
C | T | 26 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(23): Show | 26 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.4308-834C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243012 | ||||||
| chr2:97243038
|
T | C | 26 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(23): Show | 26 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.4308-808T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243038 | ||||||
| chr2:97243097
|
G | C | 72 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(69): Show | 72 | HG00423.hp2 HG00558.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.4308-749G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243097 | ||||||
| chr2:97243115
|
T | C | 26 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(23): Show | 26 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.4308-731T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243115 | ||||||
| chr2:97243126
|
G | A | 25 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(22): Show | 25 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.4308-720G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243126 | ||||||
| chr2:97243134
|
C | T | 25 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(22): Show | 25 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.4308-712C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243134 | ||||||
| chr2:97243135
|
G | A | 4 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(1): Show | 4 | HG01243.hp1 HG01891.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.4308-711G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243135 | ||||||
| chr2:97243149
|
G | T | 25 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(22): Show | 25 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.4308-697G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243149 | ||||||
| chr2:97243171
|
G | A | 25 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(22): Show | 25 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.4308-675G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243171 | ||||||
| chr2:97243173
|
G | A | 3 | a0000c0016t0006g0018a0007c0007t0001g0164a0050c0061t0001g0010 | 3 | HG01358.hp1 NA19070.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.4308-673G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243173 | ||||||
| chr2:97243179
|
C | T | 25 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(22): Show | 25 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.4308-667C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243179 | ||||||
| chr2:97243183
|
G | T | 25 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(22): Show | 25 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.4308-663G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243183 | ||||||
| chr2:97243184
|
T | C | 25 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(22): Show | 25 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.4308-662T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243184 | ||||||
| chr2:97243202
|
A | G | 65 | a0000c0016t0006g0076a0000c0016t0006g0108a0000c0016t0006g0119others(62): Show | 65 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.4308-644A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243202 | ||||||
| chr2:97243246
|
A | C | 2 | a0004c0024t0004g0038a0004c0024t0004g0040 | 2 | HG01261.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.4308-600A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243246 | ||||||
| chr2:97243247
|
C | T | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.4308-599C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243247 | ||||||
| chr2:97243252
|
G | A | 5 | a0007c0007t0001g0164a0014c0014t0001g0150a0014c0014t0001g0154others(2): Show | 5 | HG00558.hp1 HG01358.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.4308-594G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243252 | ||||||
| chr2:97243303
|
G | A | 23 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(20): Show | 23 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.4308-543G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243303 | ||||||
| chr2:97243334
|
C | G | 27 | a0001c0001t0001g0112a0002c0002t0002g0031a0002c0002t0002g0132others(24): Show | 27 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(24): Show |
intron_variant | MODIFIER | c.4308-512C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243334 | ||||||
| chr2:97243400
|
G | A | 29 | a0001c0001t0001g0070a0002c0002t0001g0017a0002c0002t0002g0031others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.4308-446G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243400 | ||||||
| chr2:97243401
|
G | A | 29 | a0001c0001t0001g0070a0002c0002t0001g0017a0002c0002t0002g0031others(26): Show | 29 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.4308-445G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243401 | ||||||
| chr2:97243447
|
G | C | 31 | a0001c0001t0001g0070a0002c0002t0001g0017a0002c0002t0002g0031others(28): Show | 31 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.4308-399G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243447 | ||||||
| chr2:97243453
|
A | G | 28 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.4308-393A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243453 | ||||||
| chr2:97243463
|
G | A | 28 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(25): Show | 28 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.4308-383G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243463 | ||||||
| chr2:97243473
|
G | A | 34 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0056others(31): Show | 34 | HG00099.hp1 HG00423.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.4308-373G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243473 | ||||||
| chr2:97243493
|
