| geneid | 9697 |
|---|---|
| ensemblid | ENSG00000065308.5 |
| hgncid | 16855 |
| symbol | TRAM2 |
| name | translocation associated membrane protein 2 |
| refseq_nuc | NM_012288.4 |
| refseq_prot | NP_036420.1 |
| ensembl_nuc | ENST00000182527.4 |
| ensembl_prot | ENSP00000182527.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 52497408 |
| end | 52577060 |
| strand | - |
| ver | v1.2 |
| region | chr6:52497408-52577060 |
| region5000 | chr6:52492408-52582060 |
| regionname0 | TRAM2_chr6_52497408_52577060 |
| regionname5000 | TRAM2_chr6_52492408_52582060 |
| 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 | 370 | 377 | 90 | 72 | 154 | 16 | 43 | 116 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0002 | 0/0 | 370 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| 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 | 1113 | 370 | 87 | 71 | 154 | 16 | 40 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| c0002 | 0/0 | 1113 | 4 | 3 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| c0003 | 0/0 | 1113 | 3 | 0 | 0 | 0 | 0 | 3 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| c0004 | 0/0 | 1113 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| 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 | 5934 | 47 | 0 | 4 | 37 | 0 | 6 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0002 | 0/0 | 5934 | 26 | 2 | 11 | 7 | 0 | 6 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0003 | 0/0 | 5933 | 25 | 0 | 9 | 11 | 1 | 4 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0004 | 0/0 | 5932 | 22 | 1 | 1 | 19 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0005 | 0/1 | 5931 | 19 | 2 | 2 | 6 | 6 | 2 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0006 | 1/0 | 5935 | 19 | 8 | 5 | 2 | 2 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0007 | 0/0 | 5932 | 17 | 0 | 0 | 17 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0008 | 0/0 | 5934 | 16 | 14 | 2 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0009 | 0/0 | 5933 | 8 | 6 | 2 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0010 | 0/0 | 5934 | 6 | 0 | 5 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0011 | 0/0 | 5935 | 6 | 0 | 0 | 6 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0012 | 0/0 | 5935 | 5 | 5 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0013 | 0/0 | 5932 | 5 | 0 | 0 | 5 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0014 | 0/0 | 5934 | 5 | 0 | 0 | 5 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0015 | 0/0 | 5932 | 5 | 0 | 0 | 2 | 0 | 3 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0016 | 0/0 | 5933 | 5 | 5 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0017 | 0/0 | 5933 | 5 | 1 | 2 | 0 | 2 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0018 | 0/0 | 5932 | 4 | 0 | 0 | 2 | 0 | 2 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0019 | 0/0 | 5934 | 4 | 4 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0020 | 0/0 | 5935 | 4 | 0 | 1 | 3 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0021 | 0/0 | 5933 | 4 | 0 | 1 | 0 | 2 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0022 | 0/0 | 5934 | 3 | 0 | 0 | 3 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0023 | 0/0 | 5933 | 3 | 0 | 1 | 0 | 0 | 2 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0024 | 0/0 | 5932 | 3 | 0 | 0 | 2 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0025 | 0/0 | 5934 | 3 | 2 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0026 | 0/0 | 5934 | 3 | 0 | 0 | 3 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0027 | 0/0 | 5931 | 3 | 0 | 2 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0028 | 0/0 | 5938 | 3 | 2 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0029 | 0/0 | 5936 | 3 | 0 | 3 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0030 | 0/0 | 5933 | 3 | 2 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0031 | 0/0 | 5934 | 3 | 3 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0032 | 0/0 | 5933 | 2 | 0 | 1 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0033 | 0/0 | 5930 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0034 | 0/0 | 5930 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0035 | 0/0 | 5927 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0036 | 0/0 | 5934 | 2 | 0 | 1 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0037 | 0/0 | 5934 | 2 | 1 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0038 | 0/0 | 5933 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0039 | 0/0 | 5933 | 2 | 0 | 1 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0040 | 0/0 | 5934 | 2 | 0 | 1 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0041 | 0/0 | 5934 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0042 | 0/0 | 5937 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0043 | 0/0 | 5934 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0044 | 0/0 | 5934 | 2 | 1 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0045 | 0/0 | 5934 | 2 | 1 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0046 | 0/0 | 5934 | 2 | 0 | 0 | 0 | 0 | 2 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0047 | 0/0 | 5933 | 2 | 0 | 1 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0048 | 0/0 | 5934 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0049 | 0/0 | 5934 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0050 | 0/0 | 5933 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0051 | 0/0 | 5932 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0052 | 0/0 | 5932 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0053 | 0/0 | 5931 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0054 | 0/0 | 5931 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0055 | 0/0 | 5932 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0056 | 0/0 | 5934 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0057 | 0/0 | 5930 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0058 | 0/0 | 5927 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0059 | 0/0 | 5927 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0060 | 0/0 | 5934 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0061 | 0/0 | 5932 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0062 | 0/0 | 5934 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0063 | 0/0 | 5932 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0064 | 0/0 | 5934 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0065 | 0/0 | 5934 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0066 | 0/0 | 5934 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0067 | 0/0 | 5935 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0068 | 0/0 | 5934 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0069 | 0/0 | 5934 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0070 | 0/0 | 5934 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0071 | 0/0 | 5933 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0072 | 0/0 | 5933 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0073 | 0/0 | 5935 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0074 | 0/0 | 5934 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0075 | 0/0 | 5932 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0076 | 0/0 | 5934 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0077 | 0/0 | 5934 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0078 | 0/0 | 5931 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0079 | 0/0 | 5935 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0080 | 0/0 | 5934 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0081 | 0/0 | 5934 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0082 | 0/0 | 5934 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0083 | 0/0 | 5935 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0084 | 0/0 | 5931 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0085 | 0/0 | 5934 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0086 | 0/0 | 5932 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0087 | 0/0 | 5931 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0088 | 0/0 | 5935 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0089 | 0/0 | 5935 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0090 | 0/0 | 5938 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0091 | 0/0 | 5938 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0092 | 0/0 | 5935 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0093 | 0/0 | 5935 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0094 | 0/0 | 5935 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0095 | 0/0 | 5935 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0096 | 0/0 | 5934 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0097 | 0/0 | 5930 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0098 | 0/0 | 5935 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0099 | 0/0 | 5934 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0100 | 0/0 | 5934 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0101 | 0/0 | 5933 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0102 | 0/0 | 5934 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0103 | 0/0 | 5934 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0104 | 0/0 | 5937 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0105 | 0/0 | 5934 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| t0106 | 0/0 | 5933 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| 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 | 4 | 0 | 0 | 4 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0179 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0265 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| 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 | 1113 | 370 | 87 | 71 | 154 | 16 | 40 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0002 | 0/0 | 1113 | 4 | 3 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0003 | 0/0 | 1113 | 3 | 0 | 0 | 0 | 0 | 3 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0002c0004 | 0/0 | 1113 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 7046 | 47 | 0 | 4 | 37 | 0 | 6 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0002 | 0/0 | 7046 | 26 | 2 | 11 | 7 | 0 | 6 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0003 | 0/0 | 7045 | 25 | 0 | 9 | 11 | 1 | 4 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0004 | 0/0 | 7044 | 22 | 1 | 1 | 19 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0005 | 0/1 | 7043 | 18 | 2 | 2 | 6 | 6 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0006 | 1/0 | 7047 | 19 | 8 | 5 | 2 | 2 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0007 | 0/0 | 7044 | 17 | 0 | 0 | 17 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0008 | 0/0 | 7046 | 16 | 14 | 2 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0009 | 0/0 | 7045 | 8 | 6 | 2 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0010 | 0/0 | 7046 | 6 | 0 | 5 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0011 | 0/0 | 7047 | 6 | 0 | 0 | 6 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0012 | 0/0 | 7047 | 5 | 5 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0013 | 0/0 | 7044 | 5 | 0 | 0 | 5 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0014 | 0/0 | 7046 | 5 | 0 | 0 | 5 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0015 | 0/0 | 7044 | 3 | 0 | 0 | 2 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0016 | 0/0 | 7045 | 5 | 5 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0017 | 0/0 | 7045 | 5 | 1 | 2 | 0 | 2 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0018 | 0/0 | 7044 | 4 | 0 | 0 | 2 | 0 | 2 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0019 | 0/0 | 7046 | 4 | 4 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0020 | 0/0 | 7047 | 4 | 0 | 1 | 3 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0021 | 0/0 | 7045 | 4 | 0 | 1 | 0 | 2 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0022 | 0/0 | 7046 | 3 | 0 | 0 | 3 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0023 | 0/0 | 7045 | 3 | 0 | 1 | 0 | 0 | 2 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0024 | 0/0 | 7044 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0025 | 0/0 | 7046 | 3 | 2 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0026 | 0/0 | 7046 | 3 | 0 | 0 | 3 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0027 | 0/0 | 7043 | 3 | 0 | 2 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0029 | 0/0 | 7048 | 3 | 0 | 3 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0030 | 0/0 | 7045 | 3 | 2 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0031 | 0/0 | 7046 | 3 | 3 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0032 | 0/0 | 7045 | 2 | 0 | 1 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0033 | 0/0 | 7042 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0034 | 0/0 | 7042 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0035 | 0/0 | 7039 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0036 | 0/0 | 7046 | 2 | 0 | 1 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0037 | 0/0 | 7046 | 2 | 1 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0038 | 0/0 | 7045 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0039 | 0/0 | 7045 | 2 | 0 | 1 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0040 | 0/0 | 7046 | 2 | 0 | 1 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0041 | 0/0 | 7046 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0042 | 0/0 | 7049 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0043 | 0/0 | 7046 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0044 | 0/0 | 7046 | 2 | 1 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0045 | 0/0 | 7046 | 2 | 1 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0046 | 0/0 | 7046 | 2 | 0 | 0 | 0 | 0 | 2 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0047 | 0/0 | 7045 | 2 | 0 | 1 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0048 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0049 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0050 | 0/0 | 7045 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0051 | 0/0 | 7044 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0052 | 0/0 | 7044 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0053 | 0/0 | 7043 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0054 | 0/0 | 7043 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0055 | 0/0 | 7044 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0056 | 0/0 | 7046 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0057 | 0/0 | 7042 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0058 | 0/0 | 7039 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0059 | 0/0 | 7039 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0060 | 0/0 | 7046 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0061 | 0/0 | 7044 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0062 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0063 | 0/0 | 7044 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0064 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0065 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0066 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0067 | 0/0 | 7047 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0068 | 0/0 | 7046 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0069 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0070 | 0/0 | 7046 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0071 | 0/0 | 7045 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0072 | 0/0 | 7045 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0073 | 0/0 | 7047 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0074 | 0/0 | 7046 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0075 | 0/0 | 7044 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0076 | 0/0 | 7046 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0077 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0078 | 0/0 | 7043 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0079 | 0/0 | 7047 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0080 | 0/0 | 7046 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0081 | 0/0 | 7046 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0082 | 0/0 | 7046 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0083 | 0/0 | 7047 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0084 | 0/0 | 7043 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0085 | 0/0 | 7046 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0086 | 0/0 | 7044 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0087 | 0/0 | 7043 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0088 | 0/0 | 7047 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0089 | 0/0 | 7047 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0090 | 0/0 | 7050 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0091 | 0/0 | 7050 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0092 | 0/0 | 7047 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0094 | 0/0 | 7047 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0095 | 0/0 | 7047 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0096 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0097 | 0/0 | 7042 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0098 | 0/0 | 7047 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0099 | 0/0 | 7046 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0100 | 0/0 | 7046 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0101 | 0/0 | 7045 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0102 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0103 | 0/0 | 7046 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0104 | 0/0 | 7049 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0105 | 0/0 | 7046 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0001t0106 | 0/0 | 7045 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0002t0028 | 0/0 | 7050 | 3 | 2 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0002t0093 | 0/0 | 7047 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0003t0005 | 0/0 | 7043 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0001c0003t0015 | 0/0 | 7044 | 2 | 0 | 0 | 0 | 0 | 2 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| a0002c0004t0024 | 0/0 | 7044 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | copy fasta | chr6 | 52492408 | 52582060 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0004g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0005g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0005g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0005g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0005g0265 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0005g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0006g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0006g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0006g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0006g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0006g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0006g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0006g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0006g0179 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0006g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0006g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0006g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0006g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0006g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0007g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0007g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0007g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0007g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0007g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0007g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0007g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0007g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0007g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0007g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0007g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0007g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0007g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0007g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0008g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0008g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0008g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0008g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0008g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0008g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0008g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0008g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0008g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0008g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0008g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0008g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0008g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0008g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0009g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0009g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0009g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0009g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0009g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0009g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0009g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0009g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0010g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0010g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0010g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0010g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0010g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0010g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0011g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0011g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0011g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0011g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0011g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0011g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0012g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0012g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0012g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0012g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0012g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0013g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0013g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0013g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0013g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0013g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0014g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0014g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0014g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0014g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0014g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0015g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0015g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0015g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0016g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0016g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0016g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0016g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0016g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0017g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0017g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0017g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0017g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0018g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0018g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0018g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0018g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0019g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0019g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0019g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0019g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0020g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0020g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0020g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0020g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0021g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0021g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0021g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0021g0363 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0022g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0022g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0022g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0023g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0023g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0023g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0024g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0024g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0025g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0025g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0025g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0026g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0026g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0026g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0027g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0027g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0027g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0029g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0030g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0030g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0030g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0031g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0031g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0031g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0032g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0032g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0033g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0033g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0034g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0034g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0035g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0035g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0036g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0036g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0037g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0037g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0038g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0038g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0039g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0039g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0040g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0040g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0041g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0041g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0042g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0042g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0043g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0043g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0044g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0044g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0045g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0045g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0046g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0046g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0047g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0047g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0048g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0049g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0050g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0051g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0052g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0053g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0054g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0055g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0056g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0057g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0058g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0059g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0060g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0061g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0062g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0063g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0064g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0065g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0066g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0067g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0068g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0069g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0070g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0071g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0072g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0073g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0074g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0075g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0076g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0077g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0078g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0079g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0080g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0081g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0082g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0083g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0084g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0085g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0086g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0087g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0088g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0089g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0090g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0091g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0092g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0094g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0095g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0096g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0097g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0098g0337 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0099g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0100g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0101g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0102g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0103g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0104g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0105g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0001t0106g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0002t0028g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0002t0028g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0002t0093g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0003t0005g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0003t0015g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0001c0003t0015g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| a0002c0004t0024g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0036 | g0321 | EUR | GBR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00099 | hp2 | a0001 | c0001 | t0021 | g0363 | EUR | GBR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00140 | hp1 | a0001 | c0001 | t0047 | g0090 | EUR | GBR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0006 | EUR | GBR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00280 | hp1 | a0001 | c0001 | t0005 | g0169 | EUR | FIN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0081 | EUR | FIN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | CHS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | CHS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00544 | hp1 | a0001 | c0001 | t0102 | g0315 | EAS | CHS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00558 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | CHS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00609 | hp1 | a0001 | c0001 | t0066 | g0335 | EAS | CHS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00609 | hp2 | a0001 | c0001 | t0022 | g0034 | EAS | CHS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00639 | hp1 | a0001 | c0001 | t0023 | g0023 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00639 | hp2 | a0001 | c0001 | t0039 | g0248 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00642 | hp1 | a0001 | c0001 | t0017 | g0010 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00642 | hp2 | a0001 | c0001 | t0006 | g0176 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00733 | hp1 | a0001 | c0001 | t0088 | g0174 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0332 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00735 | hp1 | a0001 | c0001 | t0009 | g0087 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0274 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00738 | hp2 | a0001 | c0001 | t0036 | g0088 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG00741 | hp2 | a0001 | c0001 | t0029 | g0002 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01069 | hp2 | a0001 | c0001 | t0044 | g0223 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01070 | hp2 | a0001 | c0001 | t0006 | g0065 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01071 | hp2 | a0001 | c0001 | t0006 | g0061 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01074 | hp1 | a0001 | c0001 | t0040 | g0263 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01074 | hp2 | a0001 | c0001 | t0008 | g0259 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01081 | hp1 | a0001 | c0001 | t0017 | g0171 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01099 | hp1 | a0001 | c0001 | t0009 | g0086 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0043 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01106 | hp2 | a0001 | c0001 | t0099 | g0339 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01167 | hp1 | a0001 | c0001 | t0047 | g0322 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01167 | hp2 | a0001 | c0001 | t0029 | g0002 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01169 | hp1 | a0001 | c0001 | t0029 | g0002 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0095 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01175 | hp1 | a0001 | c0001 | t0030 | g0344 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01175 | hp2 | a0001 | c0001 | t0037 | g0226 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01192 | hp1 | a0001 | c0001 | t0073 | g0243 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0354 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01243 | hp1 | a0001 | c0001 | t0078 | g0338 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01243 | hp2 | a0001 | c0002 | t0028 | g0011 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01255 | hp1 | a0001 | c0001 | t0025 | g0291 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0045 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01257 | hp1 | a0001 | c0001 | t0106 | g0324 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01257 | hp2 | a0001 | c0001 | t0027 | g0046 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01258 | hp1 | a0001 | c0001 | t0027 | g0048 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01258 | hp2 | a0001 | c0001 | t0021 | g0361 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0078 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01358 | hp1 | a0001 | c0001 | t0020 | g0247 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01358 | hp2 | a0001 | c0001 | t0053 | g0021 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01433 | hp1 | a0001 | c0001 | t0056 | g0032 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01433 | hp2 | a0001 | c0001 | t0005 | g0168 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01496 | hp1 | a0001 | c0001 | t0032 | g0031 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01515 | hp1 | a0001 | c0001 | t0021 | g0362 | EUR | IBS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0175 | EUR | IBS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0170 | EUR | IBS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01516 | hp2 | a0001 | c0001 | t0017 | g0010 | EUR | IBS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0178 | EUR | IBS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01517 | hp2 | a0001 | c0001 | t0017 | g0323 | EUR | IBS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01884 | hp1 | a0001 | c0001 | t0012 | g0279 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0195 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01891 | hp1 | a0001 | c0001 | t0042 | g0351 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01891 | hp2 | a0001 | c0001 | t0104 | g0336 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01928 | hp1 | a0001 | c0001 | t0105 | g0276 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01928 | hp2 | a0001 | c0001 | t0010 | g0026 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01934 | hp1 | a0001 | c0001 | t0006 | g0177 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01952 | hp1 | a0001 | c0001 | t0010 | g0019 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01952 | hp2 | a0001 | c0001 | t0074 | g0275 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01993 | hp2 | a0001 | c0001 | t0010 | g0028 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02004 | hp1 | a0001 | c0001 | t0060 | g0049 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02015 | hp1 | a0001 | c0001 | t0005 | g0172 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02040 | hp1 | a0001 | c0001 | t0022 | g0033 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02055 | hp1 | a0001 | c0001 | t0037 | g0316 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02055 | hp2 | a0001 | c0001 | t0008 | g0009 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02071 | hp1 | a0001 | c0001 | t0011 | g0217 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02074 | hp1 | a0001 | c0001 | t0015 | g0327 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02080 | hp1 | a0001 | c0001 | t0062 | g0320 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02080 | hp2 | a0001 | c0001 | t0014 | g0148 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02083 | hp2 | a0001 | c0001 | t0007 | g0228 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02129 | hp2 | a0001 | c0001 | t0063 | g0264 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02132 | hp1 | a0001 | c0001 | t0095 | g0216 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0319 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0342 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02145 | hp1 | a0001 | c0001 | t0009 | g0209 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02145 | hp2 | a0001 | c0001 | t0017 | g0326 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02148 | hp2 | a0001 | c0001 | t0010 | g0027 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | CDX | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02155 | hp2 | a0001 | c0001 | t0007 | g0140 | EAS | CDX | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | CDX | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02165 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | CDX | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02257 | hp1 | a0001 | c0001 | t0101 | g0292 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0191 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02258 | hp2 | a0001 | c0001 | t0059 | g0167 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02280 | hp1 | a0001 | c0001 | t0038 | g0352 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02280 | hp2 | a0001 | c0001 | t0016 | g0267 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02293 | hp2 | a0001 | c0001 | t0010 | g0025 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02300 | hp1 | a0001 | c0001 | t0076 | g0244 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0093 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02451 | hp1 | a0001 | c0001 | t0034 | g0192 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02451 | hp2 | a0001 | c0001 | t0035 | g0066 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02523 | hp1 | a0001 | c0001 | t0005 | g0328 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02523 | hp2 | a0001 | c0001 | t0069 | g0212 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02572 | hp1 | a0001 | c0001 | t0016 | g0039 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0091 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02602 | hp1 | a0001 | c0001 | t0045 | g0085 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0184 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02615 | hp2 | a0001 | c0002 | t0093 | g0272 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02622 | hp1 | a0001 | c0001 | t0009 | g0219 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0353 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02630 | hp1 | a0001 | c0001 | t0016 | g0037 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02630 | hp2 | a0001 | c0001 | t0019 | g0207 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02683 | hp1 | a0001 | c0001 | t0046 | g0075 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02683 | hp2 | a0001 | c0001 | t0018 | g0101 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0236 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02698 | hp2 | a0001 | c0001 | t0027 | g0047 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02717 | hp1 | a0001 | c0001 | t0042 | g0350 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02717 | hp2 | a0001 | c0001 | t0012 | g0268 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02723 | hp1 | a0001 | c0001 | t0043 | g0208 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02723 | hp2 | a0001 | c0001 | t0061 | g0210 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02735 | hp1 | a0002 | c0004 | t0024 | g0359 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02735 | hp2 | a0001 | c0001 | t0023 | g0022 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0068 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02738 | hp2 | a0001 | c0003 | t0015 | g0305 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02809 | hp1 | a0001 | c0001 | t0008 | g0290 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0004 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02818 | hp1 | a0001 | c0001 | t0031 | g0183 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02818 | hp2 | a0001 | c0001 | t0090 | g0273 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02886 | hp1 | a0001 | c0001 | t0025 | g0281 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02886 | hp2 | a0001 | c0001 | t0019 | g0084 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0042 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02895 | hp2 | a0001 | c0001 | t0012 | g0040 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0277 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02896 | hp2 | a0001 | c0001 | t0016 | g0194 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0041 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02897 | hp2 | a0001 | c0001 | t0016 | g0193 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0300 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02922 | hp2 | a0001 | c0001 | t0030 | g0261 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0296 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02965 | hp2 | a0001 | c0001 | t0097 | g0356 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02970 | hp1 | a0001 | c0001 | t0100 | g0067 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02970 | hp2 | a0001 | c0001 | t0025 | g0358 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03041 | hp1 | a0001 | c0001 | t0057 | g0188 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03041 | hp2 | a0001 | c0001 | t0031 | g0270 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0035 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0295 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03130 | hp1 | a0001 | c0001 | t0009 | g0232 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0297 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03139 | hp1 | a0001 | c0001 | t0038 | g0173 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03139 | hp2 | a0001 | c0001 | t0080 | g0180 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03195 | hp1 | a0001 | c0001 | t0008 | g0271 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03195 | hp2 | a0001 | c0001 | t0031 | g0182 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0283 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03209 | hp2 | a0001 | c0002 | t0028 | g0011 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03225 | hp1 | a0001 | c0002 | t0028 | g0357 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03225 | hp2 | a0001 | c0001 | t0034 | g0260 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03239 | hp1 | a0001 | c0001 | t0046 | g0076 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03239 | hp2 | a0001 | c0001 | t0051 | g0029 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03453 | hp1 | a0001 | c0001 | t0008 | g0258 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03453 | hp2 | a0001 | c0001 | t0008 | g0299 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0311 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03516 | hp1 | a0001 | c0001 | t0058 | g0189 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03516 | hp2 | a0001 | c0001 | t0035 | g0185 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03540 | hp1 | a0001 | c0001 | t0019 | g0082 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03540 | hp2 | a0001 | c0001 | t0008 | g0071 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03579 | hp1 | a0001 | c0001 | t0012 | g0280 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03579 | hp2 | a0001 | c0001 | t0030 | g0343 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03654 | hp1 | a0001 | c0001 | t0023 | g0018 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03654 | hp2 | a0001 | c0001 | t0015 | g0312 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03669 | hp1 | a0001 | c0001 | t0070 | g0097 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03688 | hp1 | a0001 | c0001 | t0082 | g0158 | SAS | STU | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03688 | hp2 | a0001 | c0003 | t0015 | g0307 | SAS | STU | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03704 | hp1 | a0001 | c0001 | t0006 | g0096 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0266 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0222 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03710 | hp2 | a0001 | c0001 | t0039 | g0318 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03831 | hp1 | a0001 | c0001 | t0098 | g0337 | SAS | BEB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03831 | hp2 | a0001 | c0001 | t0010 | g0015 | SAS | BEB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | BEB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03834 | hp2 | a0001 | c0001 | t0054 | g0016 | SAS | BEB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03942 | hp1 | a0001 | c0003 | t0005 | g0308 | SAS | BEB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03942 | hp2 | a0001 | c0001 | t0018 | g0214 | SAS | BEB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | STU | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG04115 | hp2 | a0001 | c0001 | t0055 | g0024 | SAS | STU | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0060 | SAS | BEB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG04184 | hp2 | a0001 | c0001 | t0079 | g0119 | SAS | BEB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | STU | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG04204 | hp1 | a0001 | c0001 | t0021 | g0360 | SAS | STU | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG04228 | hp1 | a0001 | c0001 | t0081 | g0129 | SAS | STU | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | STU | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18612 | hp1 | a0001 | c0001 | t0007 | g0146 | EAS | CHB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0070 | AFR | YRI | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18906 | hp2 | a0001 | c0001 | t0008 | g0293 | AFR | YRI | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18939 | hp2 | a0001 | c0001 | t0011 | g0058 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18940 | hp2 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18941 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18941 | hp2 | a0001 | c0001 | t0048 | g0013 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18943 | hp1 | a0001 | c0001 | t0015 | g0269 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18943 | hp2 | a0001 | c0001 | t0077 | g0112 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18945 | hp1 | a0001 | c0001 | t0026 | g0151 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18947 | hp1 | a0001 | c0001 | t0014 | g0130 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18947 | hp2 | a0001 | c0001 | t0005 | g0288 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18949 | hp1 | a0001 | c0001 | t0011 | g0215 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18949 | hp2 | a0001 | c0001 | t0014 | g0057 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18956 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18956 | hp2 | a0001 | c0001 | t0007 | g0255 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18959 | hp1 | a0001 | c0001 | t0011 | g0289 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18959 | hp2 | a0001 | c0001 | t0007 | g0333 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18962 | hp2 | a0001 | c0001 | t0026 | g0141 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18963 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18963 | hp2 | a0001 | c0001 | t0007 | g0251 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0284 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18965 | hp1 | a0001 | c0001 | t0050 | g0014 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18969 | hp1 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18970 | hp1 | a0001 | c0001 | t0052 | g0030 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18970 | hp2 | a0001 | c0001 | t0013 | g0073 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18972 | hp1 | a0001 | c0001 | t0018 | g0287 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18972 | hp2 | a0001 | c0001 | t0014 | g0145 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18973 | hp1 | a0001 | c0001 | t0032 | g0020 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18973 | hp2 | a0001 | c0001 | t0065 | g0202 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18981 | hp1 | a0001 | c0001 | t0007 | g0257 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18981 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18982 | hp1 | a0001 | c0001 | t0072 | g0102 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18986 | hp2 | a0001 | c0001 | t0049 | g0012 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18990 | hp1 | a0001 | c0001 | t0064 | g0111 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18990 | hp2 | a0001 | c0001 | t0013 | g0196 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18993 | hp1 | a0001 | c0001 | t0086 | g0256 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19000 | hp1 | a0001 | c0001 | t0094 | g0329 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19000 | hp2 | a0001 | c0001 | t0041 | g0109 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19004 | hp1 | a0001 | c0001 | t0007 | g0220 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19004 | hp2 | a0001 | c0001 | t0026 | g0134 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19005 | hp2 | a0001 | c0001 | t0004 | g0306 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19006 | hp1 | a0001 | c0001 | t0041 | g0159 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19006 | hp2 | a0001 | c0001 | t0020 | g0235 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0325 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19010 | hp2 | a0001 | c0001 | t0007 | g0250 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19011 | hp1 | a0001 | c0001 | t0018 | g0197 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19012 | hp1 | a0001 | c0001 | t0006 | g0309 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19012 | hp2 | a0001 | c0001 | t0005 | g0133 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19030 | hp1 | a0001 | c0001 | t0084 | g0349 | AFR | LWK | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19030 | hp2 | a0001 | c0001 | t0043 | g0345 | AFR | LWK | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19043 | hp1 | a0001 | c0001 | t0033 | g0187 | AFR | LWK | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19043 | hp2 | a0001 | c0001 | t0068 | g0313 | AFR | LWK | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19054 | hp1 | a0001 | c0001 | t0020 | g0347 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19054 | hp2 | a0001 | c0001 | t0011 | g0201 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19055 | hp1 | a0001 | c0001 | t0022 | g0017 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0105 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19057 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19062 | hp1 | a0001 | c0001 | t0007 | g0252 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0340 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19063 | hp1 | a0001 | c0001 | t0013 | g0136 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19064 | hp1 | a0001 | c0001 | t0007 | g0253 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19065 | hp1 | a0001 | c0001 | t0024 | g0303 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19065 | hp2 | a0001 | c0001 | t0007 | g0254 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19066 | hp1 | a0001 | c0001 | t0014 | g0115 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19066 | hp2 | a0001 | c0001 | t0007 | g0198 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19067 | hp1 | a0001 | c0001 | t0096 | g0155 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0104 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19070 | hp1 | a0001 | c0001 | t0013 | g0103 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19074 | hp1 | a0001 | c0001 | t0071 | g0053 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19074 | hp2 | a0001 | c0001 | t0024 | g0310 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19079 | hp1 | a0001 | c0001 | t0006 | g0331 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19080 | hp1 | a0001 | c0001 | t0013 | g0156 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19081 | hp2 | a0001 | c0001 | t0075 | g0249 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0341 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19083 | hp2 | a0001 | c0001 | t0083 | g0135 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0304 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19086 | hp1 | a0001 | c0001 | t0020 | g0240 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19087 | hp2 | a0001 | c0001 | t0092 | g0330 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19091 | hp1 | a0001 | c0001 | t0004 | g0056 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19091 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19240 | hp1 | a0001 | c0001 | t0044 | g0038 | AFR | YRI | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA19240 | hp2 | a0001 | c0001 | t0089 | g0355 | AFR | YRI | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA20129 | hp1 | a0001 | c0001 | t0008 | g0298 | AFR | ASW | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0211 | AFR | ASW | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA20752 | hp1 | a0001 | c0001 | t0006 | g0063 | EUR | TSI | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA20752 | hp2 | a0001 | c0001 | t0005 | g0006 | EUR | TSI | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA20805 | hp1 | a0001 | c0001 | t0040 | g0262 | EUR | TSI | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA20805 | hp2 | a0001 | c0001 | t0006 | g0064 | EUR | TSI | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA20905 | hp1 | a0001 | c0001 | t0087 | g0181 | SAS | GIH | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0062 | SAS | GIH | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG01123 | hp2 | a0001 | c0001 | t0008 | g0282 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02109 | hp1 | a0001 | c0001 | t0009 | g0294 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02109 | hp2 | a0001 | c0001 | t0067 | g0083 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02486 | hp1 | a0001 | c0001 | t0091 | g0301 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02486 | hp2 | a0001 | c0001 | t0019 | g0100 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0036 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG02559 | hp2 | a0001 | c0001 | t0045 | g0278 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03471 | hp1 | a0001 | c0001 | t0033 | g0186 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG06807 | hp1 | a0001 | c0001 | t0009 | g0233 | AFR | USA | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| HG06807 | hp2 | a0001 | c0001 | t0085 | g0190 | AFR | USA | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0106 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA18955 | hp2 | a0001 | c0001 | t0011 | g0230 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA20300 | hp1 | a0001 | c0001 | t0103 | g0302 | AFR | USA | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| NA20300 | hp2 | a0001 | c0001 | t0008 | g0009 | AFR | USA | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0005 | g0265 | REF | REF | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0006 | g0179 | REF | REF | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:52576872
|
T | G | 1 | a0002 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.44A>C | p.Gln15Pro | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/11 | 189/7047 | 44/1113 | 15/370 | chr6 | 52576872 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:52504610
|
C | T | 1 | a0001c0003 | 3 | HG02738.hp2 HG03688.hp2 HG03942.hp1 |
synonymous_variant | LOW | c.1020G>A | p.Arg340Arg | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 10/11 | 1165/7047 | 1020/1113 | 340/370 | chr6 | 52504610 | ||
| chr6:52504712
|
G | A | 1 | a0001c0002 | 4 | HG01243.hp2 HG02615.hp2 HG03209.hp2 others(1): Show |
synonymous_variant | LOW | c.918C>T | p.Leu306Leu | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 10/11 | 1063/7047 | 918/1113 | 306/370 | chr6 | 52504712 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:52497472
|
A | T | 1 | a0001c0001t0074 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5725T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 5725 | chr6 | 52497472 | |||||
| chr6:52497518
|
C | T | 1 | a0001c0001t0090 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5679G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 5679 | chr6 | 52497518 | |||||
| chr6:52497580
|
C | T | 1 | a0001c0001t0080 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5617G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 5617 | chr6 | 52497580 | |||||
| chr6:52497605
|
C | T | 1 | a0001c0001t0038 | 2 | HG02280.hp1 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5592G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 5592 | chr6 | 52497605 | |||||
| chr6:52497607
|
G | A | 11 | a0001c0001t0005a0001c0001t0015a0001c0001t0027others(8): Show | 33 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*5590C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 5590 | chr6 | 52497607 | |||||
| chr6:52497791
|
A | G | 1 | a0001c0001t0068 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5406T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 5406 | chr6 | 52497791 | |||||
| chr6:52497839
|
G | A | 10 | a0001c0001t0018a0001c0001t0035a0001c0001t0042others(7): Show | 15 | HG01891.hp1 HG02129.hp2 HG02258.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*5358C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 5358 | chr6 | 52497839 | |||||
| chr6:52497874
|
C | G | 2 | a0001c0001t0014a0001c0001t0041 | 7 | HG02080.hp2 NA18947.hp1 NA18949.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*5323G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 5323 | chr6 | 52497874 | |||||
| chr6:52497917
|
T | A | 7 | a0001c0001t0004a0001c0001t0013a0001c0001t0024others(4): Show | 33 | HG01192.hp2 HG02723.hp2 HG02735.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*5280A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 5280 | chr6 | 52497917 | |||||
| chr6:52498046
|
T | A | 26 | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(23): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*5151A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 5151 | chr6 | 52498046 | |||||
| chr6:52498067
|
A | T | 11 | a0001c0001t0005a0001c0001t0015a0001c0001t0027others(8): Show | 33 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*5130T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 5130 | chr6 | 52498067 | |||||
| chr6:52498253
|
T | C | 1 | a0001c0001t0013 | 5 | NA18970.hp2 NA18990.hp2 NA19063.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4944A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 4944 | chr6 | 52498253 | |||||
| chr6:52498435
|
A | G | 2 | a0001c0001t0024a0002c0004t0024 | 3 | HG02735.hp1 NA19065.hp1 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4762T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 4762 | chr6 | 52498435 | |||||
| chr6:52498567
|
G | A | 10 | a0001c0001t0017a0001c0001t0018a0001c0001t0023others(7): Show | 22 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4630C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 4630 | chr6 | 52498567 | |||||
| chr6:52498613
|
T | A | 1 | a0001c0001t0085 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4584A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 4584 | chr6 | 52498613 | |||||
| chr6:52498618
|
G | A | 2 | a0001c0002t0028a0001c0002t0093 | 4 | HG01243.hp2 HG02615.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4579C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 4579 | chr6 | 52498618 | |||||
| chr6:52498666
|
C | G | 1 | a0001c0001t0033 | 2 | HG03471.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4531G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 4531 | chr6 | 52498666 | |||||
| chr6:52498685
|
AAAAAC | A | 3 | a0001c0001t0035a0001c0001t0058a0001c0001t0059 | 4 | HG02258.hp2 HG02451.hp2 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4507_*4511delGTTT others(1): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 4507 | chr6 | 52498685 | |||||
| chr6:52498701
|
A | G | 1 | a0001c0001t0104 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4496T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 4496 | chr6 | 52498701 | |||||
| chr6:52498817
|
G | A | 7 | a0001c0001t0017a0001c0001t0023a0001c0001t0037others(4): Show | 17 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4380C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 4380 | chr6 | 52498817 | |||||
| chr6:52498817
|
G | C | 1 | a0001c0001t0027 | 3 | HG01257.hp2 HG01258.hp1 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4380C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 4380 | chr6 | 52498817 | |||||
| chr6:52498912
|
T | C | 1 | a0001c0001t0059 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4285A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 4285 | chr6 | 52498912 | |||||
| chr6:52498930
|
T | C | 45 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(42): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
3_prime_UTR_variant | MODIFIER | c.*4267A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 4267 | chr6 | 52498930 | |||||
| chr6:52498961
|
A | G | 7 | a0001c0001t0017a0001c0001t0023a0001c0001t0037others(4): Show | 17 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4236T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 4236 | chr6 | 52498961 | |||||
| chr6:52498998
|
C | T | 1 | a0001c0001t0081 | 1 | HG04228.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4199G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 4199 | chr6 | 52498998 | |||||
| chr6:52499035
|
C | T | 11 | a0001c0001t0005a0001c0001t0015a0001c0001t0027others(8): Show | 33 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*4162G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 4162 | chr6 | 52499035 | |||||
| chr6:52499051
|
C | G | 14 | a0001c0001t0004a0001c0001t0013a0001c0001t0018others(11): Show | 44 | HG01192.hp2 HG02129.hp2 HG02258.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*4146G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 4146 | chr6 | 52499051 | |||||
| chr6:52499161
|
C | T | 4 | a0001c0001t0008a0001c0001t0025a0001c0001t0080others(1): Show | 21 | HG01074.hp2 HG01123.hp2 HG01255.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*4036G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 4036 | chr6 | 52499161 | |||||
| chr6:52499204
|
A | G | 2 | a0001c0002t0028a0001c0002t0093 | 4 | HG01243.hp2 HG02615.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3993T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 3993 | chr6 | 52499204 | |||||
| chr6:52499387
|
T | C | 1 | a0001c0001t0100 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3810A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 3810 | chr6 | 52499387 | |||||
| chr6:52499391
|
T | C | 1 | a0001c0001t0054 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3806A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 3806 | chr6 | 52499391 | |||||
| chr6:52499426
|
A | G | 1 | a0001c0001t0104 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3771T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 3771 | chr6 | 52499426 | |||||
| chr6:52499457
|
A | G | 1 | a0001c0001t0092 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3740T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 3740 | chr6 | 52499457 | |||||
| chr6:52499461
|
G | A | 2 | a0001c0001t0019a0001c0001t0067 | 5 | HG02109.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3736C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 3736 | chr6 | 52499461 | |||||
| chr6:52499472
|
G | A | 97 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(94): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*3725C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 3725 | chr6 | 52499472 | |||||
| chr6:52499651
|
G | C | 1 | a0001c0001t0035 | 2 | HG02451.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3546C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 3546 | chr6 | 52499651 | |||||
| chr6:52499722
|
C | T | 7 | a0001c0001t0004a0001c0001t0013a0001c0001t0024others(4): Show | 33 | HG01192.hp2 HG02723.hp2 HG02735.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*3475G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 3475 | chr6 | 52499722 | |||||
| chr6:52499829
|
GAC | G | 4 | a0001c0001t0007a0001c0001t0071a0001c0001t0072others(1): Show | 20 | HG00558.hp1 HG02083.hp2 HG02155.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3366_*3367delGT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 3366 | chr6 | 52499829 | |||||
| chr6:52499966
|
C | T | 1 | a0001c0001t0031 | 3 | HG02818.hp1 HG03041.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3231G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 3231 | chr6 | 52499966 | |||||
| chr6:52500032
|
T | C | 1 | a0001c0001t0030 | 3 | HG01175.hp1 HG02922.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3165A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 3165 | chr6 | 52500032 | |||||
| chr6:52500047
|
C | T | 11 | a0001c0001t0003a0001c0001t0021a0001c0001t0032others(8): Show | 41 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*3150G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 3150 | chr6 | 52500047 | |||||
| chr6:52500132
|
G | A | 1 | a0001c0001t0085 | 1 | HG06807.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3065C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 3065 | chr6 | 52500132 | |||||
| chr6:52500518
|
G | GT | 7 | a0001c0001t0012a0001c0001t0067a0001c0001t0071others(4): Show | 11 | HG01192.hp1 HG01884.hp1 HG02109.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2678dupA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2678 | chr6 | 52500518 | |||||
| chr6:52500518
|
GTTTT | G | 4 | a0001c0001t0033a0001c0001t0034a0001c0001t0057others(1): Show | 6 | HG02451.hp1 HG02965.hp2 HG03041.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2675_*2678delAAAA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2675 | chr6 | 52500518 | |||||
| chr6:52500519
|
T | G | 15 | a0001c0001t0004a0001c0001t0013a0001c0001t0018others(12): Show | 45 | HG01192.hp2 HG02129.hp2 HG02258.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2678A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2678 | chr6 | 52500519 | |||||
| chr6:52500524
|
T | G | 10 | a0001c0001t0005a0001c0001t0015a0001c0001t0027others(7): Show | 32 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*2673A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2673 | chr6 | 52500524 | |||||
| chr6:52500525
|
TTTG | T | 8 | a0001c0001t0005a0001c0001t0027a0001c0001t0053others(5): Show | 27 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2669_*2671delCAA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2669 | chr6 | 52500525 | |||||
| chr6:52500526
|
TTG | T | 3 | a0001c0001t0015a0001c0001t0086a0001c0003t0015 | 6 | HG02074.hp1 HG02738.hp2 HG03654.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2669_*2670delCA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2669 | chr6 | 52500526 | |||||
| chr6:52500528
|
G | GTTT | 6 | a0001c0001t0029a0001c0001t0042a0001c0001t0090others(3): Show | 11 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2666_*2668dupAAA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2668 | chr6 | 52500528 | |||||
| chr6:52500528
|
G | T | 20 | a0001c0001t0002a0001c0001t0007a0001c0001t0020others(17): Show | 69 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*2669C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2669 | chr6 | 52500528 | |||||
| chr6:52500528
|
GT | G | 14 | a0001c0001t0003a0001c0001t0009a0001c0001t0016others(11): Show | 64 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*2668delA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2668 | chr6 | 52500528 | |||||
| chr6:52500528
|
GTT | G | 13 | a0001c0001t0004a0001c0001t0013a0001c0001t0018others(10): Show | 43 | HG01192.hp2 HG02129.hp2 HG02258.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2667_*2668delAA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2667 | chr6 | 52500528 | |||||
| chr6:52500529
|
T | G | 15 | a0001c0001t0002a0001c0001t0007a0001c0001t0022others(12): Show | 61 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*2668A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2668 | chr6 | 52500529 | |||||
| chr6:52500529
|
T | TG | 2 | a0001c0001t0020a0001c0001t0098 | 5 | HG01358.hp1 HG03831.hp1 NA19006.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2667_*2668insC | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2667 | chr6 | 52500529 | |||||
| chr6:52500530
|
T | G | 1 | a0001c0001t0064 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2667A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2667 | chr6 | 52500530 | |||||
| chr6:52500533
|
T | G | 18 | a0001c0001t0004a0001c0001t0013a0001c0001t0018others(15): Show | 48 | HG01192.hp2 HG02129.hp2 HG02258.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*2664A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2664 | chr6 | 52500533 | |||||
| chr6:52500534
|
T | G | 18 | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(15): Show | 93 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*2663A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2663 | chr6 | 52500534 | |||||
| chr6:52500537
|
T | G | 1 | a0001c0001t0071 | 1 | NA19074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2660A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2660 | chr6 | 52500537 | |||||
| chr6:52500538
|
T | G | 27 | a0001c0001t0002a0001c0001t0007a0001c0001t0012others(24): Show | 89 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*2659A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2659 | chr6 | 52500538 | |||||
| chr6:52500540
|
T | G | 3 | a0001c0001t0026a0001c0001t0049a0001c0001t0083 | 5 | NA18945.hp1 NA18962.hp2 NA18986.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2657A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2657 | chr6 | 52500540 | |||||
| chr6:52500567
|
C | T | 1 | a0001c0001t0033 | 2 | HG03471.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2630G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2630 | chr6 | 52500567 | |||||
| chr6:52500604
|
G | A | 18 | a0001c0001t0003a0001c0001t0009a0001c0001t0016others(15): Show | 67 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*2593C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2593 | chr6 | 52500604 | |||||
