Item | Value |
---|---|
geneid | 728294 |
ensemblid | ENSG00000180902.18 |
hgncid | 28358 |
symbol | D2HGDH |
name | D-2-hydroxyglutarate dehydrogenase |
refseq_nuc | NM_152783.5 |
refseq_prot | NP_689996.4 |
ensembl_nuc | ENST00000321264.9 |
ensembl_prot | ENSP00000315351.4 |
mane_status | MANE Select |
chr | chr2 |
start | 241734630 |
end | 241768811 |
strand | + |
ver | v1.2 |
region | chr2:241734630-241768811 |
region5000 | chr2:241729630-241773811 |
regionname0 | D2HGDH_chr2_241734630_241768811 |
regionname5000 | D2HGDH_chr2_241729630_241773811 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 521 | 170 | 28 | 33 | 80 | 6 | 21 | 54 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0002 | 0/0 | 521 | 104 | 26 | 22 | 46 | 4 | 6 | 39 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0003 | 0/0 | 521 | 45 | 8 | 12 | 15 | 3 | 7 | 10 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0004 | 0/0 | 521 | 26 | 13 | 3 | 7 | 0 | 3 | 5 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0005 | 0/0 | 521 | 23 | 6 | 2 | 7 | 1 | 7 | 3 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0006 | 0/0 | 521 | 15 | 0 | 3 | 12 | 0 | 0 | 10 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0007 | 0/0 | 521 | 8 | 6 | 0 | 2 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0008 | 0/0 | 521 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0009 | 0/0 | 521 | 3 | 0 | 0 | 3 | 0 | 0 | 2 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0010 | 0/0 | 521 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0011 | 0/0 | 521 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0012 | 0/0 | 521 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0013 | 0/0 | 521 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0014 | 0/0 | 521 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0015 | 0/0 | 521 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0016 | 0/0 | 521 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0017 | 0/0 | 521 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0018 | 0/0 | 521 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0019 | 0/0 | 521 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
a0020 | 0/0 | 380 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(375): Show |
chr2 | 241729630 | 241773811 |
a0021 | 0/0 | 521 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | MLPRR others(516): Show |
chr2 | 241729630 | 241773811 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1563 | 161 | 24 | 32 | 76 | 6 | 21 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0001c0012 | 0/0 | 1563 | 3 | 3 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0001c0013 | 0/0 | 1563 | 3 | 0 | 0 | 3 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0001c0026 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0001c0027 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0001c0029 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0002c0002 | 0/0 | 1563 | 97 | 20 | 21 | 46 | 4 | 6 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0002c0009 | 0/0 | 1563 | 6 | 6 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0002c0032 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0003c0003 | 0/0 | 1563 | 39 | 8 | 10 | 14 | 3 | 4 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0003c0008 | 0/0 | 1563 | 6 | 0 | 2 | 1 | 0 | 3 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0004c0005 | 0/0 | 1563 | 21 | 9 | 2 | 7 | 0 | 3 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0004c0016 | 0/0 | 1563 | 2 | 1 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0004c0021 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0004c0022 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0004c0023 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0005c0004 | 0/0 | 1563 | 22 | 5 | 2 | 7 | 1 | 7 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0005c0018 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0006c0006 | 0/0 | 1563 | 12 | 0 | 3 | 9 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0006c0015 | 0/0 | 1563 | 3 | 0 | 0 | 3 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0007c0007 | 0/0 | 1563 | 7 | 5 | 0 | 2 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0007c0017 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0008c0011 | 0/0 | 1563 | 3 | 3 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0008c0024 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0009c0014 | 0/0 | 1563 | 3 | 0 | 0 | 3 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0010c0010 | 0/0 | 1563 | 3 | 3 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0011c0028 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0012c0031 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0013c0025 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0014c0036 | 0/0 | 1563 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0015c0030 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0016c0020 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0017c0037 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0018c0034 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0019c0019 | 0/0 | 1563 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 | ||
a0020c0035 | 0/0 | 1550 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1545): Show |
chr2 | 241729630 | 241773811 | ||
a0021c0033 | 0/0 | 1563 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ATGCT others(1558): Show |
chr2 | 241729630 | 241773811 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2566 | 14 | 0 | 2 | 8 | 1 | 3 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0002 | 0/0 | 2566 | 29 | 8 | 2 | 18 | 1 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0003 | 0/1 | 2566 | 42 | 0 | 11 | 20 | 2 | 8 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0004 | 0/0 | 2566 | 11 | 0 | 2 | 7 | 0 | 2 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0005 | 0/0 | 2566 | 2 | 1 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0006 | 1/0 | 2566 | 22 | 3 | 4 | 11 | 2 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0007 | 0/0 | 2566 | 3 | 2 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0008 | 0/0 | 2566 | 2 | 2 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0009 | 0/0 | 2566 | 7 | 0 | 0 | 7 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0012 | 0/0 | 2566 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0016 | 0/0 | 2566 | 2 | 2 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0017 | 0/0 | 2566 | 2 | 0 | 0 | 2 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0018 | 0/0 | 2567 | 2 | 0 | 1 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2562): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0019 | 0/0 | 2566 | 2 | 0 | 1 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0020 | 0/0 | 2566 | 2 | 2 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0022 | 0/0 | 2566 | 2 | 0 | 1 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0025 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0028 | 0/0 | 2566 | 2 | 0 | 2 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0029 | 0/0 | 2566 | 2 | 0 | 2 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0031 | 0/0 | 2566 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0032 | 0/0 | 2566 | 2 | 1 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0035 | 0/0 | 2566 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0036 | 0/0 | 2567 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2562): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0037 | 0/0 | 2566 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0038 | 0/0 | 2548 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2543): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0040 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0041 | 0/0 | 2566 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0042 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0001t0052 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0012t0008 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0012t0030 | 0/0 | 2566 | 2 | 2 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0013t0001 | 0/0 | 2566 | 3 | 0 | 0 | 3 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0026t0002 | 0/0 | 2566 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0027t0002 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0001c0029t0002 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0002t0001 | 0/0 | 2566 | 31 | 1 | 10 | 17 | 2 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0002t0002 | 0/0 | 2566 | 10 | 5 | 0 | 5 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0002t0003 | 0/0 | 2566 | 3 | 1 | 0 | 2 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0002t0004 | 0/0 | 2566 | 26 | 0 | 6 | 18 | 0 | 2 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0002t0005 | 0/0 | 2566 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0002t0007 | 0/0 | 2566 | 11 | 6 | 3 | 0 | 2 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0002t0008 | 0/0 | 2566 | 2 | 2 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0002t0009 | 0/0 | 2566 | 2 | 0 | 0 | 2 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0002t0012 | 0/0 | 2566 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0002t0013 | 0/0 | 2566 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0002t0015 | 0/0 | 2566 | 2 | 2 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0002t0025 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0002t0026 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0002t0033 | 0/0 | 2566 | 2 | 2 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0002t0034 | 0/0 | 2566 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0002t0039 | 0/0 | 2566 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0002t0049 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0009t0008 | 0/0 | 2566 | 6 | 6 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0002c0032t0015 | 0/0 | 2566 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0003c0003t0002 | 0/0 | 2566 | 3 | 2 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0003c0003t0005 | 0/0 | 2566 | 10 | 2 | 1 | 3 | 1 | 3 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0003c0003t0007 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0003c0003t0010 | 0/0 | 2566 | 7 | 0 | 0 | 7 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0003c0003t0011 | 0/0 | 2566 | 7 | 0 | 5 | 0 | 1 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0003c0003t0013 | 0/0 | 2566 | 4 | 1 | 2 | 0 | 1 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0003c0003t0014 | 0/0 | 2566 | 3 | 0 | 0 | 3 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0003c0003t0021 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0003c0003t0024 | 0/0 | 2567 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2562): Show |
chr2 | 241729630 | 241773811 |
a0003c0003t0043 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0003c0003t0044 | 0/0 | 2567 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2562): Show |
chr2 | 241729630 | 241773811 |
a0003c0008t0001 | 0/0 | 2566 | 3 | 0 | 0 | 0 | 0 | 3 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0003c0008t0004 | 0/0 | 2566 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0003c0008t0005 | 0/0 | 2566 | 2 | 0 | 1 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0004c0005t0002 | 0/0 | 2566 | 2 | 1 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0004c0005t0003 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0004c0005t0005 | 0/0 | 2566 | 5 | 2 | 0 | 1 | 0 | 2 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0004c0005t0007 | 0/0 | 2566 | 3 | 3 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0004c0005t0009 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0004c0005t0010 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0004c0005t0012 | 0/0 | 2566 | 2 | 0 | 1 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0004c0005t0013 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0004c0005t0014 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0004c0005t0024 | 0/0 | 2567 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2562): Show |
chr2 | 241729630 | 241773811 |