C | G | 119 | a0001c0001t0001g0001a0001c0001t0001g0070a0001c0001t0001g0073others(116): Show | 119 | HG00099.hp1 HG00423.hp2 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.4308-353C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243493 | ||||||
| chr2:97243556
|
C | T | 1 | a0003c0003t0001g0166 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.4308-290C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243556 | ||||||
| chr2:97243781
|
C | T | 1 | a0002c0002t0001g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4308-65C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 69/75 | chr2 | 97243781 | ||||||
| chr2:97244039
|
T | C | 1 | a0003c0003t0001g0168 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.4491+10T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | chr2 | 97244039 | ||||||
| chr2:97244091
|
C | A | 2 | a0003c0003t0001g0167a0025c0057t0001g0134 | 2 | HG00639.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.4491+62C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | chr2 | 97244091 | ||||||
| chr2:97244103
|
G | A | 20 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(17): Show | 20 | HG00558.hp1 HG00597.hp2 HG02071.hp1 others(17): Show |
intron_variant | MODIFIER | c.4491+74G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | chr2 | 97244103 | ||||||
| chr2:97244192
|
C | T | 21 | a0007c0007t0001g0164a0008c0006t0003g0184a0008c0006t0003g0190others(18): Show | 21 | HG00558.hp1 HG00597.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.4491+163C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | chr2 | 97244192 | ||||||
| chr2:97244207
|
T | A | 1 | a0044c0038t0001g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.4491+178T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | chr2 | 97244207 | ||||||
| chr2:97244376
|
G | C | 17 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(14): Show | 17 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.4491+347G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | chr2 | 97244376 | ||||||
| chr2:97244520
|
G | C | 4 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(1): Show | 4 | HG02040.hp1 NA18965.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.4491+491G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | chr2 | 97244520 | ||||||
| chr2:97244635
|
C | T | 2 | a0020c0022t0002g0015a0020c0022t0002g0030 | 2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.4492-522C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | chr2 | 97244635 | ||||||
| chr2:97244807
|
T | TTA | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4492-349_4492-348d others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | INFO_REALIGN_3_PRIME | chr2 | 97244807 | |||||
| chr2:97245076
|
A | G | 169 | a0000c0016t0006g0018a0000c0016t0006g0076a0000c0016t0006g0108others(166): Show | 169 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.4492-81A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 70/75 | chr2 | 97245076 | ||||||
| chr2:97246274
|
A | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(168): Show | 171 | HG00099.hp1 HG00099.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.5406+203A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246274 | ||||||
| chr2:97246385
|
A | G | 11 | a0004c0005t0004g0016a0004c0005t0004g0032a0004c0005t0004g0033others(8): Show | 11 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.5406+314A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246385 | ||||||
| chr2:97246400
|
T | C | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.5406+329T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246400 | ||||||
| chr2:97246460
|
T | C | 14 | a0002c0002t0001g0017a0002c0002t0001g0068a0007c0007t0001g0137others(11): Show | 14 | HG00099.hp2 HG00558.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.5406+389T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246460 | ||||||
| chr2:97246585
|
T | C | 5 | a0013c0013t0003g0186a0013c0013t0003g0187a0013c0013t0003g0188others(2): Show | 5 | HG02071.hp1 HG02083.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.5406+514T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246585 | ||||||
| chr2:97246629
|
C | T | 5 | a0007c0007t0001g0164a0014c0014t0001g0150a0014c0014t0001g0154others(2): Show | 5 | HG00558.hp1 HG01358.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.5406+558C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246629 | ||||||
| chr2:97246654
|
A | C | 1 | a0007c0007t0001g0139 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5406+583A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246654 | ||||||
| chr2:97246679
|
C | A | 5 | a0007c0007t0001g0164a0014c0014t0001g0150a0014c0014t0001g0154others(2): Show | 5 | HG00558.hp1 HG01358.hp1 NA18946.hp1 others(2): Show |
intron_variant | MODIFIER | c.5406+608C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246679 | ||||||
| chr2:97246866
|
A | G | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.5407-610A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246866 | ||||||
| chr2:97246959
|
G | A | 11 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(8): Show | 11 | HG00597.hp2 NA18941.hp2 NA18951.hp2 others(8): Show |
intron_variant | MODIFIER | c.5407-517G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97246959 | ||||||
| chr2:97247163
|
C | G | 1 | a0015c0015t0001g0088 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.5407-313C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97247163 | ||||||
| chr2:97247276
|
C | T | 3 | a0013c0013t0003g0187a0013c0013t0003g0188a0013c0013t0003g0189 | 3 | HG03834.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.5407-200C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 71/75 | chr2 | 97247276 | ||||||
| chr2:97247725
|
T | TTTGTATT others(316): Show |
1 | a0003c0003t0001g0149 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.5559+107_5559+108i others(325): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | INFO_REALIGN_3_PRIME | chr2 | 97247725 | |||||
| chr2:97247847
|