| chr6:52500644
|
C | T | 1 | a0001c0001t0101 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2553G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2553 | chr6 | 52500644 | |||||
| chr6:52500674
|
G | C | 3 | a0001c0001t0042a0001c0001t0068a0001c0001t0085 | 4 | HG01891.hp1 HG02717.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2523C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2523 | chr6 | 52500674 | |||||
| chr6:52500691
|
G | A | 3 | a0001c0001t0009a0001c0001t0045a0001c0001t0101 | 11 | HG00735.hp1 HG01099.hp1 HG02109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2506C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2506 | chr6 | 52500691 | |||||
| chr6:52500701
|
C | T | 2 | a0001c0001t0031a0001c0001t0047 | 5 | HG00140.hp1 HG01167.hp1 HG02818.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2496G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2496 | chr6 | 52500701 | |||||
| chr6:52500818
|
G | T | 1 | a0001c0001t0070 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2379C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2379 | chr6 | 52500818 | |||||
| chr6:52500995
|
G | A | 8 | a0001c0001t0003a0001c0001t0021a0001c0001t0032others(5): Show | 37 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2202C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2202 | chr6 | 52500995 | |||||
| chr6:52501005
|
G | A | 1 | a0001c0001t0046 | 2 | HG02683.hp1 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2192C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2192 | chr6 | 52501005 | |||||
| chr6:52501015
|
G | C | 1 | a0001c0001t0104 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2182C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2182 | chr6 | 52501015 | |||||
| chr6:52501030
|
G | C | 1 | a0001c0001t0040 | 2 | HG01074.hp1 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2167C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2167 | chr6 | 52501030 | |||||
| chr6:52501075
|
A | G | 14 | a0001c0001t0004a0001c0001t0013a0001c0001t0018others(11): Show | 44 | HG01192.hp2 HG02129.hp2 HG02258.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2122T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2122 | chr6 | 52501075 | |||||
| chr6:52501137
|
C | T | 1 | a0001c0001t0031 | 3 | HG02818.hp1 HG03041.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2060G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2060 | chr6 | 52501137 | |||||
| chr6:52501178
|
G | C | 1 | a0001c0001t0031 | 3 | HG02818.hp1 HG03041.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2019C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2019 | chr6 | 52501178 | |||||
| chr6:52501190
|
G | A | 97 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(94): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*2007C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 2007 | chr6 | 52501190 | |||||
| chr6:52501353
|
A | T | 1 | a0001c0001t0088 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1844T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 1844 | chr6 | 52501353 | |||||
| chr6:52501408
|
C | T | 11 | a0001c0001t0005a0001c0001t0015a0001c0001t0027others(8): Show | 33 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1789G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 1789 | chr6 | 52501408 | |||||
| chr6:52501525
|
A | G | 1 | a0001c0001t0069 | 1 | HG02523.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1672T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 1672 | chr6 | 52501525 | |||||
| chr6:52501580
|
CTT | C | 1 | a0001c0001t0029 | 3 | HG00741.hp2 HG01167.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1615_*1616delAA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 1615 | chr6 | 52501580 | |||||
| chr6:52501633
|
G | A | 97 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(94): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*1564C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 1564 | chr6 | 52501633 | |||||
| chr6:52501705
|
C | T | 1 | a0001c0001t0077 | 1 | NA18943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1492G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 1492 | chr6 | 52501705 | |||||
| chr6:52501855
|
C | T | 1 | a0001c0001t0063 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1342G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 1342 | chr6 | 52501855 | |||||
| chr6:52501964
|
G | A | 24 | a0001c0001t0002a0001c0001t0007a0001c0001t0012others(21): Show | 86 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1233C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 1233 | chr6 | 52501964 | |||||
| chr6:52501998
|
G | A | 13 | a0001c0001t0004a0001c0001t0013a0001c0001t0018others(10): Show | 43 | HG01192.hp2 HG02129.hp2 HG02258.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1199C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 1199 | chr6 | 52501998 | |||||
| chr6:52502010
|
G | C | 11 | a0001c0001t0005a0001c0001t0011a0001c0001t0015others(8): Show | 38 | HG00140.hp2 HG00280.hp1 HG01255.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*1187C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 1187 | chr6 | 52502010 | |||||
| chr6:52502086
|
G | A | 14 | a0001c0001t0005a0001c0001t0011a0001c0001t0015others(11): Show | 43 | HG00140.hp2 HG00280.hp1 HG01255.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1111C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 1111 | chr6 | 52502086 | |||||
| chr6:52502173
|
A | G | 1 | a0001c0001t0030 | 3 | HG01175.hp1 HG02922.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1024T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 1024 | chr6 | 52502173 | |||||
| chr6:52502213
|
G | A | 1 | a0001c0001t0106 | 1 | HG01257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*984C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 984 | chr6 | 52502213 | |||||
| chr6:52502319
|
G | A | 32 | a0001c0001t0001a0001c0001t0005a0001c0001t0008others(29): Show | 130 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*878C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 878 | chr6 | 52502319 | |||||
| chr6:52502437
|
G | A | 80 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(77): Show | 287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*760C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 760 | chr6 | 52502437 | |||||
| chr6:52502440
|
TC | T | 97 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(94): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
3_prime_UTR_variant | MODIFIER | c.*756delG | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 756 | chr6 | 52502440 | |||||
| chr6:52502456
|
G | A | 1 | a0001c0001t0056 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*741C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 741 | chr6 | 52502456 | |||||
| chr6:52502478
|
C | T | 1 | a0001c0001t0060 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*719G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 719 | chr6 | 52502478 | |||||
| chr6:52502644
|
T | A | 1 | a0001c0001t0043 | 2 | HG02723.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*553A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 553 | chr6 | 52502644 | |||||
| chr6:52502714
|
C | T | 3 | a0001c0001t0035a0001c0001t0058a0001c0001t0059 | 4 | HG02258.hp2 HG02451.hp2 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*483G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 483 | chr6 | 52502714 | |||||
| chr6:52502783
|
C | A | 1 | a0001c0001t0096 | 1 | NA19067.hp1 | 3_prime_UTR_variant | MODIFIER | c.*414G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 414 | chr6 | 52502783 | |||||
| chr6:52502799
|
T | C | 1 | a0001c0001t0055 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*398A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 398 | chr6 | 52502799 | |||||
| chr6:52502879
|
G | A | 20 | a0001c0001t0003a0001c0001t0009a0001c0001t0016others(17): Show | 66 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*318C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 318 | chr6 | 52502879 | |||||
| chr6:52502939
|
G | T | 3 | a0001c0001t0033a0001c0001t0034a0001c0001t0057 | 5 | HG02451.hp1 HG03041.hp1 HG03225.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*258C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 258 | chr6 | 52502939 | |||||
| chr6:52502949
|
G | C | 1 | a0001c0001t0105 | 1 | HG01928.hp1 | 3_prime_UTR_variant | MODIFIER | c.*248C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 248 | chr6 | 52502949 | |||||
| chr6:52503047
|
C | T | 1 | a0001c0001t0051 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*150G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 150 | chr6 | 52503047 | |||||
| chr6:52503099
|
G | A | 3 | a0001c0001t0017a0001c0001t0047a0001c0001t0106 | 8 | HG00140.hp1 HG00642.hp1 HG01081.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*98C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 11/11 | 98 | chr6 | 52503099 | |||||
| chr6:52576956
|
G | T | 10 | a0001c0001t0010a0001c0001t0022a0001c0001t0023others(7): Show | 20 | HG00609.hp2 HG00639.hp1 HG01358.hp2 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-41C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/11 | 41 | chr6 | 52576956 | |||||
| chr6:52576965
|
C | T | 3 | a0001c0001t0048a0001c0001t0049a0001c0001t0050 | 3 | NA18941.hp2 NA18965.hp1 NA18986.hp2 |
5_prime_UTR_variant | MODIFIER | c.-50G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/11 | 50 | chr6 | 52576965 | |||||
| chr6:52576996
|
G | C | 1 | a0001c0001t0021 | 4 | HG00099.hp2 HG01258.hp2 HG01515.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-81C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/11 | 81 | chr6 | 52576996 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:52503324
|
G | A | 2 | a0001c0001t0019g0084a0001c0001t0067g0083 | 2 | HG02109.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1040-54C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 10/10 | chr6 | 52503324 | ||||||
| chr6:52503420
|
C | A | 4 | a0001c0001t0006g0309a0001c0001t0006g0331a0001c0001t0092g0330others(1): Show | 4 | NA19000.hp1 NA19012.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.1040-150G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 10/10 | chr6 | 52503420 | ||||||
| chr6:52503622
|
A | C | 15 | a0001c0001t0003g0069a0001c0001t0003g0074a0001c0001t0003g0077others(12): Show | 15 | HG00099.hp2 HG00738.hp1 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.1040-352T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 10/10 | chr6 | 52503622 | ||||||
| chr6:52503653
|
C | T | 1 | a0001c0001t0022g0033 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1040-383G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 10/10 | chr6 | 52503653 | ||||||
| chr6:52503680
|
C | T | 341 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(338): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.1040-410G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 10/10 | chr6 | 52503680 | ||||||
| chr6:52503960
|
C | T | 5 | a0001c0001t0033g0186a0001c0001t0033g0187a0001c0001t0034g0192others(2): Show | 5 | HG02451.hp1 HG03041.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1039+631G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 10/10 | chr6 | 52503960 | ||||||
| chr6:52504033
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1039+558C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 10/10 | chr6 | 52504033 | ||||||
| chr6:52504237
|
G | A | 1 | a0001c0001t0085g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1039+354C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 10/10 | chr6 | 52504237 | ||||||
| chr6:52504259
|
C | T | 1 | a0001c0001t0005g0172 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1039+332G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 10/10 | chr6 | 52504259 | ||||||
| chr6:52504273
|
G | T | 1 | a0001c0001t0005g0068 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1039+318C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 10/10 | chr6 | 52504273 | ||||||
| chr6:52504294
|
G | A | 37 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(34): Show | 37 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.1039+297C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 10/10 | chr6 | 52504294 | ||||||
| chr6:52504305
|
G | A | 14 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(11): Show | 15 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(12): Show |
intron_variant | MODIFIER | c.1039+286C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 10/10 | chr6 | 52504305 | ||||||
| chr6:52504309
|
C | T | 3 | a0001c0001t0003g0074a0001c0001t0003g0092a0001c0001t0003g0093 | 3 | HG01069.hp1 HG01071.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.1039+282G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 10/10 | chr6 | 52504309 | ||||||
| chr6:52504441
|
AG | A | 32 | a0001c0001t0005g0006a0001c0001t0005g0041a0001c0001t0005g0042others(29): Show | 33 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.1039+149delC | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 10/10 | chr6 | 52504441 | ||||||
| chr6:52504776
|
G | A | 1 | a0001c0001t0051g0029 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.876-22C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 9/10 | chr6 | 52504776 | ||||||
| chr6:52505102
|
T | C | 19 | a0001c0001t0004g0052a0001c0001t0004g0056a0001c0001t0004g0104others(16): Show | 19 | HG02735.hp1 HG03491.hp2 NA18944.hp1 others(16): Show |
intron_variant | MODIFIER | c.876-348A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 9/10 | chr6 | 52505102 | ||||||
| chr6:52505110
|
A | G | 1 | a0001c0001t0100g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.876-356T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 9/10 | chr6 | 52505110 | ||||||
| chr6:52505154
|
A | G | 1 | a0001c0001t0008g0299 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.876-400T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 9/10 | chr6 | 52505154 | ||||||
| chr6:52505199
|
G | A | 1 | a0001c0001t0085g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.875+400C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 9/10 | chr6 | 52505199 | ||||||
| chr6:52505202
|
T | C | 1 | a0001c0001t0001g0199 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.875+397A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 9/10 | chr6 | 52505202 | ||||||
| chr6:52505295
|
A | G | 2 | a0001c0001t0035g0066a0001c0001t0035g0185 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.875+304T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 9/10 | chr6 | 52505295 | ||||||
| chr6:52505376
|
A | G | 74 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(71): Show | 75 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(72): Show |
intron_variant | MODIFIER | c.875+223T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 9/10 | chr6 | 52505376 | ||||||
| chr6:52505828
|
G | A | 1 | a0001c0001t0037g0316 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.732-86C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 8/10 | chr6 | 52505828 | ||||||
| chr6:52505977
|
G | A | 16 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(13): Show | 17 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.731+55C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 8/10 | chr6 | 52505977 | ||||||
| chr6:52506141
|
G | A | 43 | a0001c0001t0004g0052a0001c0001t0004g0056a0001c0001t0004g0104others(40): Show | 43 | HG01192.hp2 HG02129.hp2 HG02258.hp2 others(40): Show |
splice_region_variant&intron_variant | LOW | c.627-5C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52506141 | ||||||
| chr6:52506176
|
T | C | 1 | a0001c0001t0006g0043 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.627-40A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52506176 | ||||||
| chr6:52506179
|
T | G | 4 | a0001c0001t0019g0082a0001c0001t0019g0084a0001c0001t0019g0100others(1): Show | 4 | HG02109.hp2 HG02486.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.627-43A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52506179 | ||||||
| chr6:52506267
|
G | A | 1 | a0001c0001t0001g0142 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.627-131C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52506267 | ||||||
| chr6:52506360
|
A | G | 328 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(325): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.627-224T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52506360 | ||||||
| chr6:52506372
|
T | C | 1 | a0001c0001t0045g0278 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.627-236A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52506372 | ||||||
| chr6:52506538
|
A | C | 93 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(90): Show | 95 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.627-402T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52506538 | ||||||
| chr6:52506621
|
G | A | 280 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(277): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.627-485C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52506621 | ||||||
| chr6:52506631
|
C | T | 6 | a0001c0001t0018g0101a0001c0001t0018g0197a0001c0001t0018g0214others(3): Show | 6 | HG02129.hp2 HG02683.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.627-495G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52506631 | ||||||
| chr6:52506684
|
A | G | 1 | a0001c0001t0002g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.627-548T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52506684 | ||||||
| chr6:52506698
|
C | A | 1 | a0001c0001t0097g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.627-562G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52506698 | ||||||
| chr6:52506749
|
C | T | 19 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(16): Show | 20 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.627-613G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52506749 | ||||||
| chr6:52506753
|
C | T | 9 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(6): Show | 12 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.627-617G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52506753 | ||||||
| chr6:52506783
|
A | G | 5 | a0001c0001t0019g0082a0001c0001t0019g0084a0001c0001t0019g0100others(2): Show | 5 | HG02109.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.627-647T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52506783 | ||||||
| chr6:52506896
|
G | A | 37 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(34): Show | 37 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.626+657C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52506896 | ||||||
| chr6:52507035
|
A | G | 2 | a0001c0001t0042g0350a0001c0001t0042g0351 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.626+518T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52507035 | ||||||
| chr6:52507111
|
T | C | 2 | a0001c0001t0002g0234a0001c0001t0020g0240 | 2 | NA18962.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.626+442A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52507111 | ||||||
| chr6:52507268
|
C | A | 5 | a0001c0001t0016g0037a0001c0001t0016g0039a0001c0001t0016g0193others(2): Show | 5 | HG02572.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.626+285G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52507268 | ||||||
| chr6:52507395
|
A | G | 1 | a0001c0001t0097g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.626+158T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52507395 | ||||||
| chr6:52507517
|
G | A | 2 | a0001c0001t0058g0189a0001c0001t0059g0167 | 2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.626+36C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 7/10 | chr6 | 52507517 | ||||||
| chr6:52507701
|
G | T | 1 | a0001c0001t0036g0321 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.556-78C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 6/10 | chr6 | 52507701 | ||||||
| chr6:52507950
|
T | C | 1 | a0001c0001t0019g0100 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.555+284A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 6/10 | chr6 | 52507950 | ||||||
| chr6:52508129
|
A | C | 1 | a0001c0001t0097g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.555+105T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 6/10 | chr6 | 52508129 | ||||||
| chr6:52508186
|
G | C | 3 | a0001c0001t0030g0261a0001c0001t0030g0343a0001c0001t0030g0344 | 3 | HG01175.hp1 HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.555+48C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 6/10 | chr6 | 52508186 | ||||||
| chr6:52508364
|
T | A | 5 | a0001c0001t0019g0082a0001c0001t0019g0084a0001c0001t0019g0100others(2): Show | 5 | HG02109.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.471-46A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 5/10 | chr6 | 52508364 | ||||||
| chr6:52508461
|
C | G | 1 | a0001c0001t0018g0101 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.471-143G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 5/10 | chr6 | 52508461 | ||||||
| chr6:52508464
|
C | T | 4 | a0001c0001t0042g0350a0001c0001t0042g0351a0001c0001t0068g0313others(1): Show | 4 | HG01891.hp1 HG02717.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.471-146G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 5/10 | chr6 | 52508464 | ||||||
| chr6:52508465
|
G | A | 3 | a0001c0001t0031g0182a0001c0001t0031g0183a0001c0001t0031g0270 | 3 | HG02818.hp1 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.471-147C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 5/10 | chr6 | 52508465 | ||||||
| chr6:52508553
|
G | C | 4 | a0001c0001t0035g0066a0001c0001t0035g0185a0001c0001t0058g0189others(1): Show | 4 | HG02258.hp2 HG02451.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.471-235C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 5/10 | chr6 | 52508553 | ||||||
| chr6:52508603
|
C | T | 3 | a0001c0001t0042g0350a0001c0001t0042g0351a0001c0001t0068g0313 | 3 | HG01891.hp1 HG02717.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.471-285G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 5/10 | chr6 | 52508603 | ||||||
| chr6:52508614
|
G | C | 3 | a0001c0001t0027g0046a0001c0001t0027g0047a0001c0001t0027g0048 | 3 | HG01257.hp2 HG01258.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.471-296C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 5/10 | chr6 | 52508614 | ||||||
| chr6:52508658
|
A | T | 65 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(62): Show | 72 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.471-340T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 5/10 | chr6 | 52508658 | ||||||
| chr6:52508771
|
C | T | 317 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(314): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.471-453G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 5/10 | chr6 | 52508771 | ||||||
| chr6:52509351
|
G | A | 2 | a0001c0001t0016g0267a0001c0001t0044g0223 | 2 | HG01069.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.470+177C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 5/10 | chr6 | 52509351 | ||||||
| chr6:52509410
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.470+118C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 5/10 | chr6 | 52509410 | ||||||
| chr6:52509463
|
C | T | 1 | a0001c0001t0062g0320 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.470+65G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 5/10 | chr6 | 52509463 | ||||||
| chr6:52509521
|
T | TAC | 103 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(100): Show | 105 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(102): Show |
splice_region_variant&intron_variant | LOW | c.470+5_470+6dupGT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 5/10 | chr6 | 52509521 | ||||||
| chr6:52509664
|
C | T | 5 | a0001c0001t0019g0082a0001c0001t0019g0084a0001c0001t0019g0100others(2): Show | 5 | HG02109.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.412-78G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52509664 | ||||||
| chr6:52509908
|
C | A | 1 | a0001c0001t0001g0150 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.412-322G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52509908 | ||||||
| chr6:52510025
|
C | T | 328 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(325): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.412-439G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52510025 | ||||||
| chr6:52510196
|
A | G | 5 | a0001c0001t0019g0082a0001c0001t0019g0084a0001c0001t0019g0100others(2): Show | 5 | HG02109.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.412-610T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52510196 | ||||||
| chr6:52510484
|
G | A | 3 | a0001c0001t0023g0023a0001c0001t0037g0226a0001c0001t0039g0318 | 3 | HG00639.hp1 HG01175.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.412-898C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52510484 | ||||||
| chr6:52510567
|
G | C | 1 | a0001c0003t0005g0308 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.412-981C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52510567 | ||||||
| chr6:52510774
|
G | A | 1 | a0001c0001t0003g0342 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.412-1188C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52510774 | ||||||
| chr6:52510795
|
G | A | 291 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(288): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.412-1209C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52510795 | ||||||
| chr6:52511069
|
A | G | 6 | a0001c0001t0033g0186a0001c0001t0033g0187a0001c0001t0034g0192others(3): Show | 6 | HG02451.hp1 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-1483T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511069 | ||||||
| chr6:52511210
|
T | A | 1 | a0001c0001t0008g0283 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.412-1624A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511210 | ||||||
| chr6:52511215
|
C | T | 1 | a0001c0001t0002g0242 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.412-1629G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511215 | ||||||
| chr6:52511247
|
A | G | 292 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(289): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.412-1661T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511247 | ||||||
| chr6:52511255
|
A | G | 1 | a0001c0001t0001g0059 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.412-1669T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511255 | ||||||
| chr6:52511305
|
A | G | 1 | a0001c0001t0006g0063 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.412-1719T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511305 | ||||||
| chr6:52511340
|
C | T | 1 | a0001c0001t0010g0027 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.412-1754G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511340 | ||||||
| chr6:52511384
|
T | C | 8 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(5): Show | 11 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.412-1798A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511384 | ||||||
| chr6:52511388
|
G | A | 18 | a0001c0001t0004g0052a0001c0001t0004g0056a0001c0001t0004g0104others(15): Show | 18 | HG01192.hp2 HG02735.hp1 HG02965.hp1 others(15): Show |
intron_variant | MODIFIER | c.412-1802C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511388 | ||||||
| chr6:52511428
|
G | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(85): Show | 89 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.412-1842C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511428 | ||||||
| chr6:52511456
|
T | A | 1 | a0001c0001t0001g0094 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.412-1870A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511456 | ||||||
| chr6:52511515
|
GAGA | G | 6 | a0001c0001t0019g0082a0001c0001t0019g0084a0001c0001t0019g0100others(3): Show | 6 | HG01891.hp2 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-1932_412-1930d others(5): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511515 | ||||||
| chr6:52511703
|
C | T | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.412-2117G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511703 | ||||||
| chr6:52511712
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.412-2126G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511712 | ||||||
| chr6:52511726
|
G | A | 1 | a0001c0001t0003g0314 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.412-2140C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511726 | ||||||
| chr6:52511782
|
CTTT | C | 16 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(13): Show | 19 | HG00639.hp1 HG00741.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.412-2199_412-2197d others(5): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511782 | ||||||
| chr6:52511786
|
T | A | 16 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(13): Show | 19 | HG00639.hp1 HG00741.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.412-2200A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511786 | ||||||
| chr6:52511954
|
C | T | 1 | a0001c0001t0083g0135 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.412-2368G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511954 | ||||||
| chr6:52511966
|
C | T | 291 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(288): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.412-2380G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511966 | ||||||
| chr6:52512036
|
C | T | 88 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(85): Show | 89 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.412-2450G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52512036 | ||||||
| chr6:52512050
|
A | C | 1 | a0001c0001t0018g0197 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.412-2464T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52512050 | ||||||
| chr6:52512071
|
C | T | 3 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0045 | 3 | HG01255.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.412-2485G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52512071 | ||||||
| chr6:52512364
|
C | T | 6 | a0001c0001t0018g0101a0001c0001t0018g0197a0001c0001t0018g0214others(3): Show | 6 | HG02129.hp2 HG02683.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.412-2778G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52512364 | ||||||
| chr6:52512367
|
C | T | 1 | a0001c0001t0002g0098 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.412-2781G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52512367 | ||||||
| chr6:52512513
|
C | T | 1 | a0001c0001t0097g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.412-2927G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52512513 | ||||||
| chr6:52512646
|
C | T | 7 | a0001c0001t0011g0058a0001c0001t0011g0201a0001c0001t0011g0215others(4): Show | 7 | HG02071.hp1 HG02132.hp1 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.412-3060G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52512646 | ||||||
| chr6:52512689
|
G | A | 1 | a0001c0001t0039g0248 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.412-3103C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52512689 | ||||||
| chr6:52512793
|
C | T | 1 | a0001c0001t0009g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.412-3207G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52512793 | ||||||
| chr6:52512833
|
C | A | 1 | a0001c0001t0104g0336 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.411+3173G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52512833 | ||||||
| chr6:52512883
|
C | A | 1 | a0001c0001t0080g0180 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.411+3123G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52512883 | ||||||
| chr6:52512884
|
C | T | 1 | a0001c0001t0026g0151 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.411+3122G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52512884 | ||||||
| chr6:52512942
|
C | T | 1 | a0001c0001t0005g0328 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.411+3064G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52512942 | ||||||
| chr6:52513050
|
T | C | 3 | a0001c0002t0028g0011a0001c0002t0028g0357a0001c0002t0093g0272 | 4 | HG01243.hp2 HG02615.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.411+2956A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52513050 | ||||||
| chr6:52513125
|
G | A | 5 | a0001c0001t0033g0186a0001c0001t0033g0187a0001c0001t0034g0192others(2): Show | 5 | HG02451.hp1 HG03041.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.411+2881C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52513125 | ||||||
| chr6:52513224
|
G | C | 6 | a0001c0001t0018g0101a0001c0001t0018g0197a0001c0001t0018g0214others(3): Show | 6 | HG02129.hp2 HG02683.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.411+2782C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52513224 | ||||||
| chr6:52513276
|
A | G | 1 | a0001c0001t0053g0021 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.411+2730T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52513276 | ||||||
| chr6:52513430
|
G | A | 2 | a0001c0001t0002g0239a0001c0001t0003g0060 | 2 | HG04184.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.411+2576C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52513430 | ||||||
| chr6:52513494
|
G | C | 291 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(288): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.411+2512C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52513494 | ||||||
| chr6:52513518
|
T | A | 2 | a0001c0001t0038g0173a0001c0001t0038g0352 | 2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.411+2488A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52513518 | ||||||
| chr6:52514187
|
G | A | 6 | a0001c0001t0019g0082a0001c0001t0019g0084a0001c0001t0019g0100others(3): Show | 6 | HG01891.hp2 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.411+1819C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52514187 | ||||||
| chr6:52514210
|
G | C | 1 | a0001c0001t0001g0224 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.411+1796C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52514210 | ||||||
| chr6:52514252
|
ATAT | A | 9 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(6): Show | 12 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.411+1751_411+1753d others(5): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52514252 | ||||||
| chr6:52514265
|
A | T | 5 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(2): Show | 8 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.411+1741T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52514265 | ||||||
| chr6:52514440
|
T | C | 1 | a0001c0001t0027g0047 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.411+1566A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52514440 | ||||||
| chr6:52514602
|
G | A | 16 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(13): Show | 19 | HG00639.hp1 HG00741.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.411+1404C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52514602 | ||||||
| chr6:52514780
|
C | T | 1 | a0001c0001t0097g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.411+1226G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52514780 | ||||||
| chr6:52515095
|
T | C | 43 | a0001c0001t0004g0306a0001c0001t0005g0006a0001c0001t0005g0041others(40): Show | 44 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.411+911A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52515095 | ||||||
| chr6:52515456
|
C | T | 1 | a0001c0001t0001g0118 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.411+550G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52515456 | ||||||
| chr6:52515612
|
A | C | 2 | a0001c0001t0035g0066a0001c0001t0035g0185 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.411+394T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52515612 | ||||||
| chr6:52515843
|
C | T | 291 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(288): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.411+163G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52515843 | ||||||
| chr6:52516387
|
A | G | 43 | a0001c0001t0004g0306a0001c0001t0005g0006a0001c0001t0005g0041others(40): Show | 44 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.294+241T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 3/10 | chr6 | 52516387 | ||||||
| chr6:52516434
|
G | A | 16 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(13): Show | 19 | HG00639.hp1 HG00741.hp2 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.294+194C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 3/10 | chr6 | 52516434 | ||||||
| chr6:52516504
|
