Item | Value |
---|---|
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 | 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 | MAFRR others(365): Show |
chr6 | 52492408 | 52582060 |
a0002 | 0/0 | 370 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | MAFRR others(365): Show |
chr6 | 52492408 | 52582060 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1110 | 370 | 87 | 71 | 154 | 16 | 40 | TRAM2_chr6_52492408_52582060 | TRAM2 | ATGGC others(1105): Show |
chr6 | 52492408 | 52582060 | ||
a0001c0002 | 0/0 | 1110 | 4 | 3 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | ATGGC others(1105): Show |
chr6 | 52492408 | 52582060 | ||
a0001c0003 | 0/0 | 1110 | 3 | 0 | 0 | 0 | 0 | 3 | TRAM2_chr6_52492408_52582060 | TRAM2 | ATGGC others(1105): Show |
chr6 | 52492408 | 52582060 | ||
a0002c0004 | 0/0 | 1110 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | ATGGC others(1105): Show |
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 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0002 | 0/0 | 7046 | 26 | 2 | 11 | 7 | 0 | 6 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0003 | 0/0 | 7046 | 26 | 0 | 9 | 12 | 1 | 4 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0004 | 0/0 | 7046 | 22 | 1 | 1 | 19 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0005 | 1/0 | 7047 | 21 | 10 | 5 | 2 | 2 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7042): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0006 | 0/1 | 7043 | 18 | 2 | 2 | 6 | 6 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7038): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0007 | 0/0 | 7044 | 17 | 0 | 0 | 17 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7039): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0008 | 0/0 | 7046 | 16 | 14 | 2 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0009 | 0/0 | 7046 | 10 | 7 | 2 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0010 | 0/0 | 7046 | 7 | 6 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0011 | 0/0 | 7046 | 6 | 0 | 5 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0012 | 0/0 | 7047 | 6 | 0 | 0 | 6 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7042): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0013 | 0/0 | 7047 | 5 | 5 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7042): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0014 | 0/0 | 7046 | 5 | 0 | 0 | 5 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0015 | 0/0 | 7046 | 5 | 0 | 0 | 5 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0016 | 0/0 | 7046 | 3 | 0 | 0 | 2 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0017 | 0/0 | 7046 | 5 | 1 | 2 | 0 | 2 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0018 | 0/0 | 7046 | 4 | 0 | 0 | 2 | 0 | 2 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0019 | 0/0 | 7046 | 4 | 4 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0020 | 0/0 | 7047 | 4 | 0 | 1 | 3 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7042): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0022 | 0/0 | 7046 | 4 | 0 | 1 | 0 | 2 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0023 | 0/0 | 7046 | 3 | 0 | 1 | 0 | 0 | 2 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0024 | 0/0 | 7046 | 3 | 0 | 0 | 3 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0025 | 0/0 | 7046 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0026 | 0/0 | 7046 | 3 | 2 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0027 | 0/0 | 7046 | 3 | 0 | 0 | 3 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0028 | 0/0 | 7043 | 3 | 0 | 2 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7038): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0029 | 0/0 | 7045 | 3 | 0 | 3 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7040): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0030 | 0/0 | 7046 | 3 | 2 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0031 | 0/0 | 7046 | 3 | 3 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0032 | 0/0 | 7046 | 2 | 0 | 1 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0033 | 0/0 | 7042 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7037): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0034 | 0/0 | 7042 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7037): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0035 | 0/0 | 7041 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7036): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0036 | 0/0 | 7046 | 2 | 0 | 1 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0037 | 0/0 | 7046 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0038 | 0/0 | 7046 | 2 | 0 | 1 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0039 | 0/0 | 7046 | 2 | 1 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0040 | 0/0 | 7046 | 2 | 0 | 1 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0041 | 0/0 | 7046 | 2 | 0 | 0 | 2 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0042 | 0/0 | 7046 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0043 | 0/0 | 7046 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0044 | 0/0 | 7046 | 2 | 0 | 0 | 0 | 0 | 2 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0045 | 0/0 | 7046 | 2 | 0 | 1 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0046 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0047 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0048 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0049 | 0/0 | 7046 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0050 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0051 | 0/0 | 7043 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7038): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0052 | 0/0 | 7043 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7038): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0053 | 0/0 | 7046 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0054 | 0/0 | 7046 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0055 | 0/0 | 7042 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7037): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0056 | 0/0 | 7041 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7036): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0057 | 0/0 | 7041 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7036): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0058 | 0/0 | 7046 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0059 | 0/0 | 7046 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0060 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0061 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0062 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0063 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0064 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0065 | 0/0 | 7047 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7042): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0066 | 0/0 | 7046 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0067 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0068 | 0/0 | 7046 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0069 | 0/0 | 7045 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7040): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0070 | 0/0 | 7045 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7040): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0071 | 0/0 | 7047 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7042): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0072 | 0/0 | 7046 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0073 | 0/0 | 7044 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7039): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0074 | 0/0 | 7046 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0075 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0076 | 0/0 | 7043 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7038): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0077 | 0/0 | 7047 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7042): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0078 | 0/0 | 7046 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0079 | 0/0 | 7046 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0080 | 0/0 | 7046 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0081 | 0/0 | 7047 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7042): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0082 | 0/0 | 7043 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7038): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0083 | 0/0 | 7046 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0084 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0085 | 0/0 | 7043 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7038): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0086 | 0/0 | 7047 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7042): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0087 | 0/0 | 7047 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7042): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0088 | 0/0 | 7047 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7042): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0089 | 0/0 | 7047 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7042): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0090 | 0/0 | 7047 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7042): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0091 | 0/0 | 7046 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0092 | 0/0 | 7042 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7037): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0093 | 0/0 | 7047 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7042): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0094 | 0/0 | 7046 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0095 | 0/0 | 7046 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0096 | 0/0 | 7046 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0097 | 0/0 | 7046 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0098 | 0/0 | 7046 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0099 | 0/0 | 7046 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0001t0100 | 0/0 | 7046 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0001c0002t0021 | 0/0 | 7047 | 4 | 3 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7042): Show |
chr6 | 52492408 | 52582060 |
a0001c0003t0006 | 0/0 | 7043 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7038): Show |
chr6 | 52492408 | 52582060 |
a0001c0003t0016 | 0/0 | 7046 | 2 | 0 | 0 | 0 | 0 | 2 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
a0002c0004t0025 | 0/0 | 7046 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | GAAGT others(7041): Show |
chr6 | 52492408 | 52582060 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 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 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0001g0141 | 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 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0001g0148 | 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 |
a0001c0001t0001g0151 | 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 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0001g0160 | 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 |
a0001c0001t0001g0164 | 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 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0001g0284 | 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 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0002g0004 | 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 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0002g0237 | 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 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0002g0347 | 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 |
a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 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 |
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 |
a0001c0001t0004g0122 | 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 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0004g0136 | 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 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0004g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0004g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0004g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0178 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0005g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0006g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0006g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0006g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0006g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0006g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0006g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0006g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0006g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0006g0264 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0006g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0006g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0006g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0006g0327 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0007g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0007g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0007g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0007g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0007g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0007g0249 | 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 |
a0001c0001t0007g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0007g0332 | 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 |
a0001c0001t0008g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0008g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0008g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0008g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0008g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0008g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0008g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0008g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0008g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0008g0296 | 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 |
a0001c0001t0009g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0009g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0009g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0009g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0009g0231 | 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 |
a0001c0001t0009g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0009g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0010g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0010g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0010g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0010g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0010g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0010g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0010g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0011g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0011g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0011g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0011g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0011g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0011g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0012g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0012g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0012g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0012g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0012g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0012g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0013g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0013g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0013g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0013g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0013g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0014g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0014g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0014g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0014g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0014g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0015g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0015g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0015g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0015g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0015g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0016g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0016g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0016g0326 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0017g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0017g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0017g0325 | 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 |
a0001c0001t0018g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0018g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0018g0286 | 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 |
a0001c0001t0019g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0020g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0020g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0020g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0020g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0022g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0022g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0022g0361 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0022g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0024g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0024g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0024g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0025g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0025g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0026g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0026g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0026g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0027g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0027g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0027g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0028g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0028g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0028g0048 | 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 |