T | C | 1 | a0044c0038t0001g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5559+219T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97247847 | ||||||
| chr2:97248104
|
T | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(63): Show | 66 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.5559+476T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248104 | ||||||
| chr2:97248130
|
G | A | 2 | a0005c0004t0002g0129a0044c0038t0001g0067 | 2 | HG02922.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.5559+502G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248130 | ||||||
| chr2:97248190
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.5559+562G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248190 | ||||||
| chr2:97248279
|
G | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(157): Show | 160 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.5559+651G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248279 | ||||||
| chr2:97248427
|
C | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(157): Show | 160 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(157): Show |
intron_variant | MODIFIER | c.5560-717C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248427 | ||||||
| chr2:97248515
|
C | T | 11 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(8): Show | 11 | HG00639.hp2 HG00741.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.5560-629C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248515 | ||||||
| chr2:97248528
|
G | A | 1 | a0007c0007t0001g0139 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.5560-616G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248528 | ||||||
| chr2:97248636
|
T | A | 1 | a0031c0051t0001g0085 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.5560-508T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248636 | ||||||
| chr2:97248705
|
C | T | 1 | a0001c0001t0002g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.5560-439C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248705 | ||||||
| chr2:97248852
|
G | A | 12 | a0001c0001t0001g0123a0001c0001t0002g0022a0002c0002t0001g0052others(9): Show | 12 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.5560-292G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248852 | ||||||
| chr2:97248890
|
A | G | 1 | a0002c0002t0001g0017 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.5560-254A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248890 | ||||||
| chr2:97248959
|
G | A | 1 | a0002c0002t0002g0209 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5560-185G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97248959 | ||||||
| chr2:97249030
|
T | A | 1 | a0044c0038t0001g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5560-114T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97249030 | ||||||
| chr2:97249031
|
A | T | 1 | a0044c0038t0001g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.5560-113A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97249031 | ||||||
| chr2:97249057
|
T | C | 7 | a0005c0004t0005g0199a0005c0004t0005g0200a0005c0004t0005g0201others(4): Show | 7 | HG00642.hp2 HG02630.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.5560-87T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97249057 | ||||||
| chr2:97249089
|
C | T | 3 | a0013c0013t0003g0187a0013c0013t0003g0188a0013c0013t0003g0189 | 3 | HG03834.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.5560-55C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 72/75 | chr2 | 97249089 | ||||||
| chr2:97249334
|
A | G | 1 | a0031c0051t0001g0085 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.5630+120A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 73/75 | chr2 | 97249334 | ||||||
| chr2:97249714
|
A | G | 1 | a0005c0004t0005g0200 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5724+69A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 74/75 | chr2 | 97249714 | ||||||
| chr2:97249800
|
A | G | 1 | a0030c0052t0002g0128 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.5724+155A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 74/75 | chr2 | 97249800 | ||||||
| chr2:97249832
|
G | A | 13 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(10): Show | 13 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.5724+187G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 74/75 | chr2 | 97249832 | ||||||
| chr2:97249960
|
C | T | 2 | a0001c0001t0002g0050a0001c0046t0002g0051 | 2 | NA19043.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5725-184C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 74/75 | chr2 | 97249960 | ||||||
| chr2:97249961
|
G | A | 1 | a0012c0010t0002g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.5725-183G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 74/75 | chr2 | 97249961 | ||||||
| chr2:97249984
|
G | A | 2 | a0013c0013t0003g0186a0013c0025t0003g0185 | 2 | HG02071.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.5725-160G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 74/75 | chr2 | 97249984 | ||||||
| chr2:97250013
|
T | C | 13 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(10): Show | 13 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.5725-131T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 74/75 | chr2 | 97250013 | ||||||
| chr2:97250043
|
G | A | 2 | a0005c0004t0002g0002a0048c0030t0002g0003 | 2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.5725-101G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 74/75 | chr2 | 97250043 | ||||||
| chr2:97250063
|
G | A | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.5725-81G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 74/75 | chr2 | 97250063 | ||||||
| chr2:97250204
|
A | C | 73 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.*6+31A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97250204 | ||||||
| chr2:97250346
|
A | G | 60 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(57): Show | 60 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.*6+173A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97250346 | ||||||
