| geneid | 23731 |
|---|---|
| ensemblid | ENSG00000106771.13 |
| hgncid | 1363 |
| symbol | TMEM245 |
| name | transmembrane protein 245 |
| refseq_nuc | NM_032012.4 |
| refseq_prot | NP_114401.2 |
| ensembl_nuc | ENST00000374586.8 |
| ensembl_prot | ENSP00000363714.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 109015135 |
| end | 109119947 |
| strand | - |
| ver | v1.2 |
| region | chr9:109015135-109119947 |
| region5000 | chr9:109010135-109124947 |
| regionname0 | TMEM245_chr9_109015135_109119947 |
| regionname5000 | TMEM245_chr9_109010135_109124947 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 879 | 270 | 64 | 45 | 123 | 5 | 31 | 97 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0002 | 0/0 | 879 | 75 | 0 | 23 | 43 | 4 | 5 | 35 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003 | 0/0 | 879 | 40 | 22 | 4 | 0 | 3 | 11 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0004 | 0/0 | 879 | 31 | 0 | 0 | 30 | 0 | 1 | 24 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0005 | 0/0 | 879 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0006 | 0/0 | 879 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0007 | 0/0 | 879 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0008 | 0/0 | 879 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2640 | 228 | 52 | 39 | 108 | 4 | 23 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| c0002 | 0/0 | 2640 | 75 | 0 | 23 | 43 | 4 | 5 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| c0003 | 0/0 | 2640 | 31 | 0 | 0 | 30 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| c0004 | 0/0 | 2640 | 30 | 14 | 2 | 0 | 3 | 11 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| c0005 | 0/0 | 2640 | 15 | 0 | 2 | 13 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| c0006 | 0/0 | 2640 | 13 | 12 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| c0007 | 0/0 | 2640 | 8 | 0 | 0 | 0 | 1 | 7 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| c0008 | 0/0 | 2640 | 7 | 5 | 2 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| c0009 | 0/0 | 2640 | 3 | 0 | 2 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| c0010 | 0/0 | 2640 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| c0011 | 0/0 | 2640 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| c0012 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| c0013 | 0/0 | 2640 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| c0014 | 0/0 | 2640 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| c0015 | 0/0 | 2640 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| c0016 | 0/0 | 2640 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| c0017 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| c0018 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| c0019 | 0/0 | 2640 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 5353 | 45 | 0 | 13 | 25 | 2 | 5 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0002 | 0/0 | 5360 | 39 | 0 | 10 | 22 | 2 | 5 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0003 | 0/0 | 5359 | 36 | 1 | 7 | 27 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0004 | 0/0 | 5358 | 30 | 1 | 3 | 18 | 0 | 8 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0005 | 0/0 | 5357 | 24 | 1 | 7 | 14 | 0 | 2 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0006 | 0/0 | 5359 | 13 | 0 | 0 | 9 | 1 | 3 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0007 | 0/0 | 5361 | 10 | 2 | 0 | 8 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0008 | 0/0 | 5359 | 9 | 7 | 1 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0009 | 0/0 | 5356 | 9 | 3 | 2 | 0 | 2 | 2 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0010 | 0/0 | 5355 | 8 | 7 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0011 | 0/0 | 5351 | 8 | 7 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0012 | 0/0 | 5354 | 6 | 0 | 3 | 3 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0013 | 0/0 | 5359 | 5 | 1 | 0 | 2 | 0 | 2 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0014 | 0/0 | 5361 | 5 | 0 | 2 | 2 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0015 | 0/0 | 5362 | 4 | 3 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0016 | 0/0 | 5358 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0017 | 0/0 | 5351 | 4 | 3 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0018 | 0/0 | 5355 | 4 | 0 | 2 | 0 | 1 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0019 | 0/0 | 5354 | 4 | 0 | 1 | 3 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0020 | 0/0 | 5354 | 4 | 0 | 3 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0021 | 0/0 | 5354 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0022 | 0/0 | 5357 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0023 | 0/0 | 5360 | 3 | 1 | 0 | 1 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0024 | 0/0 | 5359 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0025 | 0/0 | 5360 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0026 | 0/0 | 5359 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0027 | 0/0 | 5359 | 3 | 0 | 2 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0028 | 0/0 | 5357 | 3 | 0 | 0 | 2 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0029 | 0/0 | 5359 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0030 | 0/0 | 5363 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0031 | 0/0 | 5360 | 3 | 0 | 0 | 2 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0032 | 0/0 | 5361 | 3 | 0 | 1 | 1 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0033 | 0/0 | 5355 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0034 | 0/0 | 5358 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0035 | 0/0 | 5360 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0036 | 0/0 | 5360 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0037 | 0/0 | 5358 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0038 | 0/0 | 5358 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0039 | 0/0 | 5360 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0040 | 0/0 | 5359 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0041 | 1/0 | 5360 | 2 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0042 | 0/0 | 5363 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0043 | 0/0 | 5362 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0044 | 0/0 | 5360 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0045 | 0/0 | 5358 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0046 | 0/0 | 5362 | 2 | 0 | 1 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0047 | 0/0 | 5358 | 2 | 0 | 1 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0048 | 0/0 | 5359 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0049 | 0/0 | 5356 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0050 | 0/0 | 5354 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0051 | 0/0 | 5357 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0052 | 0/0 | 5355 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0053 | 0/0 | 5356 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0054 | 0/0 | 5351 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0055 | 0/0 | 5352 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0056 | 0/0 | 5353 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0057 | 0/0 | 5353 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0058 | 0/0 | 5357 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0059 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0060 | 0/0 | 5357 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0061 | 0/0 | 5359 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0062 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0063 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0064 | 0/0 | 5359 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0065 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0066 | 0/0 | 5360 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0067 | 0/0 | 5359 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0068 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0069 | 0/0 | 5360 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0070 | 0/0 | 5358 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0071 | 0/0 | 5357 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0072 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0073 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0074 | 0/0 | 5360 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0075 | 0/0 | 5362 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0076 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0077 | 0/0 | 5360 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0078 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0079 | 0/0 | 5360 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0080 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0081 | 0/0 | 5359 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0082 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0083 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0084 | 0/0 | 5356 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0085 | 0/0 | 5355 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0086 | 0/0 | 5359 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0087 | 0/0 | 5357 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0088 | 0/0 | 5352 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0089 | 0/0 | 5352 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0090 | 0/0 | 5358 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0091 | 0/0 | 5359 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0092 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0093 | 0/0 | 5355 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0094 | 0/0 | 5356 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0095 | 0/0 | 5350 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0096 | 0/0 | 5350 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0097 | 0/0 | 5360 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0098 | 0/0 | 5357 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0099 | 0/0 | 5357 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0100 | 0/0 | 5356 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0101 | 0/1 | 5358 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0102 | 0/0 | 5356 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0103 | 0/0 | 5355 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0104 | 0/0 | 5359 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0105 | 0/0 | 5351 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0106 | 0/0 | 5356 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0107 | 0/0 | 5357 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0108 | 0/0 | 5350 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0109 | 0/0 | 5359 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0110 | 0/0 | 5355 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0111 | 0/0 | 5352 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0112 | 0/0 | 5355 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0113 | 0/0 | 5354 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0114 | 0/0 | 5352 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0115 | 0/0 | 5353 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0116 | 0/0 | 5357 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0117 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0118 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| t0119 | 0/0 | 5359 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| 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 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0395 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0396 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0400 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0402 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0403 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0404 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0405 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0406 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0407 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0408 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0409 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0410 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0411 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0412 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0413 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0414 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0415 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0416 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0417 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0418 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0419 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| g0420 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2640 | 228 | 52 | 39 | 108 | 4 | 23 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0005 | 0/0 | 2640 | 15 | 0 | 2 | 13 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0006 | 0/0 | 2640 | 13 | 12 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0007 | 0/0 | 2640 | 8 | 0 | 0 | 0 | 1 | 7 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0009 | 0/0 | 2640 | 3 | 0 | 2 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0013 | 0/0 | 2640 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0015 | 0/0 | 2640 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0016 | 0/0 | 2640 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0002c0002 | 0/0 | 2640 | 75 | 0 | 23 | 43 | 4 | 5 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0004 | 0/0 | 2640 | 30 | 14 | 2 | 0 | 3 | 11 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0008 | 0/0 | 2640 | 7 | 5 | 2 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0012 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0017 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0018 | 0/0 | 2640 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0004c0003 | 0/0 | 2640 | 31 | 0 | 0 | 30 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0005c0010 | 0/0 | 2640 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0006c0011 | 0/0 | 2640 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0007c0014 | 0/0 | 2640 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0008c0019 | 0/0 | 2640 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 0/0 | 7999 | 13 | 0 | 8 | 0 | 2 | 3 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0003 | 0/0 | 7998 | 24 | 1 | 5 | 17 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0004 | 0/0 | 7997 | 24 | 1 | 3 | 17 | 0 | 3 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0005 | 0/0 | 7996 | 24 | 1 | 7 | 14 | 0 | 2 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0006 | 0/0 | 7998 | 13 | 0 | 0 | 9 | 1 | 3 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0007 | 0/0 | 8000 | 10 | 2 | 0 | 8 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0008 | 0/0 | 7998 | 9 | 7 | 1 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0009 | 0/0 | 7995 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0011 | 0/0 | 7990 | 4 | 3 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0013 | 0/0 | 7998 | 5 | 1 | 0 | 2 | 0 | 2 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0014 | 0/0 | 8000 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0015 | 0/0 | 8001 | 4 | 3 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0016 | 0/0 | 7997 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0022 | 0/0 | 7996 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0023 | 0/0 | 7999 | 3 | 1 | 0 | 1 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0025 | 0/0 | 7999 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0026 | 0/0 | 7998 | 3 | 3 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0027 | 0/0 | 7998 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0028 | 0/0 | 7996 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0029 | 0/0 | 7998 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0030 | 0/0 | 8002 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0031 | 0/0 | 7999 | 3 | 0 | 0 | 2 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0032 | 0/0 | 8000 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0034 | 0/0 | 7997 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0035 | 0/0 | 7999 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0036 | 0/0 | 7999 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0037 | 0/0 | 7997 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0038 | 0/0 | 7997 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0039 | 0/0 | 7999 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0040 | 0/0 | 7998 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0041 | 1/0 | 7999 | 2 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0042 | 0/0 | 8002 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0043 | 0/0 | 8001 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0044 | 0/0 | 7999 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0045 | 0/0 | 7997 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0046 | 0/0 | 8001 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0047 | 0/0 | 7997 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0053 | 0/0 | 7995 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0054 | 0/0 | 7990 | 2 | 1 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0055 | 0/0 | 7991 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0058 | 0/0 | 7996 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0059 | 0/0 | 8000 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0061 | 0/0 | 7998 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0063 | 0/0 | 8000 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0064 | 0/0 | 7998 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0065 | 0/0 | 8000 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0066 | 0/0 | 7999 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0067 | 0/0 | 7998 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0068 | 0/0 | 8000 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0069 | 0/0 | 7999 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0070 | 0/0 | 7997 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0071 | 0/0 | 7996 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0072 | 0/0 | 7997 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0073 | 0/0 | 8000 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0074 | 0/0 | 7999 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0075 | 0/0 | 8001 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0076 | 0/0 | 8000 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0077 | 0/0 | 7999 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0078 | 0/0 | 8000 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0079 | 0/0 | 7999 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0080 | 0/0 | 8000 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0081 | 0/0 | 7998 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0083 | 0/0 | 8000 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0091 | 0/0 | 7998 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0092 | 0/0 | 7997 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0093 | 0/0 | 7994 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0097 | 0/0 | 7999 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0098 | 0/0 | 7996 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0099 | 0/0 | 7996 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0100 | 0/0 | 7995 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0101 | 0/1 | 7997 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0105 | 0/0 | 7990 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0106 | 0/0 | 7995 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0107 | 0/0 | 7996 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0108 | 0/0 | 7989 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0001t0119 | 0/0 | 7998 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0005t0003 | 0/0 | 7998 | 11 | 0 | 2 | 9 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0005t0024 | 0/0 | 7998 | 3 | 0 | 0 | 3 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0005t0060 | 0/0 | 7996 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0006t0011 | 0/0 | 7990 | 4 | 4 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0006t0033 | 0/0 | 7994 | 3 | 2 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0006t0050 | 0/0 | 7993 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0006t0055 | 0/0 | 7991 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0006t0084 | 0/0 | 7995 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0006t0085 | 0/0 | 7994 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0006t0104 | 0/0 | 7998 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0007t0004 | 0/0 | 7997 | 5 | 0 | 0 | 0 | 0 | 5 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0007t0027 | 0/0 | 7998 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0007t0028 | 0/0 | 7996 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0007t0062 | 0/0 | 7997 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0009t0018 | 0/0 | 7994 | 3 | 0 | 2 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0013t0090 | 0/0 | 7997 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0015t0004 | 0/0 | 7997 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0001c0016t0030 | 0/0 | 8002 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0002c0002t0001 | 0/0 | 7992 | 44 | 0 | 12 | 25 | 2 | 5 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0002c0002t0002 | 0/0 | 7999 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0002c0002t0012 | 0/0 | 7993 | 6 | 0 | 3 | 3 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0002c0002t0019 | 0/0 | 7993 | 4 | 0 | 1 | 3 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0002c0002t0020 | 0/0 | 7993 | 4 | 0 | 3 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0002c0002t0021 | 0/0 | 7993 | 4 | 0 | 0 | 4 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0002c0002t0056 | 0/0 | 7992 | 2 | 0 | 0 | 0 | 2 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0002c0002t0057 | 0/0 | 7992 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0002c0002t0109 | 0/0 | 7998 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0002c0002t0110 | 0/0 | 7994 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0002c0002t0111 | 0/0 | 7991 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0002c0002t0112 | 0/0 | 7994 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0002c0002t0113 | 0/0 | 7993 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0002c0002t0114 | 0/0 | 7991 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0002c0002t0115 | 0/0 | 7992 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0004t0002 | 0/0 | 7999 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0004t0009 | 0/0 | 7995 | 6 | 1 | 2 | 0 | 1 | 2 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0004t0010 | 0/0 | 7994 | 8 | 7 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0004t0014 | 0/0 | 8000 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0004t0018 | 0/0 | 7994 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0004t0049 | 0/0 | 7995 | 2 | 0 | 0 | 0 | 0 | 2 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0004t0051 | 0/0 | 7996 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0004t0052 | 0/0 | 7994 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0004t0086 | 0/0 | 7998 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0004t0087 | 0/0 | 7996 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0004t0102 | 0/0 | 7995 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0004t0103 | 0/0 | 7994 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0004t0116 | 0/0 | 7996 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0004t0118 | 0/0 | 7997 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0008t0017 | 0/0 | 7990 | 4 | 3 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0008t0089 | 0/0 | 7991 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0008t0095 | 0/0 | 7989 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0008t0096 | 0/0 | 7989 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0012t0088 | 0/0 | 7991 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0017t0117 | 0/0 | 7997 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0003c0018t0094 | 0/0 | 7995 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0004c0003t0002 | 0/0 | 7999 | 22 | 0 | 0 | 22 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0004c0003t0014 | 0/0 | 8000 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0004c0003t0032 | 0/0 | 8000 | 2 | 0 | 0 | 1 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0004c0003t0043 | 0/0 | 8001 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0004c0003t0046 | 0/0 | 8001 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0004c0003t0048 | 0/0 | 7998 | 2 | 0 | 0 | 2 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0004c0003t0082 | 0/0 | 7997 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0005c0010t0003 | 0/0 | 7998 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0005c0010t0036 | 0/0 | 7999 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0006c0011t0009 | 0/0 | 7995 | 2 | 2 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0007c0014t0047 | 0/0 | 7997 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| a0008c0019t0001 | 0/0 | 7992 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | copy fasta | chr9 | 109010135 | 109124947 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0006g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0006g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0006g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0007g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0007g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0007g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0007g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0007g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0007g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0008g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0008g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0008g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0008g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0008g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0008g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0008g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0008g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0009g0030 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0011g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0011g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0011g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0011g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0013g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0013g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0013g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0013g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0013g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0014g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0014g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0015g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0015g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0015g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0015g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0016g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0016g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0016g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0016g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0022g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0022g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0022g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0023g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0023g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0023g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0025g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0025g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0025g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0026g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0026g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0026g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0027g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0027g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0028g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0028g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0029g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0029g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0029g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0030g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0030g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0031g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0031g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0031g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0032g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0034g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0034g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0034g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0035g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0035g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0036g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0037g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0037g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0038g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0038g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0039g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0039g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0040g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0040g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0041g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0041g0238 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0042g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0042g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0043g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0044g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0044g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0045g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0045g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0046g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0047g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0053g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0053g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0054g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0054g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0055g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0058g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0059g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0061g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0063g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0064g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0065g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0066g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0067g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0068g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0069g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0070g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0071g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0072g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0073g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0074g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0075g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0076g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0077g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0078g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0079g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0080g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0081g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0083g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0091g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0092g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0093g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0097g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0098g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0099g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0100g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0101g0151 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0105g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0106g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0107g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0108g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0001t0119g0420 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0005t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0005t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0005t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0005t0003g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0005t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0005t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0005t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0005t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0005t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0005t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0005t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0005t0024g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0005t0024g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0005t0024g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0005t0060g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0006t0011g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0006t0011g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0006t0011g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0006t0011g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0006t0033g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0006t0033g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0006t0033g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0006t0050g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0006t0050g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0006t0055g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0006t0084g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0006t0085g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0006t0104g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0007t0004g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0007t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0007t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0007t0004g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0007t0004g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0007t0027g0298 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0007t0028g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0007t0062g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0009t0018g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0009t0018g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0013t0090g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0015t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0001c0016t0030g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0382 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0383 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0384 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0385 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0387 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0388 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0390 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0391 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0392 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0393 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0394 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0395 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0397 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0398 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0403 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0404 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0407 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0411 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0412 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0413 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0414 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0415 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0417 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0001g0419 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0002g0409 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0002g0410 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0012g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0012g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0012g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0012g0389 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0012g0399 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0012g0401 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0019g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0019g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0019g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0019g0396 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0020g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0020g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0020g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0020g0400 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0021g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0021g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0021g0386 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0021g0405 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0056g0358 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0056g0360 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0057g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0057g0402 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0109g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0110g0418 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0111g0408 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0112g0380 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0113g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0114g0416 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0002c0002t0115g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0002g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0009g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0009g0329 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0009g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0009g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0009g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0009g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0010g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0010g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0010g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0010g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0010g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0010g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0010g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0010g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0014g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0018g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0049g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0049g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0051g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0051g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0052g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0052g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0086g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0087g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0102g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0103g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0116g0342 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0004t0118g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0008t0017g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0008t0017g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0008t0017g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0008t0017g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0008t0089g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0008t0095g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0008t0096g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0012t0088g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0017t0117g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0003c0018t0094g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0014g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0014g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0032g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0032g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0043g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0046g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0048g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0048g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0004c0003t0082g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0005c0010t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0005c0010t0036g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0006c0011t0009g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0006c0011t0009g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0007c0014t0047g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| a0008c0019t0001g0406 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0359 | EUR | GBR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00099 | hp2 | a0003 | c0004 | t0009 | g0329 | EUR | GBR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0051 | EUR | GBR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00140 | hp2 | a0001 | c0001 | t0009 | g0030 | EUR | GBR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00408 | hp1 | a0004 | c0003 | t0014 | g0073 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0150 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0377 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00438 | hp2 | a0001 | c0001 | t0037 | g0214 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00544 | hp1 | a0001 | c0001 | t0044 | g0093 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00544 | hp2 | a0001 | c0001 | t0036 | g0204 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00558 | hp1 | a0001 | c0001 | t0004 | g0216 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00558 | hp2 | a0001 | c0001 | t0016 | g0085 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00609 | hp1 | a0001 | c0001 | t0005 | g0137 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00609 | hp2 | a0001 | c0001 | t0007 | g0107 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00621 | hp1 | a0002 | c0002 | t0019 | g0350 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00621 | hp2 | a0004 | c0003 | t0046 | g0037 | EAS | CHS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00639 | hp1 | a0007 | c0014 | t0047 | g0243 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00639 | hp2 | a0001 | c0001 | t0041 | g0170 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00733 | hp1 | a0003 | c0008 | t0017 | g0308 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0274 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0390 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0364 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00738 | hp2 | a0001 | c0001 | t0014 | g0032 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG00741 | hp2 | a0008 | c0019 | t0001 | g0406 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01069 | hp2 | a0001 | c0001 | t0027 | g0236 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0249 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0366 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0235 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0145 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01081 | hp2 | a0001 | c0001 | t0065 | g0248 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01099 | hp1 | a0001 | c0001 | t0005 | g0139 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0395 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01106 | hp1 | a0003 | c0004 | t0009 | g0340 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01106 | hp2 | a0001 | c0001 | t0046 | g0039 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01109 | hp1 | a0003 | c0008 | t0095 | g0306 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01109 | hp2 | a0001 | c0013 | t0090 | g0023 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0410 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0361 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01168 | hp1 | a0001 | c0001 | t0014 | g0076 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0152 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0409 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0129 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01175 | hp2 | a0002 | c0002 | t0019 | g0396 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0393 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0164 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01243 | hp1 | a0001 | c0001 | t0011 | g0277 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01243 | hp2 | a0001 | c0001 | t0054 | g0174 | AMR | PUR | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01255 | hp1 | a0001 | c0001 | t0066 | g0187 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01255 | hp2 | a0001 | c0001 | t0119 | g0420 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0250 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01256 | hp2 | a0001 | c0001 | t0107 | g0156 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0347 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01257 | hp2 | a0001 | c0001 | t0005 | g0146 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01261 | hp1 | a0001 | c0006 | t0033 | g0290 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01261 | hp2 | a0002 | c0002 | t0020 | g0400 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0394 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0244 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01358 | hp1 | a0002 | c0002 | t0020 | g0345 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01358 | hp2 | a0003 | c0004 | t0009 | g0341 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0391 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01361 | hp2 | a0001 | c0001 | t0032 | g0191 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01433 | hp1 | a0001 | c0009 | t0018 | g0002 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01433 | hp2 | a0002 | c0002 | t0112 | g0380 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01496 | hp1 | a0001 | c0009 | t0018 | g0002 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0371 | EUR | IBS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01515 | hp2 | a0003 | c0004 | t0018 | g0325 | EUR | IBS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0047 | EUR | IBS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01516 | hp2 | a0002 | c0002 | t0056 | g0360 | EUR | IBS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01517 | hp1 | a0003 | c0004 | t0102 | g0324 | EUR | IBS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01517 | hp2 | a0002 | c0002 | t0056 | g0358 | EUR | IBS | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01884 | hp1 | a0001 | c0006 | t0055 | g0285 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01884 | hp2 | a0001 | c0001 | t0081 | g0044 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0101 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01891 | hp2 | a0001 | c0001 | t0078 | g0118 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01934 | hp1 | a0002 | c0002 | t0001 | g0346 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01934 | hp2 | a0001 | c0001 | t0005 | g0133 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01952 | hp1 | a0001 | c0001 | t0070 | g0197 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01952 | hp2 | a0002 | c0002 | t0020 | g0348 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01978 | hp1 | a0002 | c0002 | t0109 | g0344 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01978 | hp2 | a0001 | c0005 | t0003 | g0012 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02004 | hp1 | a0002 | c0002 | t0012 | g0355 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02004 | hp2 | a0001 | c0001 | t0005 | g0147 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02015 | hp1 | a0001 | c0001 | t0006 | g0092 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02015 | hp2 | a0001 | c0005 | t0060 | g0013 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0372 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02027 | hp2 | a0001 | c0001 | t0016 | g0087 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02040 | hp1 | a0001 | c0005 | t0024 | g0017 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0217 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02055 | hp1 | a0001 | c0001 | t0108 | g0083 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02055 | hp2 | a0001 | c0001 | t0059 | g0269 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0354 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02056 | hp2 | a0004 | c0003 | t0002 | g0038 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02071 | hp1 | a0001 | c0001 | t0013 | g0230 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0212 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02074 | hp1 | a0001 | c0001 | t0016 | g0086 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02074 | hp2 | a0001 | c0001 | t0013 | g0229 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02080 | hp1 | a0002 | c0002 | t0021 | g0386 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02080 | hp2 | a0004 | c0003 | t0002 | g0069 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02083 | hp2 | a0001 | c0001 | t0005 | g0134 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02129 | hp1 | a0001 | c0001 | t0006 | g0091 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02129 | hp2 | a0002 | c0002 | t0057 | g0402 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0218 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02132 | hp2 | a0001 | c0001 | t0007 | g0112 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02145 | hp1 | a0003 | c0008 | t0089 | g0305 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02145 | hp2 | a0001 | c0001 | t0025 | g0184 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02148 | hp1 | a0002 | c0002 | t0012 | g0389 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02148 | hp2 | a0001 | c0001 | t0027 | g0196 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0231 | EAS | CDX | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0403 | EAS | CDX | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02257 | hp1 | a0001 | c0001 | t0040 | g0272 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02257 | hp2 | a0003 | c0008 | t0017 | g0309 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02273 | hp2 | a0001 | c0005 | t0003 | g0019 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02293 | hp1 | a0001 | c0001 | t0064 | g0245 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0349 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02300 | hp2 | a0002 | c0002 | t0012 | g0373 | AMR | PEL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0275 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02451 | hp2 | a0003 | c0004 | t0010 | g0318 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0157 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | KHV | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02572 | hp1 | a0001 | c0006 | t0033 | g0292 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02572 | hp2 | a0001 | c0001 | t0069 | g0173 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0241 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02602 | hp2 | a0001 | c0001 | t0005 | g0154 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02615 | hp1 | a0001 | c0006 | t0011 | g0281 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02615 | hp2 | a0003 | c0004 | t0118 | g0332 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02622 | hp1 | a0001 | c0001 | t0068 | g0158 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02622 | hp2 | a0001 | c0001 | t0022 | g0005 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02630 | hp1 | a0001 | c0001 | t0008 | g0162 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02630 | hp2 | a0003 | c0004 | t0051 | g0314 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02647 | hp1 | a0001 | c0001 | t0058 | g0006 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02647 | hp2 | a0001 | c0006 | t0011 | g0280 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02698 | hp1 | a0001 | c0001 | t0099 | g0128 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02698 | hp2 | a0001 | c0001 | t0047 | g0031 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02717 | hp1 | a0001 | c0001 | t0022 | g0003 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02717 | hp2 | a0003 | c0004 | t0010 | g0317 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02723 | hp1 | a0001 | c0001 | t0040 | g0271 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02723 | hp2 | a0001 | c0001 | t0008 | g0163 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0357 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02735 | hp2 | a0001 | c0007 | t0004 | g0299 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02738 | hp1 | a0003 | c0004 | t0049 | g0331 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02738 | hp2 | a0001 | c0001 | t0013 | g0273 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02809 | hp1 | a0001 | c0001 | t0026 | g0234 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02809 | hp2 | a0001 | c0001 | t0015 | g0027 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0077 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0105 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02886 | hp1 | a0003 | c0004 | t0052 | g0320 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02886 | hp2 | a0001 | c0001 | t0015 | g0026 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02895 | hp1 | a0006 | c0011 | t0009 | g0339 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02895 | hp2 | a0001 | c0006 | t0011 | g0282 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02922 | hp1 | a0003 | c0012 | t0088 | g0022 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02965 | hp1 | a0003 | c0004 | t0010 | g0315 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02965 | hp2 | a0001 | c0001 | t0008 | g0166 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02970 | hp1 | a0001 | c0001 | t0011 | g0189 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02970 | hp2 | a0001 | c0001 | t0015 | g0028 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0168 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02976 | hp2 | a0001 | c0001 | t0026 | g0233 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03017 | hp1 | a0003 | c0004 | t0009 | g0326 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0242 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03041 | hp1 | a0003 | c0004 | t0010 | g0343 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03041 | hp2 | a0001 | c0001 | t0011 | g0278 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03098 | hp1 | a0001 | c0006 | t0084 | g0291 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03098 | hp2 | a0001 | c0001 | t0045 | g0172 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03130 | hp1 | a0003 | c0004 | t0052 | g0319 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03130 | hp2 | a0001 | c0001 | t0079 | g0119 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03139 | hp1 | a0003 | c0004 | t0010 | g0316 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03139 | hp2 | a0001 | c0001 | t0026 | g0183 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03195 | hp1 | a0001 | c0001 | t0093 | g0029 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03195 | hp2 | a0003 | c0008 | t0017 | g0304 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03209 | hp1 | a0001 | c0001 | t0022 | g0004 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03209 | hp2 | a0001 | c0001 | t0080 | g0033 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03225 | hp1 | a0001 | c0006 | t0011 | g0283 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03225 | hp2 | a0001 | c0001 | t0054 | g0176 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0382 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03239 | hp2 | a0003 | c0004 | t0009 | g0330 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03453 | hp1 | a0003 | c0004 | t0086 | g0334 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03453 | hp2 | a0003 | c0018 | t0094 | g0307 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03486 | hp1 | a0003 | c0008 | t0017 | g0310 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03486 | hp2 | a0001 | c0001 | t0045 | g0169 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0383 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03490 | hp2 | a0001 | c0007 | t0028 | g0297 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0195 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03492 | hp1 | a0001 | c0007 | t0004 | g0300 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03516 | hp1 | a0001 | c0001 | t0025 | g0198 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03516 | hp2 | a0001 | c0001 | t0077 | g0104 | AFR | ESN | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0161 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03540 | hp2 | a0006 | c0011 | t0009 | g0338 | AFR | GWD | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03579 | hp1 | a0001 | c0001 | t0008 | g0167 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0239 | AFR | MSL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03654 | hp1 | a0001 | c0001 | t0013 | g0247 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03654 | hp2 | a0003 | c0004 | t0002 | g0322 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03669 | hp1 | a0003 | c0004 | t0116 | g0342 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03669 | hp2 | a0001 | c0007 | t0004 | g0294 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03688 | hp1 | a0001 | c0001 | t0005 | g0123 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03688 | hp2 | a0003 | c0004 | t0014 | g0321 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03704 | hp1 | a0001 | c0007 | t0062 | g0295 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03704 | hp2 | a0003 | c0004 | t0103 | g0328 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03710 | hp1 | a0003 | c0004 | t0010 | g0336 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0363 | SAS | PJL | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0035 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03831 | hp2 | a0003 | c0004 | t0087 | g0327 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03834 | hp1 | a0001 | c0007 | t0004 | g0301 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03834 | hp2 | a0001 | c0001 | t0006 | g0100 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03927 | hp1 | a0004 | c0003 | t0032 | g0061 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0202 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03942 | hp1 | a0001 | c0001 | t0043 | g0050 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG03942 | hp2 | a0001 | c0001 | t0008 | g0171 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG04115 | hp1 | a0001 | c0001 | t0031 | g0079 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG04115 | hp2 | a0001 | c0009 | t0018 | g0302 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG04184 | hp1 | a0003 | c0004 | t0002 | g0323 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG04184 | hp2 | a0001 | c0001 | t0038 | g0252 | SAS | BEB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG04199 | hp1 | a0003 | c0004 | t0049 | g0333 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG04199 | hp2 | a0001 | c0001 | t0072 | g0192 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0090 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG04204 | hp2 | a0001 | c0001 | t0073 | g0177 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG04228 | hp1 | a0001 | c0001 | t0006 | g0088 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG04228 | hp2 | a0001 | c0001 | t0023 | g0259 | SAS | STU | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18522 | hp1 | a0003 | c0004 | t0010 | g0312 | AFR | YRI | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18522 | hp2 | a0003 | c0008 | t0096 | g0303 | AFR | YRI | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | CHB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18612 | hp2 | a0004 | c0003 | t0002 | g0054 | EAS | CHB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18747 | hp1 | a0004 | c0003 | t0048 | g0055 | EAS | CHB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0368 | EAS | CHB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0160 | AFR | YRI | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18906 | hp2 | a0001 | c0006 | t0033 | g0289 | AFR | YRI | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18939 | hp1 | a0001 | c0001 | t0034 | g0153 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18939 | hp2 | a0004 | c0003 | t0002 | g0040 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18940 | hp2 | a0001 | c0001 | t0030 | g0115 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18941 | hp1 | a0001 | c0001 | t0034 | g0136 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0376 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0135 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0404 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18943 | hp1 | a0004 | c0003 | t0002 | g0065 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18943 | hp2 | a0001 | c0001 | t0042 | g0114 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0374 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18944 | hp2 | a0004 | c0003 | t0002 | g0063 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18945 | hp1 | a0001 | c0005 | t0003 | g0014 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18945 | hp2 | a0004 | c0003 | t0002 | g0059 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18946 | hp1 | a0002 | c0002 | t0114 | g0416 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18946 | hp2 | a0001 | c0001 | t0007 | g0179 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18948 | hp1 | a0001 | c0001 | t0029 | g0260 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18948 | hp2 | a0001 | c0001 | t0028 | g0224 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0365 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18949 | hp2 | a0001 | c0015 | t0004 | g0268 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18950 | hp2 | a0004 | c0003 | t0014 | g0270 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18951 | hp1 | a0004 | c0003 | t0002 | g0057 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18951 | hp2 | a0001 | c0001 | t0076 | g0103 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18952 | hp2 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18954 | hp2 | a0004 | c0003 | t0002 | g0052 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0412 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18956 | hp2 | a0001 | c0001 | t0106 | g0138 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18957 | hp1 | a0001 | c0001 | t0004 | g0182 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18957 | hp2 | a0001 | c0001 | t0053 | g0279 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0411 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18959 | hp2 | a0004 | c0003 | t0002 | g0071 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18961 | hp1 | a0002 | c0002 | t0012 | g0379 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18961 | hp2 | a0001 | c0001 | t0006 | g0078 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18962 | hp1 | a0004 | c0003 | t0002 | g0041 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18963 | hp1 | a0001 | c0001 | t0030 | g0110 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18963 | hp2 | a0002 | c0002 | t0001 | g0398 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18964 | hp1 | a0001 | c0001 | t0083 | g0109 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18965 | hp1 | a0001 | c0001 | t0029 | g0199 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18965 | hp2 | a0001 | c0001 | t0071 | g0240 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18966 | hp1 | a0004 | c0003 | t0002 | g0058 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0397 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18967 | hp1 | a0002 | c0002 | t0019 | g0352 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0149 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18968 | hp1 | a0001 | c0001 | t0098 | g0132 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18968 | hp2 | a0002 | c0002 | t0021 | g0405 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18971 | hp1 | a0001 | c0001 | t0005 | g0140 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18971 | hp2 | a0002 | c0002 | t0012 | g0399 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18972 | hp1 | a0004 | c0003 | t0043 | g0062 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0155 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18973 | hp1 | a0001 | c0001 | t0007 | g0180 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0392 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18974 | hp1 | a0004 | c0003 | t0002 | g0072 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0385 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18975 | hp1 | a0001 | c0005 | t0003 | g0020 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18977 | hp1 | a0001 | c0001 | t0007 | g0106 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0387 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18979 | hp1 | a0001 | c0005 | t0003 | g0015 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18979 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18981 | hp1 | a0004 | c0003 | t0002 | g0056 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18982 | hp1 | a0004 | c0003 | t0032 | g0053 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18982 | hp2 | a0001 | c0001 | t0029 | g0211 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0414 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0351 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18984 | hp2 | a0001 | c0001 | t0006 | g0175 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18985 | hp1 | a0001 | c0001 | t0097 | g0131 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18986 | hp1 | a0001 | c0001 | t0035 | g0254 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18986 | hp2 | a0002 | c0002 | t0111 | g0408 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18988 | hp1 | a0001 | c0001 | t0034 | g0130 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18988 | hp2 | a0002 | c0002 | t0115 | g0375 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18989 | hp1 | a0001 | c0005 | t0024 | g0018 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18989 | hp2 | a0001 | c0001 | t0044 | g0080 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18990 | hp1 | a0001 | c0001 | t0092 | g0122 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0378 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18992 | hp2 | a0001 | c0001 | t0016 | g0084 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18994 | hp1 | a0001 | c0001 | t0042 | g0116 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0142 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18995 | hp1 | a0002 | c0002 | t0113 | g0353 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18998 | hp1 | a0001 | c0001 | t0006 | g0095 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18998 | hp2 | a0005 | c0010 | t0003 | g0025 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18999 | hp1 | a0001 | c0001 | t0063 | g0124 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18999 | hp2 | a0001 | c0001 | t0007 | g0108 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19000 | hp1 | a0001 | c0001 | t0031 | g0081 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19000 | hp2 | a0002 | c0002 | t0012 | g0401 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19002 | hp1 | a0001 | c0001 | t0006 | g0099 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0417 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19003 | hp1 | a0001 | c0001 | t0007 | g0111 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19003 | hp2 | a0002 | c0002 | t0021 | g0381 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0415 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19005 | hp1 | a0004 | c0003 | t0002 | g0060 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0384 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19006 | hp1 | a0001 | c0001 | t0015 | g0178 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19006 | hp2 | a0002 | c0002 | t0110 | g0418 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0407 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19007 | hp2 | a0004 | c0003 | t0002 | g0064 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19010 | hp1 | a0001 | c0001 | t0028 | g0226 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19011 | hp1 | a0001 | c0005 | t0003 | g0009 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19012 | hp1 | a0001 | c0001 | t0005 | g0148 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19012 | hp2 | a0001 | c0001 | t0006 | g0094 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19030 | hp1 | a0001 | c0001 | t0025 | g0262 | AFR | LWK | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19030 | hp2 | a0003 | c0004 | t0010 | g0313 | AFR | LWK | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19043 | hp1 | a0001 | c0001 | t0055 | g0188 | AFR | LWK | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19043 | hp2 | a0003 | c0017 | t0117 | g0311 | AFR | LWK | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19054 | hp1 | a0002 | c0002 | t0020 | g0370 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19057 | hp1 | a0001 | c0001 | t0035 | g0253 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19057 | hp2 | a0001 | c0016 | t0030 | g0293 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19060 | hp1 | a0001 | c0001 | t0023 | g0208 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19060 | hp2 | a0001 | c0005 | t0024 | g0011 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19063 | hp2 | a0001 | c0001 | t0037 | g0258 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19064 | hp1 | a0002 | c0002 | t0057 | g0369 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19064 | hp2 | a0004 | c0003 | t0002 | g0075 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0413 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19065 | hp2 | a0001 | c0001 | t0005 | g0143 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19066 | hp1 | a0001 | c0001 | t0074 | g0181 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19066 | hp2 | a0001 | c0005 | t0003 | g0007 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19070 | hp1 | a0004 | c0003 | t0002 | g0066 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19072 | hp1 | a0002 | c0002 | t0001 | g0419 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19072 | hp2 | a0001 | c0001 | t0006 | g0096 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19075 | hp1 | a0001 | c0001 | t0007 | g0113 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19075 | hp2 | a0001 | c0001 | t0091 | g0127 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19077 | hp2 | a0001 | c0001 | t0006 | g0089 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19078 | hp1 | a0002 | c0002 | t0019 | g0356 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19078 | hp2 | a0001 | c0001 | t0031 | g0097 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19080 | hp1 | a0005 | c0010 | t0036 | g0024 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19080 | hp2 | a0004 | c0003 | t0002 | g0074 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19082 | hp1 | a0001 | c0001 | t0053 | g0126 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19082 | hp2 | a0001 | c0005 | t0003 | g0016 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19084 | hp1 | a0004 | c0003 | t0002 | g0070 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19084 | hp2 | a0001 | c0001 | t0038 | g0209 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19085 | hp1 | a0001 | c0001 | t0075 | g0102 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19085 | hp2 | a0002 | c0002 | t0021 | g0367 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19086 | hp1 | a0001 | c0005 | t0003 | g0010 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19086 | hp2 | a0004 | c0003 | t0082 | g0036 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19088 | hp1 | a0001 | c0005 | t0003 | g0008 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19088 | hp2 | a0004 | c0003 | t0002 | g0068 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19090 | hp1 | a0004 | c0003 | t0002 | g0067 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0141 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19240 | hp1 | a0001 | c0006 | t0050 | g0286 | AFR | YRI | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA19240 | hp2 | a0001 | c0001 | t0061 | g0186 | AFR | YRI | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0098 | EUR | TSI | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA20805 | hp2 | a0001 | c0007 | t0027 | g0298 | EUR | TSI | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA20905 | hp1 | a0001 | c0007 | t0004 | g0296 | SAS | GIH | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0388 | SAS | GIH | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0210 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0362 | AMR | CLM | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02109 | hp1 | a0001 | c0006 | t0104 | g0284 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02109 | hp2 | a0001 | c0001 | t0067 | g0185 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02486 | hp1 | a0001 | c0001 | t0039 | g0159 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02486 | hp2 | a0001 | c0006 | t0050 | g0288 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02559 | hp1 | a0003 | c0004 | t0009 | g0337 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG02559 | hp2 | a0001 | c0001 | t0023 | g0200 | AFR | ACB | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG06807 | hp1 | a0001 | c0001 | t0105 | g0276 | AFR | USA | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| HG06807 | hp2 | a0001 | c0001 | t0039 | g0165 | AFR | USA | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18955 | hp1 | a0004 | c0003 | t0048 | g0120 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA18955 | hp2 | a0001 | c0005 | t0003 | g0021 | EAS | JPT | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA20300 | hp1 | a0001 | c0001 | t0013 | g0237 | AFR | USA | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA20300 | hp2 | a0001 | c0006 | t0085 | g0287 | AFR | USA | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA21309 | hp1 | a0003 | c0004 | t0051 | g0335 | AFR | LWK | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| NA21309 | hp2 | a0001 | c0001 | t0100 | g0144 | AFR | LWK | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0101 | g0151 | REF | REF | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0041 | g0238 | REF | REF | TMEM245_chr9_109010135_109124947 | TMEM245 | chr9 | 109010135 | 109124947 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:109015136
|
T | G | 1 | a0002 | 1 | NA18995.hp1 | splice_region_variant | LOW | c.*5324A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | chr9 | 109015136 | ||||||
| chr9:109036233
|
T | C | 1 | a0007 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.2372A>G | p.Asp791Gly | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/18 | 2406/7999 | 2372/2640 | 791/879 | chr9 | 109036233 | ||
| chr9:109091132
|
C | T | 1 | a0004 | 31 | HG00408.hp1 HG00621.hp2 HG02056.hp2 others(28): Show |
missense_variant | MODERATE | c.940G>A | p.Ala314Thr | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/18 | 974/7999 | 940/2640 | 314/879 | chr9 | 109091132 | ||
| chr9:109108507
|
G | A | 1 | a0006 | 2 | HG02895.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.643C>T | p.Arg215Cys | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/18 | 677/7999 | 643/2640 | 215/879 | chr9 | 109108507 | ||
| chr9:109108521
|
T | C | 1 | a0008 | 1 | HG00741.hp2 | missense_variant | MODERATE | c.629A>G | p.Asn210Ser | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/18 | 663/7999 | 629/2640 | 210/879 | chr9 | 109108521 | ||
| chr9:109119576
|
T | C | 2 | a0002a0008 | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
missense_variant | MODERATE | c.338A>G | p.His113Arg | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 372/7999 | 338/2640 | 113/879 | chr9 | 109119576 | ||
| chr9:109119834
|
A | G | 1 | a0005 | 2 | NA18998.hp2 NA19080.hp1 |
missense_variant | MODERATE | c.80T>C | p.Val27Ala | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 114/7999 | 80/2640 | 27/879 | chr9 | 109119834 | ||
| chr9:109119887
|
G | C | 4 | a0002a0003a0006others(1): Show | 118 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(115): Show |
missense_variant | MODERATE | c.27C>G | p.Asp9Glu | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 61/7999 | 27/2640 | 9/879 | chr9 | 109119887 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:109064522
|
C | T | 1 | a0003c0017 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1578G>A | p.Ala526Ala | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/18 | 1612/7999 | 1578/2640 | 526/879 | chr9 | 109064522 | ||
| chr9:109087295
|
G | A | 1 | a0003c0008 | 7 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(4): Show |
synonymous_variant | LOW | c.1198C>T | p.Leu400Leu | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/18 | 1232/7999 | 1198/2640 | 400/879 | chr9 | 109087295 | ||
| chr9:109091133
|
G | A | 1 | a0001c0015 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.939C>T | p.Ser313Ser | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/18 | 973/7999 | 939/2640 | 313/879 | chr9 | 109091133 | ||
| chr9:109106605
|
G | A | 2 | a0002c0002a0008c0019 | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
synonymous_variant | LOW | c.702C>T | p.Ser234Ser | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/18 | 736/7999 | 702/2640 | 234/879 | chr9 | 109106605 | ||
| chr9:109119466
|
G | A | 1 | a0001c0006 | 13 | HG01261.hp1 HG01884.hp1 HG02109.hp1 others(10): Show |
synonymous_variant | LOW | c.448C>T | p.Leu150Leu | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 482/7999 | 448/2640 | 150/879 | chr9 | 109119466 | ||
| chr9:109119530
|
G | C | 1 | a0001c0016 | 1 | NA19057.hp2 | synonymous_variant | LOW | c.384C>G | p.Leu128Leu | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 418/7999 | 384/2640 | 128/879 | chr9 | 109119530 | ||
| chr9:109119553
|
G | A | 1 | a0001c0007 | 8 | HG02735.hp2 HG03490.hp2 HG03492.hp1 others(5): Show |
synonymous_variant | LOW | c.361C>T | p.Leu121Leu | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 395/7999 | 361/2640 | 121/879 | chr9 | 109119553 | ||
| chr9:109119647
|
T | C | 5 | a0001c0009a0002c0002a0003c0004others(2): Show | 111 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(108): Show |
synonymous_variant | LOW | c.267A>G | p.Leu89Leu | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 301/7999 | 267/2640 | 89/879 | chr9 | 109119647 | ||
| chr9:109119872
|
C | T | 1 | a0001c0013 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.42G>A | p.Arg14Arg | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 76/7999 | 42/2640 | 14/879 | chr9 | 109119872 | ||
| chr9:109119890
|
C | T | 2 | a0001c0005a0003c0012 | 16 | HG01978.hp2 HG02015.hp2 HG02040.hp1 others(13): Show |
synonymous_variant | LOW | c.24G>A | p.Lys8Lys | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 58/7999 | 24/2640 | 8/879 | chr9 | 109119890 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:109015183
|
TATAA | T | 8 | a0001c0001t0054a0001c0001t0108a0003c0008t0017others(5): Show | 12 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*5273_*5276delTTAT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 5273 | chr9 | 109015183 | |||||
| chr9:109015236
|
TTAGC | T | 14 | a0002c0002t0001a0002c0002t0012a0002c0002t0019others(11): Show | 73 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*5220_*5223delGCTA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 5220 | chr9 | 109015236 | |||||
| chr9:109015705
|
T | C | 1 | a0001c0001t0054 | 2 | HG01243.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4755A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 4755 | chr9 | 109015705 | |||||
| chr9:109015735
|
C | A | 16 | a0001c0001t0009a0001c0001t0093a0001c0009t0018others(13): Show | 34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*4725G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 4725 | chr9 | 109015735 | |||||
| chr9:109015740
|
C | A | 1 | a0001c0001t0067 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4720G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 4720 | chr9 | 109015740 | |||||
| chr9:109016196
|
C | T | 2 | a0001c0001t0064a0001c0001t0070 | 2 | HG01952.hp1 HG02293.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4264G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 4264 | chr9 | 109016196 | |||||
| chr9:109016207
|
A | G | 1 | a0003c0004t0116 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4253T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 4253 | chr9 | 109016207 | |||||
| chr9:109016418
|
GA | G | 13 | a0001c0001t0005a0001c0001t0034a0001c0001t0053others(10): Show | 39 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*4041delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 4041 | chr9 | 109016418 | |||||
| chr9:109016546
|
TA | T | 15 | a0001c0001t0004a0001c0001t0013a0001c0001t0027others(12): Show | 49 | HG00558.hp1 HG00735.hp1 HG01069.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3913delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3913 | chr9 | 109016546 | |||||
| chr9:109016548
|
G | C | 15 | a0001c0001t0004a0001c0001t0013a0001c0001t0027others(12): Show | 49 | HG00558.hp1 HG00735.hp1 HG01069.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3912C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3912 | chr9 | 109016548 | |||||
| chr9:109016656
|
GTGTTTTT | G | 6 | a0001c0001t0055a0001c0006t0033a0001c0006t0050others(3): Show | 9 | HG01261.hp1 HG01884.hp1 HG02486.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3797_*3803delAAAA others(3): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3797 | chr9 | 109016656 | |||||
| chr9:109016656
|
GTGTTTTT others(1): Show |
G | 3 | a0001c0001t0011a0001c0001t0105a0001c0006t0011 | 9 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3796_*3803delAAAA others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3796 | chr9 | 109016656 | |||||
| chr9:109016658
|
GT | G | 23 | a0001c0001t0007a0001c0001t0008a0001c0001t0014others(20): Show | 48 | HG00408.hp1 HG00544.hp2 HG00609.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*3801delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3801 | chr9 | 109016658 | |||||
| chr9:109016658
|
GTT | G | 42 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(39): Show | 167 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(164): Show |
3_prime_UTR_variant | MODIFIER | c.*3800_*3801delAA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3800 | chr9 | 109016658 | |||||
| chr9:109016658
|
GTTT | G | 24 | a0001c0001t0005a0001c0001t0006a0001c0001t0031others(21): Show | 113 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*3799_*3801delAAA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3799 | chr9 | 109016658 | |||||
| chr9:109016658
|
GTTTT | G | 15 | a0001c0001t0009a0001c0001t0016a0001c0001t0022others(12): Show | 29 | HG00099.hp2 HG00140.hp2 HG00558.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*3798_*3801delAAAA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3798 | chr9 | 109016658 | |||||
| chr9:109016658
|
GTTTTT | G | 11 | a0001c0001t0054a0001c0001t0093a0001c0001t0108others(8): Show | 23 | HG01243.hp2 HG01433.hp1 HG01496.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3797_*3801delAAAA others(1): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3797 | chr9 | 109016658 | |||||
| chr9:109016658
|
GTTTTTT | G | 3 | a0003c0008t0017a0003c0008t0095a0003c0008t0096 | 6 | HG00733.hp1 HG01109.hp1 HG02257.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3796_*3801delAAAA others(2): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3796 | chr9 | 109016658 | |||||
| chr9:109016911
|
A | G | 1 | a0003c0008t0095 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3549T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3549 | chr9 | 109016911 | |||||
| chr9:109016940
|
G | GT | 15 | a0001c0001t0002a0001c0001t0014a0001c0001t0032others(12): Show | 54 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*3519dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3519 | chr9 | 109016940 | |||||
| chr9:109016940
|
GT | G | 14 | a0001c0001t0009a0001c0001t0093a0003c0004t0009others(11): Show | 30 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3519delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3519 | chr9 | 109016940 | |||||
| chr9:109016949
|
T | C | 35 | a0001c0001t0003a0001c0001t0004a0001c0001t0013others(32): Show | 115 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*3511A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3511 | chr9 | 109016949 | |||||
| chr9:109016967
|
T | C | 9 | a0001c0001t0006a0001c0001t0016a0001c0001t0031others(6): Show | 27 | HG00544.hp1 HG00558.hp2 HG00639.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3493A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3493 | chr9 | 109016967 | |||||
| chr9:109017018
|
A | T | 8 | a0001c0001t0054a0001c0001t0108a0003c0008t0017others(5): Show | 12 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3442T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3442 | chr9 | 109017018 | |||||
| chr9:109017119
|
T | A | 2 | a0001c0001t0101a0001c0001t0107 | 2 | HG01256.hp2 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3341A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3341 | chr9 | 109017119 | |||||
| chr9:109017131
|
C | A | 1 | a0001c0001t0040 | 2 | HG02257.hp1 HG02723.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3329G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3329 | chr9 | 109017131 | |||||
| chr9:109017251
|
G | T | 1 | a0001c0001t0099 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3209C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3209 | chr9 | 109017251 | |||||
| chr9:109017340
|
A | G | 2 | a0003c0012t0088a0003c0018t0094 | 2 | HG02922.hp1 HG03453.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3120T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3120 | chr9 | 109017340 | |||||
| chr9:109017346
|
G | A | 4 | a0002c0002t0012a0002c0002t0057a0002c0002t0112others(1): Show | 10 | HG01433.hp2 HG02004.hp1 HG02129.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3114C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 3114 | chr9 | 109017346 | |||||
| chr9:109017473
|
T | C | 1 | a0001c0001t0042 | 2 | NA18943.hp2 NA18994.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2987A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2987 | chr9 | 109017473 | |||||
| chr9:109017541
|
T | C | 1 | a0003c0004t0052 | 2 | HG02886.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2919A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2919 | chr9 | 109017541 | |||||
| chr9:109017568
|
G | A | 2 | a0001c0001t0022a0001c0001t0045 | 5 | HG02622.hp2 HG02717.hp1 HG03098.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2892C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2892 | chr9 | 109017568 | |||||
| chr9:109017632
|
A | C | 1 | a0002c0002t0056 | 2 | HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2828T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2828 | chr9 | 109017632 | |||||
| chr9:109017656
|
C | T | 1 | a0003c0017t0117 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2804G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2804 | chr9 | 109017656 | |||||
| chr9:109017879
|
G | A | 1 | a0001c0001t0035 | 2 | NA18986.hp1 NA19057.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2581C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2581 | chr9 | 109017879 | |||||
| chr9:109017980
|
A | C | 1 | a0001c0001t0093 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2480T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2480 | chr9 | 109017980 | |||||
| chr9:109018149
|
T | C | 1 | a0001c0001t0105 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2311A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2311 | chr9 | 109018149 | |||||
| chr9:109018240
|
G | A | 1 | a0001c0001t0077 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2220C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2220 | chr9 | 109018240 | |||||
| chr9:109018290
|
T | A | 1 | a0001c0001t0072 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2170A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2170 | chr9 | 109018290 | |||||
| chr9:109018381
|
C | A | 9 | a0001c0001t0005a0001c0001t0034a0001c0001t0091others(6): Show | 34 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2079G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 2079 | chr9 | 109018381 | |||||
| chr9:109018613
|
A | T | 2 | a0001c0006t0033a0001c0006t0084 | 4 | HG01261.hp1 HG02572.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1847T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1847 | chr9 | 109018613 | |||||
| chr9:109018739
|
C | CT | 15 | a0001c0001t0005a0001c0001t0034a0001c0001t0053others(12): Show | 42 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1720dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1720 | chr9 | 109018739 | |||||
| chr9:109018835
|
A | T | 16 | a0001c0001t0011a0001c0001t0055a0001c0001t0105others(13): Show | 28 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1625T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1625 | chr9 | 109018835 | |||||
| chr9:109018872
|
A | G | 21 | a0001c0001t0003a0001c0001t0023a0001c0001t0025others(18): Show | 67 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*1588T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1588 | chr9 | 109018872 | |||||
| chr9:109018900
|
A | AT | 63 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(60): Show | 197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*1559dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1559 | chr9 | 109018900 | |||||
| chr9:109018900
|
A | ATT | 27 | a0001c0001t0006a0001c0001t0007a0001c0001t0013others(24): Show | 66 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*1558_*1559dupAA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1559 | chr9 | 109018900 | |||||
| chr9:109018900
|
A | ATTT | 8 | a0001c0001t0015a0001c0001t0030a0001c0001t0031others(5): Show | 15 | HG02809.hp2 HG02886.hp2 HG02970.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*1557_*1559dupAAA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1559 | chr9 | 109018900 | |||||
| chr9:109018900
|
AT | A | 10 | a0001c0001t0011a0001c0001t0055a0001c0001t0105others(7): Show | 16 | HG01243.hp1 HG01256.hp2 HG01884.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1559delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1559 | chr9 | 109018900 | |||||
| chr9:109018956
|
G | A | 2 | a0002c0002t0021a0002c0002t0115 | 5 | HG02080.hp1 NA18968.hp2 NA18988.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1504C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1504 | chr9 | 109018956 | |||||
| chr9:109019004
|
C | T | 11 | a0001c0001t0007a0001c0001t0015a0001c0001t0030others(8): Show | 25 | HG00609.hp2 HG02132.hp2 HG02809.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1456G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1456 | chr9 | 109019004 | |||||
| chr9:109019068
|
C | T | 1 | a0001c0007t0062 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1392G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1392 | chr9 | 109019068 | |||||
| chr9:109019215
|
G | A | 14 | a0002c0002t0001a0002c0002t0012a0002c0002t0019others(11): Show | 73 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1245C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1245 | chr9 | 109019215 | |||||
| chr9:109019253
|