a0001c0001t0030g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0030g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0030g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0031g0181 | 0/0 | 1 | 1 | 0 | 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 |
a0001c0001t0031g0269 | 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 |
a0001c0001t0033g0185 | 0/0 | 1 | 1 | 0 | 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 |
a0001c0001t0034g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0034g0259 | 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 |
a0001c0001t0035g0184 | 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 |
a0001c0001t0036g0320 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0037g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0037g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0038g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0038g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0039g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0039g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0040g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0040g0262 | 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 |
a0001c0001t0041g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0042g0349 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0001c0001t0043g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0043g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0044g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0044g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0045g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0045g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0046g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0047g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0048g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0049g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0050g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0051g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0052g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0053g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0054g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0055g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0056g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0057g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0058g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0059g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0060g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0061g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0062g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0063g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0064g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0065g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0066g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0067g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0068g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0069g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0070g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0071g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0072g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0073g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0074g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0075g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0076g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0077g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0078g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0079g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0080g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0081g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0082g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0083g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0084g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0085g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0086g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0087g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0088g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0089g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0090g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0091g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0092g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0093g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0094g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0095g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0096g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0097g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0098g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0099g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0001t0100g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0002t0021g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0002t0021g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0002t0021g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0003t0006g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0003t0016g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0001c0003t0016g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
a0002c0004t0025g0358 | 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 | g0320 | EUR | GBR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG00099 | hp2 | a0001 | c0001 | t0022 | g0362 | EUR | GBR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG00140 | hp1 | a0001 | c0001 | t0045 | g0090 | EUR | GBR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG00140 | hp2 | a0001 | c0001 | t0006 | g0006 | EUR | GBR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG00280 | hp1 | a0001 | c0001 | t0006 | g0168 | 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 | g0143 | EAS | CHS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | CHS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0314 | 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 | g0125 | EAS | CHS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG00609 | hp1 | a0001 | c0001 | t0064 | g0334 | EAS | CHS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG00609 | hp2 | a0001 | c0001 | t0024 | g0034 | EAS | CHS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0161 | 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 | t0038 | g0247 | 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 | t0005 | g0175 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG00733 | hp1 | a0001 | c0001 | t0086 | g0173 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG00733 | hp2 | a0001 | c0001 | t0003 | g0331 | 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 | g0273 | 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 | t0010 | g0222 | 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 | t0005 | 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 | t0005 | g0061 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01074 | hp1 | a0001 | c0001 | t0040 | g0262 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01074 | hp2 | a0001 | c0001 | t0008 | g0258 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01081 | hp1 | a0001 | c0001 | t0017 | g0170 | 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 | g0217 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01106 | hp1 | a0001 | c0001 | t0005 | g0043 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01106 | hp2 | a0001 | c0001 | t0094 | g0338 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01167 | hp1 | a0001 | c0001 | t0045 | g0321 | 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 | g0236 | 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 | g0343 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01175 | hp2 | a0001 | c0001 | t0039 | g0225 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01192 | hp1 | a0001 | c0001 | t0071 | g0242 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0353 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01243 | hp1 | a0001 | c0001 | t0076 | g0337 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01243 | hp2 | a0001 | c0002 | t0021 | g0011 | AMR | PUR | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01255 | hp1 | a0001 | c0001 | t0026 | g0290 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01255 | hp2 | a0001 | c0001 | t0006 | g0045 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01257 | hp1 | a0001 | c0001 | t0100 | g0323 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01257 | hp2 | a0001 | c0001 | t0028 | g0046 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01258 | hp1 | a0001 | c0001 | t0028 | g0048 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01258 | hp2 | a0001 | c0001 | t0022 | g0360 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0004 | 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 | g0246 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01358 | hp2 | a0001 | c0001 | t0051 | g0021 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01433 | hp1 | a0001 | c0001 | t0054 | g0032 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01433 | hp2 | a0001 | c0001 | t0006 | g0167 | 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 | t0022 | g0361 | EUR | IBS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01515 | hp2 | a0001 | c0001 | t0006 | g0174 | EUR | IBS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01516 | hp1 | a0001 | c0001 | t0006 | g0169 | 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 | t0006 | g0177 | EUR | IBS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01517 | hp2 | a0001 | c0001 | t0017 | g0322 | EUR | IBS | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01884 | hp1 | a0001 | c0001 | t0013 | g0278 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0194 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01891 | hp1 | a0001 | c0001 | t0042 | g0350 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01891 | hp2 | a0001 | c0001 | t0098 | g0335 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01928 | hp1 | a0001 | c0001 | t0099 | g0275 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01928 | hp2 | a0001 | c0001 | t0011 | g0026 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01934 | hp1 | a0001 | c0001 | t0005 | g0176 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01952 | hp1 | a0001 | c0001 | t0011 | g0019 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01952 | hp2 | a0001 | c0001 | t0072 | g0274 | 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 | g0004 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG01993 | hp2 | a0001 | c0001 | t0011 | g0028 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02004 | hp1 | a0001 | c0001 | t0058 | g0049 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02015 | hp1 | a0001 | c0001 | t0006 | g0171 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0165 | 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 | g0285 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02040 | hp1 | a0001 | c0001 | t0024 | g0033 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02055 | hp1 | a0001 | c0001 | t0039 | g0315 | 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 | t0012 | g0216 | 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 | t0016 | g0326 | 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 | t0060 | g0319 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02080 | hp2 | a0001 | c0001 | t0015 | g0147 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02083 | hp2 | a0001 | c0001 | t0007 | g0227 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02129 | hp2 | a0001 | c0001 | t0061 | g0263 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02132 | hp1 | a0001 | c0001 | t0090 | g0215 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02132 | hp2 | a0001 | c0001 | t0006 | g0318 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02135 | hp1 | a0001 | c0001 | t0003 | g0341 | 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 | g0208 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02145 | hp2 | a0001 | c0001 | t0017 | g0325 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0244 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02148 | hp2 | a0001 | c0001 | t0011 | g0027 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0345 | EAS | CDX | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02155 | hp2 | a0001 | c0001 | t0007 | g0139 | EAS | CDX | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0163 | 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 | t0096 | g0291 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02257 | hp2 | a0001 | c0001 | t0005 | g0190 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02258 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02258 | hp2 | a0001 | c0001 | t0057 | g0166 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02280 | hp1 | a0001 | c0001 | t0037 | g0351 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02280 | hp2 | a0001 | c0001 | t0010 | g0266 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02293 | hp2 | a0001 | c0001 | t0011 | g0025 | AMR | PEL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02300 | hp1 | a0001 | c0001 | t0074 | g0243 | 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 | g0191 | 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 | t0006 | g0327 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02523 | hp2 | a0001 | c0001 | t0067 | g0211 | EAS | KHV | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02572 | hp1 | a0001 | c0001 | t0010 | g0039 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02572 | hp2 | a0001 | c0001 | t0013 | g0091 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02602 | hp1 | a0001 | c0001 | t0009 | g0085 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0183 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02615 | hp2 | a0001 | c0002 | t0021 | g0271 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0218 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02622 | hp2 | a0001 | c0001 | t0005 | g0352 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02630 | hp1 | a0001 | c0001 | t0010 | g0037 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02630 | hp2 | a0001 | c0001 | t0019 | g0206 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02683 | hp1 | a0001 | c0001 | t0044 | 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 | g0235 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02698 | hp2 | a0001 | c0001 | t0028 | g0047 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02717 | hp1 | a0001 | c0001 | t0042 | g0349 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02717 | hp2 | a0001 | c0001 | t0013 | g0267 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02723 | hp1 | a0001 | c0001 | t0043 | g0207 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02723 | hp2 | a0001 | c0001 | t0059 | g0209 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02735 | hp1 | a0002 | c0004 | t0025 | g0358 | 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 | t0006 | g0068 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02738 | hp2 | a0001 | c0003 | t0016 | g0304 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02809 | hp1 | a0001 | c0001 | t0008 | g0289 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02818 | hp1 | a0001 | c0001 | t0031 | g0182 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02818 | hp2 | a0001 | c0001 | t0088 | g0272 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02886 | hp1 | a0001 | c0001 | t0026 | g0280 | 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 | t0006 | g0042 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02895 | hp2 | a0001 | c0001 | t0013 | g0040 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02896 | hp1 | a0001 | c0001 | t0008 | g0276 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02896 | hp2 | a0001 | c0001 | t0010 | g0193 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0041 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02897 | hp2 | a0001 | c0001 | t0010 | g0192 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0299 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02922 | hp2 | a0001 | c0001 | t0030 | g0260 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0295 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02965 | hp2 | a0001 | c0001 | t0092 | g0355 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02970 | hp1 | a0001 | c0001 | t0095 | g0067 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02970 | hp2 | a0001 | c0001 | t0026 | g0357 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0205 | 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 | t0055 | g0187 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03041 | hp2 | a0001 | c0001 | t0031 | g0269 | AFR | GWD | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0035 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03098 | hp2 | a0001 | c0001 | t0008 | g0294 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03130 | hp1 | a0001 | c0001 | t0009 | g0231 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03130 | hp2 | a0001 | c0001 | t0008 | g0296 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03139 | hp1 | a0001 | c0001 | t0037 | g0172 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03139 | hp2 | a0001 | c0001 | t0078 | g0179 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03195 | hp1 | a0001 | c0001 | t0008 | g0270 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03195 | hp2 | a0001 | c0001 | t0031 | g0181 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03209 | hp1 | a0001 | c0001 | t0008 | g0282 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03209 | hp2 | a0001 | c0002 | t0021 | g0011 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03225 | hp1 | a0001 | c0002 | t0021 | g0356 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03225 | hp2 | a0001 | c0001 | t0034 | g0259 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03239 | hp1 | a0001 | c0001 | t0044 | g0076 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03239 | hp2 | a0001 | c0001 | t0049 | g0029 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03453 | hp1 | a0001 | c0001 | t0008 | g0257 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0298 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0310 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03516 | hp1 | a0001 | c0001 | t0056 | g0188 | AFR | ESN | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03516 | hp2 | a0001 | c0001 | t0035 | g0184 | 