a0004c0005t0031 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0004c0005t0047 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0004c0005t0050 | 0/0 | 2567 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2562): Show |
chr2 | 241729630 | 241773811 |
a0004c0016t0012 | 0/0 | 2566 | 2 | 1 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0004c0021t0008 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0004c0022t0048 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0004c0023t0002 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0005c0004t0001 | 0/0 | 2566 | 6 | 1 | 1 | 1 | 1 | 2 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0005c0004t0002 | 0/0 | 2566 | 6 | 0 | 0 | 5 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0005c0004t0003 | 0/0 | 2566 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0005c0004t0005 | 0/0 | 2566 | 3 | 3 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0005c0004t0023 | 0/0 | 2567 | 2 | 1 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2562): Show |
chr2 | 241729630 | 241773811 |
a0005c0004t0027 | 0/0 | 2566 | 2 | 0 | 0 | 0 | 0 | 2 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0005c0004t0045 | 0/0 | 2567 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2562): Show |
chr2 | 241729630 | 241773811 |
a0005c0004t0051 | 0/0 | 2567 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2562): Show |
chr2 | 241729630 | 241773811 |
a0005c0018t0008 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0006c0006t0001 | 0/0 | 2566 | 6 | 0 | 1 | 5 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0006c0006t0002 | 0/0 | 2566 | 4 | 0 | 0 | 4 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0006c0006t0004 | 0/0 | 2566 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0006c0006t0046 | 0/0 | 2567 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2562): Show |
chr2 | 241729630 | 241773811 |
a0006c0015t0001 | 0/0 | 2566 | 3 | 0 | 0 | 3 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0007c0007t0001 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0007c0007t0004 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0007c0007t0005 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0007c0007t0007 | 0/0 | 2566 | 3 | 3 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0007c0007t0026 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0007c0017t0008 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0008c0011t0002 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0008c0011t0007 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0008c0011t0021 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0008c0024t0001 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0009c0014t0003 | 0/0 | 2566 | 3 | 0 | 0 | 3 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0010c0010t0002 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0010c0010t0005 | 0/0 | 2566 | 2 | 2 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0011c0028t0004 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0012c0031t0004 | 0/0 | 2566 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0013c0025t0016 | 0/0 | 2566 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0014c0036t0001 | 0/0 | 2566 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0015c0030t0003 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0016c0020t0005 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0017c0037t0001 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0018c0034t0001 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0019c0019t0002 | 0/0 | 2566 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
a0020c0035t0001 | 0/0 | 2553 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2548): Show |
chr2 | 241729630 | 241773811 |
a0021c0033t0008 | 0/0 | 2566 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | ACTCC others(2561): Show |
chr2 | 241729630 | 241773811 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0001g0377 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0232 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0004g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0004g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0005g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0003 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0222 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0007g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0007g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0008g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0008g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0009g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0009g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0009g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0009g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0009g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0009g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0009g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0012g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0016g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0016g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0017g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0018g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0018g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0019g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0019g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0020g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0020g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0022g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0022g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0025g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0028g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0028g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0029g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0031g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0032g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0032g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0035g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0036g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0037g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0038g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0040g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0041g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0042g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0001t0052g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0012t0008g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0012t0030g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0012t0030g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0013t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0013t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0026t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0027t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0001c0029t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0014 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0005g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0007g0002 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0007g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0007g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0007g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0007g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0007g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0007g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0008g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0008g0380 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0009g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0009g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0012g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0013g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0015g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0015g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0025g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0026g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0033g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0033g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0034g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0039g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0002t0049g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0009t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0009t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0009t0008g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0009t0008g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0009t0008g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0009t0008g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0002c0032t0015g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0002g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0005g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0005g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0005g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0005g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0005g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0005g0360 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0005g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0005g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0007g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0010g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0010g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0010g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0010g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0010g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0010g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0010g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0011g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0011g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0011g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0011g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0011g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0011g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0011g0374 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0013g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0013g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0013g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0013g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0014g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0014g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0014g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0021g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0024g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0043g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0003t0044g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0008t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0008t0001g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0008t0004g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0008t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0003c0008t0005g0371 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0005g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0005g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0005g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0007g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0009g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0010g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0012g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0012g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0013g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0014g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0024g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0031g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0047g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0005t0050g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0016t0012g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0016t0012g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0021t0008g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0022t0048g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0004c0023t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0001g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0002g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0002g0370 