C | T | 1 | a0001c0001t0061 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1207G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1207 | chr9 | 109019253 | |||||
| chr9:109019281
|
G | A | 1 | a0001c0005t0024 | 3 | HG02040.hp1 NA18989.hp1 NA19060.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1179C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1179 | chr9 | 109019281 | |||||
| chr9:109019308
|
A | T | 1 | a0003c0004t0116 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1152T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1152 | chr9 | 109019308 | |||||
| chr9:109019333
|
T | A | 1 | a0001c0001t0039 | 2 | HG02486.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1127A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1127 | chr9 | 109019333 | |||||
| chr9:109019334
|
C | A | 1 | a0001c0001t0039 | 2 | HG02486.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1126G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1126 | chr9 | 109019334 | |||||
| chr9:109019337
|
T | C | 1 | a0001c0001t0039 | 2 | HG02486.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1123A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1123 | chr9 | 109019337 | |||||
| chr9:109019341
|
C | T | 1 | a0001c0001t0039 | 2 | HG02486.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1119G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1119 | chr9 | 109019341 | |||||
| chr9:109019377
|
T | C | 1 | a0003c0004t0116 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1083A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1083 | chr9 | 109019377 | |||||
| chr9:109019411
|
A | T | 2 | a0001c0001t0073a0001c0001t0074 | 2 | HG04204.hp2 NA19066.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1049T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1049 | chr9 | 109019411 | |||||
| chr9:109019413
|
G | T | 11 | a0001c0001t0007a0001c0001t0015a0001c0001t0030others(8): Show | 25 | HG00609.hp2 HG02132.hp2 HG02809.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1047C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 1047 | chr9 | 109019413 | |||||
| chr9:109019499
|
T | C | 15 | a0002c0002t0001a0002c0002t0012a0002c0002t0019others(12): Show | 74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*961A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 961 | chr9 | 109019499 | |||||
| chr9:109019509
|
A | G | 13 | a0001c0001t0003a0001c0001t0023a0001c0001t0029others(10): Show | 55 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*951T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 951 | chr9 | 109019509 | |||||
| chr9:109019630
|
G | A | 1 | a0003c0004t0116 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*830C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 830 | chr9 | 109019630 | |||||
| chr9:109019651
|
G | C | 1 | a0001c0001t0029 | 3 | NA18948.hp1 NA18965.hp1 NA18982.hp2 |
3_prime_UTR_variant | MODIFIER | c.*809C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 809 | chr9 | 109019651 | |||||
| chr9:109019769
|
G | A | 1 | a0001c0001t0083 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*691C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 691 | chr9 | 109019769 | |||||
| chr9:109019798
|
T | C | 1 | a0003c0017t0117 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*662A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 662 | chr9 | 109019798 | |||||
| chr9:109019839
|
G | A | 1 | a0003c0004t0118 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*621C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 621 | chr9 | 109019839 | |||||
| chr9:109020251
|
T | G | 40 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(37): Show | 114 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*209A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 209 | chr9 | 109020251 | |||||
| chr9:109020390
|
G | A | 63 | a0001c0001t0005a0001c0001t0009a0001c0001t0011others(60): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
3_prime_UTR_variant | MODIFIER | c.*70C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 18/18 | 70 | chr9 | 109020390 | |||||
| chr9:109119928
|
A | G | 2 | a0001c0001t0022a0001c0001t0058 | 4 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-15T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 15 | chr9 | 109119928 | |||||
| chr9:109119940
|
G | C | 1 | a0001c0001t0119 | 1 | HG01255.hp2 | 5_prime_UTR_variant | MODIFIER | c.-27C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/18 | 27 | chr9 | 109119940 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:109020534
|
T | G | 1 | a0001c0007t0004g0301 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2595-29A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109020534 | ||||||
| chr9:109020540
|
A | G | 2 | a0001c0001t0097g0131a0001c0001t0098g0132 | 2 | NA18968.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.2595-35T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109020540 | ||||||
| chr9:109020587
|
G | C | 33 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(30): Show | 34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2595-82C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109020587 | ||||||
| chr9:109020601
|
T | C | 12 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2595-96A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109020601 | ||||||
| chr9:109020664
|
T | C | 1 | a0001c0001t0003g0213 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2595-159A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109020664 | ||||||
| chr9:109020689
|
G | A | 1 | a0001c0001t0006g0099 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2595-184C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109020689 | ||||||
| chr9:109020830
|
G | A | 1 | a0003c0004t0049g0333 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2595-325C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109020830 | ||||||
| chr9:109021132
|
C | T | 1 | a0001c0001t0080g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2595-627G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021132 | ||||||
| chr9:109021142
|
C | A | 2 | a0002c0002t0001g0361a0002c0002t0001g0364 | 2 | HG00738.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.2595-637G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021142 | ||||||
| chr9:109021223
|
T | C | 1 | a0001c0013t0090g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2595-718A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021223 | ||||||
| chr9:109021421
|
A | G | 2 | a0001c0001t0007g0107a0001c0001t0083g0109 | 2 | HG00609.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.2595-916T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021421 | ||||||
| chr9:109021453
|
C | T | 3 | a0001c0007t0004g0299a0001c0007t0004g0300a0001c0007t0028g0297 | 3 | HG02735.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2595-948G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021453 | ||||||
| chr9:109021491
|
G | T | 178 | a0001c0001t0005g0101a0001c0001t0005g0121a0001c0001t0005g0123others(175): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.2595-986C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021491 | ||||||
| chr9:109021495
|
TTTTG | T | 141 | a0001c0001t0005g0101a0001c0001t0005g0121a0001c0001t0005g0123others(138): Show | 141 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.2595-994_2595-991d others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021495 | ||||||
| chr9:109021495
|
TTTTGTTT others(1): Show |
T | 33 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(30): Show | 34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2595-998_2595-991d others(10): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021495 | ||||||
| chr9:109021503
|
GTTTGTTT others(2): Show |
G | 4 | a0001c0006t0033g0289a0001c0006t0033g0290a0001c0006t0033g0292others(1): Show | 4 | HG01261.hp1 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2595-1007_2595-999 others(12): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021503 | ||||||
| chr9:109021820
|
A | C | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2595-1315T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021820 | ||||||
| chr9:109021837
|
G | A | 1 | a0001c0001t0007g0111 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2595-1332C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021837 | ||||||
| chr9:109021838
|
A | G | 1 | a0001c0001t0007g0111 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.2595-1333T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021838 | ||||||
| chr9:109021851
|
A | G | 1 | a0001c0001t0003g0250 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2595-1346T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021851 | ||||||
| chr9:109021877
|
AAAGT | A | 33 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(30): Show | 34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2595-1376_2595-137 others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109021877 | ||||||
| chr9:109022086
|
T | C | 1 | a0003c0008t0017g0310 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2595-1581A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022086 | ||||||
| chr9:109022141
|
G | A | 1 | a0001c0001t0071g0240 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2595-1636C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022141 | ||||||
| chr9:109022152
|
A | G | 1 | a0002c0002t0001g0349 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2595-1647T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022152 | ||||||
| chr9:109022167
|
A | G | 2 | a0001c0001t0040g0271a0001c0001t0040g0272 | 2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2595-1662T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022167 | ||||||
| chr9:109022289
|
C | T | 1 | a0002c0002t0012g0379 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2595-1784G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022289 | ||||||
| chr9:109022467
|
T | TTATC | 66 | a0001c0001t0003g0201a0001c0001t0003g0205a0001c0001t0003g0249others(63): Show | 66 | HG01070.hp1 HG01071.hp1 HG01109.hp2 others(63): Show |
intron_variant | MODIFIER | c.2595-1966_2595-196 others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022467 | ||||||
| chr9:109022467
|
T | TTATCTAT others(1): Show |
156 | a0001c0001t0002g0001a0001c0001t0002g0042a0001c0001t0002g0043others(153): Show | 157 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.2595-1970_2595-196 others(12): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022467 | ||||||
| chr9:109022467
|
T | TTATCTAT others(5): Show |
69 | a0001c0001t0002g0034a0001c0001t0002g0035a0001c0001t0002g0049others(66): Show | 69 | HG00609.hp2 HG00621.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.2595-1974_2595-196 others(16): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022467 | ||||||
| chr9:109022467
|
T | TTATCTAT others(9): Show |
19 | a0001c0001t0003g0251a0001c0001t0015g0027a0001c0001t0025g0198others(16): Show | 19 | HG00099.hp1 HG00738.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.2595-1978_2595-196 others(20): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022467 | ||||||
| chr9:109022467
|
T | TTATCTAT others(13): Show |
4 | a0002c0002t0001g0346a0004c0003t0002g0040a0004c0003t0002g0065others(1): Show | 4 | HG01934.hp1 NA18939.hp2 NA18943.hp1 others(1): Show |
intron_variant | MODIFIER | c.2595-1982_2595-196 others(24): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022467 | ||||||
| chr9:109022467
|
T | TTATCTAT others(17): Show |
1 | a0004c0003t0002g0060 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.2595-1986_2595-196 others(28): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022467 | ||||||
| chr9:109022467
|
TTATC | T | 37 | a0001c0001t0006g0078a0001c0001t0006g0088a0001c0001t0006g0089others(34): Show | 37 | HG00544.hp1 HG00558.hp2 HG00639.hp1 others(34): Show |
intron_variant | MODIFIER | c.2595-1966_2595-196 others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022467 | ||||||
| chr9:109022467
|
TTATCTAT others(1): Show |
T | 23 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0005t0003g0012others(20): Show | 23 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.2595-1970_2595-196 others(12): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022467 | ||||||
| chr9:109022692
|
C | G | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0018g0325others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2595-2187G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022692 | ||||||
| chr9:109022712
|
T | C | 1 | a0001c0006t0050g0286 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2595-2207A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022712 | ||||||
| chr9:109022882
|
C | G | 1 | a0001c0001t0025g0262 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2595-2377G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109022882 | ||||||
| chr9:109023354
|
C | T | 1 | a0004c0003t0032g0061 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2595-2849G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109023354 | ||||||
| chr9:109023390
|
T | C | 1 | a0001c0001t0007g0179 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2595-2885A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109023390 | ||||||
| chr9:109023598
|
G | A | 1 | a0003c0017t0117g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2595-3093C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109023598 | ||||||
| chr9:109023601
|
G | A | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2595-3096C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109023601 | ||||||
| chr9:109023605
|
C | T | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0018g0325others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2595-3100G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109023605 | ||||||
| chr9:109023836
|
C | CA | 15 | a0001c0001t0013g0273a0001c0001t0059g0269a0001c0001t0070g0197others(12): Show | 16 | HG01109.hp2 HG01433.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.2595-3332dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109023836 | ||||||
| chr9:109023836
|
CA | C | 20 | a0001c0001t0006g0091a0001c0001t0011g0189a0001c0001t0011g0275others(17): Show | 20 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.2595-3332delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109023836 | ||||||
| chr9:109023926
|
C | A | 6 | a0001c0001t0007g0106a0001c0001t0007g0108a0001c0001t0007g0111others(3): Show | 6 | HG02132.hp2 NA18940.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.2595-3421G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109023926 | ||||||
| chr9:109024075
|
G | T | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2595-3570C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109024075 | ||||||
| chr9:109024168
|
A | G | 405 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(402): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.2595-3663T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109024168 | ||||||
| chr9:109024315
|
C | T | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0018g0325others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2595-3810G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109024315 | ||||||
| chr9:109024341
|
T | G | 8 | a0001c0001t0008g0160a0001c0001t0008g0161a0001c0001t0008g0162others(5): Show | 8 | HG01192.hp2 HG02486.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2595-3836A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109024341 | ||||||
| chr9:109024422
|
C | T | 1 | a0001c0001t0003g0250 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2595-3917G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109024422 | ||||||
| chr9:109024541
|
G | A | 2 | a0001c0001t0004g0193a0001c0001t0004g0218 | 2 | HG02132.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.2595-4036C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109024541 | ||||||
| chr9:109024544
|
T | C | 10 | a0001c0001t0093g0029a0003c0004t0010g0312a0003c0004t0010g0313others(7): Show | 10 | HG02451.hp2 HG02717.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.2595-4039A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109024544 | ||||||
| chr9:109024798
|
G | C | 5 | a0001c0001t0034g0136a0001c0001t0034g0153a0001c0001t0091g0127others(2): Show | 5 | NA18939.hp1 NA18941.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.2595-4293C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109024798 | ||||||
| chr9:109024845
|
A | G | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2595-4340T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109024845 | ||||||
| chr9:109025310
|
G | A | 1 | a0003c0017t0117g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2595-4805C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109025310 | ||||||
| chr9:109025395
|
C | G | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2595-4890G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109025395 | ||||||
| chr9:109025872
|
T | A | 1 | a0001c0001t0006g0089 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2595-5367A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109025872 | ||||||
| chr9:109025888
|
T | C | 54 | a0001c0001t0005g0101a0001c0001t0005g0121a0001c0001t0005g0123others(51): Show | 54 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.2595-5383A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109025888 | ||||||
| chr9:109025948
|
T | C | 226 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(223): Show | 227 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(224): Show |
intron_variant | MODIFIER | c.2595-5443A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109025948 | ||||||
| chr9:109025963
|
G | A | 2 | a0001c0001t0007g0113a0001c0001t0030g0110 | 2 | NA18963.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.2595-5458C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109025963 | ||||||
| chr9:109026027
|
T | C | 2 | a0001c0001t0054g0174a0001c0001t0054g0176 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2595-5522A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026027 | ||||||
| chr9:109026226
|
A | AAC | 11 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0278others(8): Show | 11 | HG01884.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.2595-5723_2595-572 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026226 | ||||||
| chr9:109026278
|
T | C | 36 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0203others(33): Show | 36 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.2595-5773A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026278 | ||||||
| chr9:109026297
|
A | G | 2 | a0001c0001t0054g0174a0001c0001t0054g0176 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2595-5792T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026297 | ||||||
| chr9:109026300
|
A | G | 54 | a0001c0001t0005g0101a0001c0001t0005g0121a0001c0001t0005g0123others(51): Show | 54 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.2595-5795T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026300 | ||||||
| chr9:109026411
|
T | G | 1 | a0001c0001t0005g0134 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2595-5906A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026411 | ||||||
| chr9:109026420
|
G | A | 31 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(28): Show | 31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.2595-5915C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026420 | ||||||
| chr9:109026420
|
G | C | 3 | a0002c0002t0001g0365a0002c0002t0001g0397a0002c0002t0001g0398 | 3 | NA18949.hp1 NA18963.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.2595-5915C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026420 | ||||||
| chr9:109026517
|
G | A | 1 | a0003c0004t0118g0332 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2595-6012C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026517 | ||||||
| chr9:109026579
|
G | GA | 11 | a0001c0001t0011g0277a0001c0001t0108g0083a0003c0008t0017g0304others(8): Show | 11 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.2595-6075dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026579 | ||||||
| chr9:109026599
|
G | C | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2595-6094C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026599 | ||||||
| chr9:109026678
|
C | G | 1 | a0001c0001t0002g0047 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2595-6173G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026678 | ||||||
| chr9:109026695
|
T | C | 194 | a0001c0001t0003g0250a0001c0001t0005g0101a0001c0001t0005g0121others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.2595-6190A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026695 | ||||||
| chr9:109026724
|
G | A | 2 | a0001c0001t0054g0174a0001c0001t0054g0176 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2595-6219C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026724 | ||||||
| chr9:109026726
|
T | A | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0018g0325others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2595-6221A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026726 | ||||||
| chr9:109026996
|
G | A | 1 | a0004c0003t0002g0074 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2594+6311C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109026996 | ||||||
| chr9:109027058
|
G | T | 1 | a0001c0001t0031g0097 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2594+6249C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109027058 | ||||||
| chr9:109027239
|
T | TAAAGAGC others(303): Show |
1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2594+6067_2594+606 others(314): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109027239 | ||||||
| chr9:109027340
|
GT | G | 140 | a0001c0001t0003g0250a0001c0001t0009g0030a0001c0001t0011g0189others(137): Show | 141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.2594+5966delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109027340 | ||||||
| chr9:109027347
|
T | C | 1 | a0001c0001t0042g0114 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.2594+5960A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109027347 | ||||||
| chr9:109027526
|
CAGG | C | 4 | a0002c0002t0001g0368a0002c0002t0001g0403a0002c0002t0001g0404others(1): Show | 4 | HG02165.hp2 NA18747.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.2594+5778_2594+578 others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109027526 | ||||||
| chr9:109027534
|
T | C | 54 | a0001c0001t0005g0101a0001c0001t0005g0121a0001c0001t0005g0123others(51): Show | 54 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.2594+5773A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109027534 | ||||||
| chr9:109027678
|
C | CT | 33 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(30): Show | 34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2594+5628dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109027678 | ||||||
| chr9:109028152
|
T | C | 179 | a0001c0001t0003g0250a0001c0001t0005g0101a0001c0001t0005g0121others(176): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.2594+5155A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028152 | ||||||
| chr9:109028221
|
G | A | 31 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(28): Show | 31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.2594+5086C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028221 | ||||||
| chr9:109028269
|
G | A | 2 | a0003c0004t0009g0340a0003c0004t0103g0328 | 2 | HG01106.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2594+5038C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028269 | ||||||
| chr9:109028307
|
G | A | 27 | a0001c0001t0005g0129a0001c0001t0005g0152a0001c0001t0007g0105others(24): Show | 27 | HG00609.hp2 HG01168.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.2594+5000C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028307 | ||||||
| chr9:109028382
|
T | A | 405 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(402): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.2594+4925A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028382 | ||||||
| chr9:109028450
|
A | G | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2594+4857T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028450 | ||||||
| chr9:109028454
|
C | CA | 133 | a0001c0001t0003g0250a0001c0001t0005g0101a0001c0001t0005g0121others(130): Show | 134 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.2594+4852dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028454 | ||||||
| chr9:109028454
|
CA | C | 204 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(201): Show | 205 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(202): Show |
intron_variant | MODIFIER | c.2594+4852delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028454 | ||||||
| chr9:109028579
|
C | T | 30 | a0001c0001t0006g0078a0001c0001t0006g0088a0001c0001t0006g0089others(27): Show | 30 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.2594+4728G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028579 | ||||||
| chr9:109028732
|
C | T | 5 | a0001c0001t0022g0003a0001c0001t0022g0004a0001c0001t0022g0005others(2): Show | 5 | HG02622.hp2 HG02717.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2594+4575G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028732 | ||||||
| chr9:109028952
|
G | A | 1 | a0001c0005t0024g0011 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2594+4355C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028952 | ||||||
| chr9:109028981
|
G | A | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2594+4326C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109028981 | ||||||
| chr9:109029035
|
C | T | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2594+4272G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029035 | ||||||
| chr9:109029132
|
A | G | 1 | a0001c0001t0004g0228 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2594+4175T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029132 | ||||||
| chr9:109029368
|
T | C | 1 | a0001c0001t0011g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2594+3939A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029368 | ||||||
| chr9:109029430
|
A | G | 1 | a0001c0001t0003g0255 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2594+3877T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029430 | ||||||
| chr9:109029432
|
T | A | 1 | a0001c0001t0074g0181 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2594+3875A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029432 | ||||||
| chr9:109029443
|
T | A | 1 | a0002c0002t0114g0416 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2594+3864A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029443 | ||||||
| chr9:109029493
|
A | C | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2594+3814T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029493 | ||||||
| chr9:109029561
|
G | C | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2594+3746C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029561 | ||||||
| chr9:109029633
|
G | A | 1 | a0001c0001t0081g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2594+3674C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029633 | ||||||
| chr9:109029712
|
T | C | 52 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(49): Show | 53 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2594+3595A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029712 | ||||||
| chr9:109029828
|
C | T | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2594+3479G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029828 | ||||||
| chr9:109029883
|
G | A | 1 | a0003c0004t0010g0318 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2594+3424C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029883 | ||||||
| chr9:109029886
|
A | G | 1 | a0001c0001t0015g0028 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2594+3421T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029886 | ||||||
| chr9:109029951
|
T | C | 32 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(29): Show | 32 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.2594+3356A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029951 | ||||||
| chr9:109029959
|
G | C | 1 | a0001c0001t0011g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2594+3348C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109029959 | ||||||
| chr9:109030064
|
T | G | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2594+3243A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030064 | ||||||
| chr9:109030106
|
C | T | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0018g0325others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2594+3201G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030106 | ||||||
| chr9:109030130
|
A | C | 7 | a0003c0008t0017g0304a0003c0008t0017g0308a0003c0008t0017g0309others(4): Show | 7 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.2594+3177T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030130 | ||||||
| chr9:109030154
|
C | T | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2594+3153G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030154 | ||||||
| chr9:109030244
|
AGTCCTTA others(2): Show |
A | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2594+3054_2594+306 others(13): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030244 | ||||||
| chr9:109030286
|
T | C | 25 | a0001c0001t0003g0215a0001c0001t0003g0220a0001c0001t0003g0261others(22): Show | 25 | HG00558.hp1 HG02040.hp2 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.2594+3021A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030286 | ||||||
| chr9:109030331
|
A | AT | 32 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(29): Show | 32 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.2594+2975dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030331 | ||||||
| chr9:109030360
|
T | C | 77 | a0001c0001t0003g0250a0002c0002t0001g0346a0002c0002t0001g0347others(74): Show | 77 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.2594+2947A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030360 | ||||||
| chr9:109030408
|
A | G | 5 | a0001c0001t0003g0250a0002c0002t0001g0371a0002c0002t0001g0382others(2): Show | 5 | HG00735.hp2 HG01256.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.2594+2899T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030408 | ||||||
| chr9:109030614
|
G | A | 1 | a0001c0001t0002g0046 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2594+2693C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030614 | ||||||
| chr9:109030649
|
G | C | 2 | a0005c0010t0003g0025a0005c0010t0036g0024 | 2 | NA18998.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2594+2658C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030649 | ||||||
| chr9:109030669
|
T | C | 1 | a0005c0010t0036g0024 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.2594+2638A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030669 | ||||||
| chr9:109030782
|
C | A | 33 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(30): Show | 34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2594+2525G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030782 | ||||||
| chr9:109030993
|
C | T | 3 | a0001c0001t0108g0083a0003c0012t0088g0022a0003c0018t0094g0307 | 3 | HG02055.hp1 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2594+2314G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109030993 | ||||||
| chr9:109031049
|
A | G | 2 | a0001c0001t0039g0159a0001c0001t0039g0165 | 2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.2594+2258T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109031049 | ||||||
| chr9:109031307
|
G | C | 39 | a0001c0001t0005g0101a0001c0001t0005g0121a0001c0001t0005g0123others(36): Show | 39 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.2594+2000C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109031307 | ||||||
| chr9:109031327
|
A | T | 406 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(403): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.2594+1980T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109031327 | ||||||
| chr9:109031439
|
T | C | 77 | a0001c0001t0003g0250a0002c0002t0001g0346a0002c0002t0001g0347others(74): Show | 77 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.2594+1868A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109031439 | ||||||
| chr9:109031486
|
C | T | 2 | a0001c0001t0006g0091a0001c0001t0006g0175 | 2 | HG02129.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.2594+1821G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109031486 | ||||||
| chr9:109031512
|
G | T | 1 | a0001c0001t0004g0223 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2594+1795C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109031512 | ||||||
| chr9:109031673
|
G | A | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2594+1634C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109031673 | ||||||
| chr9:109031697
|
T | C | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2594+1610A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109031697 | ||||||
| chr9:109031987
|
T | G | 1 | a0001c0001t0013g0230 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2594+1320A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109031987 | ||||||
| chr9:109032190
|
T | C | 30 | a0001c0001t0006g0078a0001c0001t0006g0088a0001c0001t0006g0089others(27): Show | 30 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.2594+1117A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032190 | ||||||
| chr9:109032199
|
G | A | 1 | a0001c0001t0080g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2594+1108C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032199 | ||||||
| chr9:109032225
|
C | T | 1 | a0002c0002t0001g0351 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.2594+1082G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032225 | ||||||
| chr9:109032303
|
A | G | 1 | a0003c0012t0088g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2594+1004T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032303 | ||||||
| chr9:109032365
|
C | CT | 14 | a0001c0001t0008g0162a0001c0001t0014g0032a0001c0001t0081g0044others(11): Show | 14 | HG00738.hp2 HG01884.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.2594+941dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTT | 24 | a0001c0001t0002g0001a0001c0001t0002g0045a0001c0001t0002g0046others(21): Show | 25 | HG01069.hp1 HG01071.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.2594+940_2594+941d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTT | 31 | a0001c0001t0002g0049a0001c0001t0002g0051a0001c0001t0003g0232others(28): Show | 31 | HG00140.hp1 HG00735.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.2594+939_2594+941d others(5): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTTT | 34 | a0001c0001t0003g0202a0001c0001t0003g0250a0001c0001t0003g0251others(31): Show | 34 | HG00408.hp1 HG00438.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.2594+938_2594+941d others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTTTT | 17 | a0001c0001t0023g0259a0002c0002t0001g0354a0002c0002t0001g0393others(14): Show | 17 | HG00621.hp1 HG00621.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.2594+937_2594+941d others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTTTTT | 12 | a0001c0001t0003g0201a0001c0001t0003g0249a0001c0001t0003g0255others(9): Show | 12 | HG00140.hp2 HG01070.hp1 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.2594+936_2594+941d others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTTTTTT | 9 | a0001c0001t0037g0258a0001c0005t0003g0014a0002c0002t0001g0362others(6): Show | 9 | HG00738.hp1 HG01123.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.2594+935_2594+941d others(9): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTTTTTT others(1): Show |
11 | a0001c0001t0003g0205a0001c0001t0036g0204a0001c0005t0003g0015others(8): Show | 11 | HG00544.hp2 HG02015.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.2594+934_2594+941d others(10): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTTTTTT others(2): Show |
7 | a0001c0001t0003g0210a0001c0001t0023g0208a0001c0001t0038g0209others(4): Show | 7 | HG01123.hp1 HG02615.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.2594+933_2594+941d others(11): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0003g0206a0001c0005t0003g0010 | 2 | HG02273.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.2594+932_2594+941d others(12): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0037g0214a0003c0004t0009g0329a0003c0004t0009g0340 | 3 | HG00099.hp2 HG00438.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.2594+931_2594+941d others(13): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0029g0199 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2594+930_2594+941d others(14): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTTTTTT others(6): Show |
9 | a0001c0001t0003g0264a0001c0001t0003g0265a0001c0001t0003g0267others(6): Show | 9 | HG02273.hp2 HG02559.hp1 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.2594+929_2594+941d others(15): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTTTTTT others(7): Show |
3 | a0001c0001t0003g0263a0001c0001t0003g0266a0003c0004t0010g0336 | 3 | HG03710.hp1 NA18940.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.2594+928_2594+941d others(16): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTTTTTT others(8): Show |
2 | a0001c0005t0003g0008a0006c0011t0009g0338 | 2 | HG03540.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2594+927_2594+941d others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0003g0207 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2594+926_2594+941d others(18): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0003g0213a0003c0004t0052g0320 | 2 | HG02886.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.2594+925_2594+941d others(19): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTTTTTT others(12): Show |
2 | a0001c0005t0003g0007a0001c0005t0003g0012 | 2 | HG01978.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2594+923_2594+941d others(21): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTTTTTT others(13): Show |
1 | a0001c0001t0026g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2594+922_2594+941d others(22): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTTTTTT others(19): Show |
1 | a0003c0004t0087g0327 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2594+916_2594+941d others(28): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
C | CTTTTTTT others(23): Show |
1 | a0001c0001t0003g0203 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2594+912_2594+941d others(32): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
CTTTT | C | 11 | a0001c0001t0007g0107a0001c0001t0015g0028a0001c0001t0015g0178others(8): Show | 11 | HG00609.hp2 HG00733.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.2594+938_2594+941d others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
CTTTTT | C | 21 | a0001c0001t0007g0105a0001c0001t0007g0106a0001c0001t0007g0108others(18): Show | 21 | HG01243.hp2 HG02132.hp2 HG02809.hp2 others(18): Show |
intron_variant | MODIFIER | c.2594+937_2594+941d others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
CTTTTTTT | C | 15 | a0001c0001t0002g0034a0001c0001t0003g0261a0001c0001t0004g0227others(12): Show | 15 | HG00099.hp1 HG00733.hp2 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.2594+935_2594+941d others(9): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
CTTTTTTT others(1): Show |
C | 51 | a0001c0001t0003g0215a0001c0001t0003g0220a0001c0001t0004g0082others(48): Show | 51 | HG00558.hp1 HG00639.hp1 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.2594+934_2594+941d others(10): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
CTTTTTTT others(2): Show |
C | 24 | a0001c0001t0006g0078a0001c0001t0006g0088a0001c0001t0006g0089others(21): Show | 24 | HG00544.hp1 HG00558.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.2594+933_2594+941d others(11): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
CTTTTTTT others(3): Show |
C | 5 | a0001c0001t0003g0212a0001c0001t0080g0033a0002c0002t0001g0404others(2): Show | 5 | HG02071.hp2 HG03209.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.2594+932_2594+941d others(12): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
CTTTTTTT others(4): Show |
C | 6 | a0001c0001t0108g0083a0001c0009t0018g0002a0001c0009t0018g0302others(3): Show | 7 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.2594+931_2594+941d others(13): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
CTTTTTTT others(5): Show |
C | 6 | a0001c0001t0030g0115a0002c0002t0001g0385a0002c0002t0001g0392others(3): Show | 6 | HG02630.hp2 NA18940.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.2594+930_2594+941d others(14): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0026g0233a0001c0006t0033g0292a0003c0004t0086g0334 | 3 | HG02572.hp1 HG02976.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2594+929_2594+941d others(15): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
CTTTTTTT others(7): Show |
C | 17 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(14): Show | 17 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2594+928_2594+941d others(16): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
CTTTTTTT others(8): Show |
C | 4 | a0001c0001t0069g0173a0001c0006t0050g0286a0001c0006t0050g0288others(1): Show | 4 | HG02486.hp2 HG02572.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.2594+927_2594+941d others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0004g0274a0002c0002t0001g0413 | 2 | HG00735.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2594+926_2594+941d others(18): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
CTTTTTTT others(10): Show |
C | 40 | a0001c0001t0005g0101a0001c0001t0005g0121a0001c0001t0005g0123others(37): Show | 40 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.2594+925_2594+941d others(19): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
CTTTTTTT others(14): Show |
C | 2 | a0001c0001t0002g0190a0001c0001t0032g0191 | 2 | HG01175.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.2594+921_2594+941d others(23): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032365
|
CTTTTTTT others(15): Show |
C | 1 | a0001c0007t0062g0295 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2594+920_2594+941d others(24): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032365 | ||||||
| chr9:109032374
|
T | TCC | 3 | a0001c0001t0002g0042a0001c0001t0002g0043a0003c0004t0002g0322 | 3 | HG03491.hp1 HG03492.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.2594+932_2594+933i others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032374 | ||||||
| chr9:109032383
|
T | G | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2594+924A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032383 | ||||||
| chr9:109032451
|
C | T | 1 | a0002c0002t0001g0383 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2594+856G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032451 | ||||||
| chr9:109032544
|
C | T | 1 | a0003c0004t0052g0320 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2594+763G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032544 | ||||||
| chr9:109032737
|
G | A | 2 | a0001c0001t0004g0216a0001c0001t0004g0221 | 2 | HG00558.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.2594+570C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032737 | ||||||
| chr9:109032807
|
C | CT | 56 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(53): Show | 57 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.2594+499dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032807 | ||||||
| chr9:109032807
|
CT | C | 43 | a0001c0001t0003g0255a0001c0001t0005g0101a0001c0001t0005g0121others(40): Show | 43 | HG00408.hp2 HG00438.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.2594+499delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032807 | ||||||
| chr9:109032807
|
CTT | C | 71 | a0001c0001t0053g0126a0001c0001t0053g0279a0001c0001t0091g0127others(68): Show | 71 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.2594+498_2594+499d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032807 | ||||||
| chr9:109032827
|
T | A | 2 | a0001c0001t0101g0151a0001c0001t0107g0156 | 2 | HG01256.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2594+480A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032827 | ||||||
| chr9:109032827
|
TA | T | 7 | a0001c0001t0006g0096a0001c0001t0022g0003a0001c0009t0018g0002others(4): Show | 8 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.2594+479delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032827 | ||||||
| chr9:109032828
|
A | T | 56 | a0001c0001t0006g0078a0001c0001t0006g0088a0001c0001t0006g0089others(53): Show | 56 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(53): Show |
intron_variant | MODIFIER | c.2594+479T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109032828 | ||||||
| chr9:109033053
|
T | C | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2594+254A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109033053 | ||||||
| chr9:109033078
|
C | T | 1 | a0001c0013t0090g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2594+229G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109033078 | ||||||
| chr9:109033092
|
C | T | 1 | a0003c0004t0010g0343 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2594+215G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109033092 | ||||||
| chr9:109033194
|
T | C | 1 | a0001c0007t0004g0296 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2594+113A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109033194 | ||||||
| chr9:109033221
|
A | G | 3 | a0003c0004t0051g0314a0003c0004t0051g0335a0003c0004t0086g0334 | 3 | HG02630.hp2 HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2594+86T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109033221 | ||||||
| chr9:109033281
|
C | T | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2594+26G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109033281 | ||||||
| chr9:109033285
|
T | C | 29 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.2594+22A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 17/17 | chr9 | 109033285 | ||||||
| chr9:109033658
|
TAATATTG others(9): Show |
T | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2400-173_2400-158d others(18): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109033658 | ||||||
| chr9:109033913
|
T | C | 1 | a0001c0001t0003g0255 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2400-412A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109033913 | ||||||
| chr9:109033951
|
T | C | 75 | a0001c0001t0003g0250a0002c0002t0001g0346a0002c0002t0001g0347others(72): Show | 75 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.2400-450A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109033951 | ||||||