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 | t0013 | g0279 | AFR | MSL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03579 | hp2 | a0001 | c0001 | t0030 | g0342 | 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 | t0016 | g0311 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03669 | hp1 | a0001 | c0001 | t0068 | g0097 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03688 | hp1 | a0001 | c0001 | t0080 | g0157 | SAS | STU | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03688 | hp2 | a0001 | c0003 | t0016 | g0306 | SAS | STU | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03704 | hp1 | a0001 | c0001 | t0005 | g0096 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0265 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03710 | hp2 | a0001 | c0001 | t0038 | g0317 | SAS | PJL | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03831 | hp1 | a0001 | c0001 | t0093 | g0336 | SAS | BEB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03831 | hp2 | a0001 | c0001 | t0011 | 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 | t0052 | g0016 | SAS | BEB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03942 | hp1 | a0001 | c0003 | t0006 | g0307 | SAS | BEB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03942 | hp2 | a0001 | c0001 | t0018 | g0213 | 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 | t0053 | 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 | t0077 | g0119 | SAS | BEB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0220 | 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 | t0022 | g0359 | SAS | STU | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | STU | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG04228 | hp1 | a0001 | c0001 | t0079 | g0128 | 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 | g0145 | EAS | CHB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0202 | 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 | g0292 | 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 | t0012 | g0058 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18940 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18941 | hp2 | a0001 | c0001 | t0046 | g0013 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18943 | hp1 | a0001 | c0001 | t0016 | g0268 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18943 | hp2 | a0001 | c0001 | t0075 | g0112 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18944 | hp1 | a0001 | c0001 | t0004 | g0136 | 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 | t0027 | g0150 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18947 | hp1 | a0001 | c0001 | t0015 | g0129 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18947 | hp2 | a0001 | c0001 | t0006 | g0287 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18949 | hp1 | a0001 | c0001 | t0012 | g0214 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18949 | hp2 | a0001 | c0001 | t0015 | g0057 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0347 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18953 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0160 | 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 | g0254 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18959 | hp1 | a0001 | c0001 | t0012 | g0288 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18959 | hp2 | a0001 | c0001 | t0007 | g0332 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0203 | 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 | g0233 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18962 | hp2 | a0001 | c0001 | t0027 | g0140 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18963 | hp1 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18963 | hp2 | a0001 | c0001 | t0007 | g0250 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0283 | 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 | t0048 | g0014 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18970 | hp1 | a0001 | c0001 | t0050 | g0030 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18970 | hp2 | a0001 | c0001 | t0014 | g0073 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18972 | hp1 | a0001 | c0001 | t0018 | g0286 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18972 | hp2 | a0001 | c0001 | t0015 | g0144 | 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 | t0063 | g0201 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18981 | hp1 | a0001 | c0001 | t0007 | g0256 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18981 | hp2 | a0001 | c0001 | t0004 | g0159 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18982 | hp1 | a0001 | c0001 | t0070 | g0102 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18986 | hp2 | a0001 | c0001 | t0047 | g0012 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18990 | hp1 | a0001 | c0001 | t0062 | g0111 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18990 | hp2 | a0001 | c0001 | t0014 | g0195 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18993 | hp1 | a0001 | c0001 | t0084 | g0255 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19000 | hp1 | a0001 | c0001 | t0089 | g0328 | 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 | g0219 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19004 | hp2 | a0001 | c0001 | t0027 | g0133 | 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 | g0305 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19006 | hp1 | a0001 | c0001 | t0041 | g0158 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19006 | hp2 | a0001 | c0001 | t0020 | g0234 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0324 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0149 | 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 | g0249 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19011 | hp1 | a0001 | c0001 | t0018 | g0196 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19011 | hp2 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19012 | hp1 | a0001 | c0001 | t0005 | g0308 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19012 | hp2 | a0001 | c0001 | t0006 | g0132 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19030 | hp1 | a0001 | c0001 | t0082 | g0348 | AFR | LWK | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19030 | hp2 | a0001 | c0001 | t0043 | g0344 | AFR | LWK | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19043 | hp1 | a0001 | c0001 | t0033 | g0186 | AFR | LWK | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19043 | hp2 | a0001 | c0001 | t0066 | g0312 | AFR | LWK | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19054 | hp1 | a0001 | c0001 | t0020 | g0346 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19054 | hp2 | a0001 | c0001 | t0012 | g0200 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19055 | hp1 | a0001 | c0001 | t0024 | g0017 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0152 | 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 | g0230 | 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 | g0164 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19058 | hp2 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19062 | hp1 | a0001 | c0001 | t0007 | g0251 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19062 | hp2 | a0001 | c0001 | t0004 | g0339 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19063 | hp1 | a0001 | c0001 | t0014 | g0135 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19064 | hp1 | a0001 | c0001 | t0007 | g0252 | 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 | t0025 | g0302 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19065 | hp2 | a0001 | c0001 | t0007 | g0253 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19066 | hp1 | a0001 | c0001 | t0015 | g0115 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19066 | hp2 | a0001 | c0001 | t0007 | g0197 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19067 | hp1 | a0001 | c0001 | t0091 | g0154 | 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 | g0245 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19070 | hp1 | a0001 | c0001 | t0014 | g0103 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19074 | hp1 | a0001 | c0001 | t0069 | g0053 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19074 | hp2 | a0001 | c0001 | t0025 | g0309 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19079 | hp1 | a0001 | c0001 | t0005 | g0330 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19080 | hp1 | a0001 | c0001 | t0014 | g0155 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19081 | hp2 | a0001 | c0001 | t0073 | g0248 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19083 | hp2 | a0001 | c0001 | t0081 | g0134 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19085 | hp2 | a0001 | c0001 | t0006 | g0303 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19086 | hp1 | a0001 | c0001 | t0020 | g0238 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0142 | 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 | t0087 | g0329 | 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 | t0010 | g0038 | AFR | YRI | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0354 | AFR | YRI | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA20129 | hp1 | a0001 | c0001 | t0008 | g0297 | AFR | ASW | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | ASW | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA20752 | hp1 | a0001 | c0001 | t0005 | g0063 | EUR | TSI | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA20752 | hp2 | a0001 | c0001 | t0006 | g0006 | EUR | TSI | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA20805 | hp1 | a0001 | c0001 | t0040 | g0261 | EUR | TSI | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA20805 | hp2 | a0001 | c0001 | t0005 | g0064 | EUR | TSI | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA20905 | hp1 | a0001 | c0001 | t0085 | g0180 | 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 | g0281 | AMR | CLM | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02109 | hp1 | a0001 | c0001 | t0009 | g0293 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02109 | hp2 | a0001 | c0001 | t0065 | g0083 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02486 | hp1 | a0001 | c0001 | t0005 | g0300 | 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 | t0005 | g0036 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG02559 | hp2 | a0001 | c0001 | t0009 | g0277 | AFR | ACB | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG03471 | hp1 | a0001 | c0001 | t0033 | g0185 | 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 | g0232 | AFR | USA | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
HG06807 | hp2 | a0001 | c0001 | t0083 | g0189 | 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 | t0012 | g0229 | EAS | JPT | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
NA20300 | hp1 | a0001 | c0001 | t0097 | g0301 | 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 | a0001 | c0001 | t0006 | g0264 | REF | REF | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
homoSapiens | grch38p0 | a0001 | c0001 | t0005 | g0178 | REF | REF | TRAM2_chr6_52492408_52582060 | TRAM2 | chr6 | 52492408 | 52582060 |
view | 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 |
view | 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 |
view | 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 | a0001c0001t0072 | 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 | a0001c0001t0088 | 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 | a0001c0001t0078 | 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 | a0001c0001t0037 | 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 | a0001c0001t0006 a0001c0001t0016 a0001c0001t0028 others(8): Show |
32 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(29): 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 | a0001c0001t0066 | 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 | a0001c0001t0018 a0001c0001t0035 a0001c0001t0042 others(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 | a0001c0001t0015 a0001c0001t0041 |
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 | a0001c0001t0004 a0001c0001t0014 a0001c0001t0025 others(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 | 25 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0011 others(22): 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 | a0001c0001t0006 a0001c0001t0016 a0001c0001t0028 others(8): Show |
32 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(29): 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 | a0001c0001t0014 | 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 | a0001c0001t0025 a0002c0004t0025 |
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 | a0001c0001t0017 a0001c0001t0018 a0001c0001t0023 others(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 | a0001c0001t0083 | 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 | 1 | a0001c0002t0021 | 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 | a0001c0001t0035 a0001c0001t0056 a0001c0001t0057 |
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 | a0001c0001t0098 | 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 | a0001c0001t0017 a0001c0001t0023 a0001c0001t0037 others(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 | a0001c0001t0028 | 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 | a0001c0001t0057 | 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 | 44 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(41): Show |
152 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(149): 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 | a0001c0001t0017 a0001c0001t0023 a0001c0001t0037 others(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 | a0001c0001t0079 | 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 | a0001c0001t0006 a0001c0001t0016 a0001c0001t0028 others(8): Show |
32 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(29): 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 | a0001c0001t0004 a0001c0001t0014 a0001c0001t0018 others(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 | a0001c0001t0008 a0001c0001t0026 a0001c0001t0078 others(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 | 1 | a0001c0002t0021 | 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 | a0001c0001t0095 | 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 | a0001c0001t0052 | 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 | a0001c0001t0098 | 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 | a0001c0001t0087 | 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 | a0001c0001t0019 a0001c0001t0065 |
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 | 94 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(91): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): 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 | a0001c0001t0004 a0001c0001t0014 a0001c0001t0025 others(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 | a0001c0001t0007 a0001c0001t0069 a0001c0001t0070 others(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 | 10 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0032 others(7): 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 | a0001c0001t0083 | 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 | a0001c0001t0013 a0001c0001t0065 a0001c0001t0069 others(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 | a0001c0001t0033 a0001c0001t0034 a0001c0001t0055 others(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 | a0001c0001t0004 a0001c0001t0014 a0001c0001t0018 others(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 | a0001c0001t0006 a0001c0001t0016 a0001c0001t0028 others(7): Show |
31 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(28): 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 | a0001c0001t0006 a0001c0001t0028 a0001c0001t0051 others(5): Show |
26 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(23): 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 | a0001c0001t0016 a0001c0001t0084 a0001c0003t0016 |
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 | a0001c0001t0005 a0001c0001t0029 a0001c0001t0042 others(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 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(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 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0010 others(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 | a0001c0001t0004 a0001c0001t0014 a0001c0001t0018 others(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 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0024 others(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 | a0001c0001t0020 a0001c0001t0093 |
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 | a0001c0001t0062 | 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 | a0001c0001t0004 a0001c0001t0014 a0001c0001t0018 others(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 | a0001c0001t0001 a0001c0001t0008 a0001c0001t0011 others(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 | a0001c0001t0069 | 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 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0013 others(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 | a0001c0001t0027 a0001c0001t0047 a0001c0001t0081 |
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 | 15 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0010 others(12): 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 | a0001c0001t0096 | 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 | a0001c0001t0042 a0001c0001t0066 a0001c0001t0083 |
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 | 2 | a0001c0001t0009 a0001c0001t0096 |
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 | a0001c0001t0031 a0001c0001t0045 |
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 | a0001c0001t0068 | 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 | 7 | a0001c0001t0003 a0001c0001t0022 a0001c0001t0032 others(4): 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 | a0001c0001t0044 | 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 | a0001c0001t0098 | 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 | a0001c0001t0004 a0001c0001t0014 a0001c0001t0018 others(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 | 94 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(91): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): 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 | a0001c0001t0086 | 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 | a0001c0001t0006 a0001c0001t0016 a0001c0001t0028 others(8): Show |