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0005g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0005g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0023g0378 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0023g0379 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0027g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0027g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0045g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0004t0051g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0005c0018t0008g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0006c0006t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0006c0006t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0006c0006t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0006c0006t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0006c0006t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0006c0006t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0006c0006t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0006c0006t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0006c0006t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0006c0006t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0006c0006t0004g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0006c0006t0046g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0006c0015t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0006c0015t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0006c0015t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0007c0007t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0007c0007t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0007c0007t0005g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0007c0007t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0007c0007t0007g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0007c0007t0007g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0007c0007t0026g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0007c0017t0008g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0008c0011t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0008c0011t0007g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0008c0011t0021g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0008c0024t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0009c0014t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0009c0014t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0009c0014t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0010c0010t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0010c0010t0005g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0011c0028t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0012c0031t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0013c0025t0016g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0014c0036t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0015c0030t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0016c0020t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0017c0037t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0018c0034t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0019c0019t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0020c0035t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
a0021c0033t0008g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0003 | c0003 | t0011 | g0374 | EUR | GBR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0143 | EUR | GBR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | FIN | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00323 | hp2 | a0005 | c0004 | t0001 | g0352 | EUR | FIN | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00408 | hp1 | a0003 | c0008 | t0005 | g0336 | EAS | CHS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00408 | hp2 | a0006 | c0006 | t0002 | g0295 | EAS | CHS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00423 | hp1 | a0003 | c0003 | t0005 | g0023 | EAS | CHS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00423 | hp2 | a0001 | c0001 | t0006 | g0267 | EAS | CHS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00438 | hp1 | a0003 | c0003 | t0010 | g0328 | EAS | CHS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | CHS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00544 | hp2 | a0001 | c0001 | t0040 | g0214 | EAS | CHS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | CHS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00558 | hp2 | a0002 | c0002 | t0004 | g0049 | EAS | CHS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0145 | EAS | CHS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00609 | hp1 | a0001 | c0001 | t0006 | g0269 | EAS | CHS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00621 | hp1 | a0009 | c0014 | t0003 | g0292 | EAS | CHS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00621 | hp2 | a0011 | c0028 | t0004 | g0110 | EAS | CHS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00639 | hp1 | a0012 | c0031 | t0004 | g0184 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00639 | hp2 | a0003 | c0003 | t0011 | g0338 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00642 | hp1 | a0001 | c0001 | t0007 | g0213 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00642 | hp2 | a0003 | c0003 | t0011 | g0340 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | CHS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00733 | hp2 | a0003 | c0003 | t0013 | g0366 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0193 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00735 | hp2 | a0002 | c0002 | t0007 | g0137 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00738 | hp2 | a0003 | c0003 | t0002 | g0342 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00741 | hp1 | a0001 | c0001 | t0032 | g0164 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0187 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01069 | hp1 | a0002 | c0002 | t0007 | g0002 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0224 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01070 | hp1 | a0004 | c0005 | t0012 | g0217 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01071 | hp1 | a0002 | c0002 | t0007 | g0002 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0216 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01074 | hp1 | a0003 | c0003 | t0011 | g0365 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01074 | hp2 | a0013 | c0025 | t0016 | g0159 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0188 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01081 | hp2 | a0001 | c0001 | t0019 | g0247 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0228 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01099 | hp2 | a0005 | c0004 | t0023 | g0378 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01106 | hp1 | a0001 | c0001 | t0037 | g0230 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01106 | hp2 | a0004 | c0016 | t0012 | g0275 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01109 | hp1 | a0002 | c0002 | t0013 | g0150 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01109 | hp2 | a0002 | c0002 | t0034 | g0262 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01167 | hp1 | a0001 | c0001 | t0029 | g0015 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01167 | hp2 | a0002 | c0002 | t0001 | g0141 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01168 | hp1 | a0001 | c0001 | t0006 | g0021 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0252 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01169 | hp1 | a0001 | c0001 | t0029 | g0015 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01169 | hp2 | a0001 | c0001 | t0003 | g0288 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01175 | hp2 | a0002 | c0002 | t0004 | g0195 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01243 | hp2 | a0003 | c0003 | t0005 | g0362 | AMR | PUR | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0226 | AMR | CLM | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01256 | hp1 | a0001 | c0001 | t0006 | g0223 | AMR | CLM | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | CLM | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01257 | hp1 | a0003 | c0008 | t0005 | g0371 | AMR | CLM | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01257 | hp2 | a0001 | c0001 | t0006 | g0003 | AMR | CLM | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01261 | hp1 | a0001 | c0001 | t0028 | g0087 | AMR | CLM | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01261 | hp2 | a0004 | c0005 | t0002 | g0102 | AMR | CLM | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01346 | hp1 | a0006 | c0006 | t0004 | g0311 | AMR | CLM | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0186 | AMR | CLM | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01358 | hp1 | a0003 | c0003 | t0044 | g0314 | AMR | CLM | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01358 | hp2 | a0001 | c0001 | t0022 | g0073 | AMR | CLM | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0093 | AMR | CLM | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01433 | hp2 | a0003 | c0003 | t0011 | g0341 | AMR | CLM | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01496 | hp1 | a0002 | c0032 | t0015 | g0077 | AMR | CLM | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0090 | AMR | CLM | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01515 | hp1 | a0001 | c0001 | t0006 | g0003 | EUR | IBS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01515 | hp2 | a0003 | c0003 | t0013 | g0367 | EUR | IBS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01516 | hp1 | a0002 | c0002 | t0007 | g0002 | EUR | IBS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0142 | EUR | IBS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01517 | hp1 | a0002 | c0002 | t0007 | g0136 | EUR | IBS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01517 | hp2 | a0001 | c0001 | t0006 | g0003 | EUR | IBS | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01884 | hp1 | a0002 | c0009 | t0008 | g0095 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01884 | hp2 | a0008 | c0011 | t0021 | g0036 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01891 | hp1 | a0007 | c0007 | t0007 | g0337 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01891 | hp2 | a0007 | c0007 | t0007 | g0346 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01928 | hp1 | a0006 | c0006 | t0001 | g0308 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01928 | hp2 | a0002 | c0002 | t0004 | g0192 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0257 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01934 | hp2 | a0005 | c0004 | t0001 | g0323 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0189 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01943 | hp2 | a0003 | c0003 | t0011 | g0364 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01952 | hp1 | a0001 | c0001 | t0018 | g0254 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01952 | hp2 | a0006 | c0006 | t0046 | g0307 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01981 | hp1 | a0014 | c0036 | t0001 | g0304 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01993 | hp2 | a0001 | c0001 | t0006 | g0021 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02004 | hp1 | a0002 | c0002 | t0004 | g0191 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02004 | hp2 | a0001 | c0001 | t0028 | g0171 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0094 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02015 | hp2 | a0005 | c0004 | t0001 | g0315 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02040 | hp1 | a0004 | c0005 | t0047 | g0057 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02040 | hp2 | a0015 | c0030 | t0003 | g0281 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02055 | hp1 | a0005 | c0004 | t0001 | g0375 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02055 | hp2 | a0007 | c0007 | t0001 | g0358 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02056 | hp1 | a0005 | c0004 | t0002 | g0343 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02056 | hp2 | a0007 | c0007 | t0004 | g0038 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02071 | hp1 | a0004 | c0005 | t0003 | g0227 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02071 | hp2 | a0001 | c0001 | t0006 | g0280 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02074 | hp1 | a0001 | c0001 | t0009 | g0255 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02080 | hp1 | a0002 | c0002 | t0004 | g0055 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02080 | hp2 | a0001 | c0001 | t0006 | g0265 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02083 | hp1 | a0001 | c0001 | t0038 | g0253 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02083 | hp2 | a0006 | c0006 | t0002 | g0297 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02132 | hp1 | a0001 | c0001 | t0003 | g0241 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02135 | hp1 | a0003 | c0003 | t0005 | g0023 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02145 | hp1 | a0002 | c0002 | t0008 | g0380 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02145 | hp2 | a0010 | c0010 | t0002 | g0359 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02148 | hp1 | a0003 | c0008 | t0004 | g0372 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0194 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02155 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | CDX | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | CDX | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | CDX | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | CDX | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02257 | hp1 | a0001 | c0001 | t0007 | g0157 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02257 | hp2 | a0001 | c0001 | t0020 | g0085 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02258 | hp1 | a0001 | c0001 | t0052 | g0160 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02258 | hp2 | a0002 | c0002 | t0002 | g0071 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02273 | hp1 | a0001 | c0001 | t0003 | g0249 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02273 | hp2 | a0002 | c0002 | t0004 | g0017 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02280 | hp1 | a0001 | c0001 | t0008 | g0166 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02280 | hp2 | a0001 | c0001 | t0020 | g0086 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0185 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02293 | hp2 | a0002 | c0002 | t0004 | g0017 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02300 | hp1 | a0001 | c0001 | t0004 | g0176 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02300 | hp2 | a0002 | c0002 | t0004 | g0206 | AMR | PEL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02451 | hp2 | a0002 | c0002 | t0002 | g0079 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02523 | hp1 | a0003 | c0003 | t0024 | g0317 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02572 | hp1 | a0001 | c0029 | t0002 | g0156 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02572 | hp2 | a0001 | c0001 | t0007 | g0212 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02602 | hp1 | a0001 | c0001 | t0035 | g0245 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02602 | hp2 | a0002 | c0002 | t0004 | g0053 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02615 | hp1 | a0002 | c0002 | t0015 | g0134 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02615 | hp2 | a0003 | c0003 | t0007 | g0351 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02622 | hp1 | a0016 | c0020 | t0005 | g0065 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02622 | hp2 | a0002 | c0009 | t0008 | g0135 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02630 | hp1 | a0007 | c0007 | t0007 | g0347 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02630 | hp2 | a0003 | c0003 | t0005 | g0354 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02647 | hp1 | a0004 | c0005 | t0013 | g0147 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02647 | hp2 | a0004 | c0023 | t0002 | g0172 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02683 | hp1 | a0003 | c0003 | t0011 | g0339 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02683 | hp2 | a0004 | c0005 | t0005 | g0208 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02717 | hp2 | a0004 | c0005 | t0031 | g0161 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02723 | hp1 | a0004 | c0005 | t0005 | g0211 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02723 | hp2 | a0002 | c0009 | t0008 | g0100 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02735 | hp1 | a0002 | c0002 | t0012 | g0225 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02735 | hp2 | a0002 | c0002 | t0039 | g0277 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02738 | hp1 | a0001 | c0001 | t0031 | g0162 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0014 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02809 | hp1 | a0001 | c0001 | t0006 | g0084 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02809 | hp2 | a0005 | c0018 | t0008 | g0325 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02886 | hp1 | a0002 | c0009 | t0008 | g0132 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02886 | hp2 | a0002 | c0002 | t0007 | g0098 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02896 | hp1 | a0002 | c0002 | t0007 | g0005 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02896 | hp2 | a0001 | c0001 | t0025 | g0029 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02897 | hp1 | a0002 | c0002 | t0007 | g0005 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02897 | hp2 | a0002 | c0002 | t0008 | g0078 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02922 | hp1 | a0001 | c0001 | t0006 | g0170 | AFR | ESN | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02922 | hp2 | a0004 | c0022 | t0048 | g0210 | AFR | ESN | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02965 | hp1 | a0010 | c0010 | t0005 | g0026 | AFR | ESN | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02970 | hp1 | a0004 | c0005 | t0007 | g0064 | AFR | ESN | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02970 | hp2 | a0001 | c0012 | t0030 | g0312 | AFR | ESN | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02976 | hp1 | a0003 | c0003 | t0021 | g0356 | AFR | ESN | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02976 | hp2 | a0004 | c0005 | t0005 | g0152 | AFR | ESN | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03017 | hp1 | a0001 | c0001 | t0022 | g0069 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0019 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03041 | hp1 | a0002 | c0009 | t0008 | g0151 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03098 | hp1 | a0005 | c0004 | t0023 | g0379 | AFR | MSL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03098 | hp2 | a0001 | c0001 | t0042 | g0183 | AFR | MSL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03130 | hp1 | a0004 | c0005 | t0007 | g0074 | AFR | ESN | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03130 | hp2 | a0002 | c0002 | t0015 | g0146 | AFR | ESN | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0101 | AFR | ESN | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03139 | hp2 | a0003 | c0003 | t0013 | g0350 | AFR | ESN | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03195 | hp1 | a0005 | c0004 | t0005 | g0025 | AFR | ESN | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03195 | hp2 | a0004 | c0005 | t0002 | g0105 | AFR | ESN | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03209 | hp1 | a0001 | c0012 | t0008 | g0032 | AFR | MSL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03209 | hp2 | a0005 | c0004 | t0005 | g0324 | AFR | MSL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03225 | hp1 | a0002 | c0002 | t0007 | g0168 | AFR | MSL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03225 | hp2 | a0002 | c0002 | t0025 | g0169 | AFR | MSL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03239 | hp1 | a0004 | c0005 | t0012 | g0218 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0019 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03453 | hp1 | a0002 | c0002 | t0033 | g0181 | AFR | MSL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | MSL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03486 | hp1 | a0002 | c0009 | t0008 | g0133 | AFR | MSL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03486 | hp2 | a0003 | c0003 | t0043 | g0357 | AFR | MSL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03490 | hp1 | a0005 | c0004 | t0027 | g0024 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03490 | hp2 | a0005 | c0004 | t0001 | g0322 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03491 | hp1 | a0003 | c0008 | t0001 | g0028 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03491 | hp2 | a0005 | c0004 | t0001 | g0313 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03492 | hp1 | a0003 | c0008 | t0001 | g0028 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03492 | hp2 | a0005 | c0004 | t0051 | g0024 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | ESN | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03516 | hp2 | a0002 | c0002 | t0002 | g0153 | AFR | ESN | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03540 | hp1 | a0002 | c0002 | t0003 | g0082 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03540 | hp2 | a0001 | c0012 | t0030 | g0163 | AFR | GWD | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03579 | hp1 | a0004 | c0005 | t0007 | g0063 | AFR | MSL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03579 | hp2 | a0007 | c0007 | t0005 | g0348 | AFR | MSL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03654 | hp1 | a0001 | c0001 | t0019 | g0246 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03654 | hp2 | a0001 | c0001 | t0003 | g0244 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03669 | hp1 | a0002 | c0002 | t0004 | g0054 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03669 | hp2 | a0001 | c0001 | t0036 | g0290 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03688 | hp1 | a0003 | c0003 | t0005 | g0333 | SAS | STU | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03688 | hp2 | a0001 | c0001 | t0041 | g0251 | SAS | STU | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03704 | hp1 | a0003 | c0008 | t0001 | g0361 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03704 | hp2 | a0005 | c0004 | t0027 | g0369 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0008 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03710 | hp2 | a0003 | c0003 | t0005 | g0360 | SAS | PJL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03831 | hp1 | a0001 | c0001 | t0006 | g0276 | SAS | BEB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | BEB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | BEB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03834 | hp2 | a0001 | c0001 | t0012 | g0293 | SAS | BEB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03942 | hp1 | a0004 | c0005 | t0005 | g0072 | SAS | BEB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03942 | hp2 | a0005 | c0004 | t0002 | g0370 | SAS | BEB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0289 | SAS | STU | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0286 | SAS | STU | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0243 | SAS | STU | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG04199 | hp2 | a0005 | c0004 | t0003 | g0209 | SAS | STU | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0215 | SAS | STU | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG04204 | hp2 | a0002 | c0002 | t0005 | g0138 | SAS | STU | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG04228 | hp1 | a0003 | c0003 | t0005 | g0363 | SAS | STU | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18522 | hp1 | a0003 | c0003 | t0002 | g0334 | AFR | YRI | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18522 | hp2 | a0008 | c0011 | t0002 | g0103 | AFR | YRI | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | CHB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18612 | hp2 | a0001 | c0001 | t0006 | g0271 | EAS | CHB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18747 | hp1 | a0005 | c0004 | t0002 | g0345 | EAS | CHB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18747 | hp2 | a0005 | c0004 | t0002 | g0027 | EAS | CHB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18906 | hp1 | a0010 | c0010 | t0005 | g0026 | AFR | YRI | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | YRI | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18939 | hp1 | a0001 | c0001 | t0009 | g0238 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18939 | hp2 | a0004 | c0005 | t0024 | g0037 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18942 | hp1 | a0006 | c0006 | t0001 | g0301 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18942 | hp2 | a0001 | c0001 | t0006 | g0240 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18943 | hp1 | a0001 | c0001 | t0017 | g0010 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18943 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18945 | hp1 | a0004 | c0005 | t0005 | g0042 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18945 | hp2 | a0002 | c0002 | t0026 | g0044 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18946 | hp1 | a0002 | c0002 | t0004 | g0202 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18946 | hp2 | a0003 | c0003 | t0010 | g0326 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18947 | hp2 | a0001 | c0001 | t0017 | g0010 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18948 | hp1 | a0001 | c0001 | t0006 | g0234 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18949 | hp2 | a0002 | c0002 | t0004 | g0058 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18950 | hp2 | a0004 | c0005 | t0009 | g0264 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18951 | hp1 | a0005 | c0004 | t0002 | g0027 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18951 | hp2 | a0002 | c0002 | t0004 | g0046 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18952 | hp1 | a0009 | c0014 | t0003 | g0273 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18952 | hp2 | a0003 | c0003 | t0010 | g0329 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18953 | hp1 | a0001 | c0001 | t0009 | g0237 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18953 | hp2 | a0017 | c0037 | t0001 | g0299 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18957 | hp1 | a0003 | c0003 | t0010 | g0316 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18960 | hp1 | a0002 | c0002 | t0004 | g0039 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18962 | hp1 | a0006 | c0006 | t0001 | g0298 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18962 | hp2 | a0001 | c0001 | t0018 | g0270 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18963 | hp1 | a0002 | c0002 | t0004 | g0131 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18967 | hp1 | a0002 | c0002 | t0004 | g0061 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18967 | hp2 | a0002 | c0002 | t0004 | g0043 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18971 | hp1 | a0002 | c0002 | t0009 | g0261 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18972 | hp1 | a0004 | c0005 | t0014 | g0104 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18972 | hp2 | a0006 | c0006 | t0001 | g0310 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18975 | hp1 | a0002 | c0002 | t0003 | g0263 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18977 | hp2 | a0007 | c0007 | t0026 | g0047 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18979 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18979 | hp2 | a0002 | c0002 | t0049 | g0107 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18980 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18980 | hp2 | a0002 | c0002 | t0004 | g0177 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0203 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18982 | hp2 | a0002 | c0002 | t0004 | g0051 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18983 | hp1 | a0001 | c0001 | t0009 | g0235 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18983 | hp2 | a0002 | c0002 | t0004 | g0200 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18984 | hp1 | a0002 | c0002 | t0004 | g0060 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18984 | hp2 | a0003 | c0003 | t0010 | g0327 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18985 | hp1 | a0006 | c0015 | t0001 | g0309 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0377 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18992 | hp2 | a0001 | c0013 | t0001 | g0013 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18993 | hp1 | a0001 | c0001 | t0009 | g0287 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18993 | hp2 | a0009 | c0014 | t0003 | g0274 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18994 | hp1 | a0006 | c0015 | t0001 | g0305 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18995 | hp1 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18998 | hp1 | a0001 | c0013 | t0001 | g0123 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18998 | hp2 | a0002 | c0002 | t0003 | g0260 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18999 | hp1 | a0002 | c0002 | t0004 | g0207 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA18999 | hp2 | a0006 | c0006 | t0001 | g0300 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19000 | hp1 | a0005 | c0004 | t0002 | g0344 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19000 | hp2 | a0006 | c0006 | t0001 | g0303 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19002 | hp2 | a0003 | c0003 | t0014 | g0319 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19003 | hp1 | a0018 | c0034 | t0001 | g0124 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19003 | hp2 | a0006 | c0006 | t0002 | g0294 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19004 | hp2 | a0019 | c0019 | t0002 | g0097 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19005 | hp1 | a0003 | c0003 | t0014 | g0318 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19007 | hp1 | a0001 | c0001 | t0009 | g0236 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19007 | hp2 | a0002 | c0002 | t0004 | g0056 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0197 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19010 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19011 | hp1 | a0006 | c0015 | t0001 | g0306 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19011 | hp2 | a0003 | c0003 | t0010 | g0330 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19012 | hp1 | a0005 | c0004 | t0045 | g0355 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19012 | hp2 | a0001 | c0001 | t0006 | g0229 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19030 | hp1 | a0002 | c0002 | t0007 | g0130 | AFR | LWK | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19030 | hp2 | a0001 | c0001 | t0016 | g0182 | AFR | LWK | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19043 | hp1 | a0002 | c0002 | t0002 | g0139 | AFR | LWK | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19043 | hp2 | a0007 | c0017 | t0008 | g0373 | AFR | LWK | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19054 | hp1 | a0004 | c0005 | t0010 | g0041 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19054 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19060 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19063 | hp1 | a0001 | c0001 | t0009 | g0221 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19064 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19065 | hp1 | a0003 | c0003 | t0005 | g0332 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19067 | hp1 | a0001 | c0001 | t0006 | g0268 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19070 | hp1 | a0003 | c0003 | t0010 | g0331 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19070 | hp2 | a0002 | c0002 | t0004 | g0045 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19074 | hp1 | a0002 | c0002 | t0004 | g0050 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19074 | hp2 | a0001 | c0013 | t0001 | g0013 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0376 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19079 | hp2 | a0003 | c0003 | t0014 | g0320 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19081 | hp1 | a0002 | c0002 | t0009 | g0291 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19083 | hp1 | a0020 | c0035 | t0001 | g0302 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19083 | hp2 | a0002 | c0002 | t0004 | g0158 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19084 | hp1 | a0001 | c0027 | t0002 | g0012 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19085 | hp1 | a0001 | c0001 | t0006 | g0239 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19085 | hp2 | a0006 | c0006 | t0002 | g0296 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19090 | hp1 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19090 | hp2 | a0001 | c0001 | t0006 | g0283 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19240 | hp1 | a0004 | c0021 | t0008 | g0030 | AFR | YRI | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA19240 | hp2 | a0001 | c0001 | t0016 | g0179 | AFR | YRI | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA20129 | hp1 | a0001 | c0001 | t0032 | g0165 | AFR | ASW | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0014 | AFR | ASW | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0022 | EUR | TSI | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0231 | EUR | TSI | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0149 | EUR | TSI | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA20805 | hp2 | a0003 | c0003 | t0005 | g0353 | EUR | TSI | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0242 | SAS | GIH | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0008 | SAS | GIH | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01123 | hp1 | a0003 | c0003 | t0013 | g0368 | AMR | CLM | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG01123 | hp2 | a0001 | c0026 | t0002 | g0088 | AMR | CLM | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02109 | hp1 | a0003 | c0003 | t0002 | g0335 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02109 | hp2 | a0008 | c0024 | t0001 | g0035 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02486 | hp1 | a0002 | c0002 | t0002 | g0096 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02486 | hp2 | a0002 | c0002 | t0007 | g0076 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02559 | hp1 | a0005 | c0004 | t0005 | g0025 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | ACB | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03471 | hp1 | a0003 | c0003 | t0005 | g0349 | AFR | MSL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG03471 | hp2 | a0002 | c0002 | t0033 | g0180 | AFR | MSL | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG06807 | hp1 | a0008 | c0011 | t0007 | g0033 | AFR | USA | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0083 | AFR | USA | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA20300 | hp1 | a0001 | c0001 | t0008 | g0068 | AFR | USA | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA20300 | hp2 | a0004 | c0016 | t0012 | g0279 | AFR | USA | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA21309 | hp1 | a0021 | c0033 | t0008 | g0321 | AFR | LWK | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
NA21309 | hp2 | a0004 | c0005 | t0050 | g0075 | AFR | LWK | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0232 | REF | REF | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