| chr9:109034137
|
T | C | 1 | a0001c0001t0008g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2400-636A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034137 | ||||||
| chr9:109034236
|
A | G | 1 | a0003c0017t0117g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2400-735T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034236 | ||||||
| chr9:109034314
|
G | C | 3 | a0001c0006t0033g0289a0001c0006t0033g0290a0001c0006t0033g0292 | 3 | HG01261.hp1 HG02572.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2400-813C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034314 | ||||||
| chr9:109034427
|
A | C | 1 | a0001c0013t0090g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2400-926T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034427 | ||||||
| chr9:109034473
|
A | T | 141 | a0001c0001t0009g0030a0001c0001t0011g0189a0001c0001t0011g0275others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.2400-972T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034473 | ||||||
| chr9:109034477
|
C | T | 1 | a0001c0005t0060g0013 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2400-976G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034477 | ||||||
| chr9:109034561
|
C | T | 6 | a0001c0001t0007g0106a0001c0001t0007g0108a0001c0001t0007g0111others(3): Show | 6 | HG02132.hp2 NA18940.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.2400-1060G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034561 | ||||||
| chr9:109034589
|
G | A | 74 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(71): Show | 74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.2400-1088C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034589 | ||||||
| chr9:109034610
|
C | T | 36 | a0001c0001t0005g0101a0001c0001t0005g0121a0001c0001t0005g0123others(33): Show | 36 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2400-1109G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034610 | ||||||
| chr9:109034619
|
A | AT | 8 | a0001c0001t0005g0133a0001c0001t0005g0145a0001c0001t0005g0146others(5): Show | 8 | HG01081.hp1 HG01257.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.2400-1119dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034619 | ||||||
| chr9:109034619
|
A | C | 27 | a0001c0001t0007g0077a0001c0001t0007g0105a0001c0001t0007g0106others(24): Show | 27 | HG00609.hp2 HG01891.hp2 HG02132.hp2 others(24): Show |
intron_variant | MODIFIER | c.2400-1118T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034619 | ||||||
| chr9:109034684
|
G | A | 1 | a0001c0001t0080g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2400-1183C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034684 | ||||||
| chr9:109034697
|
C | T | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2400-1196G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034697 | ||||||
| chr9:109034721
|
C | T | 30 | a0001c0001t0006g0078a0001c0001t0006g0088a0001c0001t0006g0089others(27): Show | 30 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.2400-1220G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034721 | ||||||
| chr9:109034932
|
G | A | 1 | a0002c0002t0001g0349 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2399+1274C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034932 | ||||||
| chr9:109034993
|
G | C | 2 | a0001c0001t0013g0229a0001c0001t0013g0230 | 2 | HG02071.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.2399+1213C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109034993 | ||||||
| chr9:109035014
|
G | A | 3 | a0001c0001t0108g0083a0003c0012t0088g0022a0003c0018t0094g0307 | 3 | HG02055.hp1 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2399+1192C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035014 | ||||||
| chr9:109035106
|
G | A | 1 | a0001c0001t0054g0176 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2399+1100C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035106 | ||||||
| chr9:109035123
|
C | T | 1 | a0001c0001t0005g0145 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2399+1083G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035123 | ||||||
| chr9:109035156
|
C | CA | 82 | a0001c0001t0003g0213a0001c0001t0003g0220a0001c0001t0003g0255others(79): Show | 82 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.2399+1049dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035156 | ||||||
| chr9:109035156
|
CA | C | 18 | a0001c0001t0004g0221a0001c0001t0008g0162a0001c0001t0008g0163others(15): Show | 19 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.2399+1049delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035156 | ||||||
| chr9:109035156
|
CAA | C | 23 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(20): Show | 23 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.2399+1048_2399+104 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035156 | ||||||
| chr9:109035415
|
T | C | 8 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(5): Show | 8 | HG02273.hp1 NA18940.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2399+791A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035415 | ||||||
| chr9:109035737
|
C | T | 33 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(30): Show | 34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2399+469G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035737 | ||||||
| chr9:109035776
|
T | C | 32 | a0001c0001t0006g0078a0001c0001t0006g0088a0001c0001t0006g0089others(29): Show | 32 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.2399+430A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035776 | ||||||
| chr9:109035819
|
T | C | 1 | a0001c0001t0055g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2399+387A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035819 | ||||||
| chr9:109035878
|
G | C | 53 | a0001c0001t0005g0101a0001c0001t0005g0121a0001c0001t0005g0123others(50): Show | 53 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.2399+328C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035878 | ||||||
| chr9:109035879
|
G | A | 1 | a0001c0001t0011g0189 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2399+327C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035879 | ||||||
| chr9:109035913
|
G | A | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2399+293C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035913 | ||||||
| chr9:109035940
|
CA | C | 158 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(155): Show | 159 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(156): Show |
intron_variant | MODIFIER | c.2399+265delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035940 | ||||||
| chr9:109035940
|
CAA | C | 180 | a0001c0001t0002g0051a0001c0001t0005g0101a0001c0001t0005g0121others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.2399+264_2399+265d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035940 | ||||||
| chr9:109035940
|
CAAA | C | 6 | a0001c0001t0011g0278a0002c0002t0001g0368a0002c0002t0001g0403others(3): Show | 6 | HG01517.hp1 HG02165.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2399+263_2399+265d others(5): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035940 | ||||||
| chr9:109035991
|
CA | C | 355 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0042others(352): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.2399+214delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109035991 | ||||||
| chr9:109036008
|
A | C | 53 | a0001c0001t0003g0215a0001c0001t0003g0220a0001c0001t0003g0261others(50): Show | 53 | HG00558.hp1 HG00639.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.2399+198T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109036008 | ||||||
| chr9:109036045
|
C | A | 177 | a0001c0001t0005g0101a0001c0001t0005g0121a0001c0001t0005g0123others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.2399+161G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109036045 | ||||||
| chr9:109036059
|
T | C | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2399+147A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109036059 | ||||||
| chr9:109036081
|
T | C | 1 | a0001c0001t0053g0126 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2399+125A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109036081 | ||||||
| chr9:109036088
|
G | A | 1 | a0003c0004t0118g0332 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2399+118C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109036088 | ||||||
| chr9:109036135
|
T | C | 32 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(29): Show | 32 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.2399+71A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109036135 | ||||||
| chr9:109036143
|
T | TA | 36 | a0001c0001t0006g0089a0001c0001t0009g0030a0001c0001t0093g0029others(33): Show | 37 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(34): Show |
intron_variant | MODIFIER | c.2399+62dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109036143 | ||||||
| chr9:109036143
|
T | TAAAAAAA others(304): Show |
1 | a0001c0001t0003g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2399+62_2399+63ins others(311): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109036143 | ||||||
| chr9:109036143
|
TA | T | 97 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0203others(94): Show | 97 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.2399+62delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 16/17 | chr9 | 109036143 | ||||||
| chr9:109036471
|
C | T | 371 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(368): Show | 372 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(369): Show |
intron_variant | MODIFIER | c.2225-91G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109036471 | ||||||
| chr9:109036818
|
G | A | 20 | a0001c0001t0007g0106a0001c0001t0007g0107a0001c0001t0007g0108others(17): Show | 20 | HG00609.hp2 HG02132.hp2 HG04204.hp2 others(17): Show |
intron_variant | MODIFIER | c.2225-438C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109036818 | ||||||
| chr9:109037072
|
C | T | 1 | a0001c0001t0008g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2225-692G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037072 | ||||||
| chr9:109037089
|
G | T | 54 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(51): Show | 55 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(52): Show |
intron_variant | MODIFIER | c.2225-709C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037089 | ||||||
| chr9:109037283
|
A | C | 405 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(402): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.2224+734T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037283 | ||||||
| chr9:109037433
|
G | T | 1 | a0004c0003t0002g0063 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2224+584C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037433 | ||||||
| chr9:109037442
|
T | A | 1 | a0004c0003t0002g0056 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.2224+575A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037442 | ||||||
| chr9:109037459
|
G | A | 2 | a0002c0002t0012g0399a0002c0002t0113g0353 | 2 | NA18971.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.2224+558C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037459 | ||||||
| chr9:109037610
|
T | C | 2 | a0003c0004t0018g0325a0003c0004t0102g0324 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2224+407A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037610 | ||||||
| chr9:109037916
|
T | C | 15 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(12): Show | 16 | HG00140.hp1 HG00733.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.2224+101A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037916 | ||||||
| chr9:109037945
|
T | C | 29 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(26): Show | 29 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.2224+72A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037945 | ||||||
| chr9:109037954
|
G | A | 284 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(281): Show | 285 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.2224+63C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037954 | ||||||
| chr9:109037987
|
G | A | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2224+30C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 15/17 | chr9 | 109037987 | ||||||
| chr9:109038338
|
AAT | A | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0018g0325others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2124-223_2124-222d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038338 | ||||||
| chr9:109038359
|
A | T | 2 | a0002c0002t0001g0372a0002c0002t0020g0370 | 2 | HG02027.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.2124-242T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038359 | ||||||
| chr9:109038427
|
C | T | 3 | a0001c0001t0029g0199a0001c0001t0029g0211a0001c0001t0029g0260 | 3 | NA18948.hp1 NA18965.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.2124-310G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038427 | ||||||
| chr9:109038471
|
A | T | 1 | a0001c0001t0108g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2124-354T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038471 | ||||||
| chr9:109038478
|
G | A | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2124-361C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038478 | ||||||
| chr9:109038599
|
G | T | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2124-482C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038599 | ||||||
| chr9:109038683
|
T | C | 1 | a0003c0008t0017g0310 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2124-566A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038683 | ||||||
| chr9:109038687
|
T | A | 1 | a0001c0001t0006g0095 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2124-570A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038687 | ||||||
| chr9:109038876
|
A | G | 3 | a0002c0002t0001g0359a0002c0002t0056g0358a0002c0002t0056g0360 | 3 | HG00099.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2124-759T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038876 | ||||||
| chr9:109038963
|
T | C | 1 | a0002c0002t0012g0389 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.2124-846A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109038963 | ||||||
| chr9:109039005
|
T | C | 405 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(402): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.2124-888A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039005 | ||||||
| chr9:109039032
|
T | C | 1 | a0003c0017t0117g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2124-915A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039032 | ||||||
| chr9:109039045
|
G | C | 77 | a0001c0001t0003g0250a0002c0002t0001g0346a0002c0002t0001g0347others(74): Show | 77 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.2124-928C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039045 | ||||||
| chr9:109039064
|
G | A | 42 | a0001c0001t0004g0082a0001c0001t0004g0117a0001c0001t0004g0182others(39): Show | 42 | HG00558.hp1 HG00639.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.2124-947C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039064 | ||||||
| chr9:109039073
|
T | C | 77 | a0001c0001t0003g0250a0002c0002t0001g0346a0002c0002t0001g0347others(74): Show | 77 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.2124-956A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039073 | ||||||
| chr9:109039181
|
G | A | 29 | a0001c0001t0006g0078a0001c0001t0006g0088a0001c0001t0006g0089others(26): Show | 29 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(26): Show |
intron_variant | MODIFIER | c.2124-1064C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039181 | ||||||
| chr9:109039335
|
G | A | 1 | a0003c0018t0094g0307 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2124-1218C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039335 | ||||||
| chr9:109039388
|
C | A | 1 | a0001c0001t0031g0079 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2124-1271G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039388 | ||||||
| chr9:109039415
|
C | T | 1 | a0001c0001t0108g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2124-1298G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039415 | ||||||
| chr9:109039444
|
G | C | 77 | a0001c0001t0003g0250a0002c0002t0001g0346a0002c0002t0001g0347others(74): Show | 77 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.2124-1327C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039444 | ||||||
| chr9:109039469
|
G | A | 1 | a0003c0012t0088g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2124-1352C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039469 | ||||||
| chr9:109039470
|
C | A | 1 | a0003c0012t0088g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2124-1353G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039470 | ||||||
| chr9:109039612
|
C | T | 2 | a0002c0002t0001g0393a0002c0002t0001g0395 | 2 | HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.2124-1495G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039612 | ||||||
| chr9:109039820
|
G | A | 1 | a0002c0002t0001g0362 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2124-1703C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039820 | ||||||
| chr9:109039836
|
G | A | 2 | a0001c0001t0040g0271a0001c0001t0040g0272 | 2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2124-1719C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039836 | ||||||
| chr9:109039866
|
T | C | 8 | a0001c0001t0025g0184a0001c0001t0026g0183a0001c0001t0026g0233others(5): Show | 8 | HG01255.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2124-1749A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039866 | ||||||
| chr9:109039966
|
T | G | 40 | a0001c0001t0005g0101a0001c0001t0005g0121a0001c0001t0005g0123others(37): Show | 40 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.2124-1849A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109039966 | ||||||
| chr9:109040049
|
C | T | 3 | a0001c0001t0025g0198a0001c0001t0026g0234a0003c0004t0116g0342 | 3 | HG02809.hp1 HG03516.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.2124-1932G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109040049 | ||||||
| chr9:109040334
|
T | A | 75 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(72): Show | 75 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.2124-2217A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109040334 | ||||||
| chr9:109040385
|
C | T | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2124-2268G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109040385 | ||||||
| chr9:109040451
|
T | C | 65 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0203others(62): Show | 65 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(62): Show |
intron_variant | MODIFIER | c.2124-2334A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109040451 | ||||||
| chr9:109040603
|
A | G | 2 | a0001c0001t0007g0107a0001c0001t0083g0109 | 2 | HG00609.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.2124-2486T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109040603 | ||||||
| chr9:109040802
|
A | G | 1 | a0001c0001t0054g0174 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2124-2685T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109040802 | ||||||
| chr9:109040848
|
G | T | 73 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(70): Show | 73 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.2124-2731C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109040848 | ||||||
| chr9:109040942
|
G | A | 1 | a0001c0001t0005g0146 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2124-2825C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109040942 | ||||||
| chr9:109040979
|
C | T | 1 | a0003c0017t0117g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2124-2862G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109040979 | ||||||
| chr9:109041029
|
G | A | 1 | a0003c0017t0117g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2124-2912C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041029 | ||||||
| chr9:109041222
|
T | G | 5 | a0001c0001t0003g0263a0001c0001t0003g0264a0001c0001t0003g0265others(2): Show | 5 | NA18940.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.2124-3105A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041222 | ||||||
| chr9:109041270
|
G | A | 4 | a0002c0002t0001g0384a0002c0002t0001g0385a0002c0002t0001g0392others(1): Show | 4 | NA18973.hp2 NA18974.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.2124-3153C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041270 | ||||||
| chr9:109041342
|
T | C | 1 | a0002c0002t0001g0346 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2124-3225A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041342 | ||||||
| chr9:109041381
|
C | G | 7 | a0001c0007t0004g0296a0001c0007t0004g0299a0001c0007t0004g0300others(4): Show | 7 | HG02735.hp2 HG03490.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.2124-3264G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041381 | ||||||
| chr9:109041428
|
G | A | 32 | a0001c0001t0005g0101a0001c0001t0011g0189a0001c0001t0011g0275others(29): Show | 32 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.2124-3311C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041428 | ||||||
| chr9:109041453
|
A | AT | 112 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(109): Show | 114 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(111): Show |
intron_variant | MODIFIER | c.2124-3337dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041453 | ||||||
| chr9:109041453
|
A | ATT | 24 | a0001c0001t0004g0274a0001c0001t0008g0161a0001c0001t0008g0167others(21): Show | 24 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.2124-3338_2124-333 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041453 | ||||||
| chr9:109041453
|
A | ATTT | 8 | a0001c0001t0002g0042a0001c0001t0002g0043a0001c0001t0005g0101others(5): Show | 8 | HG01106.hp1 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.2124-3339_2124-333 others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041453 | ||||||
| chr9:109041453
|
AT | A | 71 | a0001c0001t0005g0121a0001c0001t0005g0125a0001c0001t0005g0129others(68): Show | 71 | HG00408.hp2 HG00544.hp1 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.2124-3337delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041453 | ||||||
| chr9:109041453
|
ATT | A | 8 | a0001c0001t0005g0123a0001c0001t0005g0152a0001c0001t0005g0157others(5): Show | 8 | HG00733.hp1 HG01109.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.2124-3338_2124-333 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041453 | ||||||
| chr9:109041453
|
ATTT | A | 7 | a0001c0001t0007g0112a0003c0008t0017g0304a0003c0008t0017g0309others(4): Show | 7 | HG02132.hp2 HG02145.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2124-3339_2124-333 others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041453 | ||||||
| chr9:109041453
|
ATTTTTTT | A | 8 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(5): Show | 8 | HG01243.hp1 HG02451.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2124-3343_2124-333 others(11): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041453 | ||||||
| chr9:109041531
|
TTGGCTCA others(1375): Show |
T | 3 | a0001c0001t0040g0271a0001c0001t0040g0272a0001c0001t0069g0173 | 3 | HG02257.hp1 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2124-4796_2124-341 others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041531 | ||||||
| chr9:109041595
|
T | C | 7 | a0001c0007t0004g0296a0001c0007t0004g0299a0001c0007t0004g0300others(4): Show | 7 | HG02735.hp2 HG03490.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.2124-3478A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041595 | ||||||
| chr9:109041959
|
G | A | 73 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(70): Show | 73 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.2124-3842C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109041959 | ||||||
| chr9:109042024
|
A | T | 2 | a0001c0001t0011g0189a0001c0001t0055g0188 | 2 | HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2124-3907T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042024 | ||||||
| chr9:109042153
|
C | T | 2 | a0001c0001t0054g0174a0001c0001t0054g0176 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2124-4036G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042153 | ||||||
| chr9:109042238
|
T | C | 30 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(27): Show | 30 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.2124-4121A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042238 | ||||||
| chr9:109042781
|
A | G | 1 | a0001c0001t0008g0161 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2124-4664T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042781 | ||||||
| chr9:109042833
|
C | T | 34 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(31): Show | 35 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.2124-4716G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042833 | ||||||
| chr9:109042839
|
A | AT | 78 | a0001c0001t0003g0232a0001c0001t0003g0250a0001c0001t0003g0251others(75): Show | 78 | HG00609.hp2 HG01109.hp2 HG01243.hp2 others(75): Show |
intron_variant | MODIFIER | c.2124-4723dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042839 | ||||||
| chr9:109042839
|
A | ATT | 34 | a0001c0001t0006g0078a0001c0001t0006g0088a0001c0001t0006g0089others(31): Show | 34 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(31): Show |
intron_variant | MODIFIER | c.2124-4724_2124-472 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042839 | ||||||
| chr9:109042839
|
AT | A | 11 | a0001c0001t0002g0047a0001c0001t0005g0141a0001c0001t0008g0166others(8): Show | 11 | HG01070.hp2 HG01516.hp1 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.2124-4723delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042839 | ||||||
| chr9:109042839
|
ATTTTTTT others(3): Show |
A | 33 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(30): Show | 34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2124-4732_2124-472 others(14): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042839 | ||||||
| chr9:109042885
|
G | A | 1 | a0001c0001t0005g0142 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2124-4768C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042885 | ||||||
| chr9:109042908
|
C | T | 53 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(50): Show | 54 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.2124-4791G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109042908 | ||||||
| chr9:109043133
|
T | C | 1 | a0001c0001t0066g0187 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2124-5016A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109043133 | ||||||
| chr9:109043206
|
A | G | 1 | a0001c0001t0003g0255 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2124-5089T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109043206 | ||||||
| chr9:109043281
|
G | T | 1 | a0001c0001t0003g0255 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2124-5164C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109043281 | ||||||
| chr9:109043284
|
G | A | 1 | a0001c0001t0004g0244 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2124-5167C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109043284 | ||||||
| chr9:109043585
|
T | C | 7 | a0001c0007t0004g0296a0001c0007t0004g0299a0001c0007t0004g0300others(4): Show | 7 | HG02735.hp2 HG03490.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.2124-5468A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109043585 | ||||||
| chr9:109043611
|
A | AATTCACA others(1): Show |
405 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(402): Show | 407 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
intron_variant | MODIFIER | c.2124-5495_2124-549 others(12): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109043611 | ||||||
| chr9:109043809
|
T | C | 381 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(378): Show | 383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.2124-5692A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109043809 | ||||||
| chr9:109043975
|
G | A | 7 | a0001c0001t0003g0215a0001c0001t0003g0220a0001c0001t0003g0261others(4): Show | 7 | NA18948.hp2 NA18952.hp2 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.2124-5858C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109043975 | ||||||
| chr9:109043995
|
A | C | 24 | a0001c0001t0006g0078a0001c0001t0006g0088a0001c0001t0006g0089others(21): Show | 24 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.2124-5878T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109043995 | ||||||
| chr9:109044127
|
C | T | 1 | a0004c0003t0046g0037 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2124-6010G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044127 | ||||||
| chr9:109044250
|
G | A | 10 | a0004c0003t0002g0040a0004c0003t0002g0060a0004c0003t0002g0065others(7): Show | 10 | NA18939.hp2 NA18943.hp1 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.2123+6033C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044250 | ||||||
| chr9:109044479
|
C | A | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2123+5804G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044479 | ||||||
| chr9:109044583
|
G | C | 37 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(34): Show | 37 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.2123+5700C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044583 | ||||||
| chr9:109044671
|
G | A | 1 | a0002c0002t0001g0362 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.2123+5612C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044671 | ||||||
| chr9:109044710
|
A | C | 8 | a0001c0001t0025g0184a0001c0001t0026g0183a0001c0001t0026g0233others(5): Show | 8 | HG01255.hp1 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2123+5573T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044710 | ||||||
| chr9:109044762
|
G | GT | 52 | a0001c0001t0002g0190a0001c0001t0003g0210a0001c0001t0003g0263others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.2123+5520dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044762 | ||||||
| chr9:109044762
|
GT | G | 34 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(31): Show | 34 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.2123+5520delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044762 | ||||||
| chr9:109044789
|
TCTCA | T | 12 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2123+5490_2123+549 others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044789 | ||||||
| chr9:109044885
|
G | T | 1 | a0001c0001t0030g0110 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.2123+5398C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044885 | ||||||
| chr9:109044892
|
T | C | 4 | a0001c0006t0033g0289a0001c0006t0033g0290a0001c0006t0033g0292others(1): Show | 4 | HG01261.hp1 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2123+5391A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044892 | ||||||
| chr9:109044993
|
C | T | 385 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(382): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.2123+5290G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109044993 | ||||||
| chr9:109045040
|
G | A | 1 | a0001c0001t0003g0206 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2123+5243C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109045040 | ||||||
| chr9:109045045
|
C | A | 1 | a0002c0002t0001g0388 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2123+5238G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109045045 | ||||||
| chr9:109045066
|
C | A | 31 | a0001c0001t0006g0078a0001c0001t0006g0088a0001c0001t0006g0089others(28): Show | 31 | HG00544.hp1 HG00558.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.2123+5217G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109045066 | ||||||
| chr9:109045114
|
A | G | 236 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(233): Show | 237 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(234): Show |
intron_variant | MODIFIER | c.2123+5169T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109045114 | ||||||
| chr9:109045534
|
G | C | 1 | a0001c0001t0002g0049 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2123+4749C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109045534 | ||||||
| chr9:109045576
|
A | T | 24 | a0001c0001t0004g0193a0001c0001t0004g0218a0001c0001t0007g0105others(21): Show | 24 | HG00609.hp2 HG02132.hp1 HG02132.hp2 others(21): Show |
intron_variant | MODIFIER | c.2123+4707T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109045576 | ||||||
| chr9:109045840
|
A | C | 1 | a0003c0004t0049g0333 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2123+4443T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109045840 | ||||||
| chr9:109045872
|
G | C | 236 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(233): Show | 237 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(234): Show |
intron_variant | MODIFIER | c.2123+4411C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109045872 | ||||||
| chr9:109046085
|
C | T | 1 | a0001c0013t0090g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2123+4198G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109046085 | ||||||
| chr9:109046086
|
G | A | 1 | a0001c0001t0008g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2123+4197C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109046086 | ||||||
| chr9:109046152
|
C | G | 54 | a0001c0001t0003g0215a0001c0001t0003g0220a0001c0001t0003g0261others(51): Show | 54 | HG00558.hp1 HG00639.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.2123+4131G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109046152 | ||||||
| chr9:109046157
|
C | A | 54 | a0001c0001t0003g0215a0001c0001t0003g0220a0001c0001t0003g0261others(51): Show | 54 | HG00558.hp1 HG00639.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.2123+4126G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109046157 | ||||||
| chr9:109046622
|
A | G | 1 | a0002c0002t0019g0352 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2123+3661T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109046622 | ||||||
| chr9:109047015
|
A | C | 77 | a0001c0001t0003g0250a0002c0002t0001g0346a0002c0002t0001g0347others(74): Show | 77 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.2123+3268T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109047015 | ||||||
| chr9:109047038
|
A | G | 33 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(30): Show | 34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.2123+3245T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109047038 | ||||||
| chr9:109047250
|
A | G | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.2123+3033T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109047250 | ||||||
| chr9:109047312
|
G | A | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0018g0325others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.2123+2971C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109047312 | ||||||
| chr9:109047840
|
T | C | 2 | a0003c0012t0088g0022a0003c0018t0094g0307 | 2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2123+2443A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109047840 | ||||||
| chr9:109047887
|
G | A | 1 | a0001c0001t0065g0248 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2123+2396C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109047887 | ||||||
| chr9:109047943
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2123+2340C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109047943 | ||||||
| chr9:109048109
|
A | G | 2 | a0003c0004t0009g0326a0003c0004t0009g0330 | 2 | HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2123+2174T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048109 | ||||||
| chr9:109048150
|
G | A | 1 | a0001c0001t0008g0167 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2123+2133C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048150 | ||||||
| chr9:109048293
|
C | G | 52 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0042others(49): Show | 53 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2123+1990G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048293 | ||||||
| chr9:109048478
|
A | C | 1 | a0002c0002t0019g0356 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2123+1805T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048478 | ||||||
| chr9:109048524
|
T | C | 406 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(403): Show | 408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.2123+1759A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048524 | ||||||
| chr9:109048525
|
G | A | 114 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0203others(111): Show | 114 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.2123+1758C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048525 | ||||||
| chr9:109048563
|
G | A | 3 | a0001c0001t0003g0212a0001c0001t0003g0213a0001c0001t0037g0214 | 3 | HG00438.hp2 HG02071.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.2123+1720C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048563 | ||||||
| chr9:109048612
|
C | T | 1 | a0001c0001t0108g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2123+1671G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048612 | ||||||
| chr9:109048619
|
A | G | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2123+1664T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048619 | ||||||
| chr9:109048837
|
G | C | 1 | a0001c0001t0015g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2123+1446C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048837 | ||||||
| chr9:109048847
|
A | T | 1 | a0001c0001t0013g0230 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2123+1436T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048847 | ||||||
| chr9:109048880
|
G | T | 1 | a0003c0004t0118g0332 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2123+1403C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048880 | ||||||
| chr9:109048929
|
G | T | 1 | a0001c0001t0105g0276 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2123+1354C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048929 | ||||||
| chr9:109048987
|
G | C | 1 | a0001c0001t0007g0077 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2123+1296C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109048987 | ||||||
| chr9:109049189
|
G | T | 1 | a0003c0004t0009g0330 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2123+1094C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109049189 | ||||||
| chr9:109049414
|
T | C | 9 | a0003c0008t0017g0304a0003c0008t0017g0308a0003c0008t0017g0309others(6): Show | 9 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2123+869A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109049414 | ||||||
| chr9:109049506
|
G | A | 56 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(53): Show | 56 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.2123+777C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109049506 | ||||||
| chr9:109049593
|
G | A | 4 | a0002c0002t0001g0361a0002c0002t0001g0362a0002c0002t0001g0363others(1): Show | 4 | HG00738.hp1 HG01123.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.2123+690C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109049593 | ||||||
| chr9:109049636
|
G | C | 1 | a0002c0002t0021g0386 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2123+647C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109049636 | ||||||
| chr9:109049848
|
G | A | 3 | a0001c0001t0003g0212a0001c0001t0003g0213a0001c0001t0037g0214 | 3 | HG00438.hp2 HG02071.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.2123+435C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109049848 | ||||||
| chr9:109049906
|
C | T | 2 | a0001c0001t0027g0196a0001c0007t0004g0294 | 2 | HG02148.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.2123+377G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109049906 | ||||||
| chr9:109049980
|
C | T | 2 | a0001c0001t0054g0174a0001c0001t0054g0176 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2123+303G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109049980 | ||||||
| chr9:109049994
|
G | A | 1 | a0001c0006t0011g0282 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2123+289C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109049994 | ||||||
| chr9:109050039
|
G | A | 2 | a0001c0001t0005g0121a0001c0001t0092g0122 | 2 | NA18979.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.2123+244C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109050039 | ||||||
| chr9:109050149
|
T | C | 2 | a0001c0001t0003g0201a0001c0001t0003g0249 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2123+134A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109050149 | ||||||
| chr9:109050175
|
A | G | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.2123+108T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 14/17 | chr9 | 109050175 | ||||||
| chr9:109050545
|
C | T | 403 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(400): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1977+25G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 13/17 | chr9 | 109050545 | ||||||
| chr9:109050740
|
A | C | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1855-48T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109050740 | ||||||
| chr9:109050743
|
T | A | 2 | a0001c0001t0005g0101a0001c0001t0108g0083 | 2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1855-51A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109050743 | ||||||
| chr9:109050831
|
T | TA | 53 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(50): Show | 53 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.1855-140dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109050831 | ||||||
| chr9:109050843
|
G | A | 1 | a0001c0001t0044g0093 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1855-151C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109050843 | ||||||
| chr9:109050928
|
A | G | 1 | a0001c0001t0053g0279 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1855-236T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109050928 | ||||||
| chr9:109050933
|
T | G | 1 | a0001c0001t0093g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1855-241A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109050933 | ||||||
| chr9:109051054
|
G | C | 1 | a0003c0004t0010g0318 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1855-362C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051054 | ||||||
| chr9:109051129
|
A | G | 2 | a0001c0001t0039g0159a0001c0001t0039g0165 | 2 | HG02486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1855-437T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051129 | ||||||
| chr9:109051241
|
G | A | 2 | a0001c0001t0003g0201a0001c0001t0003g0249 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1855-549C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051241 | ||||||
| chr9:109051295
|
A | AAC | 49 | a0001c0001t0004g0195a0001c0001t0004g0225a0001c0001t0004g0241others(46): Show | 49 | HG00408.hp2 HG00609.hp1 HG01099.hp1 others(46): Show |
intron_variant | MODIFIER | c.1855-605_1855-604d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | ||||||
| chr9:109051295
|
A | AACAC | 85 | a0001c0001t0002g0035a0001c0001t0002g0042a0001c0001t0002g0043others(82): Show | 85 | HG00609.hp2 HG00621.hp2 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.1855-607_1855-604d others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | ||||||
| chr9:109051295
|
A | AACACAC | 30 | a0001c0001t0007g0108a0001c0001t0007g0111a0001c0001t0007g0112others(27): Show | 30 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(27): Show |
intron_variant | MODIFIER | c.1855-609_1855-604d others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | ||||||
| chr9:109051295
|
A | AACACACA others(1): Show |
26 | a0001c0001t0002g0001a0001c0001t0002g0045a0001c0001t0002g0046others(23): Show | 27 | HG00140.hp1 HG01069.hp1 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1855-611_1855-604d others(10): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | ||||||
| chr9:109051295
|
A | AACACACA others(3): Show |
6 | a0003c0004t0009g0337a0003c0004t0010g0336a0003c0008t0095g0306others(3): Show | 6 | HG01109.hp1 HG02559.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1855-613_1855-604d others(12): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | ||||||
| chr9:109051295
|
A | AACACACA others(5): Show |
2 | a0003c0004t0049g0331a0003c0004t0118g0332 | 2 | HG02615.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1855-615_1855-604d others(14): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | ||||||
| chr9:109051295
|
A | AACACACA others(7): Show |
2 | a0001c0001t0080g0033a0003c0008t0017g0308 | 2 | HG00733.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1855-617_1855-604d others(16): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | ||||||
| chr9:109051295
|
A | AACACACA others(9): Show |
1 | a0004c0003t0032g0061 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1855-619_1855-604d others(18): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | ||||||
| chr9:109051295
|
A | AACACACA others(13): Show |
1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1855-623_1855-604d others(22): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | ||||||
| chr9:109051295
|
AAC | A | 104 | a0001c0001t0003g0202a0001c0001t0003g0203a0001c0001t0003g0205others(101): Show | 104 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.1855-605_1855-604d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | ||||||
| chr9:109051295
|
AACAC | A | 14 | a0001c0001t0006g0088a0001c0001t0006g0089a0001c0001t0029g0211others(11): Show | 14 | HG00438.hp2 HG04228.hp1 NA18948.hp1 others(11): Show |
intron_variant | MODIFIER | c.1855-607_1855-604d others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | ||||||
| chr9:109051295
|
AACACAC | A | 5 | a0001c0001t0003g0256a0001c0001t0022g0003a0001c0001t0022g0004others(2): Show | 5 | HG02622.hp2 HG02717.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1855-609_1855-604d others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | ||||||
| chr9:109051295
|
AACACACA others(11): Show |
A | 1 | a0001c0001t0105g0276 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1855-621_1855-604d others(20): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051295 | ||||||
| chr9:109051363
|
C | T | 4 | a0001c0001t0006g0078a0001c0001t0006g0095a0001c0001t0006g0099others(1): Show | 4 | NA18961.hp2 NA18998.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1855-671G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051363 | ||||||