32 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(29): 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 | a0001c0001t0067 | 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 | 94 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(91): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): 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 | a0001c0001t0075 | 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 | a0001c0001t0061 | 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 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0013 others(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 | a0001c0001t0004 a0001c0001t0014 a0001c0001t0018 others(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 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0016 others(8): Show |
37 | HG00140.hp2 HG00280.hp1 HG01255.hp2 others(34): 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 | a0001c0001t0006 a0001c0001t0012 a0001c0001t0016 others(11): Show |
42 | HG00140.hp2 HG00280.hp1 HG01255.hp2 others(39): 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 | a0001c0001t0100 | 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 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(29): Show |
129 | HG00140.hp2 HG00280.hp1 HG00544.hp2 others(126): 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 | 77 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(74): Show |
286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): 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 | 94 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(91): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): 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 | a0001c0001t0054 | 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 | a0001c0001t0058 | 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 | a0001c0001t0035 a0001c0001t0056 a0001c0001t0057 |
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 | a0001c0001t0091 | 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 | a0001c0001t0053 | 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 | 17 | a0001c0001t0003 a0001c0001t0009 a0001c0001t0010 others(14): 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 | a0001c0001t0033 a0001c0001t0034 a0001c0001t0055 |
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 | a0001c0001t0099 | 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 | a0001c0001t0049 | 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 | a0001c0001t0017 a0001c0001t0045 a0001c0001t0100 |
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 | a0001c0001t0011 a0001c0001t0023 a0001c0001t0024 others(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 | a0001c0001t0046 a0001c0001t0047 a0001c0001t0048 |
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 | a0001c0001t0022 | 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 |
view | 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 | a0001c0001t0019g0084 a0001c0001t0065g0083 |
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 | a0001c0001t0005g0308 a0001c0001t0005g0330 a0001c0001t0087g0329 others(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 | a0001c0001t0003g0069 a0001c0001t0003g0074 a0001c0001t0003g0077 others(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 | a0001c0001t0024g0033 | 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 | 339 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(336): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): 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 | a0001c0001t0033g0185 a0001c0001t0033g0186 a0001c0001t0034g0191 others(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 | a0001c0001t0001g0285 | 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 | a0001c0001t0083g0189 | 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 | a0001c0001t0006g0171 | 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 | a0001c0001t0006g0068 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0003g0074 a0001c0001t0003g0092 a0001c0001t0003g0093 |
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 | 31 | a0001c0001t0006g0006 a0001c0001t0006g0041 a0001c0001t0006g0042 others(28): Show |
32 | HG00140.hp2 HG00280.hp1 HG01243.hp1 others(29): Show |
intron_variant | MODIFIER | c.1039+149delC | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 10/10 | chr6 | 52504441 | |||||||
chr6:52504776 | G | A | 1 | a0001c0001t0049g0029 | 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 | a0001c0001t0004g0052 a0001c0001t0004g0056 a0001c0001t0004g0104 others(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 | a0001c0001t0095g0067 | 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 | a0001c0001t0008g0298 | 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 | a0001c0001t0083g0189 | 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 | a0001c0001t0001g0198 | 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 | a0001c0001t0035g0066 a0001c0001t0035g0184 |
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 | 73 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(70): 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 | a0001c0001t0039g0315 | 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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0004g0052 a0001c0001t0004g0056 a0001c0001t0004g0104 others(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 | a0001c0001t0005g0043 | 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 | a0001c0001t0019g0082 a0001c0001t0019g0084 a0001c0001t0019g0100 others(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 | a0001c0001t0001g0141 | 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 | 326 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(323): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): 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 | a0001c0001t0009g0277 | 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 | 92 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(89): 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 | 278 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(275): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): 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 | a0001c0001t0018g0101 a0001c0001t0018g0196 a0001c0001t0018g0213 others(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 | a0001c0001t0092g0355 | 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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0019g0082 a0001c0001t0019g0084 a0001c0001t0019g0100 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0042g0349 a0001c0001t0042g0350 |
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 | a0001c0001t0002g0233 a0001c0001t0020g0238 |
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 | a0001c0001t0010g0037 a0001c0001t0010g0038 a0001c0001t0010g0039 others(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 | a0001c0001t0092g0355 | 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 | a0001c0001t0056g0188 a0001c0001t0057g0166 |
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 | a0001c0001t0036g0320 | 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 | a0001c0001t0092g0355 | 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 | a0001c0001t0030g0260 a0001c0001t0030g0342 a0001c0001t0030g0343 |
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 | a0001c0001t0019g0082 a0001c0001t0019g0084 a0001c0001t0019g0100 others(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 | a0001c0001t0042g0349 a0001c0001t0042g0350 a0001c0001t0066g0312 others(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 | a0001c0001t0031g0181 a0001c0001t0031g0182 a0001c0001t0031g0269 |
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 | a0001c0001t0035g0066 a0001c0001t0035g0184 a0001c0001t0056g0188 others(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 | a0001c0001t0042g0349 a0001c0001t0042g0350 a0001c0001t0066g0312 |
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 | a0001c0001t0028g0046 a0001c0001t0028g0047 a0001c0001t0028g0048 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | 315 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(312): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): 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 | a0001c0001t0010g0222 a0001c0001t0010g0266 |
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 | a0001c0001t0001g0223 | 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 | a0001c0001t0060g0319 | 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 | 102 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(99): 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 | a0001c0001t0019g0082 a0001c0001t0019g0084 a0001c0001t0019g0100 others(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 | a0001c0001t0001g0149 | 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 | 326 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(323): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): 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 | a0001c0001t0019g0082 a0001c0001t0019g0084 a0001c0001t0019g0100 others(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 | a0001c0001t0023g0023 a0001c0001t0038g0317 a0001c0001t0039g0225 |
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 | a0001c0003t0006g0307 | 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 | a0001c0001t0003g0341 | 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 | 289 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(286): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): 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 | a0001c0001t0033g0185 a0001c0001t0033g0186 a0001c0001t0034g0191 others(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 | a0001c0001t0008g0282 | 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 | a0001c0001t0002g0241 | 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 | 290 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(287): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(301): 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 | a0001c0001t0005g0063 | 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 | a0001c0001t0011g0027 | 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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0004g0052 a0001c0001t0004g0056 a0001c0001t0004g0104 others(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 | 87 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(84): 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 | a0001c0001t0019g0082 a0001c0001t0019g0084 a0001c0001t0019g0100 others(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 | a0001c0001t0066g0312 | 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 | a0001c0001t0003g0313 | 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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0081g0134 | 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 | 289 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(286): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.412-2380G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52511966 | |||||||
chr6:52512036 | C | T | 87 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(84): 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 | a0001c0001t0018g0196 | 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 | a0001c0001t0006g0041 a0001c0001t0006g0042 a0001c0001t0006g0045 |
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 | a0001c0001t0018g0101 a0001c0001t0018g0196 a0001c0001t0018g0213 others(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 | a0001c0001t0092g0355 | 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 | a0001c0001t0012g0058 a0001c0001t0012g0200 a0001c0001t0012g0214 others(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 | a0001c0001t0038g0247 | 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 | a0001c0001t0098g0335 | 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 | a0001c0001t0078g0179 | 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 | a0001c0001t0027g0150 | 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 | a0001c0001t0006g0327 | 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 | a0001c0002t0021g0011 a0001c0002t0021g0271 a0001c0002t0021g0356 |
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 | a0001c0001t0033g0185 a0001c0001t0033g0186 a0001c0001t0034g0191 others(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 | a0001c0001t0018g0101 a0001c0001t0018g0196 a0001c0001t0018g0213 others(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 | a0001c0001t0051g0021 | 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 | a0001c0001t0002g0239 a0001c0001t0003g0060 |
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 | 289 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(286): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): 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 | a0001c0001t0037g0172 a0001c0001t0037g0351 |
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 | a0001c0001t0019g0082 a0001c0001t0019g0084 a0001c0001t0019g0100 others(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 | a0001c0001t0001g0223 | 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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0028g0047 | 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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0092g0355 | 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 | 42 | a0001c0001t0004g0305 a0001c0001t0006g0006 a0001c0001t0006g0041 others(39): Show |
43 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(40): 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 | a0001c0001t0035g0066 a0001c0001t0035g0184 |
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 | 289 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(286): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.411+163G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 4/10 | chr6 | 52515843 | |||||||
chr6:52516387 | A | G | 42 | a0001c0001t0004g0305 a0001c0001t0006g0006 a0001c0001t0006g0041 others(39): Show |
43 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(40): 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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0010g0037 a0001c0001t0010g0038 a0001c0001t0010g0039 others(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 | 289 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(286): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(300): 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 | a0001c0001t0008g0009 a0001c0001t0008g0070 a0001c0001t0008g0071 others(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 | a0001c0001t0002g0265 | 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 | a0001c0003t0006g0307 a0001c0003t0016g0304 a0001c0003t0016g0306 |
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 | a0001c0001t0019g0206 | 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 | a0001c0001t0034g0191 a0001c0001t0034g0259 |
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 | a0001c0001t0042g0349 a0001c0001t0042g0350 |
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 | 331 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(328): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): 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 | a0001c0001t0023g0018 a0001c0001t0023g0022 a0001c0001t0023g0023 others(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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0098g0335 | 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 | 330 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(327): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): 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 | a0001c0001t0005g0005 a0001c0001t0005g0036 a0001c0001t0005g0194 others(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 | a0001c0001t0082g0348 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0018g0101 a0001c0001t0018g0213 a0001c0001t0032g0020 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0149 a0001c0001t0003g0162 |
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 | 108 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(105): 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 | a0001c0001t0004g0105 a0001c0001t0004g0106 a0001c0001t0004g0130 others(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 | 297 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(294): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): 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 | a0001c0001t0019g0082 a0001c0001t0019g0084 a0001c0001t0019g0100 others(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 | 314 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(311): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(325): 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 | a0001c0001t0098g0335 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0001g0149 a0001c0001t0004g0122 a0001c0001t0004g0310 others(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 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | 202 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(199): 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 | a0001c0001t0013g0267 | 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 | a0001c0001t0044g0076 | 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 | a0001c0001t0023g0018 a0001c0001t0023g0022 a0001c0001t0023g0023 others(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 | a0001c0001t0003g0314 | 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 | a0001c0001t0035g0066 a0001c0001t0035g0184 |
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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | 88 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(85): 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 | a0001c0001t0019g0082 a0001c0001t0019g0084 a0001c0001t0019g0100 others(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 | 43 | a0001c0001t0004g0305 a0001c0001t0006g0006 a0001c0001t0006g0041 others(40): Show |
44 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(41): 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 | a0001c0001t0007g0249 a0001c0001t0073g0248 |
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 | a0001c0001t0034g0191 a0001c0001t0034g0259 |
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 | a0001c0001t0007g0252 | 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 | a0001c0001t0005g0300 a0001c0001t0088g0272 |
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 | a0001c0001t0008g0070 a0001c0001t0008g0071 |
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 | a0001c0001t0006g0006 a0001c0001t0006g0167 a0001c0001t0006g0168 others(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 | 46 | a0001c0001t0003g0235 a0001c0001t0004g0305 a0001c0001t0006g0006 others(43): Show |