| chr2:97250394
|
G | A | 1 | a0014c0014t0001g0154 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.*6+221G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97250394 | ||||||
| chr2:97250404
|
T | G | 2 | a0009c0009t0002g0179a0009c0009t0002g0182 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.*6+231T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97250404 | ||||||
| chr2:97250539
|
C | G | 157 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(154): Show | 157 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.*6+366C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97250539 | ||||||
| chr2:97250553
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(155): Show | 158 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.*6+380A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97250553 | ||||||
| chr2:97250627
|
ATTGACTT others(14): Show |
A | 1 | a0044c0038t0001g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*6+457_*6+477delGA others(19): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97250627 | |||||
| chr2:97250637
|
T | C | 1 | a0001c0046t0002g0051 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.*6+464T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97250637 | ||||||
| chr2:97250932
|
A | C | 3 | a0018c0018t0002g0043a0018c0018t0002g0044a0018c0018t0002g0048 | 3 | NA18951.hp1 NA18961.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.*6+759A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97250932 | ||||||
| chr2:97251067
|
C | A | 2 | a0005c0004t0002g0129a0005c0004t0002g0130 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.*6+894C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97251067 | ||||||
| chr2:97251171
|
A | G | 18 | a0002c0002t0001g0017a0002c0002t0001g0068a0002c0002t0002g0031others(15): Show | 18 | HG00423.hp1 HG02145.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.*6+998A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97251171 | ||||||
| chr2:97251285
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.*6+1112T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97251285 | ||||||
| chr2:97251388
|
C | A | 5 | a0015c0015t0001g0088a0015c0015t0001g0089a0031c0051t0001g0085others(2): Show | 5 | HG00558.hp2 NA18971.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.*6+1215C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97251388 | ||||||
| chr2:97251518
|
T | C | 7 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.*6+1345T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97251518 | ||||||
| chr2:97252133
|
C | T | 1 | a0001c0001t0001g0081 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.*6+1960C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97252133 | ||||||
| chr2:97252478
|
T | C | 2 | a0004c0005t0010g0034a0043c0039t0001g0008 | 2 | HG01123.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.*6+2305T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97252478 | ||||||
| chr2:97252579
|
G | A | 2 | a0008c0006t0003g0190a0008c0006t0003g0191 | 2 | NA18965.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.*6+2406G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97252579 | ||||||
| chr2:97252689
|
A | G | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.*6+2516A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97252689 | ||||||
| chr2:97252713
|
A | G | 72 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(69): Show | 72 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.*6+2540A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97252713 | ||||||
| chr2:97252758
|
A | G | 1 | a0004c0005t0004g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*6+2585A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97252758 | ||||||
| chr2:97252761
|
G | A | 1 | a0004c0005t0004g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.*6+2588G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97252761 | ||||||
| chr2:97253368
|
C | T | 5 | a0004c0005t0004g0037a0004c0005t0004g0039a0004c0024t0004g0038others(2): Show | 5 | HG01099.hp2 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.*6+3195C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97253368 | ||||||
| chr2:97253453
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.*6+3280T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97253453 | ||||||
| chr2:97253524
|
C | A | 1 | a0008c0006t0003g0192 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.*6+3351C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97253524 | ||||||
| chr2:97253552
|
A | G | 1 | a0037c0040t0002g0211 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.*6+3379A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97253552 | ||||||
| chr2:97253685
|
G | A | 11 | a0005c0004t0002g0002a0005c0004t0002g0129a0005c0004t0002g0130others(8): Show | 11 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.*6+3512G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97253685 | ||||||
| chr2:97253931
|
A | C | 13 | a0001c0001t0002g0050a0001c0046t0002g0051a0005c0004t0002g0002others(10): Show | 13 | HG00609.hp1 HG00642.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.*6+3758A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97253931 | ||||||
| chr2:97254539
|
C | A | 9 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(6): Show | 9 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.*6+4366C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254539 | ||||||
| chr2:97254746
|
A | G | 4 | a0001c0001t0001g0084a0001c0001t0001g0086a0010c0012t0001g0083others(1): Show | 4 | HG01169.hp1 HG01361.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.*6+4573A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254746 | ||||||
| chr2:97254758
|
C | T | 8 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(5): Show | 8 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.*6+4585C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254758 | ||||||