| chr9:109051380
|
T | C | 1 | a0001c0001t0016g0084 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1855-688A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051380 | ||||||
| chr9:109051438
|
T | C | 31 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(28): Show | 31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1855-746A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051438 | ||||||
| chr9:109051521
|
C | A | 5 | a0001c0001t0008g0160a0001c0001t0008g0162a0001c0001t0008g0163others(2): Show | 5 | HG01192.hp2 HG02630.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1855-829G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051521 | ||||||
| chr9:109051551
|
C | T | 1 | a0001c0001t0013g0237 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1855-859G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051551 | ||||||
| chr9:109051552
|
G | A | 108 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(105): Show | 109 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(106): Show |
intron_variant | MODIFIER | c.1855-860C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051552 | ||||||
| chr9:109051921
|
G | C | 2 | a0001c0001t0045g0169a0001c0001t0045g0172 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1855-1229C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109051921 | ||||||
| chr9:109052055
|
T | C | 1 | a0001c0006t0084g0291 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1855-1363A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052055 | ||||||
| chr9:109052133
|
TTATTA | T | 27 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1855-1446_1855-144 others(9): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052133 | ||||||
| chr9:109052198
|
A | G | 111 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(108): Show | 112 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(109): Show |
intron_variant | MODIFIER | c.1855-1506T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052198 | ||||||
| chr9:109052218
|
C | T | 74 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(71): Show | 74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1855-1526G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052218 | ||||||
| chr9:109052387
|
C | T | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1855-1695G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052387 | ||||||
| chr9:109052439
|
T | C | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1855-1747A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052439 | ||||||
| chr9:109052476
|
A | G | 114 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0203others(111): Show | 114 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.1855-1784T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052476 | ||||||
| chr9:109052531
|
T | A | 27 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1855-1839A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052531 | ||||||
| chr9:109052673
|
A | G | 2 | a0001c0001t0025g0198a0001c0001t0026g0234 | 2 | HG02809.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1855-1981T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052673 | ||||||
| chr9:109052795
|
T | C | 1 | a0001c0001t0003g0255 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1855-2103A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052795 | ||||||
| chr9:109052823
|
A | T | 1 | a0001c0005t0003g0014 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1855-2131T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052823 | ||||||
| chr9:109052834
|
G | C | 2 | a0001c0001t0008g0162a0001c0001t0008g0163 | 2 | HG02630.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1855-2142C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052834 | ||||||
| chr9:109052852
|
A | G | 2 | a0001c0001t0025g0262a0001c0001t0065g0248 | 2 | HG01081.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1855-2160T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052852 | ||||||
| chr9:109052888
|
C | A | 8 | a0001c0001t0011g0189a0001c0001t0055g0188a0001c0006t0011g0280others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1855-2196G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052888 | ||||||
| chr9:109052918
|
CA | C | 31 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1855-2227delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109052918 | ||||||
| chr9:109053060
|
C | A | 135 | a0001c0001t0009g0030a0001c0001t0011g0189a0001c0001t0011g0275others(132): Show | 136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1855-2368G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053060 | ||||||
| chr9:109053080
|
T | G | 1 | a0001c0001t0003g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1855-2388A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053080 | ||||||
| chr9:109053200
|
C | T | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1855-2508G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053200 | ||||||
| chr9:109053209
|
T | C | 3 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0017t0117g0311 | 4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1855-2517A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053209 | ||||||
| chr9:109053376
|
G | A | 1 | a0001c0001t0004g0244 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1855-2684C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053376 | ||||||
| chr9:109053413
|
C | G | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1855-2721G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053413 | ||||||
| chr9:109053414
|
G | A | 99 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0203others(96): Show | 99 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.1855-2722C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053414 | ||||||
| chr9:109053618
|
G | C | 1 | a0001c0001t0038g0209 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1855-2926C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053618 | ||||||
| chr9:109053637
|
G | C | 99 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0203others(96): Show | 99 | HG00438.hp2 HG00544.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.1855-2945C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053637 | ||||||
| chr9:109053703
|
T | C | 1 | a0002c0002t0001g0376 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1855-3011A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109053703 | ||||||
| chr9:109054040
|
A | G | 1 | a0001c0001t0004g0235 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1854+3151T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109054040 | ||||||
| chr9:109054099
|
G | A | 2 | a0002c0002t0001g0397a0002c0002t0001g0398 | 2 | NA18963.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1854+3092C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109054099 | ||||||
| chr9:109054233
|
A | G | 1 | a0002c0002t0001g0354 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1854+2958T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109054233 | ||||||
| chr9:109054328
|
C | T | 1 | a0003c0004t0010g0336 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1854+2863G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109054328 | ||||||
| chr9:109054401
|
C | T | 7 | a0003c0008t0017g0304a0003c0008t0017g0308a0003c0008t0017g0309others(4): Show | 7 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1854+2790G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109054401 | ||||||
| chr9:109054622
|
C | CA | 4 | a0001c0001t0047g0031a0001c0009t0018g0002a0001c0009t0018g0302others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1854+2568dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109054622 | ||||||
| chr9:109054623
|
A | T | 74 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(71): Show | 74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1854+2568T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109054623 | ||||||
| chr9:109054691
|
G | A | 2 | a0002c0002t0001g0351a0002c0002t0019g0350 | 2 | HG00621.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1854+2500C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109054691 | ||||||
| chr9:109054722
|
T | C | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1854+2469A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109054722 | ||||||
| chr9:109055102
|
T | C | 1 | a0004c0003t0002g0056 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1854+2089A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055102 | ||||||
| chr9:109055148
|
T | A | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1854+2043A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055148 | ||||||
| chr9:109055165
|
C | G | 1 | a0001c0005t0003g0016 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1854+2026G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055165 | ||||||
| chr9:109055239
|
C | T | 31 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(28): Show | 31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1854+1952G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055239 | ||||||
| chr9:109055352
|
G | GCTGA | 32 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1854+1838_1854+183 others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055352 | ||||||
| chr9:109055477
|
C | T | 1 | a0001c0005t0024g0017 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1854+1714G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055477 | ||||||
| chr9:109055545
|
A | G | 3 | a0001c0001t0007g0077a0001c0001t0078g0118a0001c0001t0079g0119 | 3 | HG01891.hp2 HG02818.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1854+1646T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055545 | ||||||
| chr9:109055637
|
CT | C | 31 | a0001c0001t0003g0249a0001c0001t0009g0030a0001c0001t0093g0029others(28): Show | 31 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1854+1553delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055637 | ||||||
| chr9:109055674
|
AC | A | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1854+1516delG | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055674 | ||||||
| chr9:109055894
|
A | C | 29 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(26): Show | 29 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1854+1297T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055894 | ||||||
| chr9:109055929
|
C | T | 54 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(51): Show | 54 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.1854+1262G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109055929 | ||||||
| chr9:109056152
|
G | A | 1 | a0001c0001t0059g0269 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1854+1039C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056152 | ||||||
| chr9:109056232
|
C | T | 8 | a0001c0001t0011g0189a0001c0001t0055g0188a0001c0006t0011g0280others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1854+959G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056232 | ||||||
| chr9:109056319
|
T | G | 1 | a0001c0001t0066g0187 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1854+872A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056319 | ||||||
| chr9:109056321
|
T | C | 404 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(401): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.1854+870A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056321 | ||||||
| chr9:109056440
|
C | CA | 131 | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0049others(128): Show | 131 | HG00140.hp1 HG00408.hp2 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.1854+750dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056440 | ||||||
| chr9:109056440
|
C | CAA | 27 | a0001c0001t0005g0121a0001c0001t0005g0129a0001c0001t0005g0137others(24): Show | 27 | HG00609.hp1 HG01109.hp2 HG01169.hp2 others(24): Show |
intron_variant | MODIFIER | c.1854+749_1854+750d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056440 | ||||||
| chr9:109056440
|
C | CAAA | 29 | a0001c0001t0004g0239a0001c0001t0005g0123a0001c0001t0007g0108others(26): Show | 29 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1854+748_1854+750d others(5): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056440 | ||||||
| chr9:109056440
|
CA | C | 43 | a0001c0001t0006g0088a0001c0001t0006g0090a0001c0001t0006g0091others(40): Show | 43 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.1854+750delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056440 | ||||||
| chr9:109056440
|
CAAAAAAA others(4): Show |
C | 5 | a0001c0001t0008g0166a0001c0001t0008g0167a0001c0001t0008g0168others(2): Show | 5 | HG02965.hp2 HG02976.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1854+740_1854+750d others(13): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056440 | ||||||
| chr9:109056476
|
T | A | 1 | a0001c0001t0004g0235 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1854+715A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056476 | ||||||
| chr9:109056488
|
T | C | 404 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(401): Show | 406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.1854+703A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056488 | ||||||
| chr9:109056558
|
G | T | 1 | a0001c0001t0006g0091 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1854+633C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056558 | ||||||
| chr9:109056594
|
C | G | 1 | a0006c0011t0009g0338 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1854+597G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056594 | ||||||
| chr9:109056635
|
T | A | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1854+556A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109056635 | ||||||
| chr9:109057049
|
AG | A | 3 | a0001c0001t0003g0212a0001c0001t0003g0213a0001c0001t0037g0214 | 3 | HG00438.hp2 HG02071.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.1854+141delC | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109057049 | ||||||
| chr9:109057057
|
T | C | 1 | a0002c0002t0001g0378 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1854+134A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 12/17 | chr9 | 109057057 | ||||||
| chr9:109057480
|
C | T | 1 | a0003c0004t0087g0327 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1723-158G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057480 | ||||||
| chr9:109057494
|
T | C | 1 | a0001c0001t0003g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1723-172A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057494 | ||||||
| chr9:109057518
|
C | T | 36 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0203others(33): Show | 36 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1723-196G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057518 | ||||||
| chr9:109057622
|
G | A | 29 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(26): Show | 29 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1723-300C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057622 | ||||||
| chr9:109057656
|
C | G | 28 | a0001c0001t0004g0117a0001c0001t0006g0078a0001c0001t0006g0088others(25): Show | 28 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1723-334G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057656 | ||||||
| chr9:109057694
|
T | C | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1723-372A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057694 | ||||||
| chr9:109057775
|
G | A | 51 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(48): Show | 52 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.1723-453C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057775 | ||||||
| chr9:109057920
|
ACTTT | A | 34 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(31): Show | 34 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.1723-602_1723-599d others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057920 | ||||||
| chr9:109057925
|
C | CT | 101 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0203others(98): Show | 101 | HG00438.hp2 HG00544.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.1723-604dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057925 | ||||||
| chr9:109057925
|
CT | C | 14 | a0001c0001t0006g0098a0001c0001t0011g0278a0001c0001t0016g0084others(11): Show | 14 | HG01099.hp2 HG02735.hp1 HG03017.hp1 others(11): Show |
intron_variant | MODIFIER | c.1723-604delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057925 | ||||||
| chr9:109057982
|
C | T | 27 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1723-660G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109057982 | ||||||
| chr9:109058005
|
A | AT | 75 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(72): Show | 75 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.1723-684dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058005 | ||||||
| chr9:109058018
|
T | G | 4 | a0001c0001t0005g0101a0001c0001t0108g0083a0004c0003t0002g0063others(1): Show | 4 | HG01891.hp1 HG02055.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.1723-696A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058018 | ||||||
| chr9:109058020
|
G | A | 138 | a0001c0001t0009g0030a0001c0001t0011g0189a0001c0001t0011g0275others(135): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.1723-698C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058020 | ||||||
| chr9:109058086
|
C | T | 1 | a0001c0001t0008g0161 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1723-764G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058086 | ||||||
| chr9:109058114
|
C | A | 2 | a0001c0001t0025g0262a0001c0001t0065g0248 | 2 | HG01081.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1723-792G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058114 | ||||||
| chr9:109058239
|
C | T | 3 | a0001c0006t0050g0286a0001c0006t0050g0288a0001c0006t0085g0287 | 3 | HG02486.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1723-917G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058239 | ||||||
| chr9:109058296
|
G | C | 1 | a0002c0002t0001g0390 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1723-974C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058296 | ||||||
| chr9:109058328
|
T | C | 54 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(51): Show | 54 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.1723-1006A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058328 | ||||||
| chr9:109058409
|
T | C | 3 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0017t0117g0311 | 4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1723-1087A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058409 | ||||||
| chr9:109058557
|
T | C | 1 | a0001c0001t0007g0077 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1723-1235A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058557 | ||||||
| chr9:109058569
|
A | T | 3 | a0001c0001t0022g0003a0001c0001t0022g0004a0001c0001t0022g0005 | 3 | HG02622.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1723-1247T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058569 | ||||||
| chr9:109058653
|
G | T | 28 | a0001c0001t0004g0117a0001c0001t0006g0078a0001c0001t0006g0088others(25): Show | 28 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1723-1331C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058653 | ||||||
| chr9:109058670
|
T | C | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1723-1348A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058670 | ||||||
| chr9:109058872
|
C | T | 7 | a0003c0008t0017g0304a0003c0008t0017g0308a0003c0008t0017g0309others(4): Show | 7 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1722+1482G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058872 | ||||||
| chr9:109058934
|
C | T | 1 | a0001c0001t0077g0104 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1722+1420G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109058934 | ||||||
| chr9:109059175
|
G | A | 1 | a0001c0001t0005g0141 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1722+1179C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059175 | ||||||
| chr9:109059183
|
C | T | 1 | a0001c0001t0008g0166 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1722+1171G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059183 | ||||||
| chr9:109059185
|
A | T | 1 | a0001c0001t0008g0166 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1722+1169T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059185 | ||||||
| chr9:109059191
|
C | T | 8 | a0001c0001t0009g0030a0003c0004t0009g0326a0003c0004t0009g0329others(5): Show | 8 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1722+1163G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059191 | ||||||
| chr9:109059215
|
T | G | 8 | a0001c0001t0011g0189a0001c0001t0055g0188a0001c0006t0011g0280others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1722+1139A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059215 | ||||||
| chr9:109059250
|
A | C | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1722+1104T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059250 | ||||||
| chr9:109059641
|
C | T | 1 | a0001c0001t0002g0046 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1722+713G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059641 | ||||||
| chr9:109059662
|
G | A | 1 | a0001c0001t0013g0247 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1722+692C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059662 | ||||||
| chr9:109059672
|
G | A | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1722+682C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059672 | ||||||
| chr9:109059787
|
T | C | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1722+567A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059787 | ||||||
| chr9:109059910
|
GA | G | 29 | a0001c0001t0007g0107a0001c0001t0009g0030a0001c0001t0093g0029others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.1722+443delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109059910 | ||||||
| chr9:109060039
|
A | G | 1 | a0002c0002t0021g0386 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1722+315T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109060039 | ||||||
| chr9:109060054
|
T | C | 1 | a0001c0001t0006g0094 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1722+300A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109060054 | ||||||
| chr9:109060123
|
C | T | 4 | a0001c0006t0033g0289a0001c0006t0033g0290a0001c0006t0033g0292others(1): Show | 4 | HG01261.hp1 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1722+231G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109060123 | ||||||
| chr9:109060200
|
T | G | 3 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0017t0117g0311 | 4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1722+154A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109060200 | ||||||
| chr9:109060218
|
A | C | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1722+136T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109060218 | ||||||
| chr9:109060228
|
T | C | 29 | a0001c0001t0004g0082a0001c0001t0004g0182a0001c0001t0007g0077others(26): Show | 29 | HG00609.hp2 HG01891.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.1722+126A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 11/17 | chr9 | 109060228 | ||||||
| chr9:109060586
|
C | T | 74 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(71): Show | 74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1624-134G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060586 | ||||||
| chr9:109060610
|
G | A | 2 | a0001c0006t0055g0285a0001c0006t0104g0284 | 2 | HG01884.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1624-158C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060610 | ||||||
| chr9:109060754
|
C | A | 3 | a0001c0006t0050g0286a0001c0006t0050g0288a0001c0006t0085g0287 | 3 | HG02486.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1624-302G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060754 | ||||||
| chr9:109060774
|
G | A | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1624-322C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060774 | ||||||
| chr9:109060803
|
T | A | 29 | a0001c0001t0004g0082a0001c0001t0004g0182a0001c0001t0007g0077others(26): Show | 29 | HG00609.hp2 HG01891.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.1624-351A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060803 | ||||||
| chr9:109060816
|
A | T | 3 | a0002c0002t0001g0365a0002c0002t0001g0397a0002c0002t0001g0398 | 3 | NA18949.hp1 NA18963.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1624-364T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060816 | ||||||
| chr9:109060838
|
T | C | 1 | a0002c0002t0001g0357 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1624-386A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060838 | ||||||
| chr9:109060848
|
T | A | 1 | a0001c0001t0006g0089 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1624-396A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060848 | ||||||
| chr9:109060861
|
T | C | 1 | a0001c0001t0005g0150 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1624-409A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060861 | ||||||
| chr9:109060884
|
G | A | 174 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(171): Show | 175 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.1624-432C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060884 | ||||||
| chr9:109060897
|
A | G | 1 | a0001c0001t0105g0276 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1624-445T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060897 | ||||||
| chr9:109060914
|
T | C | 1 | a0001c0007t0004g0301 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1624-462A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109060914 | ||||||
| chr9:109061018
|
C | T | 25 | a0001c0001t0004g0117a0001c0001t0006g0078a0001c0001t0006g0088others(22): Show | 25 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.1624-566G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061018 | ||||||
| chr9:109061096
|
G | A | 1 | a0003c0004t0010g0315 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1624-644C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061096 | ||||||
| chr9:109061225
|
A | G | 27 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1624-773T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061225 | ||||||
| chr9:109061272
|
C | T | 27 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1624-820G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061272 | ||||||
| chr9:109061418
|
T | C | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1624-966A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061418 | ||||||
| chr9:109061630
|
G | C | 31 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(28): Show | 31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1624-1178C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061630 | ||||||
| chr9:109061668
|
G | A | 3 | a0001c0001t0004g0182a0001c0001t0074g0181a0001c0006t0033g0290 | 3 | HG01261.hp1 NA18957.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1624-1216C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061668 | ||||||
| chr9:109061669
|
A | G | 3 | a0003c0004t0010g0336a0003c0004t0049g0331a0003c0004t0049g0333 | 3 | HG02738.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1624-1217T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061669 | ||||||
| chr9:109061691
|
C | T | 4 | a0002c0002t0001g0361a0002c0002t0001g0362a0002c0002t0001g0363others(1): Show | 4 | HG00738.hp1 HG01123.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.1624-1239G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061691 | ||||||
| chr9:109061714
|
G | A | 74 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(71): Show | 74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1624-1262C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061714 | ||||||
| chr9:109061753
|
G | A | 7 | a0002c0002t0012g0355a0002c0002t0012g0373a0002c0002t0012g0379others(4): Show | 7 | HG01433.hp2 HG02004.hp1 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.1624-1301C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061753 | ||||||
| chr9:109061760
|
G | A | 74 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(71): Show | 74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1624-1308C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061760 | ||||||
| chr9:109061935
|
A | C | 1 | a0001c0001t0097g0131 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1624-1483T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061935 | ||||||
| chr9:109061943
|
G | A | 28 | a0001c0001t0004g0117a0001c0001t0006g0078a0001c0001t0006g0088others(25): Show | 28 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1624-1491C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061943 | ||||||
| chr9:109061970
|
CATAA | C | 7 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(4): Show | 7 | HG01070.hp2 HG01257.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.1624-1522_1624-151 others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109061970 | ||||||
| chr9:109062347
|
A | C | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1624-1895T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109062347 | ||||||
| chr9:109062453
|
T | A | 3 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0017t0117g0311 | 4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1624-2001A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109062453 | ||||||
| chr9:109062549
|
C | T | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1623+1928G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109062549 | ||||||
| chr9:109062661
|
T | A | 401 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(398): Show | 403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1623+1816A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109062661 | ||||||
| chr9:109062799
|
C | T | 1 | a0001c0001t0043g0050 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1623+1678G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109062799 | ||||||
| chr9:109062927
|
G | A | 2 | a0001c0001t0054g0174a0001c0001t0054g0176 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1623+1550C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109062927 | ||||||
| chr9:109062934
|
C | T | 3 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0017t0117g0311 | 4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1623+1543G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109062934 | ||||||
| chr9:109062978
|
G | GA | 28 | a0001c0001t0004g0117a0001c0001t0006g0078a0001c0001t0006g0088others(25): Show | 28 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.1623+1498dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109062978 | ||||||
| chr9:109062978
|
GA | G | 31 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1623+1498delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109062978 | ||||||
| chr9:109063076
|
A | T | 31 | a0001c0001t0004g0117a0001c0001t0006g0078a0001c0001t0006g0088others(28): Show | 31 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(28): Show |
intron_variant | MODIFIER | c.1623+1401T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063076 | ||||||
| chr9:109063131
|
C | CT | 9 | a0003c0008t0017g0304a0003c0008t0017g0308a0003c0008t0017g0309others(6): Show | 9 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1623+1345dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063131 | ||||||
| chr9:109063140
|
G | A | 2 | a0006c0011t0009g0338a0006c0011t0009g0339 | 2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1623+1337C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063140 | ||||||
| chr9:109063205
|
TGCCTCCC others(25): Show |
T | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1623+1240_1623+127 others(36): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063205 | ||||||
| chr9:109063512
|
A | G | 1 | a0001c0001t0005g0157 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1623+965T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063512 | ||||||
| chr9:109063521
|
T | A | 2 | a0001c0001t0005g0101a0001c0001t0108g0083 | 2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1623+956A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063521 | ||||||
| chr9:109063694
|
A | G | 1 | a0001c0001t0054g0176 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1623+783T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063694 | ||||||
| chr9:109063752
|
A | T | 55 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(52): Show | 56 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.1623+725T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063752 | ||||||
| chr9:109063767
|
T | A | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1623+710A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063767 | ||||||
| chr9:109063835
|
C | A | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1623+642G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109063835 | ||||||
| chr9:109064128
|
AC | A | 4 | a0001c0001t0004g0242a0001c0001t0004g0244a0001c0001t0027g0196others(1): Show | 4 | HG01346.hp2 HG02148.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.1623+348delG | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109064128 | ||||||
| chr9:109064190
|
C | T | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1623+287G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109064190 | ||||||
| chr9:109064259
|
A | G | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1623+218T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109064259 | ||||||
| chr9:109064306
|
C | T | 1 | a0001c0001t0005g0157 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1623+171G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 10/17 | chr9 | 109064306 | ||||||
| chr9:109064773
|
G | A | 1 | a0001c0001t0093g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1533-206C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109064773 | ||||||
| chr9:109064773
|
G | C | 1 | a0002c0002t0001g0388 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1533-206C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109064773 | ||||||
| chr9:109064928
|
C | T | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1533-361G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109064928 | ||||||
| chr9:109064941
|
C | A | 1 | a0003c0004t0118g0332 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1533-374G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109064941 | ||||||
| chr9:109064945
|
G | A | 28 | a0001c0001t0011g0275a0001c0001t0011g0277a0001c0001t0011g0278others(25): Show | 28 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1533-378C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109064945 | ||||||
| chr9:109064974
|
T | C | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1533-407A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109064974 | ||||||
| chr9:109065298
|
G | A | 3 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0017t0117g0311 | 4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1533-731C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109065298 | ||||||
| chr9:109065334
|
G | C | 57 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(54): Show | 59 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1533-767C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109065334 | ||||||
| chr9:109065397
|
TG | T | 418 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(415): Show | 420 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(417): Show |
intron_variant | MODIFIER | c.1533-831delC | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109065397 | ||||||
| chr9:109065447
|
A | C | 3 | a0001c0001t0016g0084a0001c0001t0016g0086a0001c0001t0016g0087 | 3 | HG02027.hp2 HG02074.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1533-880T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109065447 | ||||||
| chr9:109065631
|
T | C | 2 | a0001c0001t0054g0174a0001c0001t0054g0176 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1533-1064A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109065631 | ||||||
| chr9:109065694
|
G | A | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1533-1127C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109065694 | ||||||
| chr9:109065726
|
C | T | 2 | a0002c0002t0001g0357a0008c0019t0001g0406 | 2 | HG00741.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1533-1159G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109065726 | ||||||
| chr9:109065743
|
T | G | 1 | a0001c0001t0108g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1533-1176A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109065743 | ||||||
| chr9:109065758
|
G | T | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1533-1191C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109065758 | ||||||
| chr9:109066315
|
C | A | 2 | a0003c0004t0009g0340a0003c0004t0103g0328 | 2 | HG01106.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1533-1748G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066315 | ||||||
| chr9:109066378
|
C | T | 1 | a0001c0001t0025g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1533-1811G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066378 | ||||||
| chr9:109066391
|
G | A | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1533-1824C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066391 | ||||||
| chr9:109066419
|
C | T | 3 | a0001c0001t0007g0106a0001c0001t0007g0108a0001c0001t0007g0112 | 3 | HG02132.hp2 NA18977.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1533-1852G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066419 | ||||||
| chr9:109066452
|
C | CA | 95 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0042others(92): Show | 96 | HG00408.hp1 HG00558.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.1533-1886dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | ||||||
| chr9:109066452
|
C | CAA | 35 | a0001c0001t0002g0035a0001c0001t0003g0265a0001c0001t0004g0235others(32): Show | 35 | HG00738.hp2 HG01074.hp1 HG01106.hp2 others(32): Show |
intron_variant | MODIFIER | c.1533-1887_1533-188 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | ||||||
| chr9:109066452
|
C | CAAA | 51 | a0001c0001t0013g0230a0001c0001t0029g0199a0001c0001t0071g0240others(48): Show | 51 | HG00099.hp1 HG00621.hp1 HG01070.hp2 others(48): Show |
intron_variant | MODIFIER | c.1533-1888_1533-188 others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | ||||||
| chr9:109066452
|
C | CAAAA | 18 | a0001c0001t0003g0266a0001c0001t0004g0228a0001c0001t0026g0233others(15): Show | 18 | HG00438.hp1 HG00735.hp2 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.1533-1889_1533-188 others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | ||||||
| chr9:109066452
|
C | CAAAAA | 22 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(19): Show | 22 | HG00544.hp2 HG01081.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.1533-1890_1533-188 others(9): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | ||||||
| chr9:109066452
|
C | CAAAAAA | 32 | a0001c0001t0003g0201a0001c0001t0003g0203a0001c0001t0003g0210others(29): Show | 32 | HG00438.hp2 HG01070.hp1 HG01071.hp1 others(29): Show |
intron_variant | MODIFIER | c.1533-1891_1533-188 others(10): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | ||||||
| chr9:109066452
|
C | CAAAAAAA | 13 | a0001c0001t0003g0251a0001c0001t0003g0256a0001c0001t0011g0277others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.1533-1892_1533-188 others(11): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | ||||||
| chr9:109066452
|
C | CAAAAAAA others(1): Show |
9 | a0001c0001t0003g0202a0001c0001t0038g0252a0001c0006t0011g0280others(6): Show | 9 | HG01109.hp1 HG02647.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1533-1893_1533-188 others(12): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | ||||||
| chr9:109066452
|
C | CAAAAAAA others(2): Show |
11 | a0001c0001t0011g0189a0001c0001t0055g0188a0001c0006t0011g0281others(8): Show | 11 | HG00733.hp1 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1533-1894_1533-188 others(13): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | ||||||
| chr9:109066452
|
C | CAAAAAAA others(3): Show |
3 | a0001c0001t0011g0275a0001c0001t0105g0276a0003c0008t0089g0305 | 3 | HG02145.hp1 HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1533-1895_1533-188 others(14): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | ||||||
| chr9:109066452
|
C | CAAAAAAA others(4): Show |
1 | a0001c0001t0011g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1533-1896_1533-188 others(15): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | ||||||
| chr9:109066452
|
CA | C | 6 | a0001c0001t0006g0096a0001c0001t0007g0179a0001c0001t0022g0005others(3): Show | 7 | HG01433.hp1 HG01496.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1533-1886delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | ||||||
| chr9:109066452
|
CAAAAAAA | C | 35 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(32): Show | 35 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1533-1892_1533-188 others(11): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066452 | ||||||
| chr9:109066573
|
A | C | 3 | a0001c0001t0022g0003a0001c0001t0022g0004a0001c0001t0022g0005 | 3 | HG02622.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1533-2006T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066573 | ||||||
| chr9:109066613
|
T | C | 9 | a0003c0008t0017g0304a0003c0008t0017g0308a0003c0008t0017g0309others(6): Show | 9 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1533-2046A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066613 | ||||||
| chr9:109066732
|
T | C | 1 | a0004c0003t0048g0055 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1533-2165A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066732 | ||||||
| chr9:109066885
|
G | A | 28 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(25): Show | 28 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1533-2318C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109066885 | ||||||
| chr9:109067056
|
C | CA | 137 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0203others(134): Show | 137 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.1533-2490dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067056 | ||||||
| chr9:109067056
|
CA | C | 6 | a0001c0001t0004g0235a0001c0001t0006g0096a0001c0001t0014g0076others(3): Show | 6 | HG01074.hp1 HG01168.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1533-2490delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067056 | ||||||
| chr9:109067083
|
A | T | 3 | a0001c0001t0026g0183a0001c0001t0061g0186a0001c0001t0067g0185 | 3 | HG02109.hp2 HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1533-2516T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067083 | ||||||
| chr9:109067130
|
T | C | 1 | a0001c0001t0108g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1533-2563A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067130 | ||||||
| chr9:109067292
|
G | A | 9 | a0003c0008t0017g0304a0003c0008t0017g0308a0003c0008t0017g0309others(6): Show | 9 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1533-2725C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067292 | ||||||
| chr9:109067402
|
T | G | 1 | a0003c0012t0088g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1533-2835A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067402 | ||||||
| chr9:109067407
|
A | T | 28 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(25): Show | 28 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1533-2840T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067407 | ||||||
| chr9:109067477
|
T | G | 106 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(103): Show | 106 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.1533-2910A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067477 | ||||||
| chr9:109067512
|
C | T | 80 | a0001c0009t0018g0002a0001c0009t0018g0302a0002c0002t0001g0346others(77): Show | 81 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.1533-2945G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067512 | ||||||
| chr9:109067779
|
C | T | 1 | a0003c0012t0088g0022 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1533-3212G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067779 | ||||||
| chr9:109067821
|
T | A | 2 | a0001c0001t0007g0107a0001c0001t0083g0109 | 2 | HG00609.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1533-3254A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067821 | ||||||
| chr9:109067973
|
A | G | 3 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0017t0117g0311 | 4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1533-3406T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109067973 | ||||||
| chr9:109068055
|
A | G | 1 | a0001c0001t0005g0123 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1533-3488T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068055 | ||||||
| chr9:109068090
|
G | A | 19 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(16): Show | 19 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1533-3523C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068090 | ||||||
| chr9:109068093
|
C | T | 1 | a0001c0001t0005g0146 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1533-3526G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068093 | ||||||
| chr9:109068171
|
T | C | 19 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(16): Show | 19 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1533-3604A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068171 | ||||||
| chr9:109068295
|
G | A | 1 | a0001c0001t0108g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1533-3728C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068295 | ||||||
| chr9:109068301
|
C | T | 38 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(35): Show | 38 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1533-3734G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068301 | ||||||
| chr9:109068369
|
CA | C | 305 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0203others(302): Show | 305 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(302): Show |
intron_variant | MODIFIER | c.1533-3803delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068369 | ||||||
| chr9:109068411
|
C | T | 5 | a0003c0004t0009g0337a0003c0004t0010g0336a0003c0004t0049g0331others(2): Show | 5 | HG02559.hp1 HG02615.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1533-3844G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068411 | ||||||
| chr9:109068778
|
T | C | 2 | a0001c0001t0005g0101a0001c0001t0108g0083 | 2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1533-4211A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068778 | ||||||