47 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(44): 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 | a0001c0001t0033g0185 a0001c0001t0033g0186 a0001c0001t0055g0187 |
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 | a0001c0001t0025g0309 | 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 | a0001c0001t0083g0189 | 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 | 342 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(339): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): 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 | a0001c0001t0001g0116 a0001c0001t0001g0120 a0001c0001t0001g0121 others(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 | a0001c0001t0042g0349 a0001c0001t0042g0350 |
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 | a0001c0001t0008g0009 a0001c0001t0008g0257 a0001c0001t0008g0258 others(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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | 45 | a0001c0001t0004g0305 a0001c0001t0006g0006 a0001c0001t0006g0041 others(42): Show |
46 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(43): 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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | a0001c0001t0025g0302 | 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 | a0001c0001t0005g0043 a0001c0001t0013g0267 |
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 | a0001c0002t0021g0011 a0001c0002t0021g0271 a0001c0002t0021g0356 |
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 | a0001c0001t0096g0291 | 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 | a0001c0001t0031g0181 a0001c0001t0031g0182 a0001c0001t0031g0269 |
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 | a0001c0001t0079g0128 | 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 | a0001c0001t0018g0101 a0001c0001t0018g0213 a0001c0001t0032g0020 others(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 | 89 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(86): 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 | a0001c0001t0061g0263 | 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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0040g0262 | 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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | a0001c0001t0001g0146 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0015g0147 | 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 | a0001c0001t0019g0082 a0001c0001t0019g0084 a0001c0001t0019g0100 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0149 |
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 | a0001c0001t0004g0138 | 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 | a0001c0001t0008g0292 | 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 | a0001c0001t0078g0179 | 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 | 327 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(324): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): 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 | a0001c0001t0002g0347 a0001c0001t0003g0044 a0001c0001t0003g0060 others(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 | a0001c0001t0006g0303 | 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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | a0001c0001t0037g0172 a0001c0001t0037g0351 a0001c0001t0092g0355 |
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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | a0001c0001t0013g0040 | 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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | 136 | a0001c0001t0002g0347 a0001c0001t0003g0044 a0001c0001t0003g0060 others(133): Show |
141 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): 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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0011g0028 | 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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | 88 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(85): 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 | a0001c0001t0095g0067 | 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 | a0001c0001t0085g0180 | 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 | 43 | a0001c0001t0004g0305 a0001c0001t0006g0006 a0001c0001t0006g0041 others(40): Show |
44 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.185-7753T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52524490 | |||||||
chr6:52524580 | C | T | 89 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(86): 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | 137 | a0001c0001t0002g0347 a0001c0001t0003g0044 a0001c0001t0003g0060 others(134): Show |
142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): 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 | a0001c0001t0003g0314 a0001c0001t0003g0316 a0001c0001t0003g0331 others(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 | 45 | a0001c0001t0004g0305 a0001c0001t0006g0006 a0001c0001t0006g0041 others(42): Show |
46 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(43): 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 | a0001c0001t0008g0257 | 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 | a0001c0001t0006g0171 | 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 | a0001c0001t0006g0041 a0001c0001t0006g0042 a0001c0001t0006g0045 |
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 | a0001c0001t0033g0186 | 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 | a0001c0001t0006g0132 | 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 | a0001c0001t0095g0067 | 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 | 330 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(327): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): 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 | a0001c0001t0008g0276 a0001c0001t0008g0282 a0001c0001t0099g0275 |
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 | a0001c0001t0001g0284 a0001c0001t0001g0285 |
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 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0018g0101 a0001c0001t0018g0213 a0001c0001t0032g0020 others(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 | 88 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(85): 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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | a0001c0001t0012g0288 a0001c0001t0018g0196 a0001c0001t0018g0286 others(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 | a0001c0001t0004g0305 a0001c0001t0006g0006 a0001c0001t0006g0041 others(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 | 26 | a0001c0001t0002g0221 a0001c0001t0002g0226 a0001c0001t0002g0233 others(23): Show |
27 | HG00735.hp1 HG01069.hp1 HG01071.hp1 others(24): 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 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0008 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0002g0072 a0001c0001t0003g0069 a0001c0001t0003g0077 others(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 | a0001c0001t0014g0103 a0001c0001t0018g0101 a0001c0001t0018g0213 others(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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | a0001c0001t0004g0295 a0001c0001t0004g0353 a0001c0001t0019g0082 others(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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0001g0094 a0001c0001t0001g0099 a0001c0001t0001g0202 others(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 | 84 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(81): 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 | a0001c0001t0042g0349 a0001c0001t0042g0350 |
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 | a0001c0001t0005g0061 a0001c0001t0005g0065 a0001c0001t0005g0308 others(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 | a0001c0001t0005g0064 a0001c0001t0005g0176 a0001c0001t0089g0328 |
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 | a0001c0001t0005g0096 a0001c0001t0005g0330 a0001c0001t0012g0200 others(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 | a0001c0001t0005g0352 a0001c0001t0012g0216 a0001c0001t0087g0329 others(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 | a0001c0001t0005g0043 a0001c0001t0005g0063 a0001c0001t0005g0299 others(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 | a0001c0002t0021g0271 | 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 | a0001c0001t0095g0067 a0001c0002t0021g0011 a0001c0002t0021g0356 |
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 | a0001c0001t0005g0300 | 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 | a0001c0001t0088g0272 | 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 | a0001c0001t0035g0184 | 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 | a0001c0001t0035g0066 a0001c0001t0052g0016 |
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 | a0001c0001t0052g0016 | 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 | a0001c0001t0012g0288 a0001c0001t0018g0196 a0001c0001t0018g0286 |
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 | a0001c0001t0004g0305 a0001c0001t0006g0006 a0001c0001t0006g0041 others(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 | 3 | a0001c0001t0006g0174 a0001c0001t0006g0177 a0001c0001t0009g0087 |
3 | HG00735.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.185-9435G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52526172 | |||||||
chr6:52526174 | C | G | 2 | a0001c0001t0006g0171 a0001c0001t0006g0318 |
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 | a0001c0001t0082g0348 | 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 | a0001c0001t0059g0209 | 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 | a0001c0001t0003g0331 | 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 | a0001c0001t0010g0038 a0001c0001t0010g0039 |
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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0064g0334 | 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 | a0001c0001t0001g0165 | 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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0066g0312 | 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 | 88 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(85): 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 | a0001c0001t0024g0033 a0001c0001t0024g0034 |
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 | a0001c0001t0019g0082 a0001c0001t0019g0084 a0001c0001t0019g0100 others(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 | a0001c0001t0056g0188 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | 125 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(122): 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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | 45 | a0001c0001t0004g0305 a0001c0001t0006g0006 a0001c0001t0006g0041 others(42): Show |
46 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(43): 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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | a0001c0001t0001g0003 a0001c0001t0001g0125 a0001c0001t0001g0142 others(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 | 322 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(319): Show |
338 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.184+8527G>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527256 | |||||||
chr6:52527325 | A | C | 333 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(330): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): 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 | a0001c0001t0015g0115 a0001c0001t0015g0129 a0001c0001t0015g0147 others(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 | 270 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(267): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.184+8405delT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52527377 | |||||||
chr6:52527429 | A | G | 1 | a0001c0001t0008g0270 | 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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | a0001c0001t0034g0191 a0001c0001t0034g0259 |
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 | a0001c0001t0005g0190 a0001c0001t0005g0299 a0001c0001t0005g0354 |
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 | 37 | a0001c0001t0004g0305 a0001c0001t0006g0006 a0001c0001t0006g0068 others(34): Show |
38 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(35): 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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | a0001c0001t0031g0181 a0001c0001t0031g0182 a0001c0001t0031g0269 others(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 | a0001c0001t0066g0312 | 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 | 43 | a0001c0001t0004g0305 a0001c0001t0006g0006 a0001c0001t0006g0041 others(40): Show |
44 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(41): 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 | a0001c0001t0008g0009 a0001c0001t0008g0257 a0001c0001t0008g0258 others(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 | a0001c0001t0037g0172 a0001c0001t0037g0351 |
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 | a0001c0001t0078g0179 | 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 | 286 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(283): Show |
301 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(298): 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 | a0001c0001t0024g0033 a0001c0001t0024g0034 |
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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | 112 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(109): 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | 42 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0305 others(39): Show |
43 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(40): 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 | a0001c0001t0027g0150 | 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 | 85 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(82): 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 | a0001c0001t0066g0312 | 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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0082g0348 | 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 | a0001c0001t0005g0308 a0001c0001t0009g0086 a0001c0001t0012g0214 others(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 | a0001c0001t0002g0098 a0001c0001t0010g0266 a0001c0001t0039g0225 others(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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0003g0079 a0001c0001t0003g0212 a0001c0001t0010g0037 others(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 | 114 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(111): 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 | a0001c0001t0008g0009 a0001c0001t0008g0257 a0001c0001t0008g0258 others(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 | a0001c0001t0006g0068 a0001c0001t0006g0171 a0001c0001t0006g0318 |
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 | 114 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(111): 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 | a0001c0001t0008g0009 a0001c0001t0008g0257 a0001c0001t0008g0258 others(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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0008g0009 a0001c0001t0008g0257 a0001c0001t0008g0258 others(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 | a0001c0001t0031g0181 a0001c0001t0031g0182 a0001c0001t0031g0269 |
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 | a0001c0001t0009g0218 a0001c0001t0009g0232 |
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 | 45 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0305 others(42): Show |
46 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.184+6670C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52529113 | |||||||
chr6:52529403 | C | CCTAA | 296 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(293): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): 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 | a0001c0001t0018g0101 a0001c0001t0018g0213 a0001c0001t0032g0020 others(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 | 48 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0305 others(45): Show |
49 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(46): 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 | a0001c0001t0008g0009 a0001c0001t0008g0257 a0001c0001t0008g0258 others(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 | 46 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0305 others(43): Show |
47 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(44): 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 | a0001c0001t0009g0183 | 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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0043g0344 | 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 | a0001c0001t0082g0348 | 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 | a0001c0001t0075g0112 | 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 | a0001c0001t0066g0312 a0001c0001t0078g0179 |
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 | 134 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(131): 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 | a0001c0001t0007g0253 | 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 | a0001c0001t0028g0046 a0001c0001t0028g0048 |
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 | 46 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0305 others(43): Show |
47 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.184+5154C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52530629 | |||||||
chr6:52530690 | T | C | 296 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(293): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.184+5093A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52530690 | |||||||
chr6:52530712 | A | G | 331 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(328): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): 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 | 134 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(131): 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 | 181 | a0001c0001t0001g0223 a0001c0001t0001g0284 a0001c0001t0001g0285 others(178): Show |
190 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(187): 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 | a0001c0001t0008g0009 a0001c0001t0008g0257 a0001c0001t0008g0258 others(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 | 78 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0002g0224 others(75): Show |