| chr2:97254785
|
C | CAGA | 7 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.*6+4613_*6+4614ins others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97254785 | |||||
| chr2:97254787
|
T | A | 7 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.*6+4614T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254787 | ||||||
| chr2:97254789
|
T | A | 7 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.*6+4616T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254789 | ||||||
| chr2:97254790
|
T | A | 7 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.*6+4617T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254790 | ||||||
| chr2:97254790
|
T | G | 1 | a0007c0007t0001g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.*6+4617T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254790 | ||||||
| chr2:97254791
|
G | A | 7 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.*6+4618G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254791 | ||||||
| chr2:97254845
|
A | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(140): Show | 143 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.*6+4672A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254845 | ||||||
| chr2:97254897
|
A | G | 3 | a0003c0003t0001g0142a0003c0003t0001g0143a0033c0035t0001g0136 | 3 | HG00597.hp1 NA18972.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.*6+4724A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97254897 | ||||||
| chr2:97255184
|
C | T | 3 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022 | 3 | HG01891.hp2 HG02280.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.*6+5011C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97255184 | ||||||
| chr2:97255237
|
A | G | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.*6+5064A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97255237 | ||||||
| chr2:97255720
|
G | A | 1 | a0004c0005t0004g0033 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.*6+5547G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97255720 | ||||||
| chr2:97256211
|
G | C | 81 | a0002c0002t0001g0017a0002c0002t0001g0052a0002c0002t0001g0053others(78): Show | 81 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.*6+6038G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97256211 | ||||||
| chr2:97256238
|
T | C | 66 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(63): Show | 66 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.*6+6065T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97256238 | ||||||
| chr2:97256252
|
A | G | 73 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.*6+6079A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97256252 | ||||||
| chr2:97256289
|
G | A | 12 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(9): Show | 12 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(9): Show |
intron_variant | MODIFIER | c.*6+6116G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97256289 | ||||||
| chr2:97256357
|
CA | C | 74 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(71): Show | 74 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.*6+6196delA | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97256357 | |||||
| chr2:97256449
|
GT | G | 57 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(54): Show | 57 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.*6+6279delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97256449 | |||||
| chr2:97256596
|
T | C | 73 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(70): Show | 73 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(70): Show |
intron_variant | MODIFIER | c.*6+6423T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97256596 | ||||||
| chr2:97256803
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(136): Show | 139 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.*6+6630A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97256803 | ||||||
| chr2:97256938
|
C | T | 3 | a0013c0013t0003g0187a0013c0013t0003g0188a0013c0013t0003g0189 | 3 | HG03834.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.*6+6765C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97256938 | ||||||
| chr2:97257623
|
A | G | 1 | a0047c0033t0002g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.*7-6706A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97257623 | ||||||
| chr2:97257878
|
T | G | 1 | a0003c0003t0001g0162 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.*7-6451T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97257878 | ||||||
| chr2:97258059
|
CT | C | 2 | a0003c0003t0001g0163a0003c0003t0001g0172 | 2 | HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.*7-6267delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97258059 | |||||
| chr2:97258066
|
A | G | 6 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.*7-6263A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97258066 | ||||||
| chr2:97258177
|
T | C | 68 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(65): Show | 68 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.*7-6152T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97258177 | ||||||
| chr2:97258371
|
G | A | 2 | a0005c0004t0002g0002a0048c0030t0002g0003 | 2 | HG00609.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.*7-5958G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97258371 | ||||||
| chr2:97258770
|
T | G | 1 | a0026c0058t0001g0074 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.*7-5559T>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97258770 | ||||||
| chr2:97258908
|
C | T | 1 | a0037c0040t0002g0211 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.*7-5421C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97258908 | ||||||
| chr2:97258954
|
G | T | 65 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(62): Show | 65 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.*7-5375G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97258954 | ||||||