C | A | 5 | a0001c0001t0016g0037a0001c0001t0016g0039a0001c0001t0016g0193others(2): Show | 5 | HG02572.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.294+124G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 3/10 | chr6 | 52516504 | ||||||
| chr6:52516930
|
A | T | 291 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(288): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.185-193T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52516930 | ||||||
| chr6:52517305
|
T | C | 19 | a0001c0001t0008g0009a0001c0001t0008g0070a0001c0001t0008g0071others(16): Show | 20 | HG01074.hp2 HG01123.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.185-568A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52517305 | ||||||
| chr6:52517337
|
A | G | 1 | a0001c0001t0002g0266 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.185-600T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52517337 | ||||||
| chr6:52517458
|
C | A | 3 | a0001c0003t0005g0308a0001c0003t0015g0305a0001c0003t0015g0307 | 3 | HG02738.hp2 HG03688.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.185-721G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52517458 | ||||||
| chr6:52517722
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185-985C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52517722 | ||||||
| chr6:52517919
|
C | T | 1 | a0001c0001t0032g0031 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.185-1182G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52517919 | ||||||
| chr6:52518054
|
C | T | 1 | a0001c0001t0019g0207 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.185-1317G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52518054 | ||||||
| chr6:52518101
|
C | T | 2 | a0001c0001t0034g0192a0001c0001t0034g0260 | 2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.185-1364G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52518101 | ||||||
| chr6:52518138
|
C | T | 2 | a0001c0001t0042g0350a0001c0001t0042g0351 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.185-1401G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52518138 | ||||||
| chr6:52518269
|
A | G | 333 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(330): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.185-1532T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52518269 | ||||||
| chr6:52518281
|
G | C | 5 | a0001c0001t0023g0018a0001c0001t0023g0022a0001c0001t0023g0023others(2): Show | 5 | HG00639.hp1 HG01175.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.185-1544C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52518281 | ||||||
| chr6:52518361
|
G | A | 7 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(4): Show | 8 | HG00140.hp1 HG00642.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.185-1624C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52518361 | ||||||
| chr6:52518370
|
T | C | 1 | a0001c0001t0104g0336 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.185-1633A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52518370 | ||||||
| chr6:52518433
|
T | C | 332 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(329): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.185-1696A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52518433 | ||||||
| chr6:52518472
|
G | A | 14 | a0001c0001t0006g0004a0001c0001t0006g0036a0001c0001t0006g0195others(11): Show | 17 | HG00639.hp1 HG00741.hp2 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.185-1735C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52518472 | ||||||
| chr6:52518549
|
C | T | 1 | a0001c0001t0084g0349 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.185-1812G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52518549 | ||||||
| chr6:52518878
|
G | A | 37 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(34): Show | 37 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.185-2141C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52518878 | ||||||
| chr6:52518975
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.185-2238G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52518975 | ||||||
| chr6:52519025
|
A | T | 5 | a0001c0001t0018g0101a0001c0001t0018g0214a0001c0001t0032g0020others(2): Show | 5 | HG00609.hp1 HG02129.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.185-2288T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52519025 | ||||||
| chr6:52519096
|
C | T | 3 | a0001c0001t0001g0122a0001c0001t0001g0150a0001c0001t0003g0163 | 3 | NA18971.hp2 NA18982.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.185-2359G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52519096 | ||||||
| chr6:52519217
|
C | G | 109 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(106): Show | 110 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.185-2480G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52519217 | ||||||
| chr6:52519276
|
C | T | 4 | a0001c0001t0004g0105a0001c0001t0004g0106a0001c0001t0004g0131others(1): Show | 4 | NA18940.hp2 NA18955.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.185-2539G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52519276 | ||||||
| chr6:52519488
|
A | C | 299 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(296): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.185-2751T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52519488 | ||||||
| chr6:52519529
|
T | C | 5 | a0001c0001t0019g0082a0001c0001t0019g0084a0001c0001t0019g0100others(2): Show | 5 | HG02109.hp2 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.185-2792A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52519529 | ||||||
| chr6:52519642
|
A | G | 316 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(313): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.185-2905T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52519642 | ||||||
| chr6:52519732
|
A | G | 1 | a0001c0001t0104g0336 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.185-2995T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52519732 | ||||||
| chr6:52519810
|
T | TA | 59 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(56): Show | 63 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(60): Show |
intron_variant | MODIFIER | c.185-3074dupT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52519810 | ||||||
| chr6:52519810
|
TA | T | 8 | a0001c0001t0001g0150a0001c0001t0004g0123a0001c0001t0004g0311others(5): Show | 8 | HG01099.hp1 HG01517.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.185-3074delT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52519810 | ||||||
| chr6:52519986
|
G | A | 59 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(56): Show | 66 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.185-3249C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52519986 | ||||||
| chr6:52520266
|
C | A | 203 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(200): Show | 212 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(209): Show |
intron_variant | MODIFIER | c.185-3529G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52520266 | ||||||
| chr6:52520291
|
G | A | 1 | a0001c0001t0012g0268 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.185-3554C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52520291 | ||||||
| chr6:52520425
|
C | T | 1 | a0001c0001t0046g0076 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.185-3688G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52520425 | ||||||
| chr6:52520654
|
GAA | G | 8 | a0001c0001t0023g0018a0001c0001t0023g0022a0001c0001t0023g0023others(5): Show | 8 | HG00639.hp1 HG01175.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.185-3919_185-3918d others(4): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52520654 | ||||||
| chr6:52520811
|
C | T | 1 | a0001c0001t0102g0315 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.185-4074G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52520811 | ||||||
| chr6:52520857
|
T | C | 2 | a0001c0001t0035g0066a0001c0001t0035g0185 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.185-4120A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52520857 | ||||||
| chr6:52520915
|
T | TTTTTG | 45 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(42): Show | 45 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.185-4183_185-4179d others(7): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52520915 | ||||||
| chr6:52521047
|
C | T | 89 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(86): Show | 90 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.185-4310G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521047 | ||||||
| chr6:52521175
|
G | A | 6 | a0001c0001t0019g0082a0001c0001t0019g0084a0001c0001t0019g0100others(3): Show | 6 | HG01891.hp2 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.185-4438C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521175 | ||||||
| chr6:52521190
|
G | T | 44 | a0001c0001t0004g0306a0001c0001t0005g0006a0001c0001t0005g0041others(41): Show | 45 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.185-4453C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521190 | ||||||
| chr6:52521232
|
A | T | 2 | a0001c0001t0007g0250a0001c0001t0075g0249 | 2 | NA19010.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.185-4495T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521232 | ||||||
| chr6:52521410
|
A | G | 2 | a0001c0001t0034g0192a0001c0001t0034g0260 | 2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.185-4673T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521410 | ||||||
| chr6:52521422
|
G | A | 1 | a0001c0001t0007g0253 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.185-4685C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521422 | ||||||
| chr6:52521436
|
G | A | 2 | a0001c0001t0090g0273a0001c0001t0091g0301 | 2 | HG02486.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.185-4699C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521436 | ||||||
| chr6:52521465
|
A | G | 2 | a0001c0001t0008g0070a0001c0001t0008g0071 | 2 | HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.185-4728T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521465 | ||||||
| chr6:52521481
|
C | G | 4 | a0001c0001t0005g0006a0001c0001t0005g0168a0001c0001t0005g0169others(1): Show | 5 | HG00140.hp2 HG00280.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.185-4744G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521481 | ||||||
| chr6:52521487
|
C | A | 47 | a0001c0001t0003g0236a0001c0001t0004g0306a0001c0001t0005g0006others(44): Show | 48 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.185-4750G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521487 | ||||||
| chr6:52521490
|
G | A | 3 | a0001c0001t0033g0186a0001c0001t0033g0187a0001c0001t0057g0188 | 3 | HG03041.hp1 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.185-4753C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521490 | ||||||
| chr6:52521496
|
A | T | 1 | a0001c0001t0003g0079 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.185-4759T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521496 | ||||||
| chr6:52521553
|
C | T | 1 | a0001c0001t0024g0310 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.185-4816G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521553 | ||||||
| chr6:52521570
|
A | G | 1 | a0001c0001t0085g0190 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.185-4833T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521570 | ||||||
| chr6:52521630
|
A | G | 344 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(341): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.185-4893T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521630 | ||||||
| chr6:52521646
|
G | A | 6 | a0001c0001t0001g0116a0001c0001t0001g0121a0001c0001t0001g0122others(3): Show | 6 | NA18953.hp2 NA18971.hp2 NA19005.hp1 others(3): Show |
intron_variant | MODIFIER | c.185-4909C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521646 | ||||||
| chr6:52521665
|
C | T | 2 | a0001c0001t0042g0350a0001c0001t0042g0351 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.185-4928G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521665 | ||||||
| chr6:52521668
|
G | T | 17 | a0001c0001t0008g0009a0001c0001t0008g0258a0001c0001t0008g0259others(14): Show | 18 | HG01074.hp2 HG01123.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.185-4931C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521668 | ||||||
| chr6:52521736
|
CAAAAT | C | 56 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(53): Show | 60 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.185-5004_185-5000d others(7): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521736 | ||||||
| chr6:52521743
|
A | C | 46 | a0001c0001t0004g0306a0001c0001t0005g0006a0001c0001t0005g0041others(43): Show | 47 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.185-5006T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521743 | ||||||
| chr6:52521785
|
G | A | 18 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(15): Show | 18 | HG02735.hp1 HG03491.hp2 NA18944.hp1 others(15): Show |
intron_variant | MODIFIER | c.185-5048C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521785 | ||||||
| chr6:52521826
|
C | T | 1 | a0001c0001t0024g0303 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.185-5089G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521826 | ||||||
| chr6:52521843
|
A | G | 2 | a0001c0001t0006g0043a0001c0001t0012g0268 | 2 | HG01106.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.185-5106T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521843 | ||||||
| chr6:52521849
|
C | G | 3 | a0001c0002t0028g0011a0001c0002t0028g0357a0001c0002t0093g0272 | 4 | HG01243.hp2 HG02615.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-5112G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521849 | ||||||
| chr6:52521857
|
G | A | 1 | a0001c0001t0101g0292 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.185-5120C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521857 | ||||||
| chr6:52521866
|
T | C | 3 | a0001c0001t0031g0182a0001c0001t0031g0183a0001c0001t0031g0270 | 3 | HG02818.hp1 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.185-5129A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52521866 | ||||||
| chr6:52522088
|
A | G | 1 | a0001c0001t0081g0129 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.185-5351T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52522088 | ||||||
| chr6:52522309
|
C | T | 9 | a0001c0001t0018g0101a0001c0001t0018g0214a0001c0001t0032g0020others(6): Show | 9 | HG00609.hp1 HG02129.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.185-5572G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52522309 | ||||||
| chr6:52522346
|
C | T | 90 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(87): Show | 91 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.185-5609G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52522346 | ||||||
| chr6:52522348
|
C | G | 1 | a0001c0001t0063g0264 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.185-5611G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52522348 | ||||||
| chr6:52522422
|
G | T | 8 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(5): Show | 11 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.185-5685C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52522422 | ||||||
| chr6:52522524
|
T | C | 1 | a0001c0001t0040g0263 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.185-5787A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52522524 | ||||||
| chr6:52522813
|
G | A | 20 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(17): Show | 20 | HG01192.hp2 HG02735.hp1 HG02965.hp1 others(17): Show |
intron_variant | MODIFIER | c.185-6076C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52522813 | ||||||
| chr6:52522855
|
T | A | 1 | a0001c0001t0002g0072 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.185-6118A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52522855 | ||||||
| chr6:52522896
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.185-6159G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52522896 | ||||||
| chr6:52522908
|
C | G | 1 | a0001c0001t0001g0117 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.185-6171G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52522908 | ||||||
| chr6:52522921
|
T | C | 37 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(34): Show | 37 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.185-6184A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52522921 | ||||||
| chr6:52523043
|
T | C | 1 | a0001c0001t0014g0148 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.185-6306A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52523043 | ||||||
| chr6:52523085
|
T | C | 6 | a0001c0001t0019g0082a0001c0001t0019g0084a0001c0001t0019g0100others(3): Show | 6 | HG01891.hp2 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.185-6348A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52523085 | ||||||
| chr6:52523282
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0150 | 2 | NA18971.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.185-6545C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52523282 | ||||||
| chr6:52523332
|
T | C | 1 | a0001c0001t0004g0139 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.185-6595A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52523332 | ||||||
| chr6:52523345
|
T | C | 1 | a0001c0001t0008g0293 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.185-6608A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52523345 | ||||||
| chr6:52523413
|
CACAGAAA others(6): Show |
C | 1 | a0001c0001t0080g0180 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.185-6689_185-6677d others(15): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52523413 | ||||||
| chr6:52523426
|
A | AAC | 329 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(326): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.185-6691_185-6690d others(4): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52523426 | ||||||
| chr6:52523540
|
A | C | 91 | a0001c0001t0002g0348a0001c0001t0003g0044a0001c0001t0003g0060others(88): Show | 95 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.185-6803T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52523540 | ||||||
| chr6:52523619
|
C | T | 1 | a0001c0001t0008g0071 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.185-6882G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52523619 | ||||||
| chr6:52523697
|
T | G | 1 | a0001c0001t0005g0304 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.185-6960A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52523697 | ||||||
| chr6:52523707
|
A | G | 54 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(51): Show | 58 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.185-6970T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52523707 | ||||||
| chr6:52523883
|
A | T | 3 | a0001c0001t0038g0173a0001c0001t0038g0352a0001c0001t0097g0356 | 3 | HG02280.hp1 HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.185-7146T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52523883 | ||||||
| chr6:52523896
|
C | T | 54 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(51): Show | 58 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.185-7159G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52523896 | ||||||
| chr6:52523985
|
C | A | 1 | a0001c0001t0012g0040 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.185-7248G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52523985 | ||||||
| chr6:52523985
|
C | T | 54 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(51): Show | 58 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.185-7248G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52523985 | ||||||
| chr6:52524042
|
C | T | 1 | a0001c0001t0003g0079 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.185-7305G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52524042 | ||||||
| chr6:52524077
|
G | A | 137 | a0001c0001t0002g0348a0001c0001t0003g0044a0001c0001t0003g0060others(134): Show | 142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.185-7340C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52524077 | ||||||
| chr6:52524172
|
G | A | 1 | a0001c0001t0018g0101 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.185-7435C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52524172 | ||||||
| chr6:52524233
|
C | T | 8 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(5): Show | 11 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.185-7496G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52524233 | ||||||
| chr6:52524252
|
T | C | 1 | a0001c0001t0010g0028 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.185-7515A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52524252 | ||||||
| chr6:52524284
|
A | G | 54 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(51): Show | 58 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.185-7547T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52524284 | ||||||
| chr6:52524330
|
T | C | 89 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(86): Show | 90 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.185-7593A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52524330 | ||||||
| chr6:52524474
|
C | T | 1 | a0001c0001t0100g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.185-7737G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52524474 | ||||||
| chr6:52524478
|
G | A | 1 | a0001c0001t0087g0181 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.185-7741C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52524478 | ||||||
| chr6:52524490
|
A | G | 44 | a0001c0001t0004g0306a0001c0001t0005g0006a0001c0001t0005g0041others(41): Show | 45 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.185-7753T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52524490 | ||||||
| chr6:52524580
|
C | T | 90 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(87): Show | 91 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.185-7843G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52524580 | ||||||
| chr6:52524839
|
A | G | 37 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(34): Show | 37 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.185-8102T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52524839 | ||||||
| chr6:52524913
|
C | T | 138 | a0001c0001t0002g0348a0001c0001t0003g0044a0001c0001t0003g0060others(135): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.185-8176G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52524913 | ||||||
| chr6:52524924
|
G | T | 4 | a0001c0001t0003g0317a0001c0001t0003g0332a0001c0001t0050g0014others(1): Show | 4 | HG00544.hp1 HG00733.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.185-8187C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52524924 | ||||||
| chr6:52524978
|
C | T | 46 | a0001c0001t0004g0306a0001c0001t0005g0006a0001c0001t0005g0041others(43): Show | 47 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.185-8241G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52524978 | ||||||
| chr6:52525123
|
C | T | 1 | a0001c0001t0008g0258 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.185-8386G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52525123 | ||||||
| chr6:52525158
|
G | T | 1 | a0001c0001t0005g0172 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.185-8421C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52525158 | ||||||
| chr6:52525211
|
C | G | 3 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0045 | 3 | HG01255.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.185-8474G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52525211 | ||||||
| chr6:52525495
|
G | A | 1 | a0001c0001t0033g0187 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.185-8758C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52525495 | ||||||
| chr6:52525503
|
T | C | 1 | a0001c0001t0005g0133 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.185-8766A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52525503 | ||||||
| chr6:52525571
|
A | C | 1 | a0001c0001t0100g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.185-8834T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52525571 | ||||||
| chr6:52525576
|
A | G | 332 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(329): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.185-8839T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52525576 | ||||||
| chr6:52525586
|
G | T | 3 | a0001c0001t0008g0277a0001c0001t0008g0283a0001c0001t0105g0276 | 3 | HG01928.hp1 HG02896.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.185-8849C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52525586 | ||||||
| chr6:52525602
|
G | A | 2 | a0001c0001t0001g0285a0001c0001t0001g0286 | 2 | HG02027.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.185-8865C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52525602 | ||||||
| chr6:52525621
|
A | G | 64 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(61): Show | 71 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.185-8884T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52525621 | ||||||
| chr6:52525633
|
C | T | 5 | a0001c0001t0018g0101a0001c0001t0018g0214a0001c0001t0032g0020others(2): Show | 5 | HG00609.hp1 HG02129.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.185-8896G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52525633 | ||||||
| chr6:52525650
|
A | G | 89 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(86): Show | 90 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.185-8913T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52525650 | ||||||
| chr6:52525951
|
A | G | 54 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(51): Show | 58 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.185-9214T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52525951 | ||||||
| chr6:52525952
|
C | G | 54 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(51): Show | 58 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.185-9215G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52525952 | ||||||
| chr6:52525958
|
G | C | 25 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(22): Show | 25 | HG00639.hp1 HG01175.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.185-9221C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52525958 | ||||||
| chr6:52526148
|
GACAGACA others(5): Show |
G | 6 | a0001c0001t0011g0289a0001c0001t0018g0197a0001c0001t0018g0287others(3): Show | 6 | HG02818.hp1 HG03041.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.185-9423_185-9412d others(14): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526148 | ||||||
| chr6:52526148
|
GACAGACA others(7): Show |
G | 35 | a0001c0001t0004g0306a0001c0001t0005g0006a0001c0001t0005g0041others(32): Show | 36 | HG00140.hp2 HG00280.hp1 HG01099.hp1 others(33): Show |
intron_variant | MODIFIER | c.185-9425_185-9412d others(16): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526148 | ||||||
| chr6:52526148
|
GACAGACA others(9): Show |
G | 27 | a0001c0001t0002g0222a0001c0001t0002g0227a0001c0001t0002g0234others(24): Show | 28 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.185-9427_185-9412d others(18): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526148 | ||||||
| chr6:52526148
|
GACAGACA others(11): Show |
G | 65 | a0001c0001t0002g0003a0001c0001t0002g0007a0001c0001t0002g0008others(62): Show | 72 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.185-9429_185-9412d others(20): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526148 | ||||||
| chr6:52526148
|
GACAGACA others(13): Show |
G | 37 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(34): Show | 37 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(34): Show |
intron_variant | MODIFIER | c.185-9431_185-9412d others(22): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526148 | ||||||
| chr6:52526148
|
GACAGACA others(15): Show |
G | 14 | a0001c0001t0002g0072a0001c0001t0003g0069a0001c0001t0003g0077others(11): Show | 14 | HG01074.hp1 HG01123.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.185-9433_185-9412d others(24): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526148 | ||||||
| chr6:52526148
|
GACAGACA others(17): Show |
G | 11 | a0001c0001t0013g0103a0001c0001t0018g0101a0001c0001t0018g0214others(8): Show | 11 | HG00609.hp1 HG02129.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.185-9435_185-9412d others(26): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526148 | ||||||
| chr6:52526148
|
GACAGACA others(19): Show |
G | 25 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(22): Show | 26 | HG00140.hp1 HG00642.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.185-9437_185-9412d others(28): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526148 | ||||||
| chr6:52526148
|
GACAGACA others(21): Show |
G | 11 | a0001c0001t0004g0296a0001c0001t0004g0354a0001c0001t0019g0082others(8): Show | 11 | HG01175.hp1 HG01192.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.185-9439_185-9412d others(30): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526148 | ||||||
| chr6:52526148
|
GACAGACA others(23): Show |
G | 5 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(2): Show | 8 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.185-9441_185-9412d others(32): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526148 | ||||||
| chr6:52526148
|
GACAGACA others(25): Show |
G | 5 | a0001c0001t0001g0094a0001c0001t0001g0099a0001c0001t0001g0203others(2): Show | 5 | HG00738.hp2 HG01070.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.185-9443_185-9412d others(34): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526148 | ||||||
| chr6:52526148
|
GACAGACA others(27): Show |
G | 85 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(82): Show | 86 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.185-9445_185-9412d others(36): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526148 | ||||||
| chr6:52526148
|
GACAGACA others(29): Show |
G | 2 | a0001c0001t0042g0350a0001c0001t0042g0351 | 2 | HG01891.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.185-9447_185-9412d others(38): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526148 | ||||||
| chr6:52526152
|
G | GAC | 4 | a0001c0001t0006g0061a0001c0001t0006g0065a0001c0001t0006g0309others(1): Show | 4 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-9417_185-9416d others(4): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526152 | ||||||
| chr6:52526152
|
G | GACAC | 3 | a0001c0001t0006g0064a0001c0001t0006g0177a0001c0001t0094g0329 | 3 | HG01934.hp1 NA19000.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.185-9419_185-9416d others(6): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526152 | ||||||
| chr6:52526152
|
GAC | G | 4 | a0001c0001t0006g0096a0001c0001t0006g0331a0001c0001t0011g0201others(1): Show | 4 | HG02717.hp2 HG03704.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-9417_185-9416d others(4): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526152 | ||||||
| chr6:52526152
|
GACAC | G | 4 | a0001c0001t0006g0353a0001c0001t0011g0217a0001c0001t0092g0330others(1): Show | 4 | HG02071.hp1 HG02132.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-9419_185-9416d others(6): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526152 | ||||||
| chr6:52526152
|
GACACAC | G | 6 | a0001c0001t0006g0043a0001c0001t0006g0063a0001c0001t0006g0300others(3): Show | 6 | HG01106.hp1 HG02922.hp1 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.185-9421_185-9416d others(8): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526152 | ||||||
| chr6:52526152
|
GACACACA others(3): Show |
G | 1 | a0001c0002t0093g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.185-9425_185-9416d others(12): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526152 | ||||||
| chr6:52526152
|
GACACACA others(7): Show |
G | 3 | a0001c0001t0100g0067a0001c0002t0028g0011a0001c0002t0028g0357 | 4 | HG01243.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.185-9429_185-9416d others(16): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526152 | ||||||
| chr6:52526152
|
GACACACA others(9): Show |
G | 1 | a0001c0001t0091g0301 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.185-9431_185-9416d others(18): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526152 | ||||||
| chr6:52526152
|
GACACACA others(11): Show |
G | 1 | a0001c0001t0090g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.185-9433_185-9416d others(20): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526152 | ||||||
| chr6:52526158
|
C | G | 1 | a0001c0001t0035g0185 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.185-9421G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526158 | ||||||
| chr6:52526162
|
C | G | 2 | a0001c0001t0035g0066a0001c0001t0054g0016 | 2 | HG02451.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.185-9425G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526162 | ||||||
| chr6:52526166
|
C | G | 1 | a0001c0001t0054g0016 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.185-9429G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526166 | ||||||
| chr6:52526168
|
C | G | 3 | a0001c0001t0011g0289a0001c0001t0018g0197a0001c0001t0018g0287 | 3 | NA18959.hp1 NA18972.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.185-9431G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526168 | ||||||
| chr6:52526170
|
C | G | 32 | a0001c0001t0004g0306a0001c0001t0005g0006a0001c0001t0005g0041others(29): Show | 33 | HG00140.hp2 HG00280.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.185-9433G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526170 | ||||||
| chr6:52526172
|
C | G | 4 | a0001c0001t0005g0175a0001c0001t0005g0178a0001c0001t0005g0265others(1): Show | 4 | HG00735.hp1 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.185-9435G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526172 | ||||||
| chr6:52526174
|
C | G | 2 | a0001c0001t0005g0172a0001c0001t0005g0319 | 2 | HG02015.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.185-9437G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526174 | ||||||
| chr6:52526207
|
A | G | 1 | a0001c0001t0084g0349 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.185-9470T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526207 | ||||||
| chr6:52526271
|
T | C | 1 | a0001c0001t0061g0210 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.184+9512A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526271 | ||||||
| chr6:52526363
|
G | A | 1 | a0001c0001t0003g0332 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.184+9420C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526363 | ||||||
| chr6:52526401
|
T | C | 2 | a0001c0001t0016g0039a0001c0001t0044g0038 | 2 | HG02572.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.184+9382A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526401 | ||||||
| chr6:52526432
|
G | A | 37 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(34): Show | 37 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(34): Show |
intron_variant | MODIFIER | c.184+9351C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526432 | ||||||
| chr6:52526483
|
C | A | 1 | a0001c0001t0066g0335 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.184+9300G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526483 | ||||||
| chr6:52526524
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.184+9259A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526524 | ||||||
| chr6:52526682
|
C | T | 8 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(5): Show | 11 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.184+9101G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526682 | ||||||
| chr6:52526684
|
C | T | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.184+9099G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526684 | ||||||
| chr6:52526685
|
G | A | 89 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(86): Show | 90 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.184+9098C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526685 | ||||||
| chr6:52526785
|
C | A | 2 | a0001c0001t0022g0033a0001c0001t0022g0034 | 2 | HG00609.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.184+8998G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526785 | ||||||
| chr6:52526799
|
T | G | 6 | a0001c0001t0019g0082a0001c0001t0019g0084a0001c0001t0019g0100others(3): Show | 6 | HG01891.hp2 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.184+8984A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526799 | ||||||
| chr6:52526846
|
GGCATGAC others(1731): Show |
G | 1 | a0001c0001t0058g0189 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.184+7199_184+8936d others(2): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526846 | ||||||
| chr6:52526977
|