| chr9:109068797
|
C | T | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1533-4230G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068797 | ||||||
| chr9:109068823
|
G | A | 1 | a0001c0001t0007g0113 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1533-4256C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109068823 | ||||||
| chr9:109069175
|
A | G | 1 | a0001c0001t0003g0250 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1532+4181T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109069175 | ||||||
| chr9:109069238
|
A | G | 1 | a0001c0001t0040g0271 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1532+4118T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109069238 | ||||||
| chr9:109069320
|
G | A | 84 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(81): Show | 86 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.1532+4036C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109069320 | ||||||
| chr9:109069545
|
G | A | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1532+3811C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109069545 | ||||||
| chr9:109069597
|
C | T | 1 | a0003c0017t0117g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1532+3759G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109069597 | ||||||
| chr9:109069601
|
T | C | 31 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(28): Show | 31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1532+3755A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109069601 | ||||||
| chr9:109069620
|
C | T | 4 | a0003c0008t0017g0304a0003c0008t0017g0309a0003c0008t0017g0310others(1): Show | 4 | HG02145.hp1 HG02257.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1532+3736G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109069620 | ||||||
| chr9:109069661
|
C | A | 1 | a0001c0001t0005g0101 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1532+3695G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109069661 | ||||||
| chr9:109069912
|
G | C | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1532+3444C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109069912 | ||||||
| chr9:109070130
|
A | G | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1532+3226T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070130 | ||||||
| chr9:109070175
|
C | A | 1 | a0007c0014t0047g0243 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1532+3181G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070175 | ||||||
| chr9:109070191
|
A | T | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1532+3165T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070191 | ||||||
| chr9:109070211
|
C | T | 3 | a0002c0002t0001g0365a0002c0002t0001g0397a0002c0002t0001g0398 | 3 | NA18949.hp1 NA18963.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1532+3145G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070211 | ||||||
| chr9:109070240
|
C | T | 1 | a0003c0004t0103g0328 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1532+3116G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070240 | ||||||
| chr9:109070362
|
A | G | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1532+2994T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070362 | ||||||
| chr9:109070406
|
G | C | 1 | a0001c0001t0002g0051 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1532+2950C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070406 | ||||||
| chr9:109070531
|
C | A | 2 | a0001c0001t0054g0174a0001c0001t0054g0176 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1532+2825G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070531 | ||||||
| chr9:109070550
|
G | T | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1532+2806C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070550 | ||||||
| chr9:109070650
|
TATG | T | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1532+2703_1532+270 others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070650 | ||||||
| chr9:109070779
|
A | T | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1532+2577T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070779 | ||||||
| chr9:109070849
|
C | T | 1 | a0002c0002t0020g0370 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1532+2507G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070849 | ||||||
| chr9:109070985
|
G | A | 3 | a0001c0001t0015g0026a0001c0001t0015g0027a0001c0001t0015g0028 | 3 | HG02809.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1532+2371C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109070985 | ||||||
| chr9:109071022
|
C | T | 32 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1532+2334G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071022 | ||||||
| chr9:109071171
|
C | T | 1 | a0001c0001t0069g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1532+2185G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071171 | ||||||
| chr9:109071174
|
C | T | 1 | a0001c0001t0004g0117 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1532+2182G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071174 | ||||||
| chr9:109071186
|
A | T | 1 | a0001c0005t0003g0012 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1532+2170T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071186 | ||||||
| chr9:109071231
|
G | C | 1 | a0001c0001t0011g0275 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1532+2125C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071231 | ||||||
| chr9:109071466
|
T | C | 13 | a0002c0002t0001g0365a0002c0002t0001g0397a0002c0002t0001g0398others(10): Show | 13 | HG01433.hp2 HG02004.hp1 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.1532+1890A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071466 | ||||||
| chr9:109071511
|
G | T | 74 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(71): Show | 74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1532+1845C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071511 | ||||||
| chr9:109071512
|
G | A | 74 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(71): Show | 74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1532+1844C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071512 | ||||||
| chr9:109071516
|
A | G | 1 | a0001c0001t0025g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1532+1840T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071516 | ||||||
| chr9:109071518
|
T | G | 1 | a0001c0001t0025g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1532+1838A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071518 | ||||||
| chr9:109071521
|
T | A | 1 | a0001c0001t0025g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1532+1835A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071521 | ||||||
| chr9:109071538
|
A | G | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1532+1818T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071538 | ||||||
| chr9:109071557
|
T | C | 55 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(52): Show | 56 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.1532+1799A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071557 | ||||||
| chr9:109071603
|
C | CA | 136 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(133): Show | 137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.1532+1752dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071603 | ||||||
| chr9:109071608
|
A | C | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1532+1748T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071608 | ||||||
| chr9:109071619
|
A | T | 1 | a0001c0001t0008g0166 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1532+1737T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071619 | ||||||
| chr9:109071659
|
T | A | 1 | a0002c0002t0001g0374 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1532+1697A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071659 | ||||||
| chr9:109071923
|
CTAGAGAG | C | 57 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(54): Show | 59 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.1532+1426_1532+143 others(11): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071923 | ||||||
| chr9:109071926
|
G | C | 29 | a0001c0001t0004g0082a0001c0001t0004g0182a0001c0001t0007g0077others(26): Show | 29 | HG00609.hp2 HG01891.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.1532+1430C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071926 | ||||||
| chr9:109071941
|
A | G | 2 | a0002c0002t0001g0374a0002c0002t0019g0356 | 2 | NA18944.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1532+1415T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109071941 | ||||||
| chr9:109072025
|
C | A | 31 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1532+1331G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109072025 | ||||||
| chr9:109072189
|
T | TTCCCATA others(17): Show |
1 | a0001c0001t0065g0248 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1532+1143_1532+116 others(28): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109072189 | ||||||
| chr9:109072493
|
C | T | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1532+863G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109072493 | ||||||
| chr9:109072658
|
C | G | 2 | a0003c0004t0009g0326a0003c0004t0009g0330 | 2 | HG03017.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1532+698G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109072658 | ||||||
| chr9:109072703
|
G | A | 27 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1532+653C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109072703 | ||||||
| chr9:109072754
|
T | C | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1532+602A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109072754 | ||||||
| chr9:109073125
|
T | C | 1 | a0001c0001t0007g0107 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1532+231A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109073125 | ||||||
| chr9:109073258
|
A | C | 29 | a0001c0001t0004g0082a0001c0001t0004g0182a0001c0001t0007g0077others(26): Show | 29 | HG00609.hp2 HG01891.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.1532+98T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109073258 | ||||||
| chr9:109073334
|
T | C | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1532+22A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109073334 | ||||||
| chr9:109073344
|
C | T | 1 | a0001c0001t0003g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1532+12G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 9/17 | chr9 | 109073344 | ||||||
| chr9:109073614
|
C | T | 3 | a0003c0004t0010g0312a0003c0004t0010g0313a0003c0004t0010g0343 | 3 | HG03041.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1450-176G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073614 | ||||||
| chr9:109073615
|
G | A | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1450-177C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073615 | ||||||
| chr9:109073680
|
A | G | 53 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(50): Show | 54 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1450-242T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073680 | ||||||
| chr9:109073682
|
A | T | 2 | a0001c0001t0054g0174a0001c0001t0054g0176 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1450-244T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073682 | ||||||
| chr9:109073716
|
T | C | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1450-278A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073716 | ||||||
| chr9:109073745
|
G | A | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1450-307C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073745 | ||||||
| chr9:109073833
|
T | C | 3 | a0001c0006t0050g0286a0001c0006t0050g0288a0001c0006t0085g0287 | 3 | HG02486.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1450-395A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073833 | ||||||
| chr9:109073844
|
CTTTTTTT others(8): Show |
C | 5 | a0001c0001t0003g0255a0001c0001t0003g0256a0001c0001t0035g0253others(2): Show | 5 | NA18986.hp1 NA19057.hp1 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.1450-421_1450-407d others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073844 | ||||||
| chr9:109073853
|
T | G | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0002c0002t0019g0350others(1): Show | 5 | HG00621.hp1 HG01433.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1450-415A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073853 | ||||||
| chr9:109073856
|
G | GT | 139 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(136): Show | 140 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.1450-419dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073856 | ||||||
| chr9:109073856
|
G | GTT | 13 | a0001c0001t0002g0046a0001c0001t0002g0190a0001c0016t0030g0293others(10): Show | 13 | HG00733.hp1 HG01123.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.1450-420_1450-419d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073856 | ||||||
| chr9:109073856
|
G | GTTT | 20 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0329others(17): Show | 20 | HG00099.hp2 HG00140.hp2 HG01358.hp2 others(17): Show |
intron_variant | MODIFIER | c.1450-421_1450-419d others(5): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073856 | ||||||
| chr9:109073856
|
G | T | 5 | a0001c0006t0033g0289a0001c0006t0033g0290a0001c0006t0033g0292others(2): Show | 5 | HG01261.hp1 HG02572.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1450-418C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073856 | ||||||
| chr9:109073864
|
T | G | 39 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(36): Show | 39 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.1450-426A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073864 | ||||||
| chr9:109073865
|
T | G | 48 | a0001c0001t0003g0215a0001c0001t0003g0220a0001c0001t0004g0193others(45): Show | 48 | HG00558.hp1 HG00639.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.1450-427A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073865 | ||||||
| chr9:109073867
|
T | G | 2 | a0001c0001t0054g0174a0001c0001t0054g0176 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1450-429A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073867 | ||||||
| chr9:109073903
|
C | A | 2 | a0001c0001t0054g0174a0001c0001t0054g0176 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1450-465G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073903 | ||||||
| chr9:109073978
|
A | G | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1450-540T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109073978 | ||||||
| chr9:109074104
|
T | C | 27 | a0001c0001t0004g0117a0001c0001t0006g0078a0001c0001t0006g0088others(24): Show | 27 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.1450-666A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074104 | ||||||
| chr9:109074110
|
T | C | 1 | a0001c0001t0008g0167 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1450-672A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074110 | ||||||
| chr9:109074269
|
T | C | 1 | a0001c0001t0004g0227 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1450-831A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074269 | ||||||
| chr9:109074299
|
C | T | 1 | a0001c0001t0005g0145 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1450-861G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074299 | ||||||
| chr9:109074386
|
C | T | 1 | a0001c0001t0006g0088 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1450-948G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074386 | ||||||
| chr9:109074391
|
C | A | 3 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0017t0117g0311 | 4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450-953G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074391 | ||||||
| chr9:109074462
|
G | T | 8 | a0001c0001t0003g0255a0001c0001t0003g0256a0001c0001t0003g0257others(5): Show | 8 | NA18964.hp2 NA18986.hp1 NA18998.hp2 others(5): Show |
intron_variant | MODIFIER | c.1450-1024C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074462 | ||||||
| chr9:109074477
|
A | G | 4 | a0002c0002t0001g0371a0002c0002t0001g0382a0002c0002t0001g0383others(1): Show | 4 | HG00735.hp2 HG01515.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1450-1039T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074477 | ||||||
| chr9:109074479
|
G | A | 4 | a0002c0002t0001g0371a0002c0002t0001g0382a0002c0002t0001g0383others(1): Show | 4 | HG00735.hp2 HG01515.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1450-1041C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074479 | ||||||
| chr9:109074524
|
G | A | 2 | a0001c0001t0007g0107a0001c0001t0083g0109 | 2 | HG00609.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1450-1086C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074524 | ||||||
| chr9:109074661
|
G | A | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1450-1223C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074661 | ||||||
| chr9:109074715
|
G | A | 1 | a0001c0001t0093g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1450-1277C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074715 | ||||||
| chr9:109074785
|
C | T | 38 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(35): Show | 38 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1450-1347G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074785 | ||||||
| chr9:109074814
|
G | A | 38 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(35): Show | 38 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.1450-1376C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074814 | ||||||
| chr9:109074837
|
C | T | 2 | a0001c0001t0097g0131a0001c0001t0098g0132 | 2 | NA18968.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1450-1399G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074837 | ||||||
| chr9:109074952
|
C | T | 1 | a0001c0001t0047g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1450-1514G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074952 | ||||||
| chr9:109074960
|
T | A | 1 | a0001c0001t0030g0110 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1450-1522A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109074960 | ||||||
| chr9:109075025
|
T | A | 3 | a0001c0001t0006g0090a0001c0001t0006g0100a0001c0001t0031g0079 | 3 | HG03834.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1450-1587A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075025 | ||||||
| chr9:109075030
|
C | T | 1 | a0001c0001t0007g0105 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1450-1592G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075030 | ||||||
| chr9:109075088
|
G | C | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1450-1650C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075088 | ||||||
| chr9:109075112
|
T | C | 1 | a0001c0001t0006g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1450-1674A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075112 | ||||||
| chr9:109075214
|
C | T | 6 | a0001c0001t0025g0184a0001c0001t0026g0183a0001c0001t0026g0233others(3): Show | 6 | HG01255.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1450-1776G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075214 | ||||||
| chr9:109075290
|
T | C | 1 | a0001c0001t0008g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1450-1852A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075290 | ||||||
| chr9:109075366
|
T | C | 1 | a0001c0001t0002g0051 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1450-1928A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075366 | ||||||
| chr9:109075496
|
T | C | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1450-2058A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075496 | ||||||
| chr9:109075511
|
A | T | 139 | a0001c0001t0009g0030a0001c0001t0011g0189a0001c0001t0011g0275others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1450-2073T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075511 | ||||||
| chr9:109075584
|
A | T | 39 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(36): Show | 39 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.1450-2146T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075584 | ||||||
| chr9:109075751
|
G | A | 1 | a0001c0001t0011g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1450-2313C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109075751 | ||||||
| chr9:109076185
|
T | C | 3 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0017t0117g0311 | 4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1450-2747A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076185 | ||||||
| chr9:109076255
|
C | CCAT | 403 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(400): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1450-2820_1450-281 others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076255 | ||||||
| chr9:109076312
|
T | C | 27 | a0001c0001t0004g0117a0001c0001t0006g0078a0001c0001t0006g0088others(24): Show | 27 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(24): Show |
intron_variant | MODIFIER | c.1450-2874A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076312 | ||||||
| chr9:109076322
|
C | A | 1 | a0001c0001t0008g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1450-2884G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076322 | ||||||
| chr9:109076385
|
TG | T | 403 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(400): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1450-2948delC | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076385 | ||||||
| chr9:109076435
|
A | G | 2 | a0001c0001t0101g0151a0001c0001t0107g0156 | 2 | HG01256.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1450-2997T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076435 | ||||||
| chr9:109076443
|
T | A | 32 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1450-3005A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076443 | ||||||
| chr9:109076470
|
C | T | 32 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1450-3032G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076470 | ||||||
| chr9:109076530
|
TA | T | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1450-3093delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076530 | ||||||
| chr9:109076530
|
TAA | T | 27 | a0001c0001t0093g0029a0003c0004t0009g0326a0003c0004t0009g0329others(24): Show | 27 | HG00099.hp2 HG01106.hp1 HG01358.hp2 others(24): Show |
intron_variant | MODIFIER | c.1450-3094_1450-309 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076530 | ||||||
| chr9:109076538
|
A | G | 1 | a0001c0001t0003g0257 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1450-3100T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076538 | ||||||
| chr9:109076602
|
G | A | 1 | a0001c0001t0003g0257 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1450-3164C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076602 | ||||||
| chr9:109076752
|
G | A | 1 | a0001c0007t0027g0298 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1450-3314C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076752 | ||||||
| chr9:109076846
|
A | G | 1 | a0001c0001t0091g0127 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1450-3408T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076846 | ||||||
| chr9:109076971
|
G | A | 1 | a0001c0001t0064g0245 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1450-3533C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109076971 | ||||||
| chr9:109077132
|
C | T | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1450-3694G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109077132 | ||||||
| chr9:109077142
|
T | C | 1 | a0002c0002t0001g0391 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1449+3697A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109077142 | ||||||
| chr9:109077226
|
C | T | 26 | a0001c0001t0004g0082a0001c0001t0004g0182a0001c0001t0007g0105others(23): Show | 26 | HG00609.hp2 HG02132.hp2 HG02809.hp2 others(23): Show |
intron_variant | MODIFIER | c.1449+3613G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109077226 | ||||||
| chr9:109077401
|
C | T | 2 | a0003c0004t0009g0337a0003c0004t0118g0332 | 2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1449+3438G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109077401 | ||||||
| chr9:109077466
|
T | C | 8 | a0001c0001t0011g0189a0001c0001t0055g0188a0001c0006t0011g0280others(5): Show | 8 | HG01884.hp1 HG02109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1449+3373A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109077466 | ||||||
| chr9:109077669
|
T | A | 51 | a0001c0001t0003g0215a0001c0001t0003g0220a0001c0001t0003g0261others(48): Show | 51 | HG00558.hp1 HG00639.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.1449+3170A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109077669 | ||||||
| chr9:109077873
|
T | C | 2 | a0001c0001t0005g0140a0001c0001t0005g0142 | 2 | NA18971.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1449+2966A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109077873 | ||||||
| chr9:109077956
|
G | C | 1 | a0003c0004t0051g0314 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1449+2883C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109077956 | ||||||
| chr9:109078097
|
T | G | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1449+2742A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078097 | ||||||
| chr9:109078220
|
C | T | 403 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(400): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1449+2619G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078220 | ||||||
| chr9:109078302
|
TAAAAG | T | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1449+2532_1449+253 others(9): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078302 | ||||||
| chr9:109078352
|
T | A | 1 | a0001c0001t0004g0182 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1449+2487A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078352 | ||||||
| chr9:109078353
|
C | T | 1 | a0001c0001t0004g0182 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1449+2486G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078353 | ||||||
| chr9:109078382
|
A | C | 29 | a0001c0001t0004g0082a0001c0001t0004g0182a0001c0001t0007g0077others(26): Show | 29 | HG00609.hp2 HG01891.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.1449+2457T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078382 | ||||||
| chr9:109078518
|
A | G | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1449+2321T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078518 | ||||||
| chr9:109078619
|
T | C | 1 | a0002c0002t0019g0396 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1449+2220A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078619 | ||||||
| chr9:109078690
|
G | A | 1 | a0001c0005t0024g0011 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1449+2149C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078690 | ||||||
| chr9:109078732
|
T | C | 6 | a0001c0001t0004g0182a0001c0001t0007g0179a0001c0001t0007g0180others(3): Show | 6 | HG04204.hp2 NA18946.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.1449+2107A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078732 | ||||||
| chr9:109078874
|
T | A | 28 | a0001c0001t0011g0189a0001c0001t0011g0277a0001c0001t0011g0278others(25): Show | 28 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.1449+1965A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078874 | ||||||
| chr9:109078896
|
T | C | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1449+1943A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078896 | ||||||
| chr9:109078937
|
A | G | 6 | a0001c0001t0025g0184a0001c0001t0026g0183a0001c0001t0026g0233others(3): Show | 6 | HG01255.hp1 HG02109.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1449+1902T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109078937 | ||||||
| chr9:109079014
|
T | C | 3 | a0001c0001t0009g0030a0003c0004t0009g0329a0003c0004t0009g0341 | 3 | HG00099.hp2 HG00140.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1449+1825A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079014 | ||||||
| chr9:109079019
|
A | G | 1 | a0001c0001t0081g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1449+1820T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079019 | ||||||
| chr9:109079082
|
T | C | 1 | a0001c0001t0005g0123 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1449+1757A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079082 | ||||||
| chr9:109079212
|
T | C | 192 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(189): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.1449+1627A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079212 | ||||||
| chr9:109079218
|
T | C | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1449+1621A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079218 | ||||||
| chr9:109079314
|
C | A | 3 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0017t0117g0311 | 4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1449+1525G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079314 | ||||||
| chr9:109079496
|
A | G | 6 | a0001c0001t0008g0160a0001c0001t0008g0161a0001c0001t0008g0162others(3): Show | 6 | HG01192.hp2 HG02630.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1449+1343T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079496 | ||||||
| chr9:109079508
|
G | A | 1 | a0003c0008t0017g0308 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1449+1331C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079508 | ||||||
| chr9:109079901
|
T | C | 5 | a0001c0001t0058g0006a0001c0006t0033g0289a0001c0006t0033g0290others(2): Show | 5 | HG01261.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1449+938A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079901 | ||||||
| chr9:109079914
|
A | C | 225 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(222): Show | 226 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(223): Show |
intron_variant | MODIFIER | c.1449+925T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109079914 | ||||||
| chr9:109080137
|
T | A | 27 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1449+702A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080137 | ||||||
| chr9:109080246
|
C | T | 1 | a0001c0001t0105g0276 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1449+593G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080246 | ||||||
| chr9:109080256
|
G | T | 1 | a0001c0001t0004g0217 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1449+583C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080256 | ||||||
| chr9:109080522
|
A | G | 32 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1449+317T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080522 | ||||||
| chr9:109080551
|
TA | T | 4 | a0001c0001t0008g0160a0001c0001t0008g0162a0001c0001t0008g0163others(1): Show | 4 | HG01192.hp2 HG02630.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.1449+287delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080551 | ||||||
| chr9:109080572
|
GTTC | G | 3 | a0001c0001t0022g0003a0001c0001t0022g0004a0001c0001t0022g0005 | 3 | HG02622.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1449+264_1449+266d others(5): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080572 | ||||||
| chr9:109080620
|
C | T | 1 | a0002c0002t0001g0403 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1449+219G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080620 | ||||||
| chr9:109080637
|
A | C | 1 | a0001c0001t0015g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1449+202T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080637 | ||||||
| chr9:109080756
|
GCC | G | 19 | a0001c0001t0011g0189a0001c0001t0011g0277a0001c0001t0011g0278others(16): Show | 19 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.1449+81_1449+82del others(2): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080756 | ||||||
| chr9:109080775
|
A | T | 417 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(414): Show | 419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.1449+64T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 8/17 | chr9 | 109080775 | ||||||
| chr9:109081326
|
A | C | 1 | a0001c0001t0025g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1345-383T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109081326 | ||||||
| chr9:109081332
|
G | A | 9 | a0002c0002t0001g0411a0002c0002t0001g0412a0002c0002t0001g0413others(6): Show | 9 | NA18946.hp1 NA18956.hp1 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.1345-389C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109081332 | ||||||
| chr9:109081614
|
G | C | 1 | a0001c0001t0023g0259 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1345-671C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109081614 | ||||||
| chr9:109081615
|
G | A | 1 | a0003c0004t0010g0336 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1345-672C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109081615 | ||||||
| chr9:109081625
|
T | C | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1345-682A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109081625 | ||||||
| chr9:109081682
|
A | G | 1 | a0001c0001t0011g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1345-739T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109081682 | ||||||
| chr9:109081913
|
TGATA | T | 27 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1345-974_1345-971d others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109081913 | ||||||
| chr9:109081920
|
T | C | 1 | a0001c0001t0005g0101 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1345-977A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109081920 | ||||||
| chr9:109081966
|
C | A | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1345-1023G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109081966 | ||||||
| chr9:109082302
|
G | A | 6 | a0002c0002t0001g0351a0002c0002t0001g0384a0002c0002t0001g0385others(3): Show | 6 | HG00621.hp1 NA18973.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345-1359C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082302 | ||||||
| chr9:109082336
|
CT | C | 31 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.1345-1394delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082336 | ||||||
| chr9:109082427
|
T | C | 7 | a0001c0001t0003g0215a0001c0001t0003g0220a0001c0001t0003g0261others(4): Show | 7 | NA18948.hp2 NA18952.hp2 NA18981.hp2 others(4): Show |
intron_variant | MODIFIER | c.1345-1484A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082427 | ||||||
| chr9:109082443
|
T | C | 1 | a0001c0007t0027g0298 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1345-1500A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082443 | ||||||
| chr9:109082444
|
T | A | 27 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1345-1501A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082444 | ||||||
| chr9:109082533
|
G | A | 16 | a0001c0001t0009g0030a0001c0001t0011g0189a0001c0001t0055g0188others(13): Show | 16 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.1345-1590C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082533 | ||||||
| chr9:109082568
|
C | A | 3 | a0001c0001t0022g0003a0001c0001t0022g0004a0001c0001t0022g0005 | 3 | HG02622.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1345-1625G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082568 | ||||||
| chr9:109082638
|
T | C | 1 | a0001c0001t0003g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1345-1695A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082638 | ||||||
| chr9:109082650
|
A | AT | 6 | a0001c0001t0003g0212a0001c0001t0003g0213a0001c0001t0004g0274others(3): Show | 6 | HG00438.hp2 HG00735.hp1 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1345-1708dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082650 | ||||||
| chr9:109082650
|
AT | A | 94 | a0001c0001t0003g0215a0001c0001t0004g0082a0001c0001t0004g0182others(91): Show | 94 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.1345-1708delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082650 | ||||||
| chr9:109082650
|
ATT | A | 111 | a0001c0001t0009g0030a0001c0001t0054g0174a0001c0001t0054g0176others(108): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1345-1709_1345-170 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082650 | ||||||
| chr9:109082784
|
T | C | 1 | a0003c0008t0017g0308 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1345-1841A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109082784 | ||||||
| chr9:109083128
|
C | T | 2 | a0003c0004t0009g0337a0003c0004t0118g0332 | 2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1345-2185G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083128 | ||||||
| chr9:109083173
|
A | G | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1345-2230T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083173 | ||||||
| chr9:109083175
|
T | C | 193 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(190): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1345-2232A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083175 | ||||||
| chr9:109083176
|
G | A | 1 | a0001c0001t0005g0141 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1345-2233C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083176 | ||||||
| chr9:109083223
|
C | G | 192 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(189): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1345-2280G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083223 | ||||||
| chr9:109083280
|
G | A | 1 | a0001c0001t0025g0262 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1345-2337C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083280 | ||||||
| chr9:109083298
|
G | A | 1 | a0001c0001t0002g0048 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1345-2355C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083298 | ||||||
| chr9:109083336
|
C | T | 1 | a0003c0004t0049g0333 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1345-2393G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083336 | ||||||
| chr9:109083357
|
C | T | 2 | a0001c0001t0003g0210a0003c0004t0116g0342 | 2 | HG01123.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1345-2414G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083357 | ||||||
| chr9:109083492
|
G | A | 54 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(51): Show | 54 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.1344+2505C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083492 | ||||||
| chr9:109083518
|
G | A | 36 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(33): Show | 36 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.1344+2479C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083518 | ||||||
| chr9:109083899
|
T | TACAAAAA others(6): Show |
1 | a0001c0001t0034g0130 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1344+2085_1344+209 others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083899 | ||||||
| chr9:109083901
|
C | CA | 11 | a0001c0001t0008g0161a0001c0001t0039g0165a0001c0001t0045g0172others(8): Show | 11 | HG01106.hp1 HG01515.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1344+2095dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
C | CAA | 52 | a0001c0001t0054g0176a0001c0001t0068g0158a0001c0006t0050g0286others(49): Show | 52 | HG00099.hp1 HG00438.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1344+2094_1344+209 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
C | CAAA | 29 | a0001c0001t0054g0174a0001c0006t0050g0288a0001c0006t0085g0287others(26): Show | 29 | HG00621.hp1 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.1344+2093_1344+209 others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
C | CAAAA | 9 | a0001c0001t0011g0275a0001c0001t0058g0006a0001c0006t0011g0282others(6): Show | 9 | HG01099.hp2 HG01192.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.1344+2092_1344+209 others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
C | CAAAAA | 9 | a0001c0001t0011g0277a0001c0001t0011g0278a0001c0001t0055g0188others(6): Show | 9 | HG01243.hp1 HG01261.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1344+2091_1344+209 others(9): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
C | CAAAAAAA others(1): Show |
42 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(39): Show | 42 | HG00558.hp1 HG00639.hp1 HG01074.hp1 others(39): Show |
intron_variant | MODIFIER | c.1344+2088_1344+209 others(12): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
C | CAAAAAAA others(2): Show |
45 | a0001c0001t0002g0034a0001c0001t0003g0215a0001c0001t0003g0220others(42): Show | 45 | HG00621.hp2 HG00733.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.1344+2087_1344+209 others(13): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
C | CAAAAAAA others(3): Show |
22 | a0001c0001t0002g0001a0001c0001t0002g0035a0001c0001t0002g0046others(19): Show | 23 | HG00408.hp1 HG00738.hp2 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.1344+2086_1344+209 others(14): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
C | CAAAAAAA others(4): Show |
4 | a0001c0001t0002g0045a0001c0001t0002g0051a0001c0001t0004g0225others(1): Show | 4 | HG00140.hp1 HG01496.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+2085_1344+209 others(15): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
C | CAAAAAAA others(5): Show |
4 | a0001c0001t0002g0049a0001c0001t0015g0026a0001c0001t0015g0027others(1): Show | 4 | HG00741.hp1 HG02809.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1344+2084_1344+209 others(16): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0073g0177 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1344+2078_1344+209 others(22): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0076g0103 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1344+2074_1344+209 others(26): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
C | CAAAAAAA others(18): Show |
1 | a0001c0001t0030g0115 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1344+2071_1344+209 others(29): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
C | CAAAAAAA others(6): Show |
6 | a0001c0005t0003g0007a0001c0005t0003g0009a0001c0005t0003g0010others(3): Show | 6 | HG01978.hp2 HG02273.hp2 NA19011.hp1 others(3): Show |
intron_variant | MODIFIER | c.1344+2095_1344+209 others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
C | CAAAACAA others(6): Show |
2 | a0001c0005t0003g0014a0001c0005t0003g0015 | 2 | NA18945.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.1344+2095_1344+209 others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
CAAA | C | 6 | a0001c0001t0006g0078a0001c0001t0006g0094a0001c0001t0016g0086others(3): Show | 6 | HG02027.hp2 HG02074.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.1344+2093_1344+209 others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
CAAAA | C | 11 | a0001c0001t0002g0043a0001c0001t0004g0117a0001c0001t0006g0089others(8): Show | 11 | HG00544.hp1 HG02015.hp1 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.1344+2092_1344+209 others(8): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
CAAAAA | C | 16 | a0001c0001t0002g0042a0001c0001t0006g0088a0001c0001t0006g0090others(13): Show | 17 | HG00558.hp2 HG01255.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.1344+2091_1344+209 others(9): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
CAAAAAAA others(2): Show |
C | 31 | a0001c0001t0003g0201a0001c0001t0003g0203a0001c0001t0003g0205others(28): Show | 31 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(28): Show |
intron_variant | MODIFIER | c.1344+2087_1344+209 others(13): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
CAAAAAAA others(3): Show |
C | 2 | a0001c0001t0005g0101a0001c0001t0108g0083 | 2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1344+2086_1344+209 others(14): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
CAAAAAAA others(4): Show |
C | 7 | a0003c0008t0017g0304a0003c0008t0017g0308a0003c0008t0017g0309others(4): Show | 7 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1344+2085_1344+209 others(15): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083901
|
CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0077g0104 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1344+2080_1344+209 others(20): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083901 | ||||||
| chr9:109083902
|
A | AAAAAAAA others(6): Show |
4 | a0001c0005t0024g0011a0001c0005t0024g0017a0001c0005t0024g0018others(1): Show | 4 | HG02015.hp2 HG02040.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344+2094_1344+209 others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083902 | ||||||
| chr9:109083911
|
A | C | 1 | a0001c0005t0003g0008 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1344+2086T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083911 | ||||||
| chr9:109083915
|
A | AAAAAAAA others(8): Show |
1 | a0001c0001t0005g0121 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1344+2067_1344+208 others(19): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083915 | ||||||
| chr9:109083915
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0092g0122 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1344+2081_1344+208 others(18): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083915 | ||||||
| chr9:109083916
|
A | AAAAAAAA others(8): Show |
2 | a0001c0001t0005g0142a0001c0005t0003g0020 | 2 | NA18975.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1344+2080_1344+208 others(19): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083916 | ||||||
| chr9:109083916
|
A | AAAAAAAA others(7): Show |
8 | a0001c0001t0005g0139a0001c0001t0005g0140a0001c0001t0005g0141others(5): Show | 8 | HG01099.hp1 HG02602.hp2 NA18955.hp2 others(5): Show |
intron_variant | MODIFIER | c.1344+2067_1344+208 others(18): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083916 | ||||||
| chr9:109083916
|
A | AAAAAAAA others(6): Show |
26 | a0001c0001t0005g0123a0001c0001t0005g0125a0001c0001t0005g0133others(23): Show | 26 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.1344+2080_1344+208 others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083916 | ||||||
| chr9:109083916
|
A | AAAAAAAA others(6): Show |
1 | a0001c0005t0003g0008 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1344+2080_1344+208 others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083916 | ||||||
| chr9:109083916
|
A | ACAAAAAA others(6): Show |
2 | a0001c0001t0005g0129a0001c0001t0005g0152 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1344+2080_1344+208 others(17): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083916 | ||||||
| chr9:109083916
|
A | C | 13 | a0001c0001t0034g0130a0001c0005t0003g0007a0001c0005t0003g0009others(10): Show | 13 | HG01978.hp2 HG02015.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.1344+2081T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083916 | ||||||