80 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.184+4662dupT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52531120 | |||||||
chr6:52531120 | C | CAA | 45 | a0001c0001t0003g0044 a0001c0001t0003g0062 a0001c0001t0003g0074 others(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 | a0001c0001t0003g0060 a0001c0001t0003g0069 a0001c0001t0003g0077 others(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 | 94 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(91): 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 | a0001c0001t0001g0089 a0001c0001t0002g0347 a0001c0001t0004g0052 others(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 | 114 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(111): 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 | 335 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(332): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): 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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0040g0262 | 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 | a0001c0001t0031g0181 a0001c0001t0031g0182 a0001c0001t0031g0269 others(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 | a0001c0001t0007g0219 | 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 | a0001c0001t0007g0219 | 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 | a0001c0001t0007g0219 | 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 | a0001c0001t0007g0219 | 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 | a0001c0001t0007g0219 | 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 | a0001c0001t0007g0219 | 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 | a0001c0001t0007g0219 | 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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0007g0219 | 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 | a0001c0001t0010g0037 a0001c0001t0010g0038 a0001c0001t0010g0039 others(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 | a0001c0001t0033g0185 a0001c0001t0033g0186 a0001c0001t0034g0191 others(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 | a0001c0001t0035g0066 a0001c0001t0035g0184 |
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 | 287 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(284): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): 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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | 114 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(111): 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 | 83 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(80): 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 | a0001c0001t0002g0143 a0001c0001t0002g0233 a0001c0001t0002g0237 others(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 | a0001c0001t0092g0355 | 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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0018g0101 a0001c0001t0018g0213 a0001c0001t0032g0020 others(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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | 114 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(111): 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 | a0001c0001t0018g0213 | 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 | 153 | a0001c0001t0001g0223 a0001c0001t0001g0284 a0001c0001t0001g0285 others(150): Show |
161 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(158): 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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | 208 | a0001c0001t0001g0202 a0001c0001t0001g0223 a0001c0001t0001g0284 others(205): Show |
217 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.184+1698delT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534084 | |||||||
chr6:52534100 | G | T | 1 | a0001c0001t0066g0312 | 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 | a0001c0001t0008g0282 | 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 | 171 | a0001c0001t0001g0223 a0001c0001t0001g0284 a0001c0001t0001g0285 others(168): Show |
180 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.184+1575G>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534208 | |||||||
chr6:52534317 | G | A | 171 | a0001c0001t0001g0223 a0001c0001t0001g0284 a0001c0001t0001g0285 others(168): Show |
180 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.184+1466C>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534317 | |||||||
chr6:52534449 | C | A | 151 | a0001c0001t0001g0223 a0001c0001t0001g0284 a0001c0001t0001g0285 others(148): Show |
160 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.184+1334G>T | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 2/10 | chr6 | 52534449 | |||||||
chr6:52534509 | T | G | 287 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(284): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): 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 | a0001c0001t0005g0300 | 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 | a0001c0001t0093g0336 a0001c0001t0094g0338 |
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 | a0001c0003t0016g0304 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0002g0237 | 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 | a0001c0001t0005g0035 | 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 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
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 | a0001c0001t0056g0188 | 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 | a0001c0001t0053g0024 | 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 | 92 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(89): 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 | 85 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(82): 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 | a0001c0001t0088g0272 | 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 | a0001c0001t0088g0272 | 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 | a0001c0001t0088g0272 | 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 | a0001c0001t0037g0351 a0001c0001t0042g0349 a0001c0001t0042g0350 |
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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | 135 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(132): 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 | a0001c0001t0019g0082 a0001c0001t0019g0084 a0001c0001t0019g0100 others(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 | 45 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0305 others(42): Show |
46 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(43): 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 | a0001c0001t0084g0255 | 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 | a0001c0001t0006g0174 a0001c0001t0006g0177 |
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 | a0001c0001t0005g0005 a0001c0001t0029g0002 a0001c0001t0030g0260 others(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 | a0001c0001t0018g0213 | 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 | 134 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(131): 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 | a0001c0001t0019g0082 a0001c0001t0019g0084 a0001c0001t0019g0100 others(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 | a0001c0001t0049g0029 | 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 | 339 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(336): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.121-1885delA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52537730 | |||||||
chr6:52537746 | G | A | 1 | a0001c0001t0082g0348 | 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 | 49 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0283 others(46): Show |
50 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(47): 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 | a0001c0001t0008g0009 a0001c0001t0008g0257 a0001c0001t0008g0258 others(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 | 293 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(290): Show |
308 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(305): 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 | a0001c0001t0019g0082 a0001c0001t0019g0084 a0001c0001t0019g0100 others(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 | a0001c0001t0016g0311 | 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 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0194 |
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 | a0001c0001t0055g0187 | 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 | a0001c0001t0008g0070 a0001c0001t0008g0071 |
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 | a0001c0001t0008g0257 | 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 | a0001c0001t0023g0018 a0001c0001t0023g0022 a0001c0001t0023g0023 others(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 | |||||||
chr6:52539012 | T | C | 14 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0194 others(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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0005g0043 a0001c0001t0013g0267 |
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 | a0001c0001t0009g0183 a0001c0001t0009g0208 a0001c0001t0059g0209 |
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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0001g0050 a0001c0001t0002g0347 a0001c0001t0004g0052 others(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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | a0001c0001t0004g0138 | 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 | 85 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(82): 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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0007g0227 | 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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0068g0097 | 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 | a0001c0001t0020g0246 | 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 | a0001c0001t0031g0181 a0001c0001t0031g0182 a0001c0001t0031g0269 others(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 | a0001c0001t0006g0006 a0001c0001t0006g0167 a0001c0001t0006g0168 others(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 | a0001c0001t0010g0037 a0001c0001t0010g0038 a0001c0001t0010g0039 others(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 | a0001c0001t0018g0101 a0001c0001t0018g0213 a0001c0001t0032g0020 others(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 | 224 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(221): 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 | a0001c0001t0002g0221 a0001c0001t0002g0236 |
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 | a0001c0001t0013g0267 | 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 | a0001c0001t0066g0312 | 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 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0194 others(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 | a0001c0001t0008g0296 a0001c0001t0026g0290 |
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 | a0001c0001t0082g0348 | 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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0194 others(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 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0194 others(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 | a0001c0001t0018g0101 a0001c0001t0018g0213 a0001c0001t0032g0020 others(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 | 244 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(241): Show |
255 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.121-5958dupA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52541803 | |||||||
chr6:52541803 | G | GTT | 12 | a0001c0001t0002g0217 a0001c0001t0010g0037 a0001c0001t0010g0038 others(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 | a0001c0001t0005g0005 a0001c0001t0029g0002 a0001c0001t0030g0260 others(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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0039g0315 a0001c0001t0049g0029 |
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 | a0001c0001t0018g0101 a0001c0001t0019g0084 a0001c0001t0032g0020 others(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 | a0001c0001t0018g0213 a0001c0001t0019g0082 a0001c0001t0019g0100 others(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 | a0001c0001t0066g0312 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0054g0032 | 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 | a0001c0001t0082g0348 | 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 | a0001c0001t0057g0166 | 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 | a0001c0001t0082g0348 | 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 | a0001c0001t0018g0213 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | 202 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(199): 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 | a0001c0001t0002g0240 a0001c0001t0004g0137 a0001c0001t0007g0250 others(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 | 266 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(263): Show |
277 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.121-6416C>A | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52542262 | |||||||
chr6:52542276 | T | A | 31 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0283 others(28): Show |
32 | HG00140.hp2 HG00280.hp1 HG01255.hp2 others(29): 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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0006g0287 a0001c0001t0007g0001 a0001c0001t0007g0139 others(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 | a0001c0001t0005g0005 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | 49 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0283 others(46): Show |
50 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(47): 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 | a0001c0001t0057g0166 | 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 | 84 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(81): 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 | a0001c0001t0011g0015 | 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 | a0001c0001t0060g0319 | 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 | a0001c0001t0070g0102 | 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 | 84 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(81): 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 | a0001c0001t0023g0018 a0001c0001t0023g0022 a0001c0001t0023g0023 others(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 | a0001c0001t0082g0348 | 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 | a0001c0001t0095g0067 | 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 | a0001c0001t0005g0005 a0001c0001t0029g0002 a0001c0001t0030g0260 others(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 | a0001c0001t0005g0300 a0001c0001t0088g0272 |
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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0016g0311 | 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 | a0001c0001t0044g0076 | 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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0092g0355 | 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 | a0001c0001t0092g0355 | 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 | a0001c0001t0002g0072 a0001c0001t0040g0261 a0001c0001t0040g0262 |
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 | 84 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(81): 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 | 84 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(81): 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 | 332 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(329): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): 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 | a0001c0001t0031g0181 a0001c0001t0031g0182 a0001c0001t0031g0269 others(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 | a0001c0001t0010g0037 a0001c0001t0010g0038 a0001c0001t0010g0039 others(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 | a0001c0001t0037g0172 | 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 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0194 others(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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0091g0154 | 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 | a0001c0001t0037g0172 | 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 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0194 others(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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | 84 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(81): 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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0018g0101 a0001c0001t0018g0213 a0001c0001t0032g0020 others(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 | a0001c0001t0010g0037 a0001c0001t0010g0038 a0001c0001t0010g0039 others(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 | 327 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(324): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): 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 | a0001c0001t0001g0164 a0001c0001t0004g0105 a0001c0001t0004g0106 others(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 | a0001c0001t0095g0067 | 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 | 84 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(81): 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 | a0001c0001t0095g0067 | 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 | a0001c0001t0011g0019 | 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 | a0001c0001t0066g0312 | 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 | 183 | a0001c0001t0001g0223 a0001c0001t0001g0284 a0001c0001t0001g0285 others(180): Show |
192 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(189): 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 | a0001c0001t0034g0259 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0091g0154 | 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 | a0001c0002t0021g0271 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | |||||||
chr6:52546070 | C | G | 5 | a0001c0001t0023g0018 a0001c0001t0023g0022 a0001c0001t0023g0023 others(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 | 123 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0003g0044 others(120): Show |