T | A | 36 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(33): Show | 36 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.184+8806A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526977 | ||||||
| chr6:52526984
|
T | A | 126 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(123): Show | 127 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.184+8799A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526984 | ||||||
| chr6:52527153
|
C | T | 47 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(44): Show | 48 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.184+8630G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527153 | ||||||
| chr6:52527154
|
G | A | 46 | a0001c0001t0004g0306a0001c0001t0005g0006a0001c0001t0005g0041others(43): Show | 47 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.184+8629C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527154 | ||||||
| chr6:52527203
|
A | AC | 55 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(52): Show | 59 | HG00140.hp1 HG00609.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.184+8579dupG | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527203 | ||||||
| chr6:52527239
|
G | A | 4 | a0001c0001t0001g0005a0001c0001t0001g0126a0001c0001t0001g0143others(1): Show | 5 | HG00558.hp2 HG02040.hp2 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.184+8544C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527239 | ||||||
| chr6:52527246
|
C | T | 1 | a0001c0001t0003g0069 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.184+8537G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527246 | ||||||
| chr6:52527256
|
C | T | 324 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(321): Show | 339 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(336): Show |
intron_variant | MODIFIER | c.184+8527G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527256 | ||||||
| chr6:52527325
|
A | C | 335 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(332): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.184+8458T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527325 | ||||||
| chr6:52527331
|
T | C | 4 | a0001c0001t0014g0115a0001c0001t0014g0130a0001c0001t0014g0148others(1): Show | 4 | HG02080.hp2 NA18947.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.184+8452A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527331 | ||||||
| chr6:52527377
|
CA | C | 272 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(269): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.184+8405delT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527377 | ||||||
| chr6:52527429
|
A | G | 1 | a0001c0001t0008g0271 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.184+8354T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527429 | ||||||
| chr6:52527440
|
T | C | 25 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(22): Show | 25 | HG00639.hp1 HG01175.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.184+8343A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527440 | ||||||
| chr6:52527551
|
A | G | 2 | a0001c0001t0034g0192a0001c0001t0034g0260 | 2 | HG02451.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.184+8232T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527551 | ||||||
| chr6:52527555
|
G | T | 3 | a0001c0001t0006g0191a0001c0001t0006g0300a0001c0001t0089g0355 | 3 | HG02257.hp2 HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.184+8228C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527555 | ||||||
| chr6:52527615
|
C | T | 38 | a0001c0001t0004g0306a0001c0001t0005g0006a0001c0001t0005g0068others(35): Show | 39 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.184+8168G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527615 | ||||||
| chr6:52527724
|
A | T | 50 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(47): Show | 54 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.184+8059T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527724 | ||||||
| chr6:52527760
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.184+8023G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527760 | ||||||
| chr6:52527861
|
C | T | 6 | a0001c0001t0031g0182a0001c0001t0031g0183a0001c0001t0031g0270others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.184+7922G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527861 | ||||||
| chr6:52527866
|
T | C | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.184+7917A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527866 | ||||||
| chr6:52527871
|
T | A | 44 | a0001c0001t0004g0306a0001c0001t0005g0006a0001c0001t0005g0041others(41): Show | 45 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.184+7912A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527871 | ||||||
| chr6:52528064
|
G | A | 18 | a0001c0001t0008g0009a0001c0001t0008g0258a0001c0001t0008g0259others(15): Show | 19 | HG01074.hp2 HG01123.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.184+7719C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528064 | ||||||
| chr6:52528208
|
G | A | 2 | a0001c0001t0038g0173a0001c0001t0038g0352 | 2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.184+7575C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528208 | ||||||
| chr6:52528215
|
C | T | 1 | a0001c0001t0080g0180 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.184+7568G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528215 | ||||||
| chr6:52528216
|
C | G | 288 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(285): Show | 302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.184+7567G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528216 | ||||||
| chr6:52528326
|
C | T | 2 | a0001c0001t0022g0033a0001c0001t0022g0034 | 2 | HG00609.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.184+7457G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528326 | ||||||
| chr6:52528413
|
G | T | 28 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(25): Show | 32 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.184+7370C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528413 | ||||||
| chr6:52528463
|
G | A | 113 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(110): Show | 118 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.184+7320C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528463 | ||||||
| chr6:52528549
|
C | T | 35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.184+7234G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528549 | ||||||
| chr6:52528611
|
G | A | 43 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0306others(40): Show | 44 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.184+7172C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528611 | ||||||
| chr6:52528687
|
G | A | 1 | a0001c0001t0026g0151 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.184+7096C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528687 | ||||||
| chr6:52528772
|
G | A | 86 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(83): Show | 87 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.184+7011C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528772 | ||||||
| chr6:52528772
|
G | T | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.184+7011C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528772 | ||||||
| chr6:52528793
|
C | A | 69 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(66): Show | 76 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.184+6990G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528793 | ||||||
| chr6:52528882
|
A | G | 1 | a0001c0001t0084g0349 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.184+6901T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528882 | ||||||
| chr6:52528886
|
C | CT | 8 | a0001c0001t0006g0309a0001c0001t0009g0086a0001c0001t0011g0215others(5): Show | 9 | HG01099.hp1 HG01106.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.184+6896dupA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528886 | ||||||
| chr6:52528886
|
CTT | C | 6 | a0001c0001t0002g0098a0001c0001t0016g0267a0001c0001t0037g0226others(3): Show | 6 | HG01074.hp1 HG01175.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.184+6895_184+6896d others(4): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528886 | ||||||
| chr6:52528886
|
CTTT | C | 138 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(135): Show | 145 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.184+6894_184+6896d others(5): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528886 | ||||||
| chr6:52528886
|
CTTTT | C | 7 | a0001c0001t0003g0079a0001c0001t0003g0213a0001c0001t0016g0037others(4): Show | 7 | HG02572.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.184+6893_184+6896d others(6): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528886 | ||||||
| chr6:52528886
|
CTTTTTTT others(5): Show |
C | 115 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(112): Show | 120 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.184+6885_184+6896d others(14): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528886 | ||||||
| chr6:52528914
|
C | T | 18 | a0001c0001t0008g0009a0001c0001t0008g0258a0001c0001t0008g0259others(15): Show | 19 | HG01074.hp2 HG01123.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.184+6869G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528914 | ||||||
| chr6:52528951
|
C | T | 3 | a0001c0001t0005g0068a0001c0001t0005g0172a0001c0001t0005g0319 | 3 | HG02015.hp1 HG02132.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.184+6832G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528951 | ||||||
| chr6:52528976
|
C | T | 115 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(112): Show | 120 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.184+6807G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52528976 | ||||||
| chr6:52529025
|
G | C | 19 | a0001c0001t0008g0009a0001c0001t0008g0258a0001c0001t0008g0259others(16): Show | 20 | HG01074.hp2 HG01123.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.184+6758C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52529025 | ||||||
| chr6:52529032
|
A | AC | 14 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(11): Show | 15 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.184+6750_184+6751i others(3): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52529032 | ||||||
| chr6:52529045
|
C | A | 18 | a0001c0001t0008g0009a0001c0001t0008g0258a0001c0001t0008g0259others(15): Show | 19 | HG01074.hp2 HG01123.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.184+6738G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52529045 | ||||||
| chr6:52529077
|
G | A | 3 | a0001c0001t0031g0182a0001c0001t0031g0183a0001c0001t0031g0270 | 3 | HG02818.hp1 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.184+6706C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52529077 | ||||||
| chr6:52529092
|
C | T | 2 | a0001c0001t0009g0219a0001c0001t0009g0233 | 2 | HG02622.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.184+6691G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52529092 | ||||||
| chr6:52529113
|
G | A | 46 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0306others(43): Show | 47 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.184+6670C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52529113 | ||||||
| chr6:52529403
|
C | CCTAA | 298 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(295): Show | 312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.184+6379_184+6380i others(6): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52529403 | ||||||
| chr6:52529426
|
T | C | 5 | a0001c0001t0018g0101a0001c0001t0018g0214a0001c0001t0032g0020others(2): Show | 5 | HG00609.hp1 HG02129.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.184+6357A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52529426 | ||||||
| chr6:52529443
|
C | T | 49 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0306others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.184+6340G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52529443 | ||||||
| chr6:52529881
|
T | C | 28 | a0001c0001t0008g0009a0001c0001t0008g0258a0001c0001t0008g0259others(25): Show | 29 | HG00639.hp1 HG01074.hp2 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.184+5902A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52529881 | ||||||
| chr6:52529915
|
C | T | 1 | a0001c0001t0009g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.184+5868G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52529915 | ||||||
| chr6:52529988
|
T | C | 47 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0306others(44): Show | 48 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.184+5795A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52529988 | ||||||
| chr6:52530103
|
G | A | 1 | a0001c0001t0009g0184 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.184+5680C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52530103 | ||||||
| chr6:52530172
|
C | T | 8 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(5): Show | 11 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.184+5611G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52530172 | ||||||
| chr6:52530202
|
G | A | 1 | a0001c0001t0043g0345 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.184+5581C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52530202 | ||||||
| chr6:52530268
|
C | T | 1 | a0001c0001t0084g0349 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.184+5515G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52530268 | ||||||
| chr6:52530274
|
G | C | 1 | a0001c0001t0077g0112 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.184+5509C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52530274 | ||||||
| chr6:52530410
|
T | C | 2 | a0001c0001t0068g0313a0001c0001t0080g0180 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.184+5373A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52530410 | ||||||
| chr6:52530551
|
T | G | 135 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(132): Show | 140 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.184+5232A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52530551 | ||||||
| chr6:52530590
|
T | C | 1 | a0001c0001t0007g0254 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.184+5193A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52530590 | ||||||
| chr6:52530611
|
G | A | 2 | a0001c0001t0027g0046a0001c0001t0027g0048 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.184+5172C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52530611 | ||||||
| chr6:52530629
|
G | A | 47 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0306others(44): Show | 48 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.184+5154C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52530629 | ||||||
| chr6:52530690
|
T | C | 298 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(295): Show | 312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.184+5093A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52530690 | ||||||
| chr6:52530712
|
A | G | 333 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(330): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.184+5071T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52530712 | ||||||
| chr6:52530846
|
G | C | 1 | a0001c0001t0001g0089 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.184+4937C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52530846 | ||||||
| chr6:52530906
|
A | G | 135 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(132): Show | 140 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(137): Show |
intron_variant | MODIFIER | c.184+4877T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52530906 | ||||||
| chr6:52530959
|
A | C | 182 | a0001c0001t0001g0224a0001c0001t0001g0285a0001c0001t0001g0286others(179): Show | 191 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.184+4824T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52530959 | ||||||
| chr6:52531079
|
TAAGGAAG others(1): Show |
T | 18 | a0001c0001t0008g0009a0001c0001t0008g0258a0001c0001t0008g0259others(15): Show | 19 | HG01074.hp2 HG01123.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.184+4696_184+4703d others(10): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52531079 | ||||||
| chr6:52531120
|
C | CA | 79 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0002g0225others(76): Show | 81 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.184+4662dupT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52531120 | ||||||
| chr6:52531120
|
C | CAA | 45 | a0001c0001t0003g0044a0001c0001t0003g0062a0001c0001t0003g0074others(42): Show | 45 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(42): Show |
intron_variant | MODIFIER | c.184+4661_184+4662d others(4): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52531120 | ||||||
| chr6:52531120
|
C | CAAA | 19 | a0001c0001t0003g0060a0001c0001t0003g0069a0001c0001t0003g0077others(16): Show | 22 | HG00741.hp2 HG01123.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.184+4660_184+4662d others(5): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52531120 | ||||||
| chr6:52531120
|
C | CAAAA | 95 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(92): Show | 97 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.184+4659_184+4662d others(6): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52531120 | ||||||
| chr6:52531120
|
C | CAAAAA | 24 | a0001c0001t0001g0089a0001c0001t0002g0348a0001c0001t0004g0052others(21): Show | 24 | HG00609.hp1 HG01952.hp1 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.184+4658_184+4662d others(7): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52531120 | ||||||
| chr6:52531328
|
G | T | 115 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(112): Show | 120 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.184+4455C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52531328 | ||||||
| chr6:52531369
|
T | A | 337 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(334): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.184+4414A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52531369 | ||||||
| chr6:52531704
|
C | T | 75 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(72): Show | 82 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.184+4079G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52531704 | ||||||
| chr6:52531851
|
ATCTC | A | 8 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(5): Show | 11 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.184+3928_184+3931d others(6): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52531851 | ||||||
| chr6:52531936
|
T | C | 1 | a0001c0001t0040g0263 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.184+3847A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52531936 | ||||||
| chr6:52532074
|
G | T | 1 | a0001c0001t0001g0116 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.184+3709C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52532074 | ||||||
| chr6:52532088
|
T | C | 8 | a0001c0001t0031g0182a0001c0001t0031g0183a0001c0001t0031g0270others(5): Show | 8 | HG01891.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.184+3695A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52532088 | ||||||
| chr6:52532195
|
A | T | 1 | a0001c0001t0007g0220 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.184+3588T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52532195 | ||||||
| chr6:52532221
|
T | C | 1 | a0001c0001t0007g0220 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.184+3562A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52532221 | ||||||
| chr6:52532224
|
T | G | 1 | a0001c0001t0007g0220 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.184+3559A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52532224 | ||||||
| chr6:52532240
|
C | T | 1 | a0001c0001t0007g0220 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.184+3543G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52532240 | ||||||
| chr6:52532243
|
A | AGATTAGG others(4): Show |
1 | a0001c0001t0007g0220 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.184+3539_184+3540i others(13): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52532243 | ||||||
| chr6:52532245
|
C | G | 1 | a0001c0001t0007g0220 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.184+3538G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52532245 | ||||||
| chr6:52532247
|
C | A | 1 | a0001c0001t0007g0220 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.184+3536G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52532247 | ||||||
| chr6:52532249
|
T | G | 124 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(121): Show | 132 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(129): Show |
intron_variant | MODIFIER | c.184+3534A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52532249 | ||||||
| chr6:52532252
|
A | G | 1 | a0001c0001t0007g0220 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.184+3531T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52532252 | ||||||
| chr6:52532290
|
T | C | 5 | a0001c0001t0016g0037a0001c0001t0016g0039a0001c0001t0016g0193others(2): Show | 5 | HG02572.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.184+3493A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52532290 | ||||||
| chr6:52532367
|
T | A | 5 | a0001c0001t0033g0186a0001c0001t0033g0187a0001c0001t0034g0192others(2): Show | 5 | HG02451.hp1 HG03041.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.184+3416A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52532367 | ||||||
| chr6:52532410
|
T | C | 2 | a0001c0001t0035g0066a0001c0001t0035g0185 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.184+3373A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52532410 | ||||||
| chr6:52532776
|
G | T | 289 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(286): Show | 303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.184+3007C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52532776 | ||||||
| chr6:52532808
|
AC | A | 20 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(17): Show | 21 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.184+2974delG | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52532808 | ||||||
| chr6:52532832
|
T | C | 58 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(55): Show | 65 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.184+2951A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52532832 | ||||||
| chr6:52533000
|
G | C | 115 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(112): Show | 120 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.184+2783C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52533000 | ||||||
| chr6:52533107
|
G | A | 84 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(81): Show | 85 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.184+2676C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52533107 | ||||||
| chr6:52533130
|
G | A | 24 | a0001c0001t0002g0144a0001c0001t0002g0234a0001c0001t0002g0238others(21): Show | 27 | HG00408.hp1 HG00558.hp1 HG02080.hp1 others(24): Show |
intron_variant | MODIFIER | c.184+2653C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52533130 | ||||||
| chr6:52533192
|
A | G | 1 | a0001c0001t0097g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.184+2591T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52533192 | ||||||
| chr6:52533240
|
G | T | 8 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(5): Show | 11 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.184+2543C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52533240 | ||||||
| chr6:52533385
|
C | A | 9 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(6): Show | 10 | HG00140.hp1 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.184+2398G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52533385 | ||||||
| chr6:52533440
|
C | T | 5 | a0001c0001t0018g0101a0001c0001t0018g0214a0001c0001t0032g0020others(2): Show | 5 | HG00609.hp1 HG02129.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.184+2343G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52533440 | ||||||
| chr6:52533799
|
A | G | 8 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(5): Show | 11 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.184+1984T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52533799 | ||||||
| chr6:52534041
|
C | T | 14 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(11): Show | 15 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.184+1742G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534041 | ||||||
| chr6:52534042
|
G | A | 115 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(112): Show | 120 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.184+1741C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534042 | ||||||
| chr6:52534047
|
T | C | 1 | a0001c0001t0018g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.184+1736A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534047 | ||||||
| chr6:52534080
|
C | T | 154 | a0001c0001t0001g0224a0001c0001t0001g0285a0001c0001t0001g0286others(151): Show | 162 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.184+1703G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534080 | ||||||
| chr6:52534084
|
C | CA | 16 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(13): Show | 19 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.184+1698dupT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534084 | ||||||
| chr6:52534084
|
CA | C | 209 | a0001c0001t0001g0203a0001c0001t0001g0224a0001c0001t0001g0285others(206): Show | 218 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.184+1698delT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534084 | ||||||
| chr6:52534100
|
G | T | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.184+1683C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534100 | ||||||
| chr6:52534169
|
G | A | 1 | a0001c0001t0008g0283 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.184+1614C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534169 | ||||||
| chr6:52534208
|
C | G | 172 | a0001c0001t0001g0224a0001c0001t0001g0285a0001c0001t0001g0286others(169): Show | 181 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.184+1575G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534208 | ||||||
| chr6:52534317
|
G | A | 172 | a0001c0001t0001g0224a0001c0001t0001g0285a0001c0001t0001g0286others(169): Show | 181 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.184+1466C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534317 | ||||||
| chr6:52534449
|
C | A | 152 | a0001c0001t0001g0224a0001c0001t0001g0285a0001c0001t0001g0286others(149): Show | 161 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.184+1334G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534449 | ||||||
| chr6:52534509
|
T | G | 289 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(286): Show | 303 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.184+1274A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534509 | ||||||
| chr6:52534522
|
G | A | 1 | a0001c0001t0091g0301 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.184+1261C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534522 | ||||||
| chr6:52534557
|
C | T | 2 | a0001c0001t0098g0337a0001c0001t0099g0339 | 2 | HG01106.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.184+1226G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534557 | ||||||
| chr6:52534733
|
C | T | 1 | a0001c0003t0015g0305 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.184+1050G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534733 | ||||||
| chr6:52534967
|
G | C | 35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.184+816C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534967 | ||||||
| chr6:52535055
|
CCAGT | C | 9 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(6): Show | 10 | HG00140.hp1 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.184+724_184+727del others(4): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52535055 | ||||||
| chr6:52535074
|
C | T | 1 | a0001c0001t0002g0238 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.184+709G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52535074 | ||||||
| chr6:52535129
|
C | G | 1 | a0001c0001t0006g0035 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.184+654G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52535129 | ||||||
| chr6:52535180
|
A | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG00544.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.184+603T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52535180 | ||||||
| chr6:52535409
|
G | A | 1 | a0001c0001t0058g0189 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.184+374C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52535409 | ||||||
| chr6:52535549
|
C | T | 1 | a0001c0001t0055g0024 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.184+234G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52535549 | ||||||
| chr6:52535686
|
GA | G | 93 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(90): Show | 97 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.184+96delT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52535686 | ||||||
| chr6:52535731
|
G | A | 86 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(83): Show | 87 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.184+52C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52535731 | ||||||
| chr6:52535767
|
G | GGAGAAGA others(3): Show |
1 | a0001c0001t0090g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.184+15_184+16insGC others(8): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52535767 | ||||||
| chr6:52535769
|
C | G | 1 | a0001c0001t0090g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.184+14G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52535769 | ||||||
| chr6:52535770
|
C | G | 1 | a0001c0001t0090g0273 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.184+13G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52535770 | ||||||
| chr6:52535922
|
C | G | 3 | a0001c0001t0038g0352a0001c0001t0042g0350a0001c0001t0042g0351 | 3 | HG01891.hp1 HG02280.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.121-76G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52535922 | ||||||
| chr6:52536027
|
T | C | 84 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(81): Show | 91 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.121-181A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52536027 | ||||||
| chr6:52536091
|
C | T | 136 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(133): Show | 141 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(138): Show |
intron_variant | MODIFIER | c.121-245G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52536091 | ||||||
| chr6:52536627
|
C | T | 6 | a0001c0001t0019g0082a0001c0001t0019g0084a0001c0001t0019g0100others(3): Show | 6 | HG01891.hp2 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.121-781G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52536627 | ||||||
| chr6:52536663
|
G | T | 46 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0306others(43): Show | 47 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.121-817C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52536663 | ||||||
| chr6:52536723
|
C | T | 1 | a0001c0001t0086g0256 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.121-877G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52536723 | ||||||
| chr6:52536919
|
C | A | 2 | a0001c0001t0005g0175a0001c0001t0005g0178 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.121-1073G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52536919 | ||||||
| chr6:52537109
|
C | A | 4 | a0001c0001t0006g0004a0001c0001t0029g0002a0001c0001t0030g0261others(1): Show | 7 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.121-1263G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52537109 | ||||||
| chr6:52537424
|
T | A | 1 | a0001c0001t0018g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.121-1578A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52537424 | ||||||
| chr6:52537444
|
A | C | 135 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(132): Show | 137 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(134): Show |
intron_variant | MODIFIER | c.121-1598T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52537444 | ||||||
| chr6:52537542
|
G | T | 6 | a0001c0001t0019g0082a0001c0001t0019g0084a0001c0001t0019g0100others(3): Show | 6 | HG01891.hp2 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.121-1696C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52537542 | ||||||
| chr6:52537711
|
G | A | 1 | a0001c0001t0051g0029 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.121-1865C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52537711 | ||||||
| chr6:52537730
|
GT | G | 341 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(338): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.121-1885delA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52537730 | ||||||
| chr6:52537746
|
G | A | 1 | a0001c0001t0084g0349 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.121-1900C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52537746 | ||||||
| chr6:52537798
|
G | A | 50 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0284others(47): Show | 51 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.121-1952C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52537798 | ||||||
| chr6:52537868
|
C | T | 18 | a0001c0001t0008g0009a0001c0001t0008g0258a0001c0001t0008g0259others(15): Show | 19 | HG01074.hp2 HG01123.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.121-2022G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52537868 | ||||||
| chr6:52538025
|
A | G | 295 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(292): Show | 309 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.121-2179T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52538025 | ||||||
| chr6:52538075
|
A | T | 1 | a0001c0001t0018g0101 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.121-2229T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52538075 | ||||||
| chr6:52538267
|
C | T | 6 | a0001c0001t0019g0082a0001c0001t0019g0084a0001c0001t0019g0100others(3): Show | 6 | HG01891.hp2 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.121-2421G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52538267 | ||||||
| chr6:52538343
|
A | C | 1 | a0001c0001t0015g0312 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.121-2497T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52538343 | ||||||
| chr6:52538361
|
CTGTGTGT others(10): Show |
C | 3 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0195 | 3 | HG01884.hp2 HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.121-2532_121-2516d others(19): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52538361 | ||||||
| chr6:52538486
|
C | T | 1 | a0001c0001t0057g0188 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.121-2640G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52538486 | ||||||
| chr6:52538487
|
G | A | 2 | a0001c0001t0008g0070a0001c0001t0008g0071 | 2 | HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.121-2641C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52538487 | ||||||
| chr6:52538595
|
G | C | 1 | a0001c0001t0008g0258 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.121-2749C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52538595 | ||||||
| chr6:52538744
|
T | C | 5 | a0001c0001t0023g0018a0001c0001t0023g0022a0001c0001t0023g0023others(2): Show | 5 | HG00639.hp1 HG01175.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-2898A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52538744 | ||||||
| chr6:52538835
|
T | C | 362 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(359): Show | 377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.121-2989A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52538835 | ||||||
| chr6:52539012
|
T | C | 14 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(11): Show | 15 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.121-3166A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52539012 | ||||||
| chr6:52539023
|
T | C | 4 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0195others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-3177A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52539023 | ||||||
| chr6:52539100
|
T | C | 14 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(11): Show | 15 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.121-3254A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52539100 | ||||||
| chr6:52539330
|
A | G | 2 | a0001c0001t0006g0043a0001c0001t0012g0268 | 2 | HG01106.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.121-3484T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52539330 | ||||||
| chr6:52539343
|