| chr9:109083925
|
A | AAAAAAAA others(23): Show |
1 | a0001c0001t0007g0112 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1344+2071_1344+207 others(34): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | ||||||
| chr9:109083925
|
A | AAAAAAAA others(22): Show |
1 | a0001c0001t0004g0182 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1344+2071_1344+207 others(33): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | ||||||
| chr9:109083925
|
A | AAAAAAAA others(20): Show |
1 | a0001c0001t0083g0109 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1344+2071_1344+207 others(31): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | ||||||
| chr9:109083925
|
A | AAAAAAAA others(19): Show |
2 | a0001c0001t0007g0108a0001c0001t0007g0113 | 2 | NA18999.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.1344+2071_1344+207 others(30): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | ||||||
| chr9:109083925
|
A | AAAAAAAA others(17): Show |
1 | a0001c0001t0007g0106 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1344+2071_1344+207 others(28): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | ||||||
| chr9:109083925
|
A | AAAAAAAA others(16): Show |
1 | a0001c0001t0007g0111 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1344+2071_1344+207 others(27): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | ||||||
| chr9:109083925
|
A | AAAAAAAA others(15): Show |
2 | a0001c0001t0007g0107a0001c0001t0074g0181 | 2 | HG00609.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1344+2071_1344+207 others(26): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | ||||||
| chr9:109083925
|
A | AAAAAAAA others(13): Show |
1 | a0001c0001t0075g0102 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1344+2071_1344+207 others(24): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | ||||||
| chr9:109083925
|
A | AAAAAAAA others(12): Show |
1 | a0001c0001t0007g0180 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1344+2071_1344+207 others(23): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | ||||||
| chr9:109083925
|
A | AAAAAAAA others(11): Show |
4 | a0001c0001t0007g0179a0001c0001t0015g0178a0001c0001t0030g0110others(1): Show | 4 | NA18946.hp2 NA18963.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1344+2071_1344+207 others(22): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | ||||||
| chr9:109083925
|
A | AAAAAAAA others(7): Show |
1 | a0001c0001t0004g0082 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1344+2071_1344+207 others(18): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083925 | ||||||
| chr9:109083990
|
T | C | 3 | a0003c0004t0010g0336a0003c0004t0049g0331a0003c0004t0049g0333 | 3 | HG02738.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1344+2007A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109083990 | ||||||
| chr9:109084044
|
A | G | 5 | a0001c0001t0058g0006a0001c0006t0033g0289a0001c0006t0033g0290others(2): Show | 5 | HG01261.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344+1953T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109084044 | ||||||
| chr9:109084084
|
T | TA | 207 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(204): Show | 208 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(205): Show |
intron_variant | MODIFIER | c.1344+1912dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109084084 | ||||||
| chr9:109084084
|
TA | T | 26 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(23): Show | 26 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.1344+1912delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109084084 | ||||||
| chr9:109084445
|
G | A | 27 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1344+1552C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109084445 | ||||||
| chr9:109084810
|
T | G | 1 | a0001c0001t0004g0194 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1344+1187A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109084810 | ||||||
| chr9:109084828
|
T | C | 1 | a0001c0001t0003g0215 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1344+1169A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109084828 | ||||||
| chr9:109085240
|
G | C | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344+757C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109085240 | ||||||
| chr9:109085360
|
T | C | 2 | a0001c0001t0064g0245a0001c0001t0070g0197 | 2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1344+637A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109085360 | ||||||
| chr9:109085416
|
A | G | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344+581T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109085416 | ||||||
| chr9:109085455
|
T | C | 1 | a0001c0001t0022g0003 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1344+542A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109085455 | ||||||
| chr9:109085464
|
A | G | 1 | a0001c0001t0005g0101 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1344+533T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109085464 | ||||||
| chr9:109085540
|
A | G | 1 | a0001c0001t0004g0228 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1344+457T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109085540 | ||||||
| chr9:109085653
|
A | G | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1344+344T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109085653 | ||||||
| chr9:109085720
|
A | G | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1344+277T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109085720 | ||||||
| chr9:109085944
|
C | T | 3 | a0001c0005t0003g0014a0001c0005t0003g0015a0001c0005t0003g0016 | 3 | NA18945.hp1 NA18979.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1344+53G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 7/17 | chr9 | 109085944 | ||||||
| chr9:109086029
|
T | TA | 11 | a0001c0001t0011g0189a0001c0001t0011g0277a0001c0001t0011g0278others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1321-10dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086029 | ||||||
| chr9:109086120
|
G | A | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1321-100C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086120 | ||||||
| chr9:109086120
|
GGAAACCA others(5): Show |
G | 1 | a0002c0002t0001g0366 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1321-112_1321-101d others(14): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086120 | ||||||
| chr9:109086190
|
G | A | 33 | a0001c0001t0009g0030a0001c0001t0054g0174a0001c0001t0054g0176others(30): Show | 34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1321-170C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086190 | ||||||
| chr9:109086222
|
T | C | 1 | a0003c0017t0117g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1321-202A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086222 | ||||||
| chr9:109086279
|
T | C | 1 | a0001c0001t0013g0237 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1321-259A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086279 | ||||||
| chr9:109086294
|
T | C | 5 | a0001c0001t0008g0160a0001c0001t0008g0162a0001c0001t0008g0163others(2): Show | 5 | HG01192.hp2 HG02630.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1321-274A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086294 | ||||||
| chr9:109086311
|
T | G | 1 | a0001c0001t0013g0237 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1321-291A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086311 | ||||||
| chr9:109086348
|
A | T | 1 | a0001c0001t0006g0089 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1321-328T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086348 | ||||||
| chr9:109086369
|
G | A | 3 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0017t0117g0311 | 4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1321-349C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086369 | ||||||
| chr9:109086399
|
C | T | 1 | a0001c0001t0099g0128 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1321-379G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086399 | ||||||
| chr9:109086407
|
GC | G | 3 | a0003c0004t0010g0336a0003c0004t0049g0331a0003c0004t0049g0333 | 3 | HG02738.hp1 HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1321-388delG | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086407 | ||||||
| chr9:109086427
|
G | A | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1321-407C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086427 | ||||||
| chr9:109086478
|
T | C | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1321-458A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086478 | ||||||
| chr9:109086500
|
T | C | 1 | a0001c0001t0008g0168 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1321-480A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086500 | ||||||
| chr9:109086513
|
A | G | 1 | a0001c0001t0007g0106 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1321-493T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086513 | ||||||
| chr9:109086514
|
T | C | 1 | a0003c0004t0009g0330 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1321-494A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086514 | ||||||
| chr9:109086539
|
A | G | 139 | a0001c0001t0009g0030a0001c0001t0011g0189a0001c0001t0011g0275others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1321-519T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086539 | ||||||
| chr9:109086598
|
G | C | 1 | a0001c0001t0107g0156 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1320+575C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086598 | ||||||
| chr9:109086613
|
T | G | 7 | a0003c0008t0017g0304a0003c0008t0017g0308a0003c0008t0017g0309others(4): Show | 7 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1320+560A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086613 | ||||||
| chr9:109086661
|
G | A | 11 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0207others(8): Show | 11 | HG00544.hp2 HG02273.hp1 NA18940.hp1 others(8): Show |
intron_variant | MODIFIER | c.1320+512C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086661 | ||||||
| chr9:109086817
|
A | G | 1 | a0001c0001t0093g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1320+356T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086817 | ||||||
| chr9:109086892
|
C | A | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1320+281G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086892 | ||||||
| chr9:109086920
|
A | G | 11 | a0001c0001t0007g0077a0001c0001t0025g0184a0001c0001t0025g0198others(8): Show | 11 | HG01255.hp1 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1320+253T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086920 | ||||||
| chr9:109086977
|
C | T | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1320+196G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109086977 | ||||||
| chr9:109087012
|
T | A | 1 | a0001c0001t0008g0171 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1320+161A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109087012 | ||||||
| chr9:109087066
|
T | A | 1 | a0001c0001t0003g0210 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1320+107A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 6/17 | chr9 | 109087066 | ||||||
| chr9:109087363
|
C | G | 1 | a0001c0006t0033g0289 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1151-21G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109087363 | ||||||
| chr9:109087452
|
T | G | 41 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(38): Show | 41 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(38): Show |
intron_variant | MODIFIER | c.1151-110A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109087452 | ||||||
| chr9:109087514
|
T | A | 1 | a0001c0001t0005g0143 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1151-172A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109087514 | ||||||
| chr9:109087627
|
A | T | 1 | a0001c0001t0072g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1151-285T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109087627 | ||||||
| chr9:109087635
|
C | T | 9 | a0003c0008t0017g0304a0003c0008t0017g0308a0003c0008t0017g0309others(6): Show | 9 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.1151-293G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109087635 | ||||||
| chr9:109087770
|
T | C | 1 | a0001c0001t0015g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1151-428A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109087770 | ||||||
| chr9:109087897
|
G | A | 1 | a0001c0006t0011g0283 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1151-555C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109087897 | ||||||
| chr9:109087971
|
G | C | 1 | a0001c0013t0090g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1151-629C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109087971 | ||||||
| chr9:109088157
|
C | A | 3 | a0001c0001t0022g0003a0001c0001t0022g0004a0001c0001t0022g0005 | 3 | HG02622.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1151-815G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088157 | ||||||
| chr9:109088298
|
A | G | 32 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1151-956T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088298 | ||||||
| chr9:109088386
|
C | T | 2 | a0003c0004t0018g0325a0003c0004t0102g0324 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1151-1044G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088386 | ||||||
| chr9:109088409
|
A | G | 1 | a0001c0001t0007g0111 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1151-1067T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088409 | ||||||
| chr9:109088419
|
G | A | 1 | a0001c0001t0031g0081 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1151-1077C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088419 | ||||||
| chr9:109088430
|
A | G | 139 | a0001c0001t0009g0030a0001c0001t0011g0189a0001c0001t0011g0275others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1151-1088T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088430 | ||||||
| chr9:109088605
|
A | G | 32 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1151-1263T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088605 | ||||||
| chr9:109088627
|
G | A | 27 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.1151-1285C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088627 | ||||||
| chr9:109088661
|
C | T | 1 | a0002c0002t0001g0349 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1151-1319G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088661 | ||||||
| chr9:109088678
|
G | A | 1 | a0001c0001t0047g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1151-1336C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088678 | ||||||
| chr9:109088730
|
A | G | 32 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1151-1388T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088730 | ||||||
| chr9:109088760
|
G | A | 1 | a0003c0017t0117g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1151-1418C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088760 | ||||||
| chr9:109088809
|
A | C | 32 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.1151-1467T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088809 | ||||||
| chr9:109088815
|
C | CA | 11 | a0001c0001t0011g0277a0001c0001t0013g0273a0001c0001t0015g0178others(8): Show | 11 | HG00438.hp2 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1151-1474dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088815 | ||||||
| chr9:109088815
|
CA | C | 30 | a0001c0001t0003g0201a0001c0001t0003g0215a0001c0001t0004g0195others(27): Show | 30 | HG01069.hp2 HG01071.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.1151-1474delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088815 | ||||||
| chr9:109088815
|
CAA | C | 33 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(30): Show | 34 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.1151-1475_1151-147 others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088815 | ||||||
| chr9:109088815
|
CAAA | C | 50 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(47): Show | 51 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.1151-1476_1151-147 others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088815 | ||||||
| chr9:109088842
|
G | C | 2 | a0001c0001t0007g0113a0001c0001t0030g0110 | 2 | NA18963.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1151-1500C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088842 | ||||||
| chr9:109088897
|
G | GC | 403 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(400): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1151-1556dupG | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088897 | ||||||
| chr9:109088996
|
G | A | 15 | a0001c0001t0003g0203a0001c0001t0003g0205a0001c0001t0003g0206others(12): Show | 15 | HG00544.hp2 HG02273.hp1 HG02523.hp2 others(12): Show |
intron_variant | MODIFIER | c.1151-1654C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109088996 | ||||||
| chr9:109089053
|
T | A | 139 | a0001c0001t0009g0030a0001c0001t0011g0189a0001c0001t0011g0275others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.1151-1711A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089053 | ||||||
| chr9:109089132
|
G | A | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1150+1790C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089132 | ||||||
| chr9:109089194
|
G | C | 21 | a0001c0001t0004g0082a0001c0001t0004g0182a0001c0001t0007g0106others(18): Show | 21 | HG00609.hp2 HG02132.hp2 HG04204.hp2 others(18): Show |
intron_variant | MODIFIER | c.1150+1728C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089194 | ||||||
| chr9:109089226
|
C | G | 2 | a0001c0001t0005g0101a0001c0001t0108g0083 | 2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.1150+1696G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089226 | ||||||
| chr9:109089227
|
T | C | 403 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(400): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1150+1695A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089227 | ||||||
| chr9:109089233
|
CA | C | 77 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(74): Show | 77 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.1150+1688delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089233 | ||||||
| chr9:109089242
|
A | C | 31 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(28): Show | 31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1150+1680T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089242 | ||||||
| chr9:109089475
|
T | G | 31 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(28): Show | 31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.1150+1447A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089475 | ||||||
| chr9:109089622
|
A | T | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1150+1300T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089622 | ||||||
| chr9:109089850
|
A | G | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1150+1072T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109089850 | ||||||
| chr9:109090215
|
C | G | 13 | a0001c0005t0003g0007a0001c0005t0003g0008a0001c0005t0003g0009others(10): Show | 13 | HG01978.hp2 HG02015.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.1150+707G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090215 | ||||||
| chr9:109090233
|
C | G | 1 | a0001c0001t0007g0111 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1150+689G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090233 | ||||||
| chr9:109090248
|
G | A | 4 | a0002c0002t0001g0365a0002c0002t0001g0397a0002c0002t0001g0398others(1): Show | 4 | HG03669.hp1 NA18949.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150+674C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090248 | ||||||
| chr9:109090260
|
CA | C | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1150+661delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090260 | ||||||
| chr9:109090270
|
A | C | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.1150+652T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090270 | ||||||
| chr9:109090371
|
T | C | 1 | a0004c0003t0048g0120 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1150+551A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090371 | ||||||
| chr9:109090446
|
G | A | 1 | a0001c0001t0004g0194 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1150+476C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090446 | ||||||
| chr9:109090451
|
G | A | 1 | a0002c0002t0001g0354 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1150+471C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090451 | ||||||
| chr9:109090625
|
G | A | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.1150+297C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090625 | ||||||
| chr9:109090716
|
C | CA | 74 | a0001c0001t0037g0258a0001c0001t0045g0169a0002c0002t0001g0346others(71): Show | 74 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.1150+205dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090716 | ||||||
| chr9:109090716
|
CA | C | 29 | a0001c0001t0004g0231a0001c0001t0009g0030a0001c0001t0093g0029others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1150+205delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090716 | ||||||
| chr9:109090774
|
G | A | 1 | a0001c0001t0003g0250 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1150+148C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090774 | ||||||
| chr9:109090868
|
G | GA | 3 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0017t0117g0311 | 4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150+53dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090868 | ||||||
| chr9:109090898
|
G | A | 1 | a0001c0001t0006g0096 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1150+24C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090898 | ||||||
| chr9:109090902
|
G | A | 2 | a0003c0004t0116g0342a0003c0017t0117g0311 | 2 | HG03669.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1150+20C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 5/17 | chr9 | 109090902 | ||||||
| chr9:109091199
|
T | C | 1 | a0003c0004t0010g0336 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.917-44A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091199 | ||||||
| chr9:109091266
|
T | C | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.917-111A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091266 | ||||||
| chr9:109091406
|
A | G | 403 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(400): Show | 405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.917-251T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091406 | ||||||
| chr9:109091482
|
C | G | 1 | a0001c0001t0004g0195 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.917-327G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091482 | ||||||
| chr9:109091496
|
T | C | 1 | a0001c0001t0100g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.917-341A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091496 | ||||||
| chr9:109091565
|
A | G | 1 | a0001c0001t0071g0240 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.917-410T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091565 | ||||||
| chr9:109091574
|
A | G | 1 | a0001c0001t0006g0088 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.917-419T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091574 | ||||||
| chr9:109091669
|
G | A | 3 | a0001c0001t0022g0003a0001c0001t0022g0004a0001c0001t0022g0005 | 3 | HG02622.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.917-514C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091669 | ||||||
| chr9:109091683
|
G | A | 1 | a0001c0001t0004g0194 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.917-528C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091683 | ||||||
| chr9:109091705
|
T | C | 3 | a0001c0001t0022g0003a0001c0001t0022g0004a0001c0001t0022g0005 | 3 | HG02622.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.917-550A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091705 | ||||||
| chr9:109091885
|
T | C | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.917-730A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091885 | ||||||
| chr9:109091900
|
T | C | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.917-745A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091900 | ||||||
| chr9:109091957
|
G | A | 1 | a0003c0004t0009g0337 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.917-802C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091957 | ||||||
| chr9:109091966
|
G | A | 51 | a0001c0001t0003g0215a0001c0001t0003g0220a0001c0001t0003g0261others(48): Show | 51 | HG00558.hp1 HG00639.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.917-811C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091966 | ||||||
| chr9:109091985
|
A | C | 1 | a0001c0001t0005g0145 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.917-830T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109091985 | ||||||
| chr9:109092099
|
T | C | 3 | a0001c0001t0005g0145a0001c0001t0005g0146a0001c0001t0005g0147 | 3 | HG01081.hp1 HG01257.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.917-944A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092099 | ||||||
| chr9:109092110
|
T | C | 29 | a0001c0001t0009g0030a0001c0001t0081g0044a0001c0001t0093g0029others(26): Show | 29 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.917-955A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092110 | ||||||
| chr9:109092134
|
T | G | 12 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.917-979A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092134 | ||||||
| chr9:109092204
|
A | G | 1 | a0001c0001t0119g0420 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.917-1049T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092204 | ||||||
| chr9:109092326
|
TA | T | 417 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(414): Show | 419 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(416): Show |
intron_variant | MODIFIER | c.916+1148delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092326 | ||||||
| chr9:109092343
|
A | G | 1 | a0001c0006t0011g0281 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.916+1132T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092343 | ||||||
| chr9:109092388
|
C | A | 2 | a0003c0004t0009g0337a0003c0004t0118g0332 | 2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.916+1087G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092388 | ||||||
| chr9:109092805
|
A | G | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.916+670T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092805 | ||||||
| chr9:109092899
|
G | A | 2 | a0002c0002t0001g0361a0002c0002t0001g0364 | 2 | HG00738.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.916+576C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092899 | ||||||
| chr9:109092925
|
T | C | 1 | a0001c0001t0054g0176 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.916+550A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092925 | ||||||
| chr9:109092949
|
CAG | C | 27 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.916+524_916+525del others(2): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109092949 | ||||||
| chr9:109093285
|
C | A | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.916+190G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109093285 | ||||||
| chr9:109093349
|
C | A | 2 | a0004c0003t0002g0038a0004c0003t0002g0069 | 2 | HG02056.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.916+126G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109093349 | ||||||
| chr9:109093459
|
C | T | 1 | a0001c0001t0068g0158 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.916+16G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 4/17 | chr9 | 109093459 | ||||||
| chr9:109093613
|
T | G | 4 | a0001c0001t0016g0084a0001c0001t0016g0085a0001c0001t0016g0086others(1): Show | 4 | HG00558.hp2 HG02027.hp2 HG02074.hp1 others(1): Show |
intron_variant | MODIFIER | c.800-22A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109093613 | ||||||
| chr9:109093993
|
G | C | 1 | a0001c0001t0004g0227 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.800-402C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109093993 | ||||||
| chr9:109094041
|
G | A | 27 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.800-450C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109094041 | ||||||
| chr9:109094098
|
G | A | 1 | a0001c0001t0043g0050 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.800-507C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109094098 | ||||||
| chr9:109094271
|
A | G | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.800-680T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109094271 | ||||||
| chr9:109094418
|
G | A | 1 | a0001c0001t0031g0097 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.800-827C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109094418 | ||||||
| chr9:109094452
|
A | G | 32 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.800-861T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109094452 | ||||||
| chr9:109094476
|
A | C | 1 | a0003c0017t0117g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.800-885T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109094476 | ||||||
| chr9:109094808
|
C | T | 1 | a0001c0001t0005g0157 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.800-1217G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109094808 | ||||||
| chr9:109094947
|
C | A | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.800-1356G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109094947 | ||||||
| chr9:109094969
|
T | A | 31 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.800-1378A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109094969 | ||||||
| chr9:109095070
|
G | A | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.800-1479C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095070 | ||||||
| chr9:109095111
|
G | A | 368 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(365): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.800-1520C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095111 | ||||||
| chr9:109095160
|
C | G | 191 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.800-1569G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095160 | ||||||
| chr9:109095285
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.800-1694C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095285 | ||||||
| chr9:109095353
|
C | T | 31 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.800-1762G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095353 | ||||||
| chr9:109095395
|
G | A | 31 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.800-1804C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095395 | ||||||
| chr9:109095396
|
A | C | 54 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(51): Show | 54 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(51): Show |
intron_variant | MODIFIER | c.800-1805T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095396 | ||||||
| chr9:109095585
|
T | G | 17 | a0001c0001t0008g0160a0001c0001t0008g0161a0001c0001t0008g0162others(14): Show | 17 | HG00639.hp2 HG01192.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.800-1994A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095585 | ||||||
| chr9:109095754
|
G | C | 1 | a0002c0002t0001g0349 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.800-2163C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095754 | ||||||
| chr9:109095765
|
G | A | 25 | a0001c0001t0004g0117a0001c0001t0006g0078a0001c0001t0006g0088others(22): Show | 25 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.800-2174C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095765 | ||||||
| chr9:109095871
|
A | G | 2 | a0003c0012t0088g0022a0003c0018t0094g0307 | 2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.800-2280T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109095871 | ||||||
| chr9:109096079
|
C | T | 31 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.800-2488G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096079 | ||||||
| chr9:109096114
|
G | C | 1 | a0001c0001t0005g0125 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.800-2523C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096114 | ||||||
| chr9:109096119
|
T | A | 31 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.800-2528A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096119 | ||||||
| chr9:109096122
|
A | G | 31 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.800-2531T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096122 | ||||||
| chr9:109096252
|
G | A | 1 | a0002c0002t0012g0399 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.800-2661C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096252 | ||||||
| chr9:109096286
|
C | T | 3 | a0001c0001t0029g0199a0001c0001t0029g0211a0001c0001t0029g0260 | 3 | NA18948.hp1 NA18965.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.800-2695G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096286 | ||||||
| chr9:109096349
|
C | T | 1 | a0001c0001t0038g0252 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.800-2758G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096349 | ||||||
| chr9:109096419
|
G | A | 2 | a0002c0002t0001g0361a0002c0002t0001g0364 | 2 | HG00738.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.800-2828C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096419 | ||||||
| chr9:109096420
|
T | C | 53 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0203others(50): Show | 53 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.800-2829A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096420 | ||||||
| chr9:109096426
|
G | A | 3 | a0001c0005t0003g0007a0001c0005t0003g0008a0001c0005t0003g0009 | 3 | NA19011.hp1 NA19066.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.800-2835C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096426 | ||||||
| chr9:109096947
|
A | C | 1 | a0001c0001t0015g0178 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.800-3356T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096947 | ||||||
| chr9:109096955
|
G | A | 1 | a0001c0001t0004g0239 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.800-3364C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109096955 | ||||||
| chr9:109097018
|
G | A | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.800-3427C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097018 | ||||||
| chr9:109097043
|
T | G | 53 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(50): Show | 54 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.800-3452A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097043 | ||||||
| chr9:109097158
|
A | T | 32 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.800-3567T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097158 | ||||||
| chr9:109097266
|
A | G | 32 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.800-3675T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097266 | ||||||
| chr9:109097281
|
C | T | 32 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(29): Show | 33 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.800-3690G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097281 | ||||||
| chr9:109097335
|
A | T | 1 | a0001c0001t0053g0126 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.800-3744T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097335 | ||||||
| chr9:109097374
|
G | GT | 8 | a0001c0001t0004g0235a0001c0007t0004g0296a0001c0007t0004g0299others(5): Show | 8 | HG01074.hp1 HG02735.hp2 HG03490.hp2 others(5): Show |
intron_variant | MODIFIER | c.800-3784dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097374 | ||||||
| chr9:109097389
|
G | A | 1 | a0001c0001t0093g0029 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.800-3798C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097389 | ||||||
| chr9:109097467
|
A | T | 2 | a0001c0001t0005g0101a0001c0001t0108g0083 | 2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.800-3876T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097467 | ||||||
| chr9:109097503
|
A | G | 17 | a0001c0001t0008g0160a0001c0001t0008g0161a0001c0001t0008g0162others(14): Show | 17 | HG00639.hp2 HG01192.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.800-3912T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097503 | ||||||
| chr9:109097544
|
C | T | 1 | a0002c0002t0057g0369 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.800-3953G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097544 | ||||||
| chr9:109097552
|
C | T | 3 | a0001c0001t0002g0001a0001c0001t0002g0045a0001c0001t0002g0046 | 4 | HG01069.hp1 HG01071.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-3961G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097552 | ||||||
| chr9:109097559
|
T | C | 11 | a0001c0001t0054g0174a0001c0001t0054g0176a0003c0008t0017g0304others(8): Show | 11 | HG00733.hp1 HG01109.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.800-3968A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097559 | ||||||
| chr9:109097565
|
T | C | 3 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0017t0117g0311 | 4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-3974A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097565 | ||||||
| chr9:109097636
|
T | C | 25 | a0001c0001t0004g0117a0001c0001t0006g0078a0001c0001t0006g0088others(22): Show | 25 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.800-4045A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097636 | ||||||
| chr9:109097744
|
C | T | 1 | a0001c0001t0007g0105 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.800-4153G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097744 | ||||||
| chr9:109097789
|
C | T | 1 | a0001c0001t0002g0045 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.800-4198G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097789 | ||||||
| chr9:109097813
|
T | C | 1 | a0001c0001t0022g0005 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.800-4222A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097813 | ||||||
| chr9:109097905
|
A | C | 139 | a0001c0001t0009g0030a0001c0001t0011g0189a0001c0001t0011g0275others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.800-4314T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097905 | ||||||
| chr9:109097910
|
T | C | 16 | a0001c0001t0008g0160a0001c0001t0008g0161a0001c0001t0008g0162others(13): Show | 16 | HG00639.hp2 HG01192.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.800-4319A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097910 | ||||||
| chr9:109097989
|
T | C | 1 | a0001c0001t0007g0111 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.800-4398A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109097989 | ||||||
| chr9:109098138
|
T | C | 193 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(190): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.800-4547A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109098138 | ||||||
| chr9:109098283
|
A | C | 3 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0017t0117g0311 | 4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-4692T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109098283 | ||||||
| chr9:109098517
|
C | T | 368 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(365): Show | 370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.800-4926G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109098517 | ||||||
| chr9:109098727
|
A | G | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.800-5136T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109098727 | ||||||
| chr9:109098736
|
A | C | 1 | a0001c0001t0081g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.800-5145T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109098736 | ||||||
| chr9:109098840
|
G | A | 1 | a0002c0002t0001g0366 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.800-5249C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109098840 | ||||||
| chr9:109098887
|
C | G | 2 | a0001c0005t0003g0010a0001c0005t0060g0013 | 2 | HG02015.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.800-5296G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109098887 | ||||||
| chr9:109098917
|
C | T | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.800-5326G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109098917 | ||||||
| chr9:109099065
|
T | C | 20 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(17): Show | 20 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.800-5474A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109099065 | ||||||
| chr9:109099097
|
C | T | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.800-5506G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109099097 | ||||||
| chr9:109099408
|
G | C | 2 | a0001c0001t0054g0174a0001c0001t0054g0176 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.800-5817C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109099408 | ||||||
| chr9:109099610
|
A | C | 1 | a0001c0001t0007g0077 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.800-6019T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109099610 | ||||||
| chr9:109099643
|
A | C | 1 | a0001c0001t0013g0273 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.800-6052T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109099643 | ||||||
| chr9:109100059
|
T | C | 1 | a0001c0001t0068g0158 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.799+6449A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109100059 | ||||||
| chr9:109100464
|
T | C | 1 | a0001c0001t0023g0259 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.799+6044A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109100464 | ||||||
| chr9:109100549
|
T | C | 1 | a0002c0002t0021g0367 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.799+5959A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109100549 | ||||||
| chr9:109100602
|
G | A | 1 | a0002c0002t0020g0400 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.799+5906C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109100602 | ||||||
| chr9:109100720
|
C | G | 4 | a0002c0002t0001g0361a0002c0002t0001g0362a0002c0002t0001g0363others(1): Show | 4 | HG00738.hp1 HG01123.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.799+5788G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109100720 | ||||||
| chr9:109100742
|
A | G | 27 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.799+5766T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109100742 | ||||||
| chr9:109100749
|
T | C | 27 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.799+5759A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109100749 | ||||||
| chr9:109101014
|
G | A | 27 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.799+5494C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109101014 | ||||||
| chr9:109101062
|
T | C | 2 | a0002c0002t0012g0401a0002c0002t0057g0402 | 2 | HG02129.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.799+5446A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109101062 | ||||||
| chr9:109101102
|
G | A | 1 | a0001c0001t0004g0228 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.799+5406C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109101102 | ||||||
| chr9:109101137
|
T | C | 58 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(55): Show | 59 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(56): Show |
intron_variant | MODIFIER | c.799+5371A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109101137 | ||||||
| chr9:109101316
|
G | A | 1 | a0001c0001t0003g0210 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.799+5192C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109101316 | ||||||
| chr9:109101368
|
A | G | 1 | a0001c0001t0055g0188 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.799+5140T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109101368 | ||||||
| chr9:109101945
|
T | C | 2 | a0001c0001t0013g0229a0001c0001t0013g0230 | 2 | HG02071.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.799+4563A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109101945 | ||||||
| chr9:109102014
|
G | GA | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.799+4493dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102014 | ||||||
| chr9:109102104
|
C | T | 1 | a0003c0004t0118g0332 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.799+4404G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102104 | ||||||
| chr9:109102456
|
A | T | 1 | a0003c0017t0117g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.799+4052T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102456 | ||||||
| chr9:109102522
|
C | G | 191 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(188): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.799+3986G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102522 | ||||||
| chr9:109102560
|
C | G | 3 | a0001c0001t0022g0003a0001c0001t0022g0004a0001c0001t0022g0005 | 3 | HG02622.hp2 HG02717.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.799+3948G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102560 | ||||||
| chr9:109102612
|
G | GT | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.799+3895dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102612 | ||||||
| chr9:109102704
|
A | C | 1 | a0001c0001t0003g0251 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.799+3804T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102704 | ||||||
| chr9:109102772
|
T | C | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.799+3736A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102772 | ||||||
| chr9:109102913
|
G | A | 1 | a0001c0001t0011g0275 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.799+3595C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102913 | ||||||
| chr9:109102952
|
C | A | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.799+3556G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109102952 | ||||||
| chr9:109103079
|
T | C | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.799+3429A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109103079 | ||||||
| chr9:109103086
|
C | A | 3 | a0001c0001t0029g0199a0001c0001t0029g0211a0001c0001t0029g0260 | 3 | NA18948.hp1 NA18965.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.799+3422G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109103086 | ||||||
| chr9:109103257
|
C | A | 1 | a0001c0001t0006g0098 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.799+3251G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109103257 | ||||||