| chr2:97258991
|
T | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(63): Show | 66 | HG00423.hp2 HG00558.hp2 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.*7-5338T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97258991 | ||||||
| chr2:97259024
|
C | A | 1 | a0042c0043t0002g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*7-5305C>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97259024 | ||||||
| chr2:97259046
|
G | A | 1 | a0008c0006t0003g0195 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.*7-5283G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97259046 | ||||||
| chr2:97259059
|
G | A | 1 | a0052c0026t0003g0193 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.*7-5270G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97259059 | ||||||
| chr2:97259140
|
G | T | 1 | a0042c0043t0002g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*7-5189G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97259140 | ||||||
| chr2:97259512
|
T | C | 1 | a0001c0001t0001g0081 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.*7-4817T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97259512 | ||||||
| chr2:97259574
|
G | T | 3 | a0013c0013t0003g0187a0013c0013t0003g0188a0013c0013t0003g0189 | 3 | HG03834.hp1 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.*7-4755G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97259574 | ||||||
| chr2:97259688
|
G | A | 1 | a0005c0004t0005g0205 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.*7-4641G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97259688 | ||||||
| chr2:97259755
|
G | A | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.*7-4574G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97259755 | ||||||
| chr2:97259922
|
C | T | 67 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(64): Show | 67 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.*7-4407C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97259922 | ||||||
| chr2:97260191
|
C | T | 1 | a0003c0003t0001g0172 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.*7-4138C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260191 | ||||||
| chr2:97260347
|
G | GAT | 14 | a0002c0002t0001g0068a0003c0003t0001g0142a0003c0003t0001g0143others(11): Show | 14 | HG00597.hp1 HG01123.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.*7-3950_*7-3949dup others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | |||||
| chr2:97260347
|
G | GATAT | 5 | a0003c0003t0001g0135a0003c0003t0001g0144a0003c0003t0001g0158others(2): Show | 5 | HG01515.hp2 HG02698.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.*7-3952_*7-3949dup others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | |||||
| chr2:97260347
|
G | GATATAT | 4 | a0003c0003t0001g0168a0007c0007t0001g0139a0007c0007t0001g0141others(1): Show | 4 | HG00099.hp2 HG01099.hp1 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.*7-3954_*7-3949dup others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | |||||
| chr2:97260347
|
G | GATATATA others(3): Show |
1 | a0017c0017t0001g0170 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.*7-3958_*7-3949dup others(10): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | |||||
| chr2:97260347
|
GAT | G | 23 | a0001c0001t0001g0096a0003c0003t0001g0157a0003c0003t0001g0160others(20): Show | 23 | HG01261.hp1 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.*7-3950_*7-3949del others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | |||||
| chr2:97260347
|
GATAT | G | 62 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(59): Show | 62 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(59): Show |
intron_variant | MODIFIER | c.*7-3952_*7-3949del others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | |||||
| chr2:97260347
|
GATATAT | G | 5 | a0001c0001t0001g0079a0013c0013t0003g0186a0013c0013t0003g0187others(2): Show | 5 | HG02083.hp2 HG02300.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.*7-3954_*7-3949del others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | |||||
| chr2:97260347
|
GATATATA others(3): Show |
G | 3 | a0003c0003t0001g0163a0003c0003t0001g0172a0006c0034t0001g0173 | 3 | HG02109.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.*7-3958_*7-3949del others(10): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | |||||
| chr2:97260347
|
GATATATA others(7): Show |
G | 1 | a0005c0004t0002g0002 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.*7-3962_*7-3949del others(14): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | |||||
| chr2:97260347
|
GATATATA others(11): Show |
G | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.*7-3966_*7-3949del others(18): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260347 | |||||
| chr2:97260377
|
T | C | 3 | a0001c0001t0001g0084a0010c0012t0001g0083a0040c0047t0001g0082 | 3 | HG01169.hp1 HG01361.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.*7-3952T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260377 | ||||||
| chr2:97260379
|
T | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(88): Show | 91 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.*7-3950T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260379 | ||||||
| chr2:97260379
|
T | TAC | 16 | a0002c0002t0001g0069a0002c0002t0002g0031a0002c0002t0002g0209others(13): Show | 16 | HG00597.hp2 HG01123.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.*7-3944_*7-3943dup others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260379 | |||||
| chr2:97260379
|
T | TATAC | 22 | a0001c0001t0002g0020a0001c0001t0002g0021a0002c0002t0001g0052others(19): Show | 22 | HG00642.hp2 HG01891.hp2 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.*7-3949_*7-3948ins others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260379 | |||||
| chr2:97260379
|