C | T | 3 | a0001c0001t0009g0184a0001c0001t0009g0209a0001c0001t0061g0210 | 3 | HG02145.hp1 HG02615.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.121-3497G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52539343 | ||||||
| chr6:52539462
|
A | C | 49 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(46): Show | 53 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.121-3616T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52539462 | ||||||
| chr6:52539542
|
A | AC | 29 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(26): Show | 33 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.121-3697_121-3696i others(3): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52539542 | ||||||
| chr6:52539543
|
A | C | 28 | a0001c0001t0001g0050a0001c0001t0002g0348a0001c0001t0004g0052others(25): Show | 28 | HG01192.hp2 HG01516.hp1 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.121-3697T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52539543 | ||||||
| chr6:52539545
|
A | C | 29 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(26): Show | 33 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.121-3699T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52539545 | ||||||
| chr6:52539546
|
A | C | 20 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(17): Show | 20 | HG01192.hp2 HG02735.hp1 HG02965.hp1 others(17): Show |
intron_variant | MODIFIER | c.121-3700T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52539546 | ||||||
| chr6:52539589
|
C | T | 1 | a0001c0001t0004g0139 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.121-3743G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52539589 | ||||||
| chr6:52539725
|
G | A | 86 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(83): Show | 87 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.121-3879C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52539725 | ||||||
| chr6:52540083
|
G | A | 14 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(11): Show | 15 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.121-4237C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52540083 | ||||||
| chr6:52540096
|
T | C | 1 | a0001c0001t0007g0228 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.121-4250A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52540096 | ||||||
| chr6:52540099
|
A | C | 131 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(128): Show | 139 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(136): Show |
intron_variant | MODIFIER | c.121-4253T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52540099 | ||||||
| chr6:52540210
|
C | A | 1 | a0001c0001t0070g0097 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.121-4364G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52540210 | ||||||
| chr6:52540211
|
G | A | 1 | a0001c0001t0020g0247 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.121-4365C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52540211 | ||||||
| chr6:52540261
|
T | A | 9 | a0001c0001t0031g0182a0001c0001t0031g0183a0001c0001t0031g0270others(6): Show | 9 | HG01891.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.121-4415A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52540261 | ||||||
| chr6:52540300
|
A | G | 4 | a0001c0001t0005g0006a0001c0001t0005g0168a0001c0001t0005g0169others(1): Show | 5 | HG00140.hp2 HG00280.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-4454T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52540300 | ||||||
| chr6:52540426
|
C | T | 5 | a0001c0001t0016g0037a0001c0001t0016g0039a0001c0001t0016g0193others(2): Show | 5 | HG02572.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-4580G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52540426 | ||||||
| chr6:52540480
|
C | T | 5 | a0001c0001t0018g0101a0001c0001t0018g0214a0001c0001t0032g0020others(2): Show | 5 | HG00609.hp1 HG02129.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-4634G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52540480 | ||||||
| chr6:52540617
|
A | G | 225 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(222): Show | 234 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(231): Show |
intron_variant | MODIFIER | c.121-4771T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52540617 | ||||||
| chr6:52540638
|
A | G | 2 | a0001c0001t0002g0222a0001c0001t0002g0237 | 2 | HG01168.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.121-4792T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52540638 | ||||||
| chr6:52540732
|
T | C | 1 | a0001c0001t0012g0268 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.121-4886A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52540732 | ||||||
| chr6:52540733
|
C | G | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.121-4887G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52540733 | ||||||
| chr6:52540863
|
G | A | 4 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0195others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-5017C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52540863 | ||||||
| chr6:52540924
|
A | G | 2 | a0001c0001t0008g0297a0001c0001t0025g0291 | 2 | HG01255.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.121-5078T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52540924 | ||||||
| chr6:52541059
|
G | A | 1 | a0001c0001t0084g0349 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.121-5213C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541059 | ||||||
| chr6:52541230
|
T | C | 29 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(26): Show | 33 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.121-5384A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541230 | ||||||
| chr6:52541329
|
C | CTA | 4 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0195others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-5484_121-5483i others(4): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541329 | ||||||
| chr6:52541330
|
C | G | 4 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0195others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-5484G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541330 | ||||||
| chr6:52541589
|
T | C | 1 | a0001c0001t0003g0080 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.121-5743A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541589 | ||||||
| chr6:52541658
|
C | T | 5 | a0001c0001t0018g0101a0001c0001t0018g0214a0001c0001t0032g0020others(2): Show | 5 | HG00609.hp1 HG02129.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-5812G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541658 | ||||||
| chr6:52541756
|
C | T | 1 | a0001c0001t0001g0116 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.121-5910G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541756 | ||||||
| chr6:52541803
|
G | GT | 246 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(243): Show | 256 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.121-5958dupA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541803 | ||||||
| chr6:52541803
|
G | GTT | 12 | a0001c0001t0002g0218a0001c0001t0010g0025a0001c0001t0013g0136others(9): Show | 12 | HG01099.hp2 HG02293.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.121-5959_121-5958d others(4): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541803 | ||||||
| chr6:52541803
|
G | GTTT | 4 | a0001c0001t0006g0004a0001c0001t0029g0002a0001c0001t0030g0261others(1): Show | 7 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.121-5960_121-5958d others(5): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541803 | ||||||
| chr6:52541803
|
G | GTTTTTTT others(6): Show |
7 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(4): Show | 8 | HG00140.hp1 HG00642.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.121-5970_121-5958d others(15): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541803 | ||||||
| chr6:52541803
|
G | GTTTTTTT others(7): Show |
2 | a0001c0001t0037g0316a0001c0001t0051g0029 | 2 | HG02055.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.121-5971_121-5958d others(16): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541803 | ||||||
| chr6:52541803
|
G | GTTTTTTT others(9): Show |
6 | a0001c0001t0018g0101a0001c0001t0019g0084a0001c0001t0032g0020others(3): Show | 6 | HG00609.hp1 HG02109.hp2 HG02129.hp2 others(3): Show |
intron_variant | MODIFIER | c.121-5958_121-5957i others(18): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541803 | ||||||
| chr6:52541803
|
G | GTTTTTTT others(10): Show |
5 | a0001c0001t0018g0214a0001c0001t0019g0082a0001c0001t0019g0100others(2): Show | 5 | HG01891.hp2 HG02486.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.121-5958_121-5957i others(19): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541803 | ||||||
| chr6:52541803
|
G | GTTTTTTT others(12): Show |
1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.121-5958_121-5957i others(21): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541803 | ||||||
| chr6:52541803
|
GT | G | 34 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(31): Show | 34 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.121-5958delA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541803 | ||||||
| chr6:52541875
|
G | A | 1 | a0001c0001t0056g0032 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.121-6029C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541875 | ||||||
| chr6:52541875
|
G | C | 1 | a0001c0001t0084g0349 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.121-6029C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541875 | ||||||
| chr6:52541975
|
C | A | 1 | a0001c0001t0059g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.121-6129G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541975 | ||||||
| chr6:52541981
|
G | C | 1 | a0001c0001t0084g0349 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.121-6135C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541981 | ||||||
| chr6:52542058
|
G | C | 1 | a0001c0001t0018g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.121-6212C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542058 | ||||||
| chr6:52542258
|
T | C | 36 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(33): Show | 36 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.121-6412A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542258 | ||||||
| chr6:52542261
|
G | GT | 203 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(200): Show | 212 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(209): Show |
intron_variant | MODIFIER | c.121-6416_121-6415i others(3): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542261 | ||||||
| chr6:52542261
|
G | GTT | 7 | a0001c0001t0002g0241a0001c0001t0004g0138a0001c0001t0007g0251others(4): Show | 7 | HG02080.hp2 NA18940.hp1 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.121-6416_121-6415i others(4): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542261 | ||||||
| chr6:52542262
|
G | T | 268 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(265): Show | 278 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.121-6416C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542262 | ||||||
| chr6:52542276
|
T | A | 32 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0284others(29): Show | 33 | HG00140.hp2 HG00280.hp1 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.121-6430A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542276 | ||||||
| chr6:52542277
|
A | T | 181 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(178): Show | 194 | HG00140.hp1 HG00408.hp1 HG00558.hp1 others(191): Show |
intron_variant | MODIFIER | c.121-6431T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542277 | ||||||
| chr6:52542278
|
A | T | 137 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(134): Show | 146 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(143): Show |
intron_variant | MODIFIER | c.121-6432T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542278 | ||||||
| chr6:52542279
|
A | T | 125 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(122): Show | 134 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.121-6433T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542279 | ||||||
| chr6:52542280
|
A | C | 29 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(26): Show | 33 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.121-6434T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542280 | ||||||
| chr6:52542280
|
A | T | 40 | a0001c0001t0005g0288a0001c0001t0007g0001a0001c0001t0007g0140others(37): Show | 44 | HG00558.hp1 HG00639.hp2 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.121-6434T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542280 | ||||||
| chr6:52542335
|
C | T | 29 | a0001c0001t0006g0004a0001c0001t0006g0035a0001c0001t0006g0036others(26): Show | 33 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.121-6489G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542335 | ||||||
| chr6:52542345
|
C | T | 50 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0284others(47): Show | 51 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.121-6499G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542345 | ||||||
| chr6:52542358
|
G | C | 1 | a0001c0001t0059g0167 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.121-6512C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542358 | ||||||
| chr6:52542361
|
G | A | 85 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(82): Show | 86 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.121-6515C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542361 | ||||||
| chr6:52542459
|
T | C | 1 | a0001c0001t0010g0015 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.121-6613A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542459 | ||||||
| chr6:52542467
|
G | C | 1 | a0001c0001t0062g0320 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.121-6621C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542467 | ||||||
| chr6:52542499
|
G | A | 1 | a0001c0001t0072g0102 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.121-6653C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542499 | ||||||
| chr6:52542625
|
C | T | 85 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(82): Show | 86 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.121-6779G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542625 | ||||||
| chr6:52542719
|
T | C | 5 | a0001c0001t0023g0018a0001c0001t0023g0022a0001c0001t0023g0023others(2): Show | 5 | HG00639.hp1 HG01175.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-6873A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542719 | ||||||
| chr6:52542741
|
G | A | 1 | a0001c0001t0084g0349 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.121-6895C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542741 | ||||||
| chr6:52542902
|
T | C | 1 | a0001c0001t0100g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.121-7056A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542902 | ||||||
| chr6:52542972
|
G | A | 4 | a0001c0001t0006g0004a0001c0001t0029g0002a0001c0001t0030g0261others(1): Show | 7 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.121-7126C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542972 | ||||||
| chr6:52543001
|
C | T | 2 | a0001c0001t0090g0273a0001c0001t0091g0301 | 2 | HG02486.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.121-7155G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52543001 | ||||||
| chr6:52543042
|
C | T | 9 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(6): Show | 10 | HG00140.hp1 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.121-7196G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52543042 | ||||||
| chr6:52543111
|
G | A | 2 | a0001c0001t0001g0113a0001c0001t0001g0114 | 2 | HG00544.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.121-7265C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52543111 | ||||||
| chr6:52543129
|
G | C | 35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.121-7283C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52543129 | ||||||
| chr6:52543150
|
TAATA | T | 60 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(57): Show | 67 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.121-7308_121-7305d others(6): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52543150 | ||||||
| chr6:52543153
|
T | C | 1 | a0001c0001t0015g0312 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.121-7307A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52543153 | ||||||
| chr6:52543179
|
A | C | 1 | a0001c0001t0004g0104 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.121-7333T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52543179 | ||||||
| chr6:52543287
|
A | C | 1 | a0001c0001t0004g0104 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.121-7441T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52543287 | ||||||
| chr6:52543391
|
A | C | 1 | a0001c0001t0004g0104 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.121-7545T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52543391 | ||||||
| chr6:52543460
|
G | A | 1 | a0001c0001t0046g0076 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.121-7614C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52543460 | ||||||
| chr6:52543694
|
G | A | 9 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(6): Show | 10 | HG00140.hp1 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.121-7848C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52543694 | ||||||
| chr6:52543737
|
T | A | 1 | a0001c0001t0097g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.121-7891A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52543737 | ||||||
| chr6:52544033
|
T | C | 1 | a0001c0001t0097g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.121-8187A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544033 | ||||||
| chr6:52544038
|
C | G | 3 | a0001c0001t0002g0072a0001c0001t0040g0262a0001c0001t0040g0263 | 3 | HG01074.hp1 HG03471.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.121-8192G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544038 | ||||||
| chr6:52544052
|
G | C | 85 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(82): Show | 86 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.121-8206C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544052 | ||||||
| chr6:52544089
|
A | T | 85 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(82): Show | 86 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.121-8243T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544089 | ||||||
| chr6:52544096
|
A | G | 334 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(331): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.121-8250T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544096 | ||||||
| chr6:52544144
|
T | C | 9 | a0001c0001t0031g0182a0001c0001t0031g0183a0001c0001t0031g0270others(6): Show | 9 | HG01891.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.121-8298A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544144 | ||||||
| chr6:52544153
|
C | T | 5 | a0001c0001t0016g0037a0001c0001t0016g0039a0001c0001t0016g0193others(2): Show | 5 | HG02572.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-8307G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544153 | ||||||
| chr6:52544185
|
G | A | 1 | a0001c0001t0038g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.121-8339C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544185 | ||||||
| chr6:52544206
|
G | C | 24 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0195others(21): Show | 25 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.121-8360C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544206 | ||||||
| chr6:52544330
|
ATC | A | 68 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(65): Show | 75 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.121-8486_121-8485d others(4): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544330 | ||||||
| chr6:52544373
|
A | T | 1 | a0001c0001t0096g0155 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.121-8527T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544373 | ||||||
| chr6:52544388
|
G | C | 1 | a0001c0001t0038g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.121-8542C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544388 | ||||||
| chr6:52544475
|
G | A | 4 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0195others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-8629C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544475 | ||||||
| chr6:52544524
|
G | A | 20 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(17): Show | 20 | HG01192.hp2 HG02735.hp1 HG02965.hp1 others(17): Show |
intron_variant | MODIFIER | c.121-8678C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544524 | ||||||
| chr6:52544545
|
G | A | 85 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(82): Show | 86 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.121-8699C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544545 | ||||||
| chr6:52544627
|
G | A | 19 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(16): Show | 22 | HG00621.hp1 HG00735.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.121-8781C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544627 | ||||||
| chr6:52544639
|
G | A | 5 | a0001c0001t0018g0101a0001c0001t0018g0214a0001c0001t0032g0020others(2): Show | 5 | HG00609.hp1 HG02129.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-8793C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544639 | ||||||
| chr6:52544712
|
T | G | 5 | a0001c0001t0016g0037a0001c0001t0016g0039a0001c0001t0016g0193others(2): Show | 5 | HG02572.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-8866A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544712 | ||||||
| chr6:52544822
|
A | G | 329 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(326): Show | 340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.121-8976T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544822 | ||||||
| chr6:52544844
|
C | T | 10 | a0001c0001t0001g0165a0001c0001t0004g0105a0001c0001t0004g0106others(7): Show | 10 | NA18940.hp2 NA18955.hp1 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.121-8998G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544844 | ||||||
| chr6:52544918
|
C | T | 1 | a0001c0001t0100g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.121-9072G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544918 | ||||||
| chr6:52544943
|
A | G | 85 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(82): Show | 86 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.121-9097T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52544943 | ||||||
| chr6:52545013
|
G | A | 1 | a0001c0001t0100g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.121-9167C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52545013 | ||||||
| chr6:52545201
|
A | C | 1 | a0001c0001t0010g0019 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.121-9355T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52545201 | ||||||
| chr6:52545260
|
G | C | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.121-9414C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52545260 | ||||||
| chr6:52545312
|
G | C | 184 | a0001c0001t0001g0224a0001c0001t0001g0285a0001c0001t0001g0286others(181): Show | 193 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.121-9466C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52545312 | ||||||
| chr6:52545343
|
C | A | 1 | a0001c0001t0034g0260 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.121-9497G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52545343 | ||||||
| chr6:52545466
|
G | A | 36 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(33): Show | 36 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.121-9620C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52545466 | ||||||
| chr6:52545514
|
A | G | 68 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(65): Show | 75 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.121-9668T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52545514 | ||||||
| chr6:52545541
|
G | A | 1 | a0001c0001t0096g0155 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.121-9695C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52545541 | ||||||
| chr6:52545644
|
G | A | 1 | a0001c0002t0093g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.121-9798C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52545644 | ||||||
| chr6:52545658
|
G | A | 35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.121-9812C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52545658 | ||||||
| chr6:52545979
|
T | C | 1 | a0001c0001t0005g0265 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.121-10133A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52545979 | ||||||
| chr6:52546070
|
C | G | 5 | a0001c0001t0023g0018a0001c0001t0023g0022a0001c0001t0023g0023others(2): Show | 5 | HG00639.hp1 HG01175.hp2 HG02735.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-10224G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52546070 | ||||||
| chr6:52546324
|
A | C | 124 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0003g0044others(121): Show | 129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.121-10478T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52546324 | ||||||
| chr6:52546531
|
G | T | 1 | a0001c0001t0096g0155 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.121-10685C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52546531 | ||||||
| chr6:52546619
|
A | T | 35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.121-10773T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52546619 | ||||||
| chr6:52546657
|
TA | T | 4 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0195others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-10812delT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52546657 | ||||||
| chr6:52546704
|
G | A | 4 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0195others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-10858C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52546704 | ||||||
| chr6:52546829
|
G | A | 1 | a0001c0001t0063g0264 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.121-10983C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52546829 | ||||||
| chr6:52546874
|
G | C | 4 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0195others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-11028C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52546874 | ||||||
| chr6:52546905
|
G | C | 154 | a0001c0001t0001g0224a0001c0001t0001g0285a0001c0001t0001g0286others(151): Show | 162 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.121-11059C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52546905 | ||||||
| chr6:52546915
|
C | T | 36 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(33): Show | 36 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.121-11069G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52546915 | ||||||
| chr6:52546969
|
G | A | 2 | a0001c0002t0028g0011a0001c0002t0028g0357 | 3 | HG01243.hp2 HG03209.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.121-11123C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52546969 | ||||||
| chr6:52546998
|
ACTGGTAA others(3): Show |
A | 19 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(16): Show | 22 | HG00621.hp1 HG00735.hp2 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.121-11162_121-1115 others(14): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52546998 | ||||||
| chr6:52547148
|
G | A | 5 | a0001c0001t0031g0182a0001c0001t0031g0183a0001c0001t0031g0270others(2): Show | 5 | HG02451.hp2 HG02818.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-11302C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52547148 | ||||||
| chr6:52547170
|
G | A | 1 | a0001c0001t0004g0106 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.121-11324C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52547170 | ||||||
| chr6:52547213
|
G | T | 1 | a0001c0001t0084g0349 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.121-11367C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52547213 | ||||||
| chr6:52547229
|
C | T | 1 | a0001c0001t0045g0085 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.121-11383G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52547229 | ||||||
| chr6:52547327
|
A | C | 7 | a0001c0001t0007g0146a0001c0001t0014g0115a0001c0001t0014g0130others(4): Show | 7 | HG02080.hp2 NA18612.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.121-11481T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52547327 | ||||||
| chr6:52547344
|
T | A | 223 | a0001c0001t0001g0224a0001c0001t0001g0285a0001c0001t0001g0286others(220): Show | 232 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.121-11498A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52547344 | ||||||
| chr6:52547382
|
T | C | 4 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0195others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-11536A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52547382 | ||||||
| chr6:52547462
|
G | A | 1 | a0001c0001t0008g0299 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.121-11616C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52547462 | ||||||
| chr6:52547476
|
C | G | 14 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(11): Show | 15 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.121-11630G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52547476 | ||||||
| chr6:52547756
|
C | T | 1 | a0001c0001t0062g0320 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.121-11910G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52547756 | ||||||
| chr6:52548321
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.121-12475T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52548321 | ||||||
| chr6:52548377
|
C | T | 2 | a0001c0001t0002g0098a0001c0001t0019g0082 | 2 | HG03540.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.121-12531G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52548377 | ||||||
| chr6:52548401
|
A | C | 1 | a0001c0001t0100g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.121-12555T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52548401 | ||||||
| chr6:52548667
|
T | C | 31 | a0001c0001t0006g0300a0001c0001t0008g0009a0001c0001t0008g0258others(28): Show | 32 | HG00639.hp1 HG01074.hp2 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.121-12821A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52548667 | ||||||
| chr6:52548784
|
T | C | 1 | a0001c0001t0003g0342 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.121-12938A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52548784 | ||||||
| chr6:52548837
|
A | G | 50 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0284others(47): Show | 51 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.121-12991T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52548837 | ||||||
| chr6:52548913
|
G | C | 10 | a0001c0001t0001g0165a0001c0001t0004g0105a0001c0001t0004g0106others(7): Show | 10 | NA18940.hp2 NA18955.hp1 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.121-13067C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52548913 | ||||||
| chr6:52548920
|
C | A | 4 | a0001c0001t0054g0016a0001c0003t0005g0308a0001c0003t0015g0305others(1): Show | 4 | HG02738.hp2 HG03688.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-13074G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52548920 | ||||||
| chr6:52548969
|
C | T | 85 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(82): Show | 86 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.121-13123G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52548969 | ||||||
| chr6:52548988
|
C | G | 335 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(332): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.121-13142G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52548988 | ||||||
| chr6:52549113
|
C | G | 1 | a0001c0001t0036g0321 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.121-13267G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52549113 | ||||||
| chr6:52549114
|
G | C | 5 | a0001c0001t0016g0037a0001c0001t0016g0039a0001c0001t0016g0193others(2): Show | 5 | HG02572.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-13268C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52549114 | ||||||
| chr6:52549118
|
G | A | 50 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0284others(47): Show | 51 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.121-13272C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52549118 | ||||||
| chr6:52549153
|
T | G | 21 | a0001c0001t0006g0300a0001c0001t0008g0009a0001c0001t0008g0258others(18): Show | 22 | HG01074.hp2 HG01123.hp2 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.121-13307A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52549153 | ||||||
| chr6:52549196
|
C | T | 5 | a0001c0001t0006g0004a0001c0001t0029g0002a0001c0001t0030g0261others(2): Show | 8 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.121-13350G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52549196 | ||||||
| chr6:52549236
|
T | TCCTTCCC others(10): Show |
1 | a0001c0001t0097g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.121-13407_121-1339 others(21): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52549236 | ||||||
| chr6:52549236
|
TCCTTCCC others(10): Show |
T | 11 | a0001c0001t0006g0309a0001c0001t0006g0331a0001c0001t0011g0058others(8): Show | 11 | HG01433.hp1 HG02071.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.121-13407_121-1339 others(21): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52549236 | ||||||
| chr6:52549278
|
C | CCCTT | 101 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(98): Show | 108 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(105): Show |
intron_variant | MODIFIER | c.121-13436_121-1343 others(8): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52549278 | ||||||
| chr6:52549282
|
T | C | 1 | a0001c0001t0080g0180 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.121-13436A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52549282 | ||||||
| chr6:52549445
|
C | T | 23 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0195others(20): Show | 24 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.121-13599G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52549445 | ||||||
| chr6:52549566
|
T | C | 1 | a0001c0001t0029g0002 | 3 | HG00741.hp2 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.121-13720A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52549566 | ||||||
| chr6:52549573
|
C | T | 1 | a0001c0001t0039g0318 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.121-13727G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52549573 | ||||||
| chr6:52549662
|
C | T | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.121-13816G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52549662 | ||||||
| chr6:52549681
|
C | T | 3 | a0001c0001t0008g0277a0001c0001t0008g0283a0001c0001t0105g0276 | 3 | HG01928.hp1 HG02896.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.121-13835G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52549681 | ||||||
| chr6:52549913
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.121-14067T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52549913 | ||||||
| chr6:52550044
|
T | C | 5 | a0001c0001t0016g0037a0001c0001t0016g0039a0001c0001t0016g0193others(2): Show | 5 | HG02572.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-14198A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550044 | ||||||
| chr6:52550130
|
G | C | 6 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0284others(3): Show | 6 | HG02027.hp2 NA18959.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.121-14284C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550130 | ||||||
| chr6:52550225
|
C | T | 35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.121-14379G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550225 | ||||||
| chr6:52550244
|
A | G | 2 | a0001c0001t0002g0221a0001c0001t0003g0236 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.121-14398T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550244 | ||||||
| chr6:52550262
|
C | T | 5 | a0001c0001t0016g0037a0001c0001t0016g0039a0001c0001t0016g0193others(2): Show | 5 | HG02572.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-14416G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550262 | ||||||
| chr6:52550289
|
A | G | 35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.121-14443T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550289 | ||||||
| chr6:52550303
|
C | G | 1 | a0001c0001t0003g0163 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.121-14457G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550303 | ||||||
| chr6:52550329
|