| chr9:109103363
|
A | G | 1 | a0001c0001t0003g0250 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.799+3145T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109103363 | ||||||
| chr9:109103482
|
A | C | 7 | a0003c0008t0017g0304a0003c0008t0017g0308a0003c0008t0017g0309others(4): Show | 7 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.799+3026T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109103482 | ||||||
| chr9:109103753
|
C | T | 2 | a0001c0001t0005g0101a0001c0001t0108g0083 | 2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.799+2755G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109103753 | ||||||
| chr9:109103778
|
T | G | 16 | a0001c0001t0008g0160a0001c0001t0008g0161a0001c0001t0008g0162others(13): Show | 16 | HG00639.hp2 HG01192.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.799+2730A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109103778 | ||||||
| chr9:109103861
|
G | A | 1 | a0001c0001t0004g0246 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.799+2647C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109103861 | ||||||
| chr9:109103978
|
G | A | 4 | a0001c0001t0004g0082a0001c0001t0007g0179a0001c0001t0007g0180others(1): Show | 4 | NA18946.hp2 NA18973.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.799+2530C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109103978 | ||||||
| chr9:109104011
|
G | C | 4 | a0001c0001t0022g0003a0001c0001t0022g0004a0001c0001t0022g0005others(1): Show | 4 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.799+2497C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104011 | ||||||
| chr9:109104049
|
C | A | 4 | a0002c0002t0001g0368a0002c0002t0001g0403a0002c0002t0001g0404others(1): Show | 4 | HG02165.hp2 NA18747.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.799+2459G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104049 | ||||||
| chr9:109104154
|
A | C | 1 | a0002c0002t0001g0346 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.799+2354T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104154 | ||||||
| chr9:109104194
|
T | C | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.799+2314A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104194 | ||||||
| chr9:109104262
|
T | C | 1 | a0003c0004t0049g0331 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.799+2246A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104262 | ||||||
| chr9:109104315
|
CCTA | C | 4 | a0001c0006t0033g0289a0001c0006t0033g0290a0001c0006t0033g0292others(1): Show | 4 | HG01261.hp1 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.799+2190_799+2192d others(5): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104315 | ||||||
| chr9:109104357
|
A | C | 30 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(27): Show | 30 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.799+2151T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104357 | ||||||
| chr9:109104469
|
C | T | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.799+2039G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104469 | ||||||
| chr9:109104529
|
T | C | 2 | a0001c0001t0002g0042a0001c0001t0002g0043 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.799+1979A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104529 | ||||||
| chr9:109104614
|
G | C | 1 | a0001c0001t0007g0112 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.799+1894C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104614 | ||||||
| chr9:109104636
|
AT | A | 3 | a0001c0001t0005g0148a0001c0001t0005g0149a0001c0001t0005g0155 | 3 | NA18967.hp2 NA18972.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.799+1871delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104636 | ||||||
| chr9:109104991
|
A | G | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.799+1517T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109104991 | ||||||
| chr9:109105010
|
T | C | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.799+1498A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105010 | ||||||
| chr9:109105081
|
G | A | 1 | a0002c0002t0012g0355 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.799+1427C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105081 | ||||||
| chr9:109105095
|
C | A | 19 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(16): Show | 19 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.799+1413G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105095 | ||||||
| chr9:109105097
|
T | C | 1 | a0001c0001t0005g0150 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.799+1411A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105097 | ||||||
| chr9:109105159
|
A | G | 2 | a0001c0001t0023g0200a0001c0001t0059g0269 | 2 | HG02055.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.799+1349T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105159 | ||||||
| chr9:109105275
|
C | A | 3 | a0001c0001t0003g0212a0001c0001t0003g0213a0001c0001t0037g0214 | 3 | HG00438.hp2 HG02071.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.799+1233G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105275 | ||||||
| chr9:109105327
|
G | C | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.799+1181C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105327 | ||||||
| chr9:109105356
|
G | T | 6 | a0001c0001t0008g0160a0001c0001t0008g0161a0001c0001t0008g0162others(3): Show | 6 | HG01192.hp2 HG02622.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.799+1152C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105356 | ||||||
| chr9:109105359
|
T | C | 1 | a0001c0001t0025g0184 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.799+1149A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105359 | ||||||
| chr9:109105464
|
A | G | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.799+1044T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105464 | ||||||
| chr9:109105478
|
C | T | 1 | a0001c0001t0011g0275 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.799+1030G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105478 | ||||||
| chr9:109105496
|
C | T | 1 | a0001c0001t0004g0239 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.799+1012G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105496 | ||||||
| chr9:109105510
|
G | T | 1 | a0001c0001t0077g0104 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.799+998C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105510 | ||||||
| chr9:109105521
|
G | A | 31 | a0004c0003t0002g0038a0004c0003t0002g0040a0004c0003t0002g0041others(28): Show | 31 | HG00408.hp1 HG00621.hp2 HG02056.hp2 others(28): Show |
intron_variant | MODIFIER | c.799+987C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105521 | ||||||
| chr9:109105566
|
T | C | 16 | a0001c0001t0008g0160a0001c0001t0008g0161a0001c0001t0008g0162others(13): Show | 16 | HG00639.hp2 HG01192.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.799+942A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105566 | ||||||
| chr9:109105615
|
G | T | 2 | a0001c0001t0030g0115a0001c0001t0076g0103 | 2 | NA18940.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.799+893C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105615 | ||||||
| chr9:109105768
|
T | C | 1 | a0004c0003t0002g0070 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.799+740A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109105768 | ||||||
| chr9:109106004
|
C | T | 26 | a0001c0001t0004g0082a0001c0001t0004g0182a0001c0001t0007g0105others(23): Show | 26 | HG00609.hp2 HG02132.hp2 HG02809.hp2 others(23): Show |
intron_variant | MODIFIER | c.799+504G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106004 | ||||||
| chr9:109106018
|
T | C | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.799+490A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106018 | ||||||
| chr9:109106032
|
A | G | 2 | a0003c0004t0018g0325a0003c0004t0102g0324 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.799+476T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106032 | ||||||
| chr9:109106064
|
G | A | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.799+444C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106064 | ||||||
| chr9:109106092
|
T | C | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.799+416A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106092 | ||||||
| chr9:109106199
|
T | TG | 419 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(416): Show | 421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.799+308dupC | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106199 | ||||||
| chr9:109106225
|
A | AAAAAATA others(22): Show |
86 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(83): Show | 87 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.799+254_799+282dup others(29): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106225 | ||||||
| chr9:109106225
|
A | AAAAAATA others(51): Show |
1 | a0001c0001t0108g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.799+282_799+283ins others(58): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106225 | ||||||
| chr9:109106403
|
T | C | 1 | a0001c0001t0006g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.799+105A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106403 | ||||||
| chr9:109106418
|
A | G | 28 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(25): Show | 28 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.799+90T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106418 | ||||||
| chr9:109106462
|
C | G | 4 | a0002c0002t0001g0361a0002c0002t0001g0362a0002c0002t0001g0363others(1): Show | 4 | HG00738.hp1 HG01123.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.799+46G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106462 | ||||||
| chr9:109106464
|
A | C | 1 | a0003c0004t0087g0327 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.799+44T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106464 | ||||||
| chr9:109106497
|
C | T | 16 | a0001c0001t0008g0160a0001c0001t0008g0161a0001c0001t0008g0162others(13): Show | 16 | HG00639.hp2 HG01192.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.799+11G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 3/17 | chr9 | 109106497 | ||||||
| chr9:109106657
|
A | G | 2 | a0001c0001t0005g0101a0001c0001t0108g0083 | 2 | HG01891.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.698-48T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109106657 | ||||||
| chr9:109106736
|
C | CA | 5 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(2): Show | 6 | HG01433.hp1 HG01496.hp1 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.698-128dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109106736 | ||||||
| chr9:109106837
|
T | C | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.698-228A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109106837 | ||||||
| chr9:109106911
|
G | T | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.698-302C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109106911 | ||||||
| chr9:109106944
|
C | G | 3 | a0001c0001t0015g0026a0001c0001t0015g0027a0001c0001t0015g0028 | 3 | HG02809.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.698-335G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109106944 | ||||||
| chr9:109106952
|
G | A | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.698-343C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109106952 | ||||||
| chr9:109107013
|
CTT | C | 36 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(33): Show | 36 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.698-406_698-405del others(2): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107013 | ||||||
| chr9:109107180
|
G | A | 62 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0203others(59): Show | 62 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.698-571C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107180 | ||||||
| chr9:109107242
|
A | T | 1 | a0001c0001t0091g0127 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.698-633T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107242 | ||||||
| chr9:109107243
|
A | T | 2 | a0001c0001t0002g0042a0001c0001t0002g0043 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.698-634T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107243 | ||||||
| chr9:109107331
|
G | A | 19 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(16): Show | 19 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.698-722C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107331 | ||||||
| chr9:109107398
|
CA | C | 38 | a0001c0001t0003g0264a0001c0001t0009g0030a0001c0001t0093g0029others(35): Show | 39 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.698-790delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107398 | ||||||
| chr9:109107417
|
A | AT | 50 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0129others(47): Show | 50 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.698-809_698-808ins others(1): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107417 | ||||||
| chr9:109107417
|
A | T | 319 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(316): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.698-808T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107417 | ||||||
| chr9:109107418
|
G | A | 1 | a0002c0002t0021g0405 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.698-809C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107418 | ||||||
| chr9:109107430
|
C | T | 1 | a0001c0001t0005g0123 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.698-821G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107430 | ||||||
| chr9:109107470
|
C | T | 5 | a0001c0001t0004g0117a0001c0001t0016g0084a0001c0001t0016g0085others(2): Show | 5 | HG00558.hp2 HG02027.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.698-861G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107470 | ||||||
| chr9:109107629
|
C | T | 19 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(16): Show | 19 | HG01243.hp1 HG01261.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.697+824G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107629 | ||||||
| chr9:109107654
|
T | C | 30 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(27): Show | 30 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.697+799A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107654 | ||||||
| chr9:109107675
|
T | C | 1 | a0001c0001t0047g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.697+778A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107675 | ||||||
| chr9:109107801
|
C | T | 1 | a0001c0001t0013g0237 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.697+652G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107801 | ||||||
| chr9:109107805
|
G | A | 39 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(36): Show | 39 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.697+648C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107805 | ||||||
| chr9:109107988
|
C | G | 1 | a0001c0006t0011g0283 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.697+465G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109107988 | ||||||
| chr9:109108121
|
G | A | 6 | a0003c0004t0010g0315a0003c0004t0010g0316a0003c0004t0010g0317others(3): Show | 6 | HG02451.hp2 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.697+332C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109108121 | ||||||
| chr9:109108246
|
T | C | 12 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.697+207A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109108246 | ||||||
| chr9:109108420
|
T | TA | 44 | a0001c0001t0008g0161a0001c0001t0008g0162a0001c0001t0008g0163others(41): Show | 44 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.697+32dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109108420 | ||||||
| chr9:109108420
|
T | TAAA | 35 | a0001c0001t0005g0123a0001c0001t0005g0125a0001c0001t0005g0129others(32): Show | 35 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.697+30_697+32dupTT others(1): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109108420 | ||||||
| chr9:109108420
|
TA | T | 22 | a0001c0001t0003g0232a0001c0001t0003g0249a0001c0001t0004g0193others(19): Show | 22 | HG01069.hp2 HG01070.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.697+32delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109108420 | ||||||
| chr9:109108441
|
G | A | 39 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(36): Show | 39 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.697+12C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 2/17 | chr9 | 109108441 | ||||||
| chr9:109108614
|
A | C | 2 | a0001c0001t0004g0274a0001c0001t0013g0273 | 2 | HG00735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.580-44T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109108614 | ||||||
| chr9:109108730
|
G | A | 1 | a0001c0001t0013g0247 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.580-160C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109108730 | ||||||
| chr9:109108898
|
T | C | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.580-328A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109108898 | ||||||
| chr9:109109061
|
A | T | 177 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.580-491T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109061 | ||||||
| chr9:109109235
|
G | C | 62 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0203others(59): Show | 62 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(59): Show |
intron_variant | MODIFIER | c.580-665C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109235 | ||||||
| chr9:109109276
|
C | T | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.580-706G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109276 | ||||||
| chr9:109109280
|
T | A | 1 | a0008c0019t0001g0406 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.580-710A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109280 | ||||||
| chr9:109109386
|
A | C | 1 | a0001c0001t0026g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.580-816T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109386 | ||||||
| chr9:109109436
|
C | CA | 44 | a0001c0001t0008g0160a0001c0001t0008g0161a0001c0001t0008g0162others(41): Show | 44 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.580-867dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109436 | ||||||
| chr9:109109504
|
A | C | 3 | a0003c0004t0010g0312a0003c0004t0010g0313a0003c0004t0010g0343 | 3 | HG03041.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.580-934T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109504 | ||||||
| chr9:109109523
|
A | G | 1 | a0001c0001t0026g0233 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.580-953T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109523 | ||||||
| chr9:109109584
|
T | C | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.580-1014A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109584 | ||||||
| chr9:109109585
|
C | T | 30 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(27): Show | 30 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.580-1015G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109585 | ||||||
| chr9:109109817
|
A | G | 52 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(49): Show | 53 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.580-1247T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109817 | ||||||
| chr9:109109914
|
A | T | 1 | a0001c0001t0072g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.580-1344T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109109914 | ||||||
| chr9:109110125
|
G | C | 1 | a0001c0001t0011g0278 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.580-1555C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109110125 | ||||||
| chr9:109110277
|
C | T | 1 | a0001c0001t0003g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.580-1707G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109110277 | ||||||
| chr9:109110465
|
A | G | 4 | a0002c0002t0001g0361a0002c0002t0001g0362a0002c0002t0001g0363others(1): Show | 4 | HG00738.hp1 HG01123.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-1895T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109110465 | ||||||
| chr9:109110529
|
A | C | 52 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(49): Show | 53 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.580-1959T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109110529 | ||||||
| chr9:109110564
|
T | C | 50 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0203others(47): Show | 50 | HG00438.hp2 HG00544.hp2 HG01070.hp1 others(47): Show |
intron_variant | MODIFIER | c.580-1994A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109110564 | ||||||
| chr9:109110570
|
T | TA | 246 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(243): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.580-2001dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109110570 | ||||||
| chr9:109110717
|
G | A | 7 | a0001c0007t0004g0296a0001c0007t0004g0299a0001c0007t0004g0300others(4): Show | 7 | HG02735.hp2 HG03490.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-2147C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109110717 | ||||||
| chr9:109110916
|
A | C | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.580-2346T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109110916 | ||||||
| chr9:109110947
|
A | G | 31 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(28): Show | 31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.580-2377T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109110947 | ||||||
| chr9:109111049
|
TA | T | 31 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.580-2480delT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109111049 | ||||||
| chr9:109111058
|
T | C | 1 | a0001c0015t0004g0268 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.580-2488A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109111058 | ||||||
| chr9:109111098
|
A | G | 2 | a0001c0001t0075g0102a0001c0016t0030g0293 | 2 | NA19057.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.580-2528T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109111098 | ||||||
| chr9:109111552
|
GTTTAAAA others(7): Show |
G | 29 | a0001c0001t0004g0082a0001c0001t0004g0182a0001c0001t0007g0077others(26): Show | 29 | HG00609.hp2 HG01891.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.580-2996_580-2983d others(16): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109111552 | ||||||
| chr9:109111582
|
C | T | 3 | a0002c0002t0001g0359a0002c0002t0056g0358a0002c0002t0056g0360 | 3 | HG00099.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.580-3012G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109111582 | ||||||
| chr9:109111694
|
T | A | 2 | a0001c0001t0042g0114a0001c0001t0042g0116 | 2 | NA18943.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.580-3124A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109111694 | ||||||
| chr9:109111829
|
C | CA | 29 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(26): Show | 29 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.580-3260dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109111829 | ||||||
| chr9:109111928
|
T | C | 2 | a0001c0001t0101g0151a0001c0001t0107g0156 | 2 | HG01256.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.580-3358A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109111928 | ||||||
| chr9:109111934
|
A | G | 31 | a0001c0001t0011g0189a0001c0001t0011g0275a0001c0001t0011g0277others(28): Show | 31 | HG00733.hp1 HG01109.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.580-3364T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109111934 | ||||||
| chr9:109112113
|
C | T | 1 | a0002c0002t0001g0357 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.580-3543G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112113 | ||||||
| chr9:109112296
|
T | A | 3 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0017t0117g0311 | 4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-3726A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112296 | ||||||
| chr9:109112338
|
C | G | 1 | a0001c0001t0053g0279 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.580-3768G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112338 | ||||||
| chr9:109112466
|
A | G | 177 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(174): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.580-3896T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112466 | ||||||
| chr9:109112473
|
G | A | 1 | a0001c0001t0006g0099 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.580-3903C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112473 | ||||||
| chr9:109112502
|
T | C | 29 | a0001c0001t0004g0082a0001c0001t0004g0182a0001c0001t0007g0077others(26): Show | 29 | HG00609.hp2 HG01891.hp2 HG02132.hp2 others(26): Show |
intron_variant | MODIFIER | c.580-3932A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112502 | ||||||
| chr9:109112541
|
C | CA | 46 | a0001c0001t0004g0231a0001c0001t0008g0160a0001c0001t0008g0161others(43): Show | 46 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.580-3972dupT | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112541 | ||||||
| chr9:109112648
|
T | C | 1 | a0003c0004t0116g0342 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.580-4078A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112648 | ||||||
| chr9:109112675
|
A | C | 1 | a0001c0001t0080g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.580-4105T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112675 | ||||||
| chr9:109112781
|
G | A | 1 | a0001c0001t0054g0174 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.580-4211C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112781 | ||||||
| chr9:109112800
|
G | A | 1 | a0001c0001t0006g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.580-4230C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112800 | ||||||
| chr9:109112805
|
C | T | 113 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(110): Show | 114 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.580-4235G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112805 | ||||||
| chr9:109112935
|
G | A | 1 | a0002c0002t0001g0407 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.580-4365C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112935 | ||||||
| chr9:109112938
|
T | C | 2 | a0001c0001t0005g0157a0001c0001t0063g0124 | 2 | HG02523.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.580-4368A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112938 | ||||||
| chr9:109112939
|
G | A | 2 | a0001c0001t0040g0271a0001c0001t0040g0272 | 2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.580-4369C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112939 | ||||||
| chr9:109112968
|
C | T | 1 | a0001c0001t0003g0232 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.580-4398G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109112968 | ||||||
| chr9:109113043
|
T | C | 1 | a0001c0001t0030g0115 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.580-4473A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109113043 | ||||||
| chr9:109113130
|
C | T | 3 | a0001c0006t0050g0286a0001c0006t0050g0288a0001c0006t0085g0287 | 3 | HG02486.hp2 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.580-4560G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109113130 | ||||||
| chr9:109113183
|
G | A | 190 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.580-4613C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109113183 | ||||||
| chr9:109113312
|
C | T | 16 | a0001c0001t0008g0160a0001c0001t0008g0161a0001c0001t0008g0162others(13): Show | 16 | HG00639.hp2 HG01192.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.580-4742G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109113312 | ||||||
| chr9:109113391
|
G | C | 1 | a0001c0001t0005g0125 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.580-4821C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109113391 | ||||||
| chr9:109113760
|
T | C | 1 | a0001c0001t0042g0116 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.580-5190A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109113760 | ||||||
| chr9:109113918
|
C | T | 31 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.580-5348G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109113918 | ||||||
| chr9:109113995
|
G | C | 1 | a0001c0001t0047g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.579+5340C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109113995 | ||||||
| chr9:109114024
|
C | T | 28 | a0001c0001t0004g0117a0001c0001t0006g0078a0001c0001t0006g0088others(25): Show | 28 | HG00544.hp1 HG00558.hp2 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.579+5311G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114024 | ||||||
| chr9:109114037
|
T | C | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.579+5298A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114037 | ||||||
| chr9:109114076
|
CCAAAA | C | 25 | a0001c0001t0003g0215a0001c0001t0003g0220a0001c0001t0003g0261others(22): Show | 25 | HG00558.hp1 HG00735.hp1 HG01515.hp2 others(22): Show |
intron_variant | MODIFIER | c.579+5254_579+5258d others(7): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114076 | ||||||
| chr9:109114243
|
A | G | 76 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(73): Show | 76 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.579+5092T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114243 | ||||||
| chr9:109114259
|
T | C | 9 | a0003c0008t0017g0304a0003c0008t0017g0308a0003c0008t0017g0309others(6): Show | 9 | HG00733.hp1 HG01109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.579+5076A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114259 | ||||||
| chr9:109114491
|
AGAG | A | 8 | a0001c0001t0008g0166a0001c0001t0008g0167a0001c0001t0008g0168others(5): Show | 8 | HG00639.hp2 HG02572.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.579+4841_579+4843d others(5): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114491 | ||||||
| chr9:109114543
|
A | C | 21 | a0001c0001t0003g0215a0001c0001t0003g0220a0001c0001t0003g0261others(18): Show | 21 | HG00558.hp1 HG02040.hp2 HG02071.hp1 others(18): Show |
intron_variant | MODIFIER | c.579+4792T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114543 | ||||||
| chr9:109114558
|
G | C | 3 | a0004c0003t0002g0074a0004c0003t0002g0075a0004c0003t0014g0073 | 3 | HG00408.hp1 NA19064.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.579+4777C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114558 | ||||||
| chr9:109114741
|
G | A | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+4594C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114741 | ||||||
| chr9:109114744
|
G | A | 31 | a0001c0001t0009g0030a0001c0001t0093g0029a0001c0009t0018g0002others(28): Show | 32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.579+4591C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114744 | ||||||
| chr9:109114852
|
AT | A | 172 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.579+4482delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109114852 | ||||||
| chr9:109115134
|
G | A | 1 | a0003c0008t0095g0306 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.579+4201C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115134 | ||||||
| chr9:109115148
|
A | C | 27 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.579+4187T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115148 | ||||||
| chr9:109115176
|
G | A | 17 | a0001c0001t0008g0160a0001c0001t0008g0161a0001c0001t0008g0162others(14): Show | 17 | HG00639.hp2 HG01192.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.579+4159C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115176 | ||||||
| chr9:109115203
|
A | G | 1 | a0001c0001t0108g0083 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.579+4132T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115203 | ||||||
| chr9:109115228
|
T | C | 2 | a0001c0001t0004g0182a0001c0001t0074g0181 | 2 | NA18957.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.579+4107A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115228 | ||||||
| chr9:109115318
|
T | C | 2 | a0003c0004t0052g0319a0003c0004t0052g0320 | 2 | HG02886.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.579+4017A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115318 | ||||||
| chr9:109115357
|
G | A | 2 | a0001c0001t0014g0076a0001c0001t0046g0039 | 2 | HG01106.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.579+3978C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115357 | ||||||
| chr9:109115431
|
A | C | 39 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(36): Show | 39 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.579+3904T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115431 | ||||||
| chr9:109115522
|
C | CT | 50 | a0001c0001t0003g0201a0001c0001t0003g0202a0001c0001t0003g0203others(47): Show | 51 | HG00438.hp2 HG00544.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.579+3812dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115522 | ||||||
| chr9:109115522
|
C | CTT | 6 | a0001c0001t0003g0263a0001c0006t0011g0280a0002c0002t0019g0350others(3): Show | 6 | HG00621.hp1 HG02257.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.579+3811_579+3812d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115522 | ||||||
| chr9:109115522
|
C | CTTT | 17 | a0001c0001t0093g0029a0003c0004t0009g0337a0003c0004t0010g0312others(14): Show | 17 | HG02451.hp2 HG02559.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.579+3810_579+3812d others(5): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115522 | ||||||
| chr9:109115522
|
C | CTTTT | 7 | a0001c0001t0009g0030a0003c0004t0009g0326a0003c0004t0009g0329others(4): Show | 7 | HG00099.hp2 HG00140.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+3809_579+3812d others(6): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115522 | ||||||
| chr9:109115522
|
CT | C | 144 | a0001c0001t0002g0001a0001c0001t0002g0042a0001c0001t0002g0043others(141): Show | 145 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.579+3812delA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115522 | ||||||
| chr9:109115522
|
CTT | C | 8 | a0001c0001t0005g0152a0001c0001t0005g0154a0001c0001t0005g0155others(5): Show | 8 | HG01168.hp2 HG01256.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.579+3811_579+3812d others(4): Show |
TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115522 | ||||||
| chr9:109115593
|
C | T | 5 | a0001c0001t0003g0263a0001c0001t0003g0264a0001c0001t0003g0265others(2): Show | 5 | NA18940.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+3742G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115593 | ||||||
| chr9:109115594
|
G | A | 1 | a0001c0001t0004g0117 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.579+3741C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115594 | ||||||
| chr9:109115606
|
T | C | 27 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0009g0326others(24): Show | 27 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.579+3729A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115606 | ||||||
| chr9:109115683
|
T | C | 303 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.579+3652A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115683 | ||||||
| chr9:109115712
|
T | C | 2 | a0003c0012t0088g0022a0003c0018t0094g0307 | 2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.579+3623A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115712 | ||||||
| chr9:109115750
|
G | A | 1 | a0001c0001t0069g0173 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.579+3585C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115750 | ||||||
| chr9:109115762
|
T | C | 2 | a0001c0009t0018g0002a0001c0009t0018g0302 | 3 | HG01433.hp1 HG01496.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.579+3573A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115762 | ||||||
| chr9:109115782
|
G | A | 1 | a0002c0002t0111g0408 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.579+3553C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115782 | ||||||
| chr9:109115798
|
G | A | 2 | a0001c0001t0078g0118a0001c0001t0079g0119 | 2 | HG01891.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.579+3537C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115798 | ||||||
| chr9:109115892
|
G | T | 53 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(50): Show | 54 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.579+3443C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109115892 | ||||||
| chr9:109116058
|
A | G | 1 | a0001c0013t0090g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.579+3277T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109116058 | ||||||
| chr9:109116244
|
T | C | 5 | a0001c0001t0003g0263a0001c0001t0003g0264a0001c0001t0003g0265others(2): Show | 5 | NA18940.hp1 NA18952.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+3091A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109116244 | ||||||
| chr9:109116498
|
T | C | 1 | a0001c0015t0004g0268 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.579+2837A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109116498 | ||||||
| chr9:109116540
|
C | CT | 32 | a0001c0001t0014g0032a0001c0001t0093g0029a0001c0006t0011g0280others(29): Show | 32 | HG00738.hp2 HG01109.hp1 HG01261.hp1 others(29): Show |
intron_variant | MODIFIER | c.579+2794dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109116540 | ||||||
| chr9:109116602
|
A | T | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+2733T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109116602 | ||||||
| chr9:109116676
|
G | A | 77 | a0001c0001t0059g0269a0002c0002t0001g0346a0002c0002t0001g0347others(74): Show | 77 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.579+2659C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109116676 | ||||||
| chr9:109117043
|
T | G | 114 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(111): Show | 115 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.579+2292A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117043 | ||||||
| chr9:109117069
|
C | T | 2 | a0001c0001t0054g0174a0001c0001t0054g0176 | 2 | HG01243.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.579+2266G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117069 | ||||||
| chr9:109117117
|
G | T | 1 | a0001c0005t0003g0010 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.579+2218C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117117 | ||||||
| chr9:109117118
|
T | G | 81 | a0001c0001t0054g0174a0001c0009t0018g0002a0001c0009t0018g0302others(78): Show | 82 | HG00099.hp1 HG00438.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.579+2217A>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117118 | ||||||
| chr9:109117133
|
G | T | 1 | a0001c0001t0026g0183 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.579+2202C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117133 | ||||||
| chr9:109117158
|
G | A | 32 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0002g0322others(29): Show | 32 | HG00099.hp2 HG00140.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.579+2177C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117158 | ||||||
| chr9:109117160
|
A | C | 1 | a0001c0001t0068g0158 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.579+2175T>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117160 | ||||||
| chr9:109117258
|
C | T | 1 | a0001c0001t0072g0192 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.579+2077G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117258 | ||||||
| chr9:109117276
|
A | AT | 120 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(117): Show | 121 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.579+2058dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117276 | ||||||
| chr9:109117510
|
C | G | 1 | a0001c0001t0006g0175 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.579+1825G>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117510 | ||||||
| chr9:109117679
|
G | A | 2 | a0003c0008t0017g0309a0003c0008t0017g0310 | 2 | HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.579+1656C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117679 | ||||||
| chr9:109117746
|
T | C | 115 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(112): Show | 117 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.579+1589A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117746 | ||||||
| chr9:109117894
|
T | A | 4 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0004t0116g0342others(1): Show | 5 | HG01433.hp1 HG01496.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+1441A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117894 | ||||||
| chr9:109117942
|
G | A | 3 | a0001c0009t0018g0002a0001c0009t0018g0302a0003c0017t0117g0311 | 4 | HG01433.hp1 HG01496.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+1393C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109117942 | ||||||
| chr9:109118072
|
A | T | 39 | a0001c0001t0005g0121a0001c0001t0005g0123a0001c0001t0005g0125others(36): Show | 39 | HG00408.hp2 HG00609.hp1 HG01081.hp1 others(36): Show |
intron_variant | MODIFIER | c.579+1263T>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118072 | ||||||
| chr9:109118128
|
G | A | 1 | a0004c0003t0048g0120 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.579+1207C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118128 | ||||||
| chr9:109118168
|
C | T | 3 | a0003c0004t0010g0312a0003c0004t0010g0313a0003c0004t0010g0343 | 3 | HG03041.hp1 NA18522.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.579+1167G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118168 | ||||||
| chr9:109118186
|
C | T | 6 | a0001c0006t0011g0280a0001c0006t0011g0281a0001c0006t0011g0282others(3): Show | 6 | HG01884.hp1 HG02109.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+1149G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118186 | ||||||
| chr9:109118373
|
G | T | 1 | a0001c0001t0047g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.579+962C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118373 | ||||||
| chr9:109118385
|
T | C | 5 | a0001c0001t0058g0006a0001c0006t0033g0289a0001c0006t0033g0290others(2): Show | 5 | HG01261.hp1 HG02572.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+950A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118385 | ||||||
| chr9:109118413
|
T | C | 113 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(110): Show | 114 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.579+922A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118413 | ||||||
| chr9:109118433
|
A | G | 111 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(108): Show | 112 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.579+902T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118433 | ||||||
| chr9:109118436
|
T | C | 1 | a0001c0001t0006g0175 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.579+899A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118436 | ||||||
| chr9:109118443
|
G | GT | 6 | a0002c0002t0001g0346a0002c0002t0001g0347a0002c0002t0001g0349others(3): Show | 6 | HG01257.hp1 HG01358.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+891dupA | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118443 | ||||||
| chr9:109118456
|
T | C | 303 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.579+879A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118456 | ||||||
| chr9:109118529
|
T | C | 1 | a0003c0004t0010g0343 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.579+806A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118529 | ||||||
| chr9:109118558
|
G | A | 9 | a0002c0002t0001g0411a0002c0002t0001g0412a0002c0002t0001g0413others(6): Show | 9 | NA18946.hp1 NA18956.hp1 NA18959.hp1 others(6): Show |
intron_variant | MODIFIER | c.579+777C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118558 | ||||||
| chr9:109118620
|
G | A | 1 | a0003c0017t0117g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.579+715C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118620 | ||||||
| chr9:109118629
|
T | C | 1 | a0001c0001t0054g0176 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.579+706A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118629 | ||||||
| chr9:109118990
|
C | T | 3 | a0001c0005t0003g0007a0001c0005t0003g0008a0001c0005t0003g0009 | 3 | NA19011.hp1 NA19066.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.579+345G>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109118990 | ||||||
| chr9:109119018
|
C | A | 6 | a0001c0001t0004g0182a0001c0001t0007g0179a0001c0001t0007g0180others(3): Show | 6 | HG04204.hp2 NA18946.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+317G>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109119018 | ||||||
| chr9:109119070
|
A | G | 43 | a0001c0001t0009g0030a0001c0001t0093g0029a0003c0004t0002g0322others(40): Show | 43 | HG00099.hp2 HG00140.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.579+265T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109119070 | ||||||
| chr9:109119071
|
T | C | 2 | a0001c0001t0040g0271a0001c0001t0040g0272 | 2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.579+264A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109119071 | ||||||
| chr9:109119089
|
T | A | 4 | a0001c0001t0011g0275a0001c0001t0011g0277a0001c0001t0011g0278others(1): Show | 4 | HG01243.hp1 HG02451.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.579+246A>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109119089 | ||||||
| chr9:109119117
|
G | A | 2 | a0001c0001t0004g0274a0001c0001t0013g0273 | 2 | HG00735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.579+218C>T | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109119117 | ||||||
| chr9:109119120
|
A | G | 303 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0035others(300): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.579+215T>C | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109119120 | ||||||
| chr9:109119166
|
G | C | 5 | a0001c0001t0011g0275a0001c0001t0011g0277a0001c0001t0011g0278others(2): Show | 5 | HG01243.hp1 HG02451.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+169C>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109119166 | ||||||
| chr9:109119275
|
T | C | 1 | a0001c0001t0053g0279 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.579+60A>G | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109119275 | ||||||
| chr9:109119289
|
G | T | 3 | a0001c0001t0015g0026a0001c0001t0015g0027a0001c0001t0015g0028 | 3 | HG02809.hp2 HG02886.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.579+46C>A | TMEM245 | ENSG00000106771.13 | transcript | ENST00000374586.8 | protein_coding | 1/17 | chr9 | 109119289 |