homoSapiens | grch38p0 | a0001 | c0001 | t0006 | g0222 | REF | REF | D2HGDH_chr2_241729630_241773811 | D2HGDH | chr2 | 241729630 | 241773811 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241735134 | C | G | 3 | a0001 a0004 a0013 |
12 | HG00741.hp1 HG01074.hp2 HG01167.hp1 others(9): Show |
splice_region_variant | LOW | c.-91C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/10 | chr2 | 241735134 | |||||||
chr2:241735267 | C | G | 4 | a0006 a0014 a0017 others(1): Show |
18 | HG00408.hp2 HG01346.hp1 HG01928.hp1 others(15): Show |
missense_variant | MODERATE | c.43C>G | p.Arg15Gly | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/10 | 201/2566 | 43/1566 | 15/521 | chr2 | 241735267 | |||
chr2:241735388 | G | A | 4 | a0003 a0005 a0007 others(1): Show |
79 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(76): Show |
missense_variant | MODERATE | c.164G>A | p.Arg55Gln | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/10 | 322/2566 | 164/1566 | 55/521 | chr2 | 241735388 | |||
chr2:241735451 | G | C | 1 | a0018 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.227G>C | p.Gly76Ala | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/10 | 385/2566 | 227/1566 | 76/521 | chr2 | 241735451 | |||
chr2:241743648 | G | A | 1 | a0019 | 1 | NA19004.hp2 | missense_variant | MODERATE | c.517G>A | p.Val173Ile | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 5/10 | 675/2566 | 517/1566 | 173/521 | chr2 | 241743648 | |||
chr2:241743790 | A | G | 1 | a0021 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.659A>G | p.His220Arg | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 5/10 | 817/2566 | 659/1566 | 220/521 | chr2 | 241743790 | |||
chr2:241751260 | G | A | 5 | a0003 a0004 a0008 others(2): Show |
79 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(76): Show |
missense_variant | MODERATE | c.1012G>A | p.Val338Ile | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/10 | 1170/2566 | 1012/1566 | 338/521 | chr2 | 241751260 | |||
chr2:241751314 | C | T | 2 | a0008 a0010 |
7 | HG01884.hp2 HG02109.hp2 HG02145.hp2 others(4): Show |
missense_variant | MODERATE | c.1066C>T | p.His356Tyr | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/10 | 1224/2566 | 1066/1566 | 356/521 | chr2 | 241751314 | |||
chr2:241751330 | C | T | 7 | a0002 a0007 a0009 others(4): Show |
119 | HG00140.hp2 HG00558.hp2 HG00597.hp2 others(116): Show |
missense_variant | MODERATE | c.1082C>T | p.Ala361Val | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/10 | 1240/2566 | 1082/1566 | 361/521 | chr2 | 241751330 | |||
chr2:241751375 | AGAGGAAA others(67): Show |
A | 1 | a0020 | 1 | NA19083.hp1 | frameshift_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.1130_1140+63delGGA others(71): Show |
p.Arg377fs | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/10 | 1288/2566 | 1130/1566 | 377/521 | INFO_REALIGN_3_PRIME | chr2 | 241751375 | ||
chr2:241755891 | C | T | 1 | a0009 | 3 | HG00621.hp1 NA18952.hp1 NA18993.hp2 |
missense_variant | MODERATE | c.1183C>T | p.Arg395Trp | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/10 | 1341/2566 | 1183/1566 | 395/521 | chr2 | 241755891 | |||
chr2:241755945 | G | A | 1 | a0015 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.1237G>A | p.Asp413Asn | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/10 | 1395/2566 | 1237/1566 | 413/521 | chr2 | 241755945 | |||
chr2:241755966 | G | A | 1 | a0013 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.1258G>A | p.Ala420Thr | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/10 | 1416/2566 | 1258/1566 | 420/521 | chr2 | 241755966 | |||
chr2:241767721 | C | G | 1 | a0011 | 1 | HG00621.hp2 | missense_variant | MODERATE | c.1318C>G | p.Leu440Val | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 1476/2566 | 1318/1566 | 440/521 | chr2 | 241767721 | |||
chr2:241767737 | C | T | 1 | a0012 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.1334C>T | p.Thr445Met | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 1492/2566 | 1334/1566 | 445/521 | chr2 | 241767737 | |||
chr2:241767790 | G | A | 1 | a0016 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.1387G>A | p.Glu463Lys | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 1545/2566 | 1387/1566 | 463/521 | chr2 | 241767790 | |||
chr2:241767817 | G | A | 1 | a0014 | 1 | HG01981.hp1 | missense_variant | MODERATE | c.1414G>A | p.Val472Ile | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 1572/2566 | 1414/1566 | 472/521 | chr2 | 241767817 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241735362 | G | A | 1 | a0007c0017 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.138G>A | p.Pro46Pro | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/10 | 296/2566 | 138/1566 | 46/521 | chr2 | 241735362 | |||
chr2:241735449 | C | G | 1 | a0018c0034 | 1 | NA19003.hp1 | synonymous_variant | LOW | c.225C>G | p.Pro75Pro | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/10 | 383/2566 | 225/1566 | 75/521 | chr2 | 241735449 | |||
chr2:241735452 | C | G | 1 | a0018c0034 | 1 | NA19003.hp1 | synonymous_variant | LOW | c.228C>G | p.Gly76Gly | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/10 | 386/2566 | 228/1566 | 76/521 | chr2 | 241735452 | |||
chr2:241744864 | C | T | 1 | a0002c0032 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.840C>T | p.Asn280Asn | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/10 | 998/2566 | 840/1566 | 280/521 | chr2 | 241744864 | |||
chr2:241751355 | T | C | 2 | a0003c0008 a0004c0016 |
8 | HG00408.hp1 HG01106.hp2 HG01257.hp1 others(5): Show |
synonymous_variant | LOW | c.1107T>C | p.Asp369Asp | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/10 | 1265/2566 | 1107/1566 | 369/521 | chr2 | 241751355 | |||
chr2:241751370 | C | T | 1 | a0008c0024 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.1122C>T | p.Thr374Thr | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/10 | 1280/2566 | 1122/1566 | 374/521 | chr2 | 241751370 | |||
chr2:241767711 | A | G | 2 | a0001c0029 a0004c0023 |
2 | HG02572.hp1 HG02647.hp2 |
splice_region_variant&synonymous_variant | LOW | c.1308A>G | p.Gly436Gly | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 1466/2566 | 1308/1566 | 436/521 | chr2 | 241767711 | |||
chr2:241767780 | C | A | 1 | a0001c0026 | 1 | HG01123.hp2 | synonymous_variant | LOW | c.1377C>A | p.Pro459Pro | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 1535/2566 | 1377/1566 | 459/521 | chr2 | 241767780 | |||
chr2:241767789 | C | T | 3 | a0001c0013 a0006c0015 a0018c0034 |
7 | NA18985.hp1 NA18992.hp2 NA18994.hp1 others(4): Show |
synonymous_variant | LOW | c.1386C>T | p.Tyr462Tyr | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 1544/2566 | 1386/1566 | 462/521 | chr2 | 241767789 | |||
chr2:241767798 | G | A | 5 | a0001c0012 a0002c0009 a0004c0021 others(2): Show |
12 | HG01884.hp1 HG02622.hp2 HG02723.hp2 others(9): Show |
synonymous_variant | LOW | c.1395G>A | p.Thr465Thr | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 1553/2566 | 1395/1566 | 465/521 | chr2 | 241767798 | |||
chr2:241767801 | C | G | 1 | a0001c0027 | 1 | NA19084.hp1 | synonymous_variant | LOW | c.1398C>G | p.Ala466Ala | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 1556/2566 | 1398/1566 | 466/521 | chr2 | 241767801 | |||
chr2:241767879 | G | A | 1 | a0004c0022 | 1 | HG02922.hp2 | synonymous_variant | LOW | c.1476G>A | p.Pro492Pro | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 1634/2566 | 1476/1566 | 492/521 | chr2 | 241767879 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241734670 | G | A | 1 | a0001c0001t0017 | 2 | NA18943.hp1 NA18947.hp2 |
5_prime_UTR_variant | MODIFIER | c.-118G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 1/10 | 555 | chr2 | 241734670 | ||||||
chr2:241734678 | C | T | 1 | a0002c0002t0033 | 2 | HG03453.hp1 HG03471.hp2 |
5_prime_UTR_variant | MODIFIER | c.-110C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 1/10 | 547 | chr2 | 241734678 | ||||||
chr2:241734689 | A | G | 98 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(95): Show |
309 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(306): Show |
5_prime_UTR_variant | MODIFIER | c.-99A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 1/10 | 536 | chr2 | 241734689 | ||||||
chr2:241767971 | G | A | 1 | a0001c0001t0042 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 2 | chr2 | 241767971 | ||||||
chr2:241767995 | C | T | 1 | a0001c0001t0028 | 2 | HG01261.hp1 HG02004.hp2 |
3_prime_UTR_variant | MODIFIER | c.*26C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 26 | chr2 | 241767995 | ||||||
chr2:241767996 | C | T | 3 | a0001c0001t0041 a0005c0004t0027 a0005c0004t0051 |
4 | HG03490.hp1 HG03492.hp2 HG03688.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*27C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 27 | chr2 | 241767996 | ||||||
chr2:241768009 | C | T | 2 | a0002c0002t0015 a0002c0032t0015 |
3 | HG01496.hp1 HG02615.hp1 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*40C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 40 | chr2 | 241768009 | ||||||
chr2:241768020 | C | G | 1 | a0004c0005t0050 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*51C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 51 | chr2 | 241768020 | ||||||
chr2:241768021 | G | C | 1 | a0004c0005t0050 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*52G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 52 | chr2 | 241768021 | ||||||
chr2:241768052 | G | A | 1 | a0003c0003t0043 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*83G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 83 | chr2 | 241768052 | ||||||
chr2:241768062 | T | C | 6 | a0002c0002t0013 a0002c0002t0034 a0003c0003t0011 others(3): Show |
15 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*93T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 93 | chr2 | 241768062 | ||||||
chr2:241768191 | G | C | 1 | a0001c0001t0035 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*222G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 222 | chr2 | 241768191 | ||||||
chr2:241768222 | C | CG | 10 | a0001c0001t0018 a0001c0001t0036 a0003c0003t0024 others(7): Show |
12 | HG01099.hp2 HG01358.hp1 HG01952.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*257dupG | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 258 | INFO_REALIGN_3_PRIME | chr2 | 241768222 | |||||
chr2:241768223 | G | A | 9 | a0001c0001t0007 a0001c0001t0022 a0002c0002t0007 others(6): Show |
26 | HG00642.hp1 HG00735.hp2 HG01069.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*254G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 254 | chr2 | 241768223 | ||||||
chr2:241768235 | G | A | 4 | a0003c0003t0010 a0004c0005t0010 a0004c0005t0047 others(1): Show |
10 | HG00438.hp1 HG02040.hp1 NA18946.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*266G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 266 | chr2 | 241768235 | ||||||
chr2:241768271 | C | T | 1 | a0002c0002t0049 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*302C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 302 | chr2 | 241768271 | ||||||
chr2:241768379 | G | A | 1 | a0001c0001t0019 | 2 | HG01081.hp2 HG03654.hp1 |
3_prime_UTR_variant | MODIFIER | c.*410G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 410 | chr2 | 241768379 | ||||||
chr2:241768385 | C | T | 1 | a0001c0001t0040 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*416C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 416 | chr2 | 241768385 | ||||||
chr2:241768396 | G | A | 5 | a0001c0001t0020 a0001c0001t0025 a0001c0001t0029 others(2): Show |
8 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*427G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 427 | chr2 | 241768396 | ||||||
chr2:241768402 | G | T | 2 | a0003c0003t0014 a0004c0005t0014 |
4 | NA18972.hp1 NA19002.hp2 NA19005.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*433G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 433 | chr2 | 241768402 | ||||||
chr2:241768418 | C | A | 1 | a0001c0001t0037 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*449C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 449 | chr2 | 241768418 | ||||||
chr2:241768418 | C | T | 56 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(53): Show |