128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): 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 | a0001c0001t0091g0154 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0194 others(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 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0194 others(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 | a0001c0001t0061g0263 | 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 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0194 others(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 | 153 | a0001c0001t0001g0223 a0001c0001t0001g0284 a0001c0001t0001g0285 others(150): Show |
161 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(158): 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0002t0021g0011 a0001c0002t0021g0356 |
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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0031g0181 a0001c0001t0031g0182 a0001c0001t0031g0269 others(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 | a0001c0001t0082g0348 | 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 | a0001c0001t0009g0085 | 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 | a0001c0001t0007g0145 a0001c0001t0015g0115 a0001c0001t0015g0129 others(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 | 222 | a0001c0001t0001g0223 a0001c0001t0001g0284 a0001c0001t0001g0285 others(219): Show |
231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): 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 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0194 others(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 | a0001c0001t0008g0298 | 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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0060g0319 | 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 | a0001c0001t0002g0098 a0001c0001t0019g0082 |
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 | a0001c0001t0095g0067 | 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 | a0001c0001t0005g0299 a0001c0001t0008g0009 a0001c0001t0008g0257 others(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 | a0001c0001t0003g0341 | 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 | 49 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0283 others(46): Show |
50 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(47): 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 | a0001c0001t0001g0164 a0001c0001t0004g0105 a0001c0001t0004g0106 others(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 | a0001c0001t0052g0016 a0001c0003t0006g0307 a0001c0003t0016g0304 others(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 | 84 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(81): 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 | 333 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(330): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): 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 | a0001c0001t0036g0320 | 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 | a0001c0001t0010g0037 a0001c0001t0010g0038 a0001c0001t0010g0039 others(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 | 49 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0283 others(46): Show |
50 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(47): 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 | a0001c0001t0005g0299 a0001c0001t0008g0009 a0001c0001t0008g0257 others(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 | a0001c0001t0005g0005 a0001c0001t0029g0002 a0001c0001t0030g0260 others(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 | a0001c0001t0092g0355 | 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 | a0001c0001t0005g0308 a0001c0001t0005g0330 a0001c0001t0012g0058 others(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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0078g0179 | 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 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0194 others(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 | a0001c0001t0038g0317 | 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 | a0001c0001t0066g0312 | 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 | a0001c0001t0008g0276 a0001c0001t0008g0282 a0001c0001t0099g0275 |
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 | a0001c0001t0001g0161 | 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 | a0001c0001t0010g0037 a0001c0001t0010g0038 a0001c0001t0010g0039 others(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 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0283 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0002g0220 a0001c0001t0003g0235 |
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 | a0001c0001t0010g0037 a0001c0001t0010g0038 a0001c0001t0010g0039 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0003g0162 | 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 | a0001c0001t0009g0085 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0001g0156 | 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 | a0001c0001t0033g0185 a0001c0001t0033g0186 |
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 | a0001c0001t0019g0082 a0001c0001t0019g0084 a0001c0001t0019g0100 others(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 | a0001c0001t0010g0037 a0001c0001t0010g0038 a0001c0001t0010g0039 others(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 | 343 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(340): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.121-14850T>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52550696 | |||||||
chr6:52550712 | C | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(81): 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 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0194 others(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 | 48 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0283 others(45): Show |
49 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(46): 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 | a0001c0001t0023g0018 a0001c0001t0023g0022 a0001c0001t0023g0023 others(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 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0283 others(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 | a0001c0001t0046g0013 a0001c0001t0047g0012 |
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 | 276 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(273): Show |
288 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(285): 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0023g0023 a0001c0001t0038g0317 |
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 | 84 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(81): 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 | 84 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(81): 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 | a0001c0001t0024g0033 a0001c0001t0024g0034 |
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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | 84 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(81): 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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | 48 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0283 others(45): Show |
49 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(46): 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 | a0001c0001t0008g0281 | 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 | a0001c0001t0004g0305 | 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 | a0001c0001t0023g0018 a0001c0001t0023g0022 a0001c0001t0023g0023 others(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 | a0001c0001t0001g0199 a0001c0001t0001g0204 a0001c0001t0001g0205 |
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 | a0001c0001t0082g0348 | 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 | 166 | a0001c0001t0001g0223 a0001c0001t0001g0284 a0001c0001t0001g0285 others(163): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.121-17484A>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52553330 | |||||||
chr6:52553577 | C | T | 48 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0283 others(45): Show |
49 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(46): 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 | a0001c0001t0005g0063 a0001c0001t0005g0096 a0001c0001t0009g0086 others(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 | a0001c0001t0012g0216 | 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 | a0001c0001t0005g0005 a0001c0001t0017g0010 a0001c0001t0017g0170 others(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 | a0001c0001t0023g0018 a0001c0001t0023g0022 a0001c0001t0023g0023 others(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 | a0001c0001t0069g0053 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0019g0082 a0001c0001t0019g0084 a0001c0001t0019g0100 others(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 | a0001c0001t0028g0047 | 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 | 48 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0283 others(45): Show |
49 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(46): 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 | a0001c0001t0043g0344 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0003g0230 a0001c0001t0005g0005 a0001c0001t0029g0002 others(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 | 60 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(57): 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 | a0001c0001t0001g0089 a0001c0001t0001g0094 a0001c0001t0001g0099 others(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 | a0001c0001t0007g0249 a0001c0001t0073g0248 |
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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0006g0287 a0001c0001t0007g0001 a0001c0001t0007g0139 others(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 | 217 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(214): 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 | a0001c0001t0004g0104 a0001c0001t0004g0110 a0001c0001t0004g0136 others(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 | a0001c0001t0005g0300 | 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 | 84 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(81): 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 | a0001c0001t0037g0351 a0001c0001t0042g0349 a0001c0001t0042g0350 |
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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | a0001c0001t0066g0312 | 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 | a0001c0001t0001g0153 a0001c0001t0001g0333 a0001c0001t0006g0132 others(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 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0194 others(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 | 84 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(81): 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 | a0001c0001t0005g0299 a0001c0001t0008g0009 a0001c0001t0008g0257 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | 276 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(273): Show |
288 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(285): 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 | a0001c0001t0023g0018 a0001c0001t0023g0022 a0001c0001t0023g0023 others(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 | a0001c0001t0066g0312 | 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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0037g0351 a0001c0001t0042g0349 a0001c0001t0042g0350 |
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 | a0001c0001t0022g0362 | 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 | a0001c0001t0066g0312 | 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 | a0001c0001t0009g0293 | 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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0002t0021g0271 | 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 | 48 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0283 others(45): Show |
49 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(46): 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 | a0001c0001t0006g0168 | 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 | 76 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0283 others(73): Show |
81 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(78): Show |
intron_variant | MODIFIER | c.120+19868dupT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52556927 | |||||||
chr6:52556927 | CA | C | 149 | a0001c0001t0001g0003 a0001c0001t0001g0051 a0001c0001t0001g0054 others(146): 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 | a0001c0001t0037g0172 | 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 | a0001c0001t0005g0299 a0001c0001t0008g0009 a0001c0001t0008g0257 others(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 | a0001c0001t0066g0312 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0005g0005 a0001c0001t0017g0010 a0001c0001t0017g0170 others(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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0031g0181 a0001c0001t0031g0182 a0001c0001t0031g0269 others(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 | a0001c0002t0021g0271 | 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 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0194 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0005g0308 a0001c0001t0005g0330 a0001c0001t0087g0329 others(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 | a0001c0001t0049g0029 | 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0066g0312 | 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 | a0001c0001t0082g0348 | 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 | a0001c0001t0005g0005 a0001c0001t0029g0002 a0001c0001t0030g0260 |
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 | a0001c0001t0003g0077 a0001c0001t0003g0078 a0001c0001t0003g0095 |
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 | a0001c0001t0028g0046 a0001c0001t0028g0048 |
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 | a0001c0001t0002g0347 a0001c0001t0004g0052 a0001c0001t0004g0056 others(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 | a0001c0001t0005g0005 a0001c0001t0019g0082 a0001c0001t0019g0084 others(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 | a0001c0002t0021g0271 | 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 | a0001c0001t0005g0064 | 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 | a0001c0001t0092g0355 | 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 | a0001c0001t0010g0266 | 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 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0194 others(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 | a0001c0002t0021g0271 | 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 | a0001c0001t0005g0354 | 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 | a0001c0001t0005g0005 a0001c0001t0029g0002 a0001c0001t0030g0260 others(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 | a0001c0001t0006g0132 | 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 | 197 | a0001c0001t0001g0223 a0001c0001t0001g0284 a0001c0001t0001g0285 others(194): Show |
205 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(202): 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 | a0001c0001t0003g0313 | 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 | a0001c0002t0021g0271 | 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 | a0001c0001t0005g0300 | 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 | 212 | a0001c0001t0001g0223 a0001c0001t0001g0284 a0001c0001t0001g0285 others(209): Show |
225 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(222): 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 | a0001c0001t0001g0125 | 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 | a0001c0001t0005g0096 | 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 | a0001c0001t0005g0299 a0001c0001t0008g0289 a0001c0001t0009g0293 others(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 | a0001c0001t0005g0005 a0001c0001t0007g0332 a0001c0001t0018g0196 others(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 | 221 | a0001c0001t0001g0223 a0001c0001t0001g0284 a0001c0001t0001g0285 others(218): Show |
230 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.120+16514T>C | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52560282 | |||||||
chr6:52560391 | A | G | 306 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(303): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(314): 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 | a0001c0001t0007g0249 a0001c0001t0073g0248 |
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 | a0001c0001t0005g0300 a0001c0001t0088g0272 |
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 | 86 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(83): 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 | 85 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(82): 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 | a0001c0002t0021g0271 | 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 | a0001c0001t0008g0070 a0001c0001t0008g0071 a0001c0001t0083g0189 |
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 | a0001c0001t0054g0032 | 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 | a0001c0001t0001g0204 | 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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0003g0079 a0001c0001t0003g0212 |
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 | a0001c0001t0066g0312 | 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 | 103 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(100): 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 | 81 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0003g0044 others(78): Show |
82 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.120+15308delA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52561487 | |||||||
chr6:52561525 | G | A | 2 | a0001c0001t0037g0351 a0001c0001t0042g0350 |
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 | 85 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(82): 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 | a0001c0001t0095g0067 | 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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0003g0074 a0001c0001t0003g0092 a0001c0001t0003g0093 |