T | TATATAC | 6 | a0002c0002t0001g0055a0002c0002t0001g0056a0002c0002t0001g0058others(3): Show | 6 | HG02257.hp1 HG03130.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.*7-3949_*7-3948ins others(6): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260379 | |||||
| chr2:97260379
|
T | TATATATA others(1): Show |
3 | a0002c0002t0001g0057a0002c0002t0001g0065a0005c0004t0005g0202 | 3 | HG02451.hp2 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.*7-3949_*7-3948ins others(8): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260379 | |||||
| chr2:97260379
|
T | TATATATA others(3): Show |
3 | a0001c0001t0002g0022a0001c0046t0002g0051a0024c0060t0002g0024 | 3 | HG01891.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.*7-3949_*7-3948ins others(10): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260379 | |||||
| chr2:97260379
|
T | TATATATA others(5): Show |
1 | a0044c0038t0001g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*7-3949_*7-3948ins others(12): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260379 | |||||
| chr2:97260379
|
T | TATATATA others(7): Show |
1 | a0001c0001t0002g0050 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.*7-3949_*7-3948ins others(14): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260379 | |||||
| chr2:97260379
|
T | TATATATA others(9): Show |
1 | a0029c0055t0002g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.*7-3949_*7-3948ins others(16): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260379 | |||||
| chr2:97260387
|
T | C | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.*7-3942T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260387 | ||||||
| chr2:97260388
|
A | G | 68 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(65): Show | 68 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.*7-3941A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260388 | ||||||
| chr2:97260389
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0115a0001c0001t0001g0117 | 3 | HG01070.hp1 HG01257.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.*7-3940T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260389 | ||||||
| chr2:97260410
|
A | G | 66 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(63): Show | 66 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.*7-3919A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260410 | ||||||
| chr2:97260425
|
AAC | A | 84 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(81): Show | 84 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.*7-3885_*7-3884del others(2): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260425 | |||||
| chr2:97260425
|
AACAC | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(63): Show | 66 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.*7-3887_*7-3884del others(4): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260425 | |||||
| chr2:97260488
|
G | A | 2 | a0037c0040t0002g0211a0042c0043t0002g0210 | 2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.*7-3841G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260488 | ||||||
| chr2:97260759
|
T | C | 3 | a0001c0001t0001g0014a0001c0001t0001g0115a0001c0001t0001g0117 | 3 | HG01070.hp1 HG01257.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.*7-3570T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260759 | ||||||
| chr2:97260845
|
C | T | 7 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(4): Show | 7 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.*7-3484C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260845 | ||||||
| chr2:97260855
|
T | C | 1 | a0002c0002t0001g0069 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.*7-3474T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260855 | ||||||
| chr2:97260977
|
T | TTAC | 148 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(145): Show | 148 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.*7-3350_*7-3349ins others(3): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97260977 | |||||
| chr2:97260980
|
G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(145): Show | 148 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.*7-3349G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97260980 | ||||||
| chr2:97261214
|
C | T | 1 | a0042c0043t0002g0210 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.*7-3115C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97261214 | ||||||
| chr2:97261296
|
C | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.*7-3033C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97261296 | ||||||
| chr2:97261388
|
G | A | 3 | a0014c0014t0001g0150a0014c0014t0001g0154a0014c0014t0001g0155 | 3 | HG00558.hp1 NA18946.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.*7-2941G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97261388 | ||||||
| chr2:97261452
|
C | T | 136 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(133): Show | 136 | HG00423.hp1 HG00423.hp2 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.*7-2877C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97261452 | ||||||
| chr2:97261462
|
G | A | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.*7-2867G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97261462 | ||||||
| chr2:97261567
|
A | C | 1 | a0050c0061t0001g0010 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.*7-2762A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97261567 | ||||||
| chr2:97261672
|
G | C | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.*7-2657G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97261672 | ||||||
| chr2:97261689
|
C | T | 2 | a0002c0002t0001g0017a0002c0002t0001g0068 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.*7-2640C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97261689 | ||||||
| chr2:97261828
|
C | G | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.*7-2501C>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97261828 | ||||||
| chr2:97262618
|
A | G | 147 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.*7-1711A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262618 | ||||||
| chr2:97262698