224 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(221): Show |
3_prime_UTR_variant | MODIFIER | c.*449C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 449 | chr2 | 241768418 | ||||||
chr2:241768419 | G | T | 1 | a0001c0001t0037 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*450G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 450 | chr2 | 241768419 | ||||||
chr2:241768443 | C | T | 1 | a0002c0002t0039 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*474C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 474 | chr2 | 241768443 | ||||||
chr2:241768630 | C | T | 3 | a0002c0002t0034 a0003c0003t0011 a0003c0003t0044 |
9 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*661C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 661 | chr2 | 241768630 | ||||||
chr2:241768640 | T | A | 1 | a0005c0004t0023 | 2 | HG01099.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*671T>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 671 | chr2 | 241768640 | ||||||
chr2:241768653 | G | A | 1 | a0004c0005t0050 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*684G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 684 | chr2 | 241768653 | ||||||
chr2:241768657 | G | A | 10 | a0001c0001t0007 a0001c0001t0052 a0002c0002t0007 others(7): Show |
26 | HG00642.hp1 HG00735.hp2 HG01069.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*688G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 688 | chr2 | 241768657 | ||||||
chr2:241768669 | GAGGGCCC others(11): Show |
G | 1 | a0001c0001t0038 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*707_*724delCCGGCA others(12): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 707 | INFO_REALIGN_3_PRIME | chr2 | 241768669 | |||||
chr2:241768747 | C | T | 39 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(36): Show |
110 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*778C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 778 | chr2 | 241768747 | ||||||
chr2:241768765 | A | T | 1 | a0001c0001t0037 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*796A>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 796 | chr2 | 241768765 | ||||||
chr2:241768770 | A | G | 30 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0009 others(27): Show |
90 | HG00140.hp1 HG00558.hp2 HG00621.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*801A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 801 | chr2 | 241768770 | ||||||
chr2:241768796 | T | C | 1 | a0004c0005t0047 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*827T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 10/10 | 827 | chr2 | 241768796 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:241734711 | C | G | 1 | a0002c0002t0008g0380 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-93+16C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 1/9 | chr2 | 241734711 | |||||||
chr2:241734756 | G | GGGTCGGG others(10): Show |
1 | a0001c0001t0025g0029 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-93+74_-93+75insCG others(15): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 241734756 | ||||||
chr2:241734853 | AAC | A | 75 | a0001c0001t0001g0376 a0001c0001t0001g0377 a0001c0012t0030g0312 others(72): Show |
80 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.-93+161_-93+162del others(2): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr2 | 241734853 | ||||||
chr2:241734868 | C | T | 18 | a0006c0006t0001g0298 a0006c0006t0001g0300 a0006c0006t0001g0301 others(15): Show |
18 | HG00408.hp2 HG01346.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.-93+173C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 1/9 | chr2 | 241734868 | |||||||
chr2:241734889 | C | A | 1 | a0002c0002t0008g0380 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-93+194C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 1/9 | chr2 | 241734889 | |||||||
chr2:241734898 | A | C | 75 | a0001c0001t0001g0376 a0001c0001t0001g0377 a0001c0012t0030g0312 others(72): Show |
80 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.-93+203A>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 1/9 | chr2 | 241734898 | |||||||
chr2:241734936 | C | G | 75 | a0001c0001t0001g0376 a0001c0001t0001g0377 a0001c0012t0030g0312 others(72): Show |
80 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.-92-197C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 1/9 | chr2 | 241734936 | |||||||
chr2:241735032 | G | A | 18 | a0006c0006t0001g0298 a0006c0006t0001g0300 a0006c0006t0001g0301 others(15): Show |
18 | HG00408.hp2 HG01346.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-101G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 1/9 | chr2 | 241735032 | |||||||
chr2:241735058 | C | G | 18 | a0006c0006t0001g0298 a0006c0006t0001g0300 a0006c0006t0001g0301 others(15): Show |
18 | HG00408.hp2 HG01346.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.-92-75C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 1/9 | chr2 | 241735058 | |||||||
chr2:241735094 | A | G | 2 | a0005c0004t0023g0378 a0005c0004t0023g0379 |
2 | HG01099.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-92-39A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 1/9 | chr2 | 241735094 | |||||||
chr2:241735525 | G | A | 8 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0012t0008g0032 others(5): Show |
9 | HG01884.hp2 HG02109.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+9G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241735525 | |||||||
chr2:241735544 | T | G | 293 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0070 others(290): Show |
314 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.292+28T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241735544 | |||||||
chr2:241735709 | TTTG | T | 3 | a0001c0001t0007g0212 a0001c0001t0007g0213 a0004c0005t0005g0211 |
3 | HG00642.hp1 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.292+208_292+210del others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 241735709 | ||||||
chr2:241735802 | C | G | 8 | a0006c0006t0001g0308 a0006c0006t0001g0310 a0006c0006t0004g0311 others(5): Show |
8 | HG01346.hp1 HG01928.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.292+286C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241735802 | |||||||
chr2:241735845 | C | T | 1 | a0004c0022t0048g0210 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.292+329C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241735845 | |||||||
chr2:241735867 | A | T | 6 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0012t0008g0032 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+351A>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241735867 | |||||||
chr2:241735907 | C | T | 8 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0012t0008g0032 others(5): Show |
9 | HG01884.hp2 HG02109.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+391C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241735907 | |||||||
chr2:241736045 | G | A | 2 | a0005c0004t0023g0378 a0005c0004t0023g0379 |
2 | HG01099.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.292+529G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241736045 | |||||||
chr2:241736082 | G | A | 1 | a0001c0001t0040g0214 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.292+566G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241736082 | |||||||
chr2:241736085 | G | C | 17 | a0006c0006t0001g0298 a0006c0006t0001g0300 a0006c0006t0001g0301 others(14): Show |
17 | HG00408.hp2 HG01928.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.292+569G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241736085 | |||||||
chr2:241736117 | G | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0215 a0001c0001t0003g0216 |
4 | HG01070.hp2 HG01071.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+601G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241736117 | |||||||
chr2:241736381 | C | G | 1 | a0005c0004t0001g0375 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.292+865C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241736381 | |||||||
chr2:241736414 | G | T | 1 | a0001c0001t0012g0293 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.292+898G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241736414 | |||||||
chr2:241736432 | C | CCCTCCGC others(2): Show |
72 | a0003c0003t0002g0334 a0003c0003t0002g0335 a0003c0003t0002g0342 others(69): Show |
77 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.292+921_292+922ins others(9): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 241736432 | ||||||
chr2:241736443 | C | T | 1 | a0003c0003t0011g0374 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.292+927C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241736443 | |||||||
chr2:241736546 | TCTC | T | 26 | a0001c0001t0001g0196 a0002c0002t0001g0016 a0002c0002t0001g0185 others(23): Show |
28 | HG00639.hp1 HG00735.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.292+1031_292+1033d others(5): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241736546 | |||||||
chr2:241736656 | A | G | 3 | a0001c0001t0007g0212 a0001c0001t0007g0213 a0004c0005t0005g0211 |
3 | HG00642.hp1 HG02572.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.292+1140A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241736656 | |||||||
chr2:241736670 | C | CT | 69 | a0003c0003t0002g0334 a0003c0003t0002g0335 a0003c0003t0002g0342 others(66): Show |
74 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.292+1154_292+1155i others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241736670 | |||||||
chr2:241736671 | G | GT | 51 | a0001c0001t0001g0167 a0001c0001t0002g0173 a0001c0001t0002g0174 others(48): Show |
52 | HG00408.hp2 HG00621.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.292+1169dupT | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 241736671 | ||||||
chr2:241736671 | G | GTT | 8 | a0001c0001t0016g0182 a0001c0001t0042g0183 a0002c0002t0033g0180 others(5): Show |
8 | HG01928.hp1 HG03098.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.292+1168_292+1169d others(4): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 241736671 | ||||||
chr2:241736671 | G | T | 80 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0012t0008g0032 others(77): Show |
86 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.292+1155G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241736671 | |||||||
chr2:241736727 | T | C | 80 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0012t0008g0032 others(77): Show |
86 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.292+1211T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241736727 | |||||||
chr2:241736763 | G | A | 1 | a0001c0001t0003g0019 | 2 | HG03017.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.292+1247G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241736763 | |||||||
chr2:241736809 | C | T | 1 | a0001c0001t0042g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.292+1293C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241736809 | |||||||
chr2:241736822 | G | A | 17 | a0006c0006t0001g0298 a0006c0006t0001g0300 a0006c0006t0001g0301 others(14): Show |
17 | HG00408.hp2 HG01928.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.292+1306G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241736822 | |||||||
chr2:241737005 | G | A | 8 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0012t0008g0032 others(5): Show |
9 | HG01884.hp2 HG02109.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.292+1489G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241737005 | |||||||
chr2:241737021 | T | C | 8 | a0003c0003t0010g0316 a0003c0003t0014g0318 a0003c0003t0014g0319 others(5): Show |
8 | HG02015.hp2 HG02523.hp1 HG02683.hp2 others(5): Show |
intron_variant | MODIFIER | c.292+1505T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241737021 | |||||||
chr2:241737114 | G | A | 1 | a0005c0004t0003g0209 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.292+1598G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241737114 | |||||||
chr2:241737117 | C | T | 5 | a0006c0006t0001g0300 a0006c0006t0001g0301 a0006c0006t0001g0303 others(2): Show |