C | T | 1 | a0001c0001t0045g0085 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.121-14483G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550329 | ||||||
| chr6:52550438
|
G | T | 1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.121-14592C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550438 | ||||||
| chr6:52550440
|
T | A | 1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.121-14594A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550440 | ||||||
| chr6:52550441
|
G | C | 1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.121-14595C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550441 | ||||||
| chr6:52550442
|
G | C | 1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.121-14596C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550442 | ||||||
| chr6:52550443
|
G | C | 1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.121-14597C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550443 | ||||||
| chr6:52550445
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.121-14599G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550445 | ||||||
| chr6:52550446
|
T | A | 1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.121-14600A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550446 | ||||||
| chr6:52550447
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.121-14601G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550447 | ||||||
| chr6:52550448
|
T | A | 1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.121-14602A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550448 | ||||||
| chr6:52550449
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.121-14603C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550449 | ||||||
| chr6:52550452
|
T | A | 1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.121-14606A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550452 | ||||||
| chr6:52550453
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.121-14607C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550453 | ||||||
| chr6:52550455
|
T | A | 1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.121-14609A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550455 | ||||||
| chr6:52550456
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.121-14610C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550456 | ||||||
| chr6:52550457
|
G | C | 1 | a0001c0001t0001g0157 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.121-14611C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550457 | ||||||
| chr6:52550461
|
T | C | 2 | a0001c0001t0033g0186a0001c0001t0033g0187 | 2 | HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.121-14615A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550461 | ||||||
| chr6:52550509
|
C | T | 5 | a0001c0001t0019g0082a0001c0001t0019g0084a0001c0001t0019g0100others(2): Show | 5 | HG01891.hp2 HG02109.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-14663G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550509 | ||||||
| chr6:52550583
|
C | T | 5 | a0001c0001t0016g0037a0001c0001t0016g0039a0001c0001t0016g0193others(2): Show | 5 | HG02572.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.121-14737G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550583 | ||||||
| chr6:52550696
|
A | C | 345 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(342): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.121-14850T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550696 | ||||||
| chr6:52550712
|
C | T | 85 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(82): Show | 86 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.121-14866G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550712 | ||||||
| chr6:52550713
|
G | A | 4 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0195others(1): Show | 4 | HG01884.hp2 HG02559.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.121-14867C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550713 | ||||||
| chr6:52550792
|
TCCACCTG others(10): Show |
T | 49 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0284others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.121-14963_121-1494 others(21): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550792 | ||||||
| chr6:52550890
|
C | T | 4 | a0001c0001t0023g0018a0001c0001t0023g0022a0001c0001t0023g0023others(1): Show | 4 | HG00639.hp1 HG02735.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-15044G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550890 | ||||||
| chr6:52550968
|
G | C | 6 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0284others(3): Show | 6 | HG02027.hp2 NA18959.hp1 NA18964.hp1 others(3): Show |
intron_variant | MODIFIER | c.121-15122C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550968 | ||||||
| chr6:52550994
|
A | G | 2 | a0001c0001t0048g0013a0001c0001t0049g0012 | 2 | NA18941.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.121-15148T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550994 | ||||||
| chr6:52551008
|
A | G | 278 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(275): Show | 289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.121-15162T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52551008 | ||||||
| chr6:52551241
|
T | G | 46 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(43): Show | 46 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.121-15395A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52551241 | ||||||
| chr6:52551436
|
G | T | 2 | a0001c0001t0023g0023a0001c0001t0039g0318 | 2 | HG00639.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.121-15590C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52551436 | ||||||
| chr6:52551461
|
G | C | 85 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(82): Show | 86 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.121-15615C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52551461 | ||||||
| chr6:52551534
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.121-15688C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52551534 | ||||||
| chr6:52552009
|
G | A | 85 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(82): Show | 86 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.121-16163C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52552009 | ||||||
| chr6:52552023
|
C | T | 2 | a0001c0001t0022g0033a0001c0001t0022g0034 | 2 | HG00609.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.121-16177G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52552023 | ||||||
| chr6:52552215
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.121-16369A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52552215 | ||||||
| chr6:52552235
|
G | T | 9 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(6): Show | 10 | HG00140.hp1 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.121-16389C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52552235 | ||||||
| chr6:52552302
|
G | A | 85 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(82): Show | 86 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.121-16456C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52552302 | ||||||
| chr6:52552713
|
C | T | 67 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(64): Show | 74 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.121-16867G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52552713 | ||||||
| chr6:52552757
|
A | G | 49 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0284others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.121-16911T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52552757 | ||||||
| chr6:52552786
|
A | G | 1 | a0001c0001t0008g0282 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.121-16940T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52552786 | ||||||
| chr6:52552896
|
T | C | 1 | a0001c0001t0004g0306 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.121-17050A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52552896 | ||||||
| chr6:52553132
|
C | T | 4 | a0001c0001t0023g0018a0001c0001t0023g0022a0001c0001t0023g0023others(1): Show | 4 | HG00639.hp1 HG02735.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-17286G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52553132 | ||||||
| chr6:52553135
|
C | T | 3 | a0001c0001t0001g0200a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG02602.hp2 HG03017.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.121-17289G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52553135 | ||||||
| chr6:52553178
|
C | T | 1 | a0001c0001t0003g0080 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.121-17332G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52553178 | ||||||
| chr6:52553181
|
C | G | 1 | a0001c0001t0084g0349 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.121-17335G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52553181 | ||||||
| chr6:52553330
|
T | C | 167 | a0001c0001t0001g0224a0001c0001t0001g0285a0001c0001t0001g0286others(164): Show | 178 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.121-17484A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52553330 | ||||||
| chr6:52553577
|
C | T | 49 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0284others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.121-17731G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52553577 | ||||||
| chr6:52553604
|
T | A | 6 | a0001c0001t0006g0063a0001c0001t0006g0096a0001c0001t0009g0086others(3): Show | 6 | HG00735.hp1 HG01099.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.121-17758A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52553604 | ||||||
| chr6:52553711
|
T | C | 1 | a0001c0001t0011g0217 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.121-17865A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52553711 | ||||||
| chr6:52553907
|
A | G | 24 | a0001c0001t0006g0004a0001c0001t0017g0010a0001c0001t0017g0171others(21): Show | 28 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.121-18061T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52553907 | ||||||
| chr6:52554051
|
C | T | 4 | a0001c0001t0023g0018a0001c0001t0023g0022a0001c0001t0023g0023others(1): Show | 4 | HG00639.hp1 HG02735.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.121-18205G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554051 | ||||||
| chr6:52554063
|
C | T | 1 | a0001c0001t0071g0053 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.121-18217G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554063 | ||||||
| chr6:52554158
|
T | C | 35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.121-18312A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554158 | ||||||
| chr6:52554264
|
C | G | 6 | a0001c0001t0019g0082a0001c0001t0019g0084a0001c0001t0019g0100others(3): Show | 6 | HG01891.hp2 HG02109.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.121-18418G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554264 | ||||||
| chr6:52554346
|
G | A | 1 | a0001c0001t0027g0047 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.121-18500C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554346 | ||||||
| chr6:52554391
|
G | A | 49 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0284others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.121-18545C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554391 | ||||||
| chr6:52554464
|
G | A | 1 | a0001c0001t0043g0345 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.121-18618C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554464 | ||||||
| chr6:52554475
|
ATGTCACT others(11): Show |
A | 36 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(33): Show | 36 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.121-18647_121-1863 others(22): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554475 | ||||||
| chr6:52554519
|
C | CA | 39 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(36): Show | 39 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.121-18674dupT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554519 | ||||||
| chr6:52554519
|
C | CAA | 5 | a0001c0001t0003g0231a0001c0001t0006g0004a0001c0001t0029g0002others(2): Show | 8 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.121-18675_121-1867 others(6): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554519 | ||||||
| chr6:52554519
|
CA | C | 61 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(58): Show | 63 | HG00140.hp1 HG00558.hp2 HG00621.hp2 others(60): Show |
intron_variant | MODIFIER | c.121-18674delT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554519 | ||||||
| chr6:52554519
|
CAA | C | 148 | a0001c0001t0001g0089a0001c0001t0001g0094a0001c0001t0001g0099others(145): Show | 155 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(152): Show |
intron_variant | MODIFIER | c.121-18675_121-1867 others(6): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554519 | ||||||
| chr6:52554531
|
A | G | 2 | a0001c0001t0007g0250a0001c0001t0075g0249 | 2 | NA19010.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.121-18685T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554531 | ||||||
| chr6:52554535
|
A | G | 115 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(112): Show | 122 | HG00408.hp1 HG00558.hp1 HG00609.hp2 others(119): Show |
intron_variant | MODIFIER | c.121-18689T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554535 | ||||||
| chr6:52554572
|
C | T | 18 | a0001c0001t0005g0288a0001c0001t0007g0001a0001c0001t0007g0140others(15): Show | 21 | HG00558.hp1 HG02083.hp2 HG02155.hp2 others(18): Show |
intron_variant | MODIFIER | c.121-18726G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554572 | ||||||
| chr6:52554766
|
C | CT | 218 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(215): Show | 228 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.121-18921dupA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554766 | ||||||
| chr6:52554766
|
C | CTT | 19 | a0001c0001t0004g0104a0001c0001t0004g0110a0001c0001t0004g0137others(16): Show | 22 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(19): Show |
intron_variant | MODIFIER | c.121-18922_121-1892 others(6): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554766 | ||||||
| chr6:52554846
|
ACAGCCTC others(7): Show |
A | 1 | a0001c0001t0091g0301 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.121-19014_121-1900 others(18): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554846 | ||||||
| chr6:52554993
|
T | C | 85 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(82): Show | 86 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.121-19147A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52554993 | ||||||
| chr6:52555029
|
C | G | 3 | a0001c0001t0038g0352a0001c0001t0042g0350a0001c0001t0042g0351 | 3 | HG01891.hp1 HG02280.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.121-19183G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52555029 | ||||||
| chr6:52555071
|
T | C | 20 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(17): Show | 20 | HG01192.hp2 HG02735.hp1 HG02965.hp1 others(17): Show |
intron_variant | MODIFIER | c.121-19225A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52555071 | ||||||
| chr6:52555108
|
T | G | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.121-19262A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52555108 | ||||||
| chr6:52555391
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.121-19545T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52555391 | ||||||
| chr6:52555558
|
C | T | 6 | a0001c0001t0001g0154a0001c0001t0001g0334a0001c0001t0005g0133others(3): Show | 6 | NA18945.hp2 NA18962.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.121-19712G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52555558 | ||||||
| chr6:52555578
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.121-19732G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52555578 | ||||||
| chr6:52555776
|
A | G | 8 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0195others(5): Show | 8 | HG01884.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.121-19930T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52555776 | ||||||
| chr6:52555883
|
G | A | 85 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(82): Show | 86 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.121-20037C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52555883 | ||||||
| chr6:52555945
|
C | A | 24 | a0001c0001t0006g0300a0001c0001t0008g0009a0001c0001t0008g0258others(21): Show | 25 | HG01074.hp1 HG01074.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.121-20099G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52555945 | ||||||
| chr6:52555954
|
A | G | 35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.121-20108T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52555954 | ||||||
| chr6:52556285
|
CTT | C | 278 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(275): Show | 289 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.121-20441_121-2044 others(6): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556285 | ||||||
| chr6:52556449
|
T | C | 4 | a0001c0001t0023g0018a0001c0001t0023g0022a0001c0001t0023g0023others(1): Show | 4 | HG00639.hp1 HG02735.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+20347A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556449 | ||||||
| chr6:52556466
|
G | C | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.120+20330C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556466 | ||||||
| chr6:52556540
|
A | C | 14 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(11): Show | 15 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+20256T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556540 | ||||||
| chr6:52556597
|
T | C | 3 | a0001c0001t0038g0352a0001c0001t0042g0350a0001c0001t0042g0351 | 3 | HG01891.hp1 HG02280.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.120+20199A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556597 | ||||||
| chr6:52556609
|
G | A | 1 | a0001c0001t0021g0363 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.120+20187C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556609 | ||||||
| chr6:52556621
|
G | A | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.120+20175C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556621 | ||||||
| chr6:52556667
|
C | T | 1 | a0001c0001t0001g0050 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.120+20129G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556667 | ||||||
| chr6:52556709
|
C | T | 1 | a0001c0001t0009g0294 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.120+20087G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556709 | ||||||
| chr6:52556762
|
T | C | 56 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(53): Show | 57 | HG00639.hp1 HG01074.hp1 HG01074.hp2 others(54): Show |
intron_variant | MODIFIER | c.120+20034A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556762 | ||||||
| chr6:52556805
|
G | A | 35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.120+19991C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556805 | ||||||
| chr6:52556829
|
G | A | 1 | a0001c0002t0093g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.120+19967C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556829 | ||||||
| chr6:52556845
|
T | A | 49 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0284others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.120+19951A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556845 | ||||||
| chr6:52556846
|
T | C | 1 | a0001c0001t0005g0169 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.120+19950A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556846 | ||||||
| chr6:52556927
|
C | CA | 77 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0284others(74): Show | 82 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.120+19868dupT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556927 | ||||||
| chr6:52556927
|
CA | C | 150 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0054others(147): Show | 158 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(155): Show |
intron_variant | MODIFIER | c.120+19868delT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556927 | ||||||
| chr6:52556960
|
G | A | 1 | a0001c0001t0038g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.120+19836C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556960 | ||||||
| chr6:52556967
|
G | A | 24 | a0001c0001t0006g0300a0001c0001t0008g0009a0001c0001t0008g0258others(21): Show | 25 | HG01074.hp1 HG01074.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.120+19829C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556967 | ||||||
| chr6:52556985
|
G | T | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.120+19811C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556985 | ||||||
| chr6:52557171
|
A | C | 35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.120+19625T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52557171 | ||||||
| chr6:52557176
|
A | G | 35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.120+19620T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52557176 | ||||||
| chr6:52557180
|
A | G | 35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.120+19616T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52557180 | ||||||
| chr6:52557182
|
A | G | 35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.120+19614T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52557182 | ||||||
| chr6:52557192
|
C | CAAAAAAA others(5): Show |
35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.120+19603_120+1960 others(16): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52557192 | ||||||
| chr6:52557207
|
T | C | 25 | a0001c0001t0006g0004a0001c0001t0017g0010a0001c0001t0017g0171others(22): Show | 29 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.120+19589A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52557207 | ||||||
| chr6:52557624
|
T | G | 14 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(11): Show | 15 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+19172A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52557624 | ||||||
| chr6:52557791
|
T | C | 8 | a0001c0001t0031g0182a0001c0001t0031g0183a0001c0001t0031g0270others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.120+19005A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52557791 | ||||||
| chr6:52557930
|
G | A | 1 | a0001c0002t0093g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.120+18866C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52557930 | ||||||
| chr6:52558016
|
T | C | 8 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0195others(5): Show | 8 | HG01884.hp2 HG02559.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.120+18780A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52558016 | ||||||
| chr6:52558175
|
G | A | 35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.120+18621C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52558175 | ||||||
| chr6:52558181
|
C | A | 4 | a0001c0001t0006g0309a0001c0001t0006g0331a0001c0001t0092g0330others(1): Show | 4 | NA19000.hp1 NA19012.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+18615G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52558181 | ||||||
| chr6:52558317
|
C | T | 1 | a0001c0001t0051g0029 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.120+18479G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52558317 | ||||||
| chr6:52558380
|
C | G | 35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.120+18416G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52558380 | ||||||
| chr6:52558485
|
T | C | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.120+18311A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52558485 | ||||||
| chr6:52558843
|
G | C | 1 | a0001c0001t0084g0349 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.120+17953C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52558843 | ||||||
| chr6:52558949
|
C | T | 3 | a0001c0001t0006g0004a0001c0001t0029g0002a0001c0001t0030g0261 | 6 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.120+17847G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52558949 | ||||||
| chr6:52558961
|
CAG | C | 3 | a0001c0001t0003g0077a0001c0001t0003g0078a0001c0001t0003g0095 | 3 | HG01168.hp1 HG01169.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.120+17833_120+1783 others(6): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52558961 | ||||||
| chr6:52559058
|
T | C | 2 | a0001c0001t0027g0046a0001c0001t0027g0048 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.120+17738A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52559058 | ||||||
| chr6:52559113
|
T | C | 24 | a0001c0001t0002g0348a0001c0001t0004g0052a0001c0001t0004g0056others(21): Show | 24 | HG00639.hp1 HG01192.hp2 HG02735.hp1 others(21): Show |
intron_variant | MODIFIER | c.120+17683A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52559113 | ||||||
| chr6:52559217
|
G | A | 10 | a0001c0001t0006g0004a0001c0001t0019g0082a0001c0001t0019g0084others(7): Show | 13 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.120+17579C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52559217 | ||||||
| chr6:52559272
|
G | T | 1 | a0001c0002t0093g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.120+17524C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52559272 | ||||||
| chr6:52559326
|
A | G | 1 | a0001c0001t0006g0064 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.120+17470T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52559326 | ||||||
| chr6:52559337
|
C | G | 1 | a0001c0001t0097g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.120+17459G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52559337 | ||||||
| chr6:52559417
|
C | T | 1 | a0001c0001t0004g0108 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.120+17379G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52559417 | ||||||
| chr6:52559434
|
C | T | 1 | a0001c0001t0016g0267 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.120+17362G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52559434 | ||||||
| chr6:52559442
|
T | C | 32 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0195others(29): Show | 33 | HG01074.hp1 HG01074.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.120+17354A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52559442 | ||||||
| chr6:52559742
|
C | T | 1 | a0001c0002t0093g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.120+17054G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52559742 | ||||||
| chr6:52559780
|
T | C | 1 | a0001c0001t0089g0355 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.120+17016A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52559780 | ||||||
| chr6:52559852
|
T | C | 4 | a0001c0001t0006g0004a0001c0001t0029g0002a0001c0001t0030g0261others(1): Show | 7 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.120+16944A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52559852 | ||||||
| chr6:52559905
|
A | C | 1 | a0001c0001t0005g0133 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.120+16891T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52559905 | ||||||
| chr6:52559920
|
C | T | 198 | a0001c0001t0001g0224a0001c0001t0001g0285a0001c0001t0001g0286others(195): Show | 206 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.120+16876G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52559920 | ||||||
| chr6:52559962
|
C | T | 1 | a0001c0001t0003g0314 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.120+16834G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52559962 | ||||||
| chr6:52559963
|
G | A | 1 | a0001c0002t0093g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.120+16833C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52559963 | ||||||
| chr6:52560007
|
G | A | 1 | a0001c0001t0091g0301 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.120+16789C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52560007 | ||||||
| chr6:52560039
|
C | A | 213 | a0001c0001t0001g0224a0001c0001t0001g0285a0001c0001t0001g0286others(210): Show | 226 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(223): Show |
intron_variant | MODIFIER | c.120+16757G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52560039 | ||||||
| chr6:52560170
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.120+16626C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52560170 | ||||||
| chr6:52560175
|
C | T | 1 | a0001c0001t0006g0096 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.120+16621G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52560175 | ||||||
| chr6:52560249
|
T | TA | 10 | a0001c0001t0006g0300a0001c0001t0008g0290a0001c0001t0009g0294others(7): Show | 10 | HG00639.hp2 HG02109.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.120+16546dupT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52560249 | ||||||
| chr6:52560249
|
TA | T | 11 | a0001c0001t0006g0004a0001c0001t0007g0333a0001c0001t0018g0197others(8): Show | 14 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.120+16546delT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52560249 | ||||||
| chr6:52560282
|
A | G | 222 | a0001c0001t0001g0224a0001c0001t0001g0285a0001c0001t0001g0286others(219): Show | 231 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.120+16514T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52560282 | ||||||
| chr6:52560391
|
A | G | 308 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(305): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(315): Show |
intron_variant | MODIFIER | c.120+16405T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52560391 | ||||||
| chr6:52560463
|
C | T | 2 | a0001c0001t0007g0250a0001c0001t0075g0249 | 2 | NA19010.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.120+16333G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52560463 | ||||||
| chr6:52560577
|
T | C | 2 | a0001c0001t0090g0273a0001c0001t0091g0301 | 2 | HG02486.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.120+16219A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52560577 | ||||||
| chr6:52560595
|
G | A | 87 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(84): Show | 88 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.120+16201C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52560595 | ||||||
| chr6:52560658
|
C | T | 86 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(83): Show | 87 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.120+16138G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52560658 | ||||||
| chr6:52560722
|
A | G | 1 | a0001c0002t0093g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.120+16074T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52560722 | ||||||
| chr6:52560879
|
C | G | 3 | a0001c0001t0008g0070a0001c0001t0008g0071a0001c0001t0085g0190 | 3 | HG03540.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.120+15917G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52560879 | ||||||
| chr6:52560944
|
C | T | 1 | a0001c0001t0056g0032 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.120+15852G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52560944 | ||||||
| chr6:52561284
|
C | T | 1 | a0001c0001t0001g0205 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.120+15512G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52561284 | ||||||
| chr6:52561395
|
G | A | 65 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(62): Show | 72 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.120+15401C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52561395 | ||||||
| chr6:52561427
|
T | C | 2 | a0001c0001t0003g0079a0001c0001t0003g0213 | 2 | NA18941.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.120+15369A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52561427 | ||||||
| chr6:52561434
|
C | T | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.120+15362G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52561434 | ||||||
| chr6:52561487
|
C | CT | 104 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(101): Show | 108 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.120+15308dupA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52561487 | ||||||
| chr6:52561487
|
CT | C | 82 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0003g0044others(79): Show | 83 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(80): Show |
intron_variant | MODIFIER | c.120+15308delA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52561487 | ||||||
| chr6:52561525
|
G | A | 2 | a0001c0001t0038g0352a0001c0001t0042g0351 | 2 | HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.120+15271C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52561525 | ||||||
| chr6:52561578
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.120+15218G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52561578 | ||||||
| chr6:52561611
|
G | A | 86 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(83): Show | 87 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.120+15185C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52561611 | ||||||
| chr6:52561724
|
C | T | 1 | a0001c0001t0100g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.120+15072G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52561724 | ||||||
| chr6:52561736
|
G | A | 9 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(6): Show | 10 | HG00140.hp1 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.120+15060C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52561736 | ||||||
| chr6:52561853
|
C | T | 3 | a0001c0001t0003g0074a0001c0001t0003g0092a0001c0001t0003g0093 | 3 | HG01069.hp1 HG01071.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.120+14943G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52561853 | ||||||
| chr6:52561854
|
C | T | 65 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(62): Show | 72 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.120+14942G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52561854 | ||||||
| chr6:52561887
|
C | T | 1 | a0001c0001t0097g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.120+14909G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52561887 | ||||||
| chr6:52561958
|
G | A | 1 | a0001c0001t0016g0267 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.120+14838C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52561958 | ||||||
| chr6:52561961
|
G | A | 66 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(63): Show | 73 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.120+14835C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52561961 | ||||||
| chr6:52561983
|
CTAAAAAT others(17): Show |
C | 162 | a0001c0001t0001g0224a0001c0001t0001g0285a0001c0001t0001g0286others(159): Show | 170 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(167): Show |
intron_variant | MODIFIER | c.120+14789_120+1481 others(28): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52561983 | ||||||
| chr6:52562079
|
T | G | 1 | a0001c0001t0002g0227 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.120+14717A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52562079 | ||||||
| chr6:52562081
|
C | A | 1 | a0001c0001t0018g0287 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.120+14715G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52562081 | ||||||
| chr6:52562081
|
C | CA | 140 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0200others(137): Show | 148 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(145): Show |
intron_variant | MODIFIER | c.120+14714dupT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52562081 | ||||||
| chr6:52562278
|
G | A | 3 | a0001c0001t0038g0352a0001c0001t0042g0350a0001c0001t0042g0351 | 3 | HG01891.hp1 HG02280.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.120+14518C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52562278 | ||||||
| chr6:52562386
|
A | G | 1 | a0001c0001t0003g0069 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.120+14410T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52562386 | ||||||
| chr6:52562396
|
G | A | 1 | a0001c0001t0066g0335 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.120+14400C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52562396 | ||||||
| chr6:52562466
|
G | C | 12 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0006g0195others(9): Show | 12 | HG00639.hp1 HG01884.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.120+14330C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52562466 | ||||||
| chr6:52562540
|
C | T | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.120+14256G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52562540 | ||||||
| chr6:52562585
|
G | T | 1 | a0001c0001t0006g0004 | 2 | HG02258.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.120+14211C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52562585 | ||||||
| chr6:52562598
|
T | C | 1 | a0001c0001t0097g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.120+14198A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52562598 | ||||||