|
C | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.*7-1631C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262698 | ||||||
| chr2:97262710
|
T | C | 7 | a0009c0009t0002g0174a0009c0009t0002g0175a0009c0009t0002g0176others(4): Show | 7 | HG01261.hp1 HG01358.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.*7-1619T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262710 | ||||||
| chr2:97262761
|
C | T | 14 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(11): Show | 14 | HG02055.hp2 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.*7-1568C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262761 | ||||||
| chr2:97262779
|
G | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.*7-1550G>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262779 | ||||||
| chr2:97262785
|
T | TC | 147 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.*7-1543dupC | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97262785 | |||||
| chr2:97262930
|
C | T | 1 | a0029c0055t0002g0023 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.*7-1399C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262930 | ||||||
| chr2:97262943
|
A | ACCTAGTC others(21): Show |
61 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(58): Show | 61 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.*7-1386_*7-1385ins others(28): Show |
ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262943 | ||||||
| chr2:97262944
|
A | T | 61 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(58): Show | 61 | HG00423.hp2 HG00558.hp2 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.*7-1385A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262944 | ||||||
| chr2:97262963
|
A | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.*7-1366A>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262963 | ||||||
| chr2:97262998
|
G | A | 31 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0022others(28): Show | 31 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.*7-1331G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97262998 | ||||||
| chr2:97263074
|
T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.*7-1255T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263074 | ||||||
| chr2:97263123
|
T | A | 147 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.*7-1206T>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263123 | ||||||
| chr2:97263174
|
T | C | 147 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0019others(144): Show | 147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.*7-1155T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263174 | ||||||
| chr2:97263185
|
A | G | 1 | a0026c0058t0001g0074 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.*7-1144A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263185 | ||||||
| chr2:97263317
|
G | A | 6 | a0012c0010t0002g0026a0012c0010t0002g0027a0012c0010t0002g0028others(3): Show | 6 | HG01891.hp1 HG02559.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.*7-1012G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263317 | ||||||
| chr2:97263339
|
A | G | 1 | a0047c0033t0002g0025 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.*7-990A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263339 | ||||||
| chr2:97263578
|
C | T | 1 | a0026c0058t0001g0074 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.*7-751C>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263578 | ||||||
| chr2:97263580
|
CTT | C | 25 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(22): Show | 25 | HG00099.hp1 HG00423.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.*7-746_*7-745delTT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97263580 | |||||
| chr2:97263590
|
A | C | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.*7-739A>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263590 | ||||||
| chr2:97263713
|
T | C | 3 | a0003c0003t0001g0163a0003c0003t0001g0172a0006c0034t0001g0173 | 3 | HG02109.hp1 HG02897.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.*7-616T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263713 | ||||||
| chr2:97263815
|
A | AT | 10 | a0004c0005t0004g0016a0004c0005t0004g0032a0004c0005t0004g0033others(7): Show | 10 | HG00099.hp1 HG01099.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.*7-504dupT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97263815 | |||||
| chr2:97263815
|
AT | A | 16 | a0008c0006t0003g0184a0008c0006t0003g0190a0008c0006t0003g0191others(13): Show | 16 | HG00597.hp2 HG02071.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.*7-504delT | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | INFO_REALIGN_3_PRIME | chr2 | 97263815 | |||||
| chr2:97263939
|
G | A | 1 | a0044c0038t0001g0067 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.*7-390G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263939 | ||||||
| chr2:97263964
|
G | A | 9 | a0005c0004t0002g0129a0005c0004t0002g0130a0005c0004t0005g0199others(6): Show | 9 | HG00642.hp2 HG02258.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.*7-365G>A | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97263964 | ||||||
| chr2:97264107
|
A | G | 15 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(12): Show | 15 | HG00423.hp1 HG02572.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.*7-222A>G | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97264107 | ||||||
| chr2:97264123
|
G | T | 43 | a0002c0002t0002g0031a0002c0002t0002g0132a0002c0002t0002g0209others(40): Show | 43 | HG00099.hp1 HG00423.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.*7-206G>T | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97264123 | ||||||
| chr2:97264249
|
T | C | 7 | a0002c0002t0001g0052a0002c0002t0001g0053a0002c0002t0001g0054others(4): Show | 7 | HG02257.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.*7-80T>C | ANKRD36 | ENSG00000135976.21 | transcript | ENST00000420699.9 | protein_coding | 75/75 | chr2 | 97264249 |