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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0092g0355 | 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 | a0001c0001t0010g0266 | 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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | 161 | a0001c0001t0001g0223 a0001c0001t0001g0284 a0001c0001t0001g0285 others(158): Show |
169 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(166): 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 | a0001c0001t0002g0226 | 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 | a0001c0001t0018g0286 | 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 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0199 others(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 | a0001c0001t0037g0351 a0001c0001t0042g0349 a0001c0001t0042g0350 |
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 | a0001c0001t0064g0334 | 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 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0194 others(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 | a0001c0001t0066g0312 | 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 | a0001c0001t0005g0005 | 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 | a0001c0001t0092g0355 | 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 | a0001c0001t0066g0312 | 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 | 155 | a0001c0001t0001g0223 a0001c0001t0001g0284 a0001c0001t0001g0285 others(152): Show |
163 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(160): 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 | a0001c0001t0004g0159 | 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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0092g0355 | 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 | a0001c0001t0079g0128 | 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 | a0001c0001t0005g0005 a0001c0001t0019g0082 a0001c0001t0019g0084 others(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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0026g0357 | 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 | 48 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0283 others(45): Show |
49 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(46): 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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0003t0016g0306 | 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 | a0001c0001t0033g0185 a0001c0001t0033g0186 a0001c0001t0055g0187 |
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 | 80 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0054 others(77): 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 | a0001c0001t0001g0051 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0002g0072 a0001c0001t0002g0217 a0001c0001t0003g0044 others(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 | 91 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0283 others(88): Show |
97 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(94): 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 | a0001c0001t0006g0287 a0001c0001t0007g0001 a0001c0001t0007g0139 others(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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0004g0052 a0001c0001t0004g0056 a0001c0001t0004g0138 others(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 | a0001c0001t0004g0136 a0001c0001t0004g0137 a0001c0001t0014g0073 others(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 | 74 | a0001c0001t0001g0131 a0001c0001t0001g0161 a0001c0001t0001g0284 others(71): Show |
79 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.120+12944delA | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563851 | |||||||
chr6:52563877 | G | A | 1 | a0001c0001t0012g0058 | 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 | 322 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(319): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.120+12895dupT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52563900 | |||||||
chr6:52563989 | G | A | 1 | a0001c0001t0082g0348 | 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 | a0001c0001t0037g0172 | 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 | a0001c0001t0048g0014 | 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 | a0001c0001t0005g0005 a0001c0001t0029g0002 |
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 | a0001c0001t0005g0299 a0001c0001t0008g0009 a0001c0001t0008g0257 others(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 | 332 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(329): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0003g0163 | 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 | a0001c0001t0006g0169 a0001c0001t0017g0010 a0001c0001t0017g0170 others(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 | a0001c0001t0005g0005 a0001c0001t0029g0002 a0001c0001t0078g0179 |
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 | a0001c0002t0021g0356 | 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 | a0001c0001t0003g0069 a0001c0001t0003g0077 a0001c0001t0003g0078 others(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 | a0001c0001t0003g0044 a0001c0001t0003g0060 a0001c0001t0003g0062 others(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 | a0001c0001t0005g0194 | 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 | a0001c0001t0005g0299 a0001c0001t0008g0009 a0001c0001t0008g0257 others(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 | a0001c0002t0021g0271 | 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 | a0001c0002t0021g0271 | 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 | a0001c0001t0040g0261 a0001c0001t0040g0262 |
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 | 150 | a0001c0001t0001g0223 a0001c0001t0001g0284 a0001c0001t0001g0285 others(147): Show |
161 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(158): 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 | a0001c0001t0036g0320 | 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 | 118 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(115): 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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | 85 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(82): 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 | a0001c0001t0005g0299 a0001c0001t0008g0009 a0001c0001t0008g0257 others(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 | a0001c0001t0023g0023 a0001c0001t0038g0317 |
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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | 48 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0283 others(45): Show |
49 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(46): 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 | a0001c0001t0030g0343 | 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 | 92 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(89): 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 | a0001c0001t0067g0211 | 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 | a0001c0001t0001g0153 a0001c0001t0001g0333 a0001c0001t0006g0132 others(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 | 48 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0283 others(45): Show |
49 | HG00140.hp2 HG00280.hp1 HG00735.hp1 others(46): 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 | a0001c0001t0092g0355 | 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 | a0001c0001t0001g0094 a0001c0001t0003g0044 a0001c0001t0003g0060 others(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 | a0001c0001t0005g0299 a0001c0001t0008g0009 a0001c0001t0008g0257 others(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 | 267 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(264): Show |
281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): 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 | a0001c0001t0005g0299 a0001c0001t0008g0009 a0001c0001t0008g0257 others(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 | a0001c0001t0001g0094 a0001c0001t0003g0069 a0001c0001t0003g0077 others(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 | 150 | a0001c0001t0001g0223 a0001c0001t0001g0284 a0001c0001t0001g0285 others(147): Show |
161 | HG00140.hp2 HG00280.hp1 HG00558.hp1 others(158): 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 | a0001c0002t0021g0271 | 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 | a0001c0001t0008g0070 a0001c0001t0008g0071 a0001c0001t0083g0189 |
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 | 84 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(81): 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 | a0001c0001t0023g0018 a0001c0001t0023g0022 a0001c0001t0023g0023 others(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 | a0001c0001t0001g0094 a0001c0001t0003g0044 a0001c0001t0003g0060 others(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 | a0001c0001t0001g0223 a0001c0001t0002g0004 a0001c0001t0002g0007 others(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 | a0001c0001t0019g0206 a0001c0001t0043g0207 a0001c0001t0043g0344 others(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 | a0001c0001t0017g0010 a0001c0001t0017g0170 a0001c0001t0017g0322 others(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 | a0001c0001t0033g0185 a0001c0001t0033g0186 a0001c0001t0055g0187 |
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 | 178 | a0001c0001t0001g0094 a0001c0001t0001g0223 a0001c0001t0001g0284 others(175): Show |
189 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.120+7407delT | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52569388 | |||||||
chr6:52569388 | TAA | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(139): 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 | a0001c0001t0001g0165 a0001c0001t0019g0082 a0001c0001t0019g0084 others(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 | a0001c0001t0001g0094 a0001c0001t0003g0069 a0001c0001t0003g0074 others(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 | a0001c0001t0005g0299 a0001c0001t0008g0009 a0001c0001t0008g0257 others(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 | a0001c0001t0066g0312 | 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 | a0001c0001t0005g0300 a0001c0001t0088g0272 |
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 | 84 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(81): 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 | a0001c0001t0082g0348 a0001c0001t0095g0067 |
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 | a0001c0001t0066g0312 | 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 | a0001c0001t0091g0154 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0223 a0001c0001t0001g0284 others(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 | a0001c0001t0001g0094 a0001c0001t0003g0044 a0001c0001t0003g0060 others(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 | a0001c0001t0066g0312 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0099 a0001c0001t0001g0164 others(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 | a0001c0001t0001g0089 a0001c0001t0002g0072 a0001c0001t0003g0044 others(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 | a0001c0001t0002g0210 a0001c0001t0011g0019 a0001c0001t0011g0025 others(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 | 54 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(51): 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 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0141 others(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 | a0001c0001t0001g0156 a0001c0001t0004g0056 a0001c0001t0004g0310 others(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 | a0001c0001t0015g0057 | 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 | a0001c0001t0002g0265 | 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 | 146 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(143): 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 | a0001c0001t0003g0340 a0001c0001t0003g0341 |
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 | a0001c0001t0006g0068 a0001c0001t0011g0019 a0001c0001t0011g0025 others(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 | a0001c0001t0001g0333 a0001c0001t0003g0331 a0001c0001t0005g0330 others(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 | a0001c0001t0002g0072 a0001c0001t0005g0035 a0001c0001t0005g0036 others(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 | a0001c0001t0076g0337 a0001c0001t0093g0336 a0001c0001t0094g0338 |
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 | a0001c0001t0055g0187 | 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 | a0001c0001t0005g0190 a0001c0001t0033g0185 a0001c0001t0033g0186 others(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 | a0001c0001t0003g0340 a0001c0001t0003g0341 |
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 | a0001c0001t0008g0276 a0001c0001t0099g0275 |
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 | a0001c0001t0001g0345 a0001c0001t0002g0347 a0001c0001t0020g0346 |
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 | 348 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(345): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): 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 | a0001c0001t0001g0345 a0001c0001t0002g0347 a0001c0001t0020g0346 |
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 | a0001c0001t0009g0277 a0001c0001t0011g0015 a0001c0001t0011g0019 others(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 | a0001c0001t0001g0089 a0001c0001t0001g0094 a0001c0001t0001g0099 others(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 | 102 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(99): 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 | 111 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0202 others(108): Show |
120 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.120+4569C>G | TRAM2 | ENSG00000065308.5 | transcript | ENST00000182527.4 | protein_coding | 1/10 | chr6 | 52572227 | |||||||
chr6:52572402 | A | G | 351 | a0001c0001t0001g0003 a0001c0001t0001g0050 a0001c0001t0001g0051 others(348): Show |
367 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(364): 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 | a0001c0001t0005g0190 a0001c0001t0026g0280 a0001c0001t0033g0185 others(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 | a0001c0001t0009g0183 a0001c0001t0031g0181 a0001c0001t0031g0182 others(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 | a0001c0001t0003g0340 a0001c0001t0003g0341 a0001c0001t0004g0339 |
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 | a0001c0001t0011g0015 a0001c0001t0011g0019 a0001c0001t0011g0025 others(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 | 111 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0202 others(108): Show |
120 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(117): 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 | a0001c0001t0037g0351 a0001c0001t0042g0349 a0001c0001t0042g0350 |
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 | a0001c0001t0037g0351 a0001c0001t0042g0349 a0001c0001t0042g0350 |
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 | 154 | a0001c0001t0001g0089 a0001c0001t0001g0094 a0001c0001t0001g0099 others(151): Show |
166 | HG00140.hp1 HG00280.hp2 HG00558.hp1 others(163): 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 | a0001c0001t0008g0270 a0001c0001t0088g0272 a0001c0002t0021g0271 |
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 | a0001c0001t0001g0345 a0001c0001t0002g0347 a0001c0001t0020g0346 |
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 | a0002c0004t0025g0358 | 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 | a0001c0001t0006g0068 | 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 | a0001c0001t0078g0179 | 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 | a0001c0001t0035g0066 a0001c0001t0095g0067 |
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 | a0001c0001t0072g0274 | 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 | a0001c0001t0004g0353 a0001c0001t0005g0352 a0001c0001t0005g0354 |
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 | a0001c0001t0054g0032 | 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 | a0001c0001t0003g0060 a0001c0001t0003g0062 a0001c0001t0005g0061 others(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 | a0001c0001t0003g0273 | 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 | a0001c0001t0030g0342 a0001c0001t0030g0343 a0001c0001t0043g0344 |
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 | a0001c0001t0092g0355 a0001c0002t0021g0011 a0001c0002t0021g0356 |
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 | 97 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0202 others(94): Show |
105 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(102): 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 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0345 a0001c0001t0002g0347 a0001c0001t0009g0183 others(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 | a0001c0001t0072g0274 | 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 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0333 others(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 | a0001c0001t0005g0190 a0001c0001t0009g0183 a0001c0001t0031g0181 others(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 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0004g0283 others(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 | 95 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0202 others(92): Show |
103 | HG00558.hp1 HG00609.hp2 HG00621.hp1 others(100): 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 | a0001c0001t0008g0276 a0001c0001t0008g0281 a0001c0001t0009g0277 others(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 | a0001c0001t0008g0282 | 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 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0333 others(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 | a0001c0001t0082g0348 | 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 | a0001c0001t0005g0035 | 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 | a0001c0001t0010g0037 a0001c0001t0010g0038 a0001c0001t0010g0039 |
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 | a0001c0001t0004g0353 a0001c0001t0005g0352 a0001c0001t0005g0354 others(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 | a0001c0001t0026g0357 | 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 | a0001c0001t0013g0040 | 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 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0010g0037 others(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 |