| chr6:52562808
|
T | C | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.120+13988A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52562808 | ||||||
| chr6:52562941
|
G | A | 156 | a0001c0001t0001g0224a0001c0001t0001g0285a0001c0001t0001g0286others(153): Show | 164 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.120+13855C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52562941 | ||||||
| chr6:52563113
|
C | G | 1 | a0001c0001t0004g0160 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.120+13683G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563113 | ||||||
| chr6:52563238
|
T | A | 14 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(11): Show | 15 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+13558A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563238 | ||||||
| chr6:52563263
|
T | C | 1 | a0001c0001t0097g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.120+13533A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563263 | ||||||
| chr6:52563280
|
T | G | 1 | a0001c0001t0081g0129 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.120+13516A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563280 | ||||||
| chr6:52563332
|
A | G | 9 | a0001c0001t0006g0004a0001c0001t0019g0082a0001c0001t0019g0084others(6): Show | 12 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.120+13464T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563332 | ||||||
| chr6:52563335
|
G | C | 14 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(11): Show | 15 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+13461C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563335 | ||||||
| chr6:52563441
|
C | T | 1 | a0001c0001t0025g0358 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.120+13355G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563441 | ||||||
| chr6:52563505
|
G | A | 49 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0284others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.120+13291C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563505 | ||||||
| chr6:52563514
|
T | C | 35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.120+13282A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563514 | ||||||
| chr6:52563592
|
G | A | 1 | a0001c0003t0015g0307 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.120+13204C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563592 | ||||||
| chr6:52563603
|
C | CAGCT | 3 | a0001c0001t0033g0186a0001c0001t0033g0187a0001c0001t0057g0188 | 3 | HG03041.hp1 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.120+13189_120+1319 others(8): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563603 | ||||||
| chr6:52563694
|
C | CA | 81 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0054others(78): Show | 82 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.120+13101dupT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563694 | ||||||
| chr6:52563694
|
C | CAA | 11 | a0001c0001t0001g0051a0001c0001t0001g0153a0001c0001t0001g0154others(8): Show | 11 | HG02027.hp1 NA18940.hp2 NA18941.hp2 others(8): Show |
intron_variant | MODIFIER | c.120+13100_120+1310 others(6): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563694 | ||||||
| chr6:52563694
|
CA | C | 60 | a0001c0001t0002g0072a0001c0001t0002g0218a0001c0001t0003g0044others(57): Show | 60 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.120+13101delT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563694 | ||||||
| chr6:52563694
|
CAA | C | 92 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0284others(89): Show | 98 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.120+13100_120+1310 others(6): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563694 | ||||||
| chr6:52563736
|
G | A | 18 | a0001c0001t0005g0288a0001c0001t0007g0001a0001c0001t0007g0140others(15): Show | 21 | HG00558.hp1 HG02083.hp2 HG02155.hp2 others(18): Show |
intron_variant | MODIFIER | c.120+13060C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563736 | ||||||
| chr6:52563851
|
A | AT | 84 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(81): Show | 91 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.120+12944dupA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563851 | ||||||
| chr6:52563851
|
A | ATT | 12 | a0001c0001t0004g0052a0001c0001t0004g0056a0001c0001t0004g0139others(9): Show | 12 | HG02735.hp1 HG03491.hp2 HG03540.hp2 others(9): Show |
intron_variant | MODIFIER | c.120+12943_120+1294 others(6): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563851 | ||||||
| chr6:52563851
|
A | ATTT | 7 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0013g0073others(4): Show | 7 | NA18944.hp1 NA18953.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+12942_120+1294 others(7): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563851 | ||||||
| chr6:52563851
|
AT | A | 75 | a0001c0001t0001g0132a0001c0001t0001g0162a0001c0001t0001g0285others(72): Show | 80 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.120+12944delA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563851 | ||||||
| chr6:52563877
|
G | A | 1 | a0001c0001t0011g0058 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.120+12919C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563877 | ||||||
| chr6:52563900
|
C | CA | 324 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(321): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.120+12895dupT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563900 | ||||||
| chr6:52563989
|
G | A | 1 | a0001c0001t0084g0349 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.120+12807C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563989 | ||||||
| chr6:52564099
|
T | C | 1 | a0001c0001t0038g0173 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.120+12697A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52564099 | ||||||
| chr6:52564179
|
G | A | 1 | a0001c0001t0050g0014 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.120+12617C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52564179 | ||||||
| chr6:52564252
|
G | A | 2 | a0001c0001t0006g0004a0001c0001t0029g0002 | 5 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+12544C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52564252 | ||||||
| chr6:52564325
|
G | A | 25 | a0001c0001t0006g0300a0001c0001t0008g0009a0001c0001t0008g0258others(22): Show | 26 | HG01074.hp1 HG01074.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.120+12471C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52564325 | ||||||
| chr6:52564664
|
C | T | 334 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(331): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.120+12132G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52564664 | ||||||
| chr6:52565072
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.120+11724G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52565072 | ||||||
| chr6:52565292
|
T | G | 1 | a0001c0001t0003g0164 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.120+11504A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52565292 | ||||||
| chr6:52565423
|
G | A | 31 | a0001c0001t0005g0170a0001c0001t0017g0010a0001c0001t0017g0171others(28): Show | 32 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.120+11373C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52565423 | ||||||
| chr6:52565709
|
C | T | 3 | a0001c0001t0006g0004a0001c0001t0029g0002a0001c0001t0080g0180 | 6 | HG00741.hp2 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.120+11087G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52565709 | ||||||
| chr6:52565748
|
A | C | 1 | a0001c0002t0028g0357 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.120+11048T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52565748 | ||||||
| chr6:52565805
|
G | A | 4 | a0001c0001t0003g0069a0001c0001t0003g0077a0001c0001t0003g0078others(1): Show | 4 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+10991C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52565805 | ||||||
| chr6:52565947
|
G | A | 35 | a0001c0001t0003g0044a0001c0001t0003g0060a0001c0001t0003g0062others(32): Show | 35 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.120+10849C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52565947 | ||||||
| chr6:52565984
|
T | C | 1 | a0001c0001t0003g0078 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.120+10812A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52565984 | ||||||
| chr6:52566043
|
G | A | 1 | a0001c0001t0006g0195 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.120+10753C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52566043 | ||||||
| chr6:52566109
|
A | G | 1 | a0001c0001t0004g0105 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.120+10687T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52566109 | ||||||
| chr6:52566125
|
G | T | 24 | a0001c0001t0006g0300a0001c0001t0008g0009a0001c0001t0008g0258others(21): Show | 25 | HG01074.hp1 HG01074.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.120+10671C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52566125 | ||||||
| chr6:52566163
|
G | A | 1 | a0001c0002t0093g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.120+10633C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52566163 | ||||||
| chr6:52566294
|
T | C | 1 | a0001c0002t0093g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.120+10502A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52566294 | ||||||
| chr6:52566443
|
C | A | 2 | a0001c0001t0040g0262a0001c0001t0040g0263 | 2 | HG01074.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.120+10353G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52566443 | ||||||
| chr6:52566487
|
A | T | 151 | a0001c0001t0001g0224a0001c0001t0001g0285a0001c0001t0001g0286others(148): Show | 162 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.120+10309T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52566487 | ||||||
| chr6:52566510
|
G | T | 1 | a0001c0001t0036g0321 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.120+10286C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52566510 | ||||||
| chr6:52566605
|
C | T | 119 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(116): Show | 121 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(118): Show |
intron_variant | MODIFIER | c.120+10191G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52566605 | ||||||
| chr6:52566640
|
C | T | 14 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(11): Show | 15 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+10156G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52566640 | ||||||
| chr6:52566661
|
A | T | 86 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(83): Show | 87 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.120+10135T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52566661 | ||||||
| chr6:52566710
|
C | T | 25 | a0001c0001t0006g0300a0001c0001t0008g0009a0001c0001t0008g0258others(22): Show | 26 | HG01074.hp1 HG01074.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.120+10086G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52566710 | ||||||
| chr6:52566884
|
G | A | 2 | a0001c0001t0023g0023a0001c0001t0039g0318 | 2 | HG00639.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.120+9912C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52566884 | ||||||
| chr6:52566920
|
G | A | 1 | a0001c0001t0032g0031 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.120+9876C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52566920 | ||||||
| chr6:52567040
|
T | C | 1 | a0001c0001t0003g0081 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.120+9756A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52567040 | ||||||
| chr6:52567089
|
A | G | 20 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(17): Show | 21 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.120+9707T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52567089 | ||||||
| chr6:52567154
|
T | C | 7 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(4): Show | 8 | HG00140.hp1 HG00642.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.120+9642A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52567154 | ||||||
| chr6:52567220
|
C | T | 14 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(11): Show | 15 | HG00140.hp1 HG00609.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.120+9576G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52567220 | ||||||
| chr6:52567221
|
G | A | 49 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0284others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.120+9575C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52567221 | ||||||
| chr6:52567229
|
T | C | 1 | a0001c0001t0030g0344 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.120+9567A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52567229 | ||||||
| chr6:52567323
|
C | A | 93 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(90): Show | 94 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.120+9473G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52567323 | ||||||
| chr6:52567365
|
T | C | 1 | a0001c0001t0069g0212 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.120+9431A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52567365 | ||||||
| chr6:52567409
|
G | A | 6 | a0001c0001t0001g0154a0001c0001t0001g0334a0001c0001t0005g0133others(3): Show | 6 | NA18945.hp2 NA18962.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.120+9387C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52567409 | ||||||
| chr6:52567546
|
T | C | 49 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0284others(46): Show | 50 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.120+9250A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52567546 | ||||||
| chr6:52567599
|
T | C | 1 | a0001c0001t0097g0356 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.120+9197A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52567599 | ||||||
| chr6:52567910
|
A | G | 36 | a0001c0001t0001g0094a0001c0001t0003g0044a0001c0001t0003g0060others(33): Show | 36 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.120+8886T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52567910 | ||||||
| chr6:52567949
|
C | T | 25 | a0001c0001t0006g0300a0001c0001t0008g0009a0001c0001t0008g0258others(22): Show | 26 | HG01074.hp1 HG01074.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.120+8847G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52567949 | ||||||
| chr6:52567975
|
G | A | 269 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(266): Show | 282 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.120+8821C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52567975 | ||||||
| chr6:52568000
|
C | T | 25 | a0001c0001t0006g0300a0001c0001t0008g0009a0001c0001t0008g0258others(22): Show | 26 | HG01074.hp1 HG01074.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.120+8796G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52568000 | ||||||
| chr6:52568053
|
T | C | 5 | a0001c0001t0001g0094a0001c0001t0003g0069a0001c0001t0003g0077others(2): Show | 5 | HG01070.hp1 HG01123.hp1 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+8743A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52568053 | ||||||
| chr6:52568139
|
C | A | 151 | a0001c0001t0001g0224a0001c0001t0001g0285a0001c0001t0001g0286others(148): Show | 162 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.120+8657G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52568139 | ||||||
| chr6:52568140
|
C | T | 1 | a0001c0002t0093g0272 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.120+8656G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52568140 | ||||||
| chr6:52568165
|
G | A | 3 | a0001c0001t0008g0070a0001c0001t0008g0071a0001c0001t0085g0190 | 3 | HG03540.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.120+8631C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52568165 | ||||||
| chr6:52568676
|
T | C | 85 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(82): Show | 86 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.120+8120A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52568676 | ||||||
| chr6:52568949
|
C | T | 4 | a0001c0001t0023g0018a0001c0001t0023g0022a0001c0001t0023g0023others(1): Show | 4 | HG00639.hp1 HG02735.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+7847G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52568949 | ||||||
| chr6:52569039
|
T | G | 1 | a0001c0001t0035g0066 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.120+7757A>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52569039 | ||||||
| chr6:52569096
|
A | G | 36 | a0001c0001t0001g0094a0001c0001t0003g0044a0001c0001t0003g0060others(33): Show | 36 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.120+7700T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52569096 | ||||||
| chr6:52569159
|
C | A | 66 | a0001c0001t0001g0224a0001c0001t0002g0003a0001c0001t0002g0007others(63): Show | 73 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.120+7637G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52569159 | ||||||
| chr6:52569212
|
T | C | 4 | a0001c0001t0019g0207a0001c0001t0043g0208a0001c0001t0043g0345others(1): Show | 4 | HG01358.hp2 HG02630.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.120+7584A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52569212 | ||||||
| chr6:52569280
|
C | A | 9 | a0001c0001t0017g0010a0001c0001t0017g0171a0001c0001t0017g0323others(6): Show | 10 | HG00140.hp1 HG00642.hp1 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.120+7516G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52569280 | ||||||
| chr6:52569315
|
G | T | 3 | a0001c0001t0033g0186a0001c0001t0033g0187a0001c0001t0057g0188 | 3 | HG03041.hp1 HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.120+7481C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52569315 | ||||||
| chr6:52569388
|
TA | T | 179 | a0001c0001t0001g0094a0001c0001t0001g0224a0001c0001t0001g0285others(176): Show | 190 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.120+7407delT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52569388 | ||||||
| chr6:52569388
|
TAA | T | 143 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(140): Show | 146 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.120+7406_120+7407d others(4): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52569388 | ||||||
| chr6:52569388
|
TAAA | T | 9 | a0001c0001t0001g0166a0001c0001t0019g0082a0001c0001t0019g0084others(6): Show | 9 | HG01167.hp1 HG01891.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.120+7405_120+7407d others(5): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52569388 | ||||||
| chr6:52569404
|
A | G | 16 | a0001c0001t0001g0094a0001c0001t0003g0069a0001c0001t0003g0074others(13): Show | 16 | HG00099.hp2 HG01069.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.120+7392T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52569404 | ||||||
| chr6:52569409
|
A | G | 25 | a0001c0001t0006g0300a0001c0001t0008g0009a0001c0001t0008g0258others(22): Show | 26 | HG01074.hp1 HG01074.hp2 HG01123.hp2 others(23): Show |
intron_variant | MODIFIER | c.120+7387T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52569409 | ||||||
| chr6:52569499
|
A | G | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.120+7297T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52569499 | ||||||
| chr6:52569567
|
C | A | 2 | a0001c0001t0090g0273a0001c0001t0091g0301 | 2 | HG02486.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.120+7229G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52569567 | ||||||
| chr6:52569628
|
C | T | 85 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(82): Show | 86 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.120+7168G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52569628 | ||||||
| chr6:52569659
|
C | T | 2 | a0001c0001t0084g0349a0001c0001t0100g0067 | 2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.120+7137G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52569659 | ||||||
| chr6:52569800
|
G | C | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.120+6996C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52569800 | ||||||
| chr6:52570062
|
G | A | 1 | a0001c0001t0096g0155 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.120+6734C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52570062 | ||||||
| chr6:52570200
|
C | G | 183 | a0001c0001t0001g0094a0001c0001t0001g0224a0001c0001t0001g0285others(180): Show | 194 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.120+6596G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52570200 | ||||||
| chr6:52570445
|
C | G | 39 | a0001c0001t0001g0094a0001c0001t0003g0044a0001c0001t0003g0060others(36): Show | 39 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.120+6351G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52570445 | ||||||
| chr6:52570460
|
T | C | 1 | a0001c0001t0068g0313 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.120+6336A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52570460 | ||||||
| chr6:52570795
|
A | AC | 63 | a0001c0001t0001g0094a0001c0001t0001g0099a0001c0001t0001g0165others(60): Show | 65 | HG00099.hp1 HG00609.hp2 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.120+6000dupG | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52570795 | ||||||
| chr6:52570795
|
A | ACC | 45 | a0001c0001t0001g0089a0001c0001t0002g0072a0001c0001t0003g0044others(42): Show | 46 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(43): Show |
intron_variant | MODIFIER | c.120+5999_120+6000d others(4): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52570795 | ||||||
| chr6:52570800
|
C | T | 12 | a0001c0001t0002g0211a0001c0001t0010g0019a0001c0001t0010g0025others(9): Show | 12 | HG00639.hp1 HG01928.hp2 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.120+5996G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52570800 | ||||||
| chr6:52570803
|
C | CCCCCG | 55 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(52): Show | 56 | HG00544.hp2 HG00558.hp2 HG01258.hp2 others(53): Show |
intron_variant | MODIFIER | c.120+5992_120+5993i others(7): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52570803 | ||||||
| chr6:52570803
|
C | CCCCG | 52 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0142others(49): Show | 53 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.120+5992_120+5993i others(6): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52570803 | ||||||
| chr6:52570803
|
C | CCCG | 28 | a0001c0001t0001g0157a0001c0001t0004g0056a0001c0001t0004g0311others(25): Show | 28 | HG00280.hp1 HG01106.hp1 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.120+5992_120+5993i others(5): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52570803 | ||||||
| chr6:52570803
|
C | G | 1 | a0001c0001t0014g0057 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.120+5993G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52570803 | ||||||
| chr6:52570805
|
C | A | 1 | a0001c0001t0002g0266 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.120+5991G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52570805 | ||||||
| chr6:52570807
|
A | C | 147 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(144): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.120+5989T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52570807 | ||||||
| chr6:52570974
|
T | A | 2 | a0001c0001t0003g0341a0001c0001t0003g0342 | 2 | HG02135.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.120+5822A>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52570974 | ||||||
| chr6:52570976
|
T | C | 12 | a0001c0001t0005g0068a0001c0001t0010g0019a0001c0001t0010g0025others(9): Show | 12 | HG00639.hp1 HG01358.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.120+5820A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52570976 | ||||||
| chr6:52571025
|
G | A | 29 | a0001c0001t0001g0334a0001c0001t0003g0332a0001c0001t0005g0068others(26): Show | 29 | HG00609.hp1 HG00639.hp1 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.120+5771C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52571025 | ||||||
| chr6:52571069
|
TC | T | 13 | a0001c0001t0002g0072a0001c0001t0006g0035a0001c0001t0006g0036others(10): Show | 13 | HG01884.hp2 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.120+5726delG | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52571069 | ||||||
| chr6:52571076
|
C | A | 3 | a0001c0001t0078g0338a0001c0001t0098g0337a0001c0001t0099g0339 | 3 | HG01106.hp2 HG01243.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.120+5720G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52571076 | ||||||
| chr6:52571216
|
T | C | 1 | a0001c0001t0057g0188 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.120+5580A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52571216 | ||||||
| chr6:52571231
|
C | T | 7 | a0001c0001t0006g0191a0001c0001t0033g0186a0001c0001t0033g0187others(4): Show | 7 | HG02257.hp2 HG02451.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.120+5565G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52571231 | ||||||
| chr6:52571294
|
G | C | 2 | a0001c0001t0003g0341a0001c0001t0003g0342 | 2 | HG02135.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.120+5502C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52571294 | ||||||
| chr6:52571357
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.120+5439C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52571357 | ||||||
| chr6:52571432
|
G | A | 2 | a0001c0001t0008g0277a0001c0001t0105g0276 | 2 | HG01928.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.120+5364C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52571432 | ||||||
| chr6:52571432
|
G | C | 3 | a0001c0001t0001g0346a0001c0001t0002g0348a0001c0001t0020g0347 | 3 | HG02155.hp1 NA18952.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.120+5364C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52571432 | ||||||
| chr6:52571556
|
A | T | 350 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(347): Show | 365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.120+5240T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52571556 | ||||||
| chr6:52571687
|
G | C | 3 | a0001c0001t0001g0346a0001c0001t0002g0348a0001c0001t0020g0347 | 3 | HG02155.hp1 NA18952.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.120+5109C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52571687 | ||||||
| chr6:52571850
|
G | A | 21 | a0001c0001t0010g0015a0001c0001t0010g0019a0001c0001t0010g0025others(18): Show | 21 | HG00639.hp1 HG01358.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.120+4946C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52571850 | ||||||
| chr6:52571866
|
G | A | 42 | a0001c0001t0001g0089a0001c0001t0001g0094a0001c0001t0001g0099others(39): Show | 45 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.120+4930C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52571866 | ||||||
| chr6:52571894
|
A | C | 103 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(100): Show | 104 | HG00099.hp2 HG00408.hp1 HG00544.hp2 others(101): Show |
intron_variant | MODIFIER | c.120+4902T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52571894 | ||||||
| chr6:52572227
|
G | C | 112 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0203others(109): Show | 121 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.120+4569C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52572227 | ||||||
| chr6:52572402
|
A | G | 353 | a0001c0001t0001g0005a0001c0001t0001g0050a0001c0001t0001g0051others(350): Show | 368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.120+4394T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52572402 | ||||||
| chr6:52572451
|
A | C | 7 | a0001c0001t0006g0191a0001c0001t0025g0281a0001c0001t0033g0186others(4): Show | 7 | HG02257.hp2 HG02886.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.120+4345T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52572451 | ||||||
| chr6:52572584
|
C | G | 5 | a0001c0001t0009g0184a0001c0001t0031g0182a0001c0001t0031g0183others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.120+4212G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52572584 | ||||||
| chr6:52572746
|
G | A | 3 | a0001c0001t0003g0341a0001c0001t0003g0342a0001c0001t0004g0340 | 3 | HG02135.hp1 NA19062.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.120+4050C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52572746 | ||||||
| chr6:52572869
|
C | G | 15 | a0001c0001t0010g0015a0001c0001t0010g0019a0001c0001t0010g0025others(12): Show | 15 | HG00639.hp1 HG01358.hp2 HG01928.hp2 others(12): Show |
intron_variant | MODIFIER | c.120+3927G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52572869 | ||||||
| chr6:52572996
|
C | G | 112 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0203others(109): Show | 121 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(118): Show |
intron_variant | MODIFIER | c.120+3800G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52572996 | ||||||
| chr6:52573047
|
C | T | 3 | a0001c0001t0038g0352a0001c0001t0042g0350a0001c0001t0042g0351 | 3 | HG01891.hp1 HG02280.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.120+3749G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52573047 | ||||||
| chr6:52573240
|
C | T | 3 | a0001c0001t0038g0352a0001c0001t0042g0350a0001c0001t0042g0351 | 3 | HG01891.hp1 HG02280.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.120+3556G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52573240 | ||||||
| chr6:52573305
|
A | G | 155 | a0001c0001t0001g0089a0001c0001t0001g0094a0001c0001t0001g0099others(152): Show | 167 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(164): Show |
intron_variant | MODIFIER | c.120+3491T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52573305 | ||||||
| chr6:52573552
|
G | C | 3 | a0001c0001t0008g0271a0001c0001t0090g0273a0001c0002t0093g0272 | 3 | HG02615.hp2 HG02818.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.120+3244C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52573552 | ||||||
| chr6:52573577
|
G | A | 3 | a0001c0001t0001g0346a0001c0001t0002g0348a0001c0001t0020g0347 | 3 | HG02155.hp1 NA18952.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.120+3219C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52573577 | ||||||
| chr6:52573594
|
C | T | 1 | a0002c0004t0024g0359 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.120+3202G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52573594 | ||||||
| chr6:52573701
|
A | T | 1 | a0001c0001t0005g0068 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.120+3095T>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52573701 | ||||||
| chr6:52573789
|
G | A | 1 | a0001c0001t0080g0180 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.120+3007C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52573789 | ||||||
| chr6:52573871
|
C | T | 2 | a0001c0001t0035g0066a0001c0001t0100g0067 | 2 | HG02451.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.120+2925G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52573871 | ||||||
| chr6:52573946
|
A | G | 1 | a0001c0001t0074g0275 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.120+2850T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52573946 | ||||||
| chr6:52573956
|
G | A | 3 | a0001c0001t0004g0354a0001c0001t0006g0353a0001c0001t0089g0355 | 3 | HG01192.hp2 HG02622.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.120+2840C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52573956 | ||||||
| chr6:52574059
|
C | A | 1 | a0001c0001t0056g0032 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.120+2737G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52574059 | ||||||
| chr6:52574059
|
C | T | 6 | a0001c0001t0003g0060a0001c0001t0003g0062a0001c0001t0006g0061others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.120+2737G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52574059 | ||||||
| chr6:52574231
|
C | A | 1 | a0001c0001t0003g0274 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.120+2565G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52574231 | ||||||
| chr6:52574269
|
T | C | 3 | a0001c0001t0030g0343a0001c0001t0030g0344a0001c0001t0043g0345 | 3 | HG01175.hp1 HG03579.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.120+2527A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52574269 | ||||||
| chr6:52574428
|
C | T | 3 | a0001c0001t0097g0356a0001c0002t0028g0011a0001c0002t0028g0357 | 4 | HG01243.hp2 HG02965.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.120+2368G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52574428 | ||||||
| chr6:52574607
|
T | C | 98 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0203others(95): Show | 106 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.120+2189A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52574607 | ||||||
| chr6:52574643
|
A | G | 11 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0054others(8): Show | 11 | HG01496.hp2 HG01975.hp1 HG02004.hp1 others(8): Show |
intron_variant | MODIFIER | c.120+2153T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52574643 | ||||||
| chr6:52574934
|
C | T | 11 | a0001c0001t0001g0346a0001c0001t0002g0348a0001c0001t0009g0184others(8): Show | 11 | HG02155.hp1 HG02615.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.120+1862G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52574934 | ||||||
| chr6:52575049
|
C | A | 1 | a0001c0001t0074g0275 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.120+1747G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52575049 | ||||||
| chr6:52575061
|
C | T | 74 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0334others(71): Show | 76 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.120+1735G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52575061 | ||||||
| chr6:52575311
|
G | A | 10 | a0001c0001t0006g0191a0001c0001t0009g0184a0001c0001t0031g0182others(7): Show | 10 | HG02257.hp2 HG02615.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.120+1485C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52575311 | ||||||
| chr6:52575375
|
C | T | 6 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0004g0284others(3): Show | 6 | HG02027.hp2 NA18947.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.120+1421G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52575375 | ||||||
| chr6:52575540
|
CCT | C | 96 | a0001c0001t0001g0199a0001c0001t0001g0200a0001c0001t0001g0203others(93): Show | 104 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.120+1254_120+1255d others(4): Show |
TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52575540 | ||||||
| chr6:52575809
|
T | C | 7 | a0001c0001t0008g0277a0001c0001t0008g0282a0001c0001t0012g0279others(4): Show | 7 | HG01123.hp2 HG01884.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.120+987A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52575809 | ||||||
| chr6:52576012
|
T | C | 1 | a0001c0001t0008g0283 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.120+784A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52576012 | ||||||
| chr6:52576172
|
G | A | 70 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0334others(67): Show | 72 | HG00099.hp1 HG00408.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.120+624C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52576172 | ||||||
| chr6:52576271
|
G | A | 1 | a0001c0001t0084g0349 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.120+525C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52576271 | ||||||
| chr6:52576280
|
C | T | 1 | a0001c0001t0006g0035 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.120+516G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52576280 | ||||||
| chr6:52576431
|
G | A | 3 | a0001c0001t0016g0037a0001c0001t0016g0039a0001c0001t0044g0038 | 3 | HG02572.hp1 HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.120+365C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52576431 | ||||||
| chr6:52576630
|
G | A | 9 | a0001c0001t0004g0354a0001c0001t0006g0353a0001c0001t0038g0352others(6): Show | 10 | HG01192.hp2 HG01243.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.120+166C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52576630 | ||||||
| chr6:52576689
|
G | C | 1 | a0001c0001t0025g0358 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.120+107C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52576689 | ||||||
| chr6:52576751
|
A | G | 1 | a0001c0001t0012g0040 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.120+45T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52576751 | ||||||
| chr6:52576785
|
C | T | 5 | a0001c0001t0006g0035a0001c0001t0006g0036a0001c0001t0016g0037others(2): Show | 5 | HG02559.hp1 HG02572.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.120+11G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52576785 |