5 | NA18942.hp1 NA18953.hp2 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.292+1601C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241737117 | |||||||
chr2:241737126 | G | A | 122 | a0001c0001t0001g0040 a0001c0001t0002g0031 a0001c0001t0002g0034 others(119): Show |
129 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.292+1610G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241737126 | |||||||
chr2:241737170 | T | C | 2 | a0002c0002t0004g0060 a0002c0002t0004g0061 |
2 | NA18967.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.292+1654T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241737170 | |||||||
chr2:241737300 | G | C | 1 | a0001c0001t0002g0062 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.292+1784G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241737300 | |||||||
chr2:241737417 | A | G | 2 | a0005c0004t0023g0378 a0005c0004t0023g0379 |
2 | HG01099.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.292+1901A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241737417 | |||||||
chr2:241737496 | T | TTTTA | 158 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0070 others(155): Show |
167 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.292+1984_292+1987d others(6): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 241737496 | ||||||
chr2:241737496 | T | TTTTTA | 128 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0092 others(125): Show |
140 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(137): Show |
intron_variant | MODIFIER | c.292+1983_292+1984i others(7): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 241737496 | ||||||
chr2:241737531 | T | C | 17 | a0006c0006t0001g0298 a0006c0006t0001g0300 a0006c0006t0001g0301 others(14): Show |
17 | HG00408.hp2 HG01928.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.292+2015T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241737531 | |||||||
chr2:241737536 | G | A | 9 | a0001c0001t0029g0015 a0001c0001t0031g0162 a0001c0001t0032g0164 others(6): Show |
10 | HG00741.hp1 HG01074.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.292+2020G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241737536 | |||||||
chr2:241737767 | G | A | 5 | a0001c0001t0002g0062 a0004c0005t0007g0063 a0004c0005t0007g0064 others(2): Show |
5 | HG02622.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.292+2251G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241737767 | |||||||
chr2:241737769 | G | A | 118 | a0001c0001t0001g0089 a0001c0001t0001g0091 a0001c0001t0001g0092 others(115): Show |
129 | HG00140.hp2 HG00438.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.292+2253G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241737769 | |||||||
chr2:241737846 | G | A | 240 | a0001c0001t0001g0040 a0001c0001t0001g0089 a0001c0001t0001g0091 others(237): Show |
258 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.292+2330G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241737846 | |||||||
chr2:241738001 | G | A | 2 | a0001c0001t0028g0087 a0001c0001t0028g0171 |
2 | HG01261.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.292+2485G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241738001 | |||||||
chr2:241738208 | G | T | 1 | a0001c0001t0002g0081 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.292+2692G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241738208 | |||||||
chr2:241738282 | C | T | 1 | a0002c0002t0001g0080 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.293-2751C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241738282 | |||||||
chr2:241738304 | C | T | 2 | a0002c0002t0033g0180 a0002c0002t0033g0181 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.293-2729C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241738304 | |||||||
chr2:241738409 | C | T | 6 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0012t0008g0032 others(3): Show |
6 | HG01884.hp2 HG02109.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-2624C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241738409 | |||||||
chr2:241738452 | C | T | 4 | a0004c0005t0007g0063 a0004c0005t0007g0064 a0004c0022t0048g0210 others(1): Show |
4 | HG02622.hp1 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-2581C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241738452 | |||||||
chr2:241738457 | C | G | 5 | a0001c0001t0003g0004 a0001c0001t0003g0282 a0001c0001t0003g0284 others(2): Show |
7 | HG00558.hp1 NA18977.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-2576C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241738457 | |||||||
chr2:241738592 | C | T | 2 | a0005c0004t0023g0378 a0005c0004t0023g0379 |
2 | HG01099.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.293-2441C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241738592 | |||||||
chr2:241738602 | C | G | 1 | a0001c0001t0002g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.293-2431C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241738602 | |||||||
chr2:241738657 | C | A | 4 | a0001c0001t0025g0029 a0001c0001t0042g0183 a0005c0004t0023g0378 others(1): Show |
4 | HG01099.hp2 HG02896.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-2376C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241738657 | |||||||
chr2:241738658 | C | T | 1 | a0005c0004t0003g0209 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.293-2375C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241738658 | |||||||
chr2:241738689 | G | A | 2 | a0002c0002t0007g0005 a0004c0021t0008g0030 |
3 | HG02896.hp1 HG02897.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.293-2344G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241738689 | |||||||
chr2:241738728 | C | T | 1 | a0015c0030t0003g0281 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.293-2305C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241738728 | |||||||
chr2:241738756 | G | A | 1 | a0001c0026t0002g0088 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.293-2277G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241738756 | |||||||
chr2:241739024 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.293-2009G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739024 | |||||||
chr2:241739054 | C | T | 2 | a0004c0022t0048g0210 a0007c0017t0008g0373 |
2 | HG02922.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.293-1979C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739054 | |||||||
chr2:241739082 | T | C | 1 | a0021c0033t0008g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.293-1951T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739082 | |||||||
chr2:241739110 | C | G | 1 | a0001c0001t0006g0280 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.293-1923C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739110 | |||||||
chr2:241739183 | G | T | 1 | a0005c0004t0001g0375 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.293-1850G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739183 | |||||||
chr2:241739239 | C | T | 23 | a0001c0001t0007g0157 a0001c0001t0007g0212 a0001c0001t0007g0213 others(20): Show |
24 | HG00140.hp1 HG00642.hp1 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.293-1794C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739239 | |||||||
chr2:241739372 | C | T | 1 | a0001c0001t0003g0278 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.293-1661C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739372 | |||||||
chr2:241739408 | C | T | 65 | a0001c0001t0001g0040 a0001c0001t0002g0154 a0001c0001t0004g0155 others(62): Show |
66 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.293-1625C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739408 | |||||||
chr2:241739463 | T | G | 3 | a0001c0001t0008g0068 a0001c0001t0008g0166 a0002c0002t0007g0168 |
3 | HG02280.hp1 HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.293-1570T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739463 | |||||||
chr2:241739483 | C | G | 289 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0070 others(286): Show |
309 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(306): Show |
intron_variant | MODIFIER | c.293-1550C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739483 | |||||||
chr2:241739519 | A | T | 1 | a0008c0024t0001g0035 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.293-1514A>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739519 | |||||||
chr2:241739561 | T | A | 255 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0070 others(252): Show |
275 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.293-1472T>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739561 | |||||||
chr2:241739584 | C | G | 1 | a0003c0003t0005g0353 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.293-1449C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739584 | |||||||
chr2:241739734 | C | T | 2 | a0005c0004t0023g0378 a0005c0004t0023g0379 |
2 | HG01099.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.293-1299C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739734 | |||||||
chr2:241739754 | G | A | 6 | a0001c0001t0006g0276 a0003c0003t0011g0374 a0003c0008t0004g0372 others(3): Show |
6 | HG00140.hp1 HG01106.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-1279G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739754 | |||||||
chr2:241739772 | C | T | 1 | a0002c0002t0007g0098 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.293-1261C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739772 | |||||||
chr2:241739820 | A | G | 375 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0070 others(372): Show |
402 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(399): Show |
intron_variant | MODIFIER | c.293-1213A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739820 | |||||||
chr2:241739864 | G | A | 1 | a0003c0003t0005g0354 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.293-1169G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739864 | |||||||
chr2:241739866 | C | T | 1 | a0003c0008t0004g0372 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.293-1167C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739866 | |||||||
chr2:241739962 | T | C | 4 | a0001c0001t0007g0157 a0001c0001t0007g0212 a0001c0001t0007g0213 others(1): Show |
4 | HG00642.hp1 HG02257.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-1071T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739962 | |||||||
chr2:241739966 | G | A | 2 | a0002c0002t0033g0180 a0002c0002t0033g0181 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.293-1067G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241739966 | |||||||
chr2:241740098 | T | C | 1 | a0001c0001t0002g0154 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.293-935T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241740098 | |||||||
chr2:241740162 | G | A | 56 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0070 others(53): Show |
60 | HG00323.hp1 HG00408.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.293-871G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241740162 | |||||||
chr2:241740266 | G | GC | 69 | a0001c0001t0002g0062 a0001c0001t0002g0148 a0001c0001t0004g0155 others(66): Show |
73 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.293-766dupC | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr2 | 241740266 | ||||||
chr2:241740294 | G | A | 5 | a0001c0001t0002g0031 a0002c0002t0002g0071 a0002c0002t0007g0098 others(2): Show |
5 | HG02258.hp2 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-739G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241740294 | |||||||
chr2:241740449 | A | G | 19 | a0001c0001t0004g0155 a0001c0001t0042g0183 a0001c0001t0052g0160 others(16): Show |
19 | HG00408.hp2 HG02083.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.293-584A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241740449 | |||||||
chr2:241740453 | A | G | 1 | a0002c0002t0007g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.293-580A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241740453 | |||||||
chr2:241740475 | C | T | 44 | a0001c0001t0052g0160 a0002c0002t0001g0006 a0002c0002t0001g0048 others(41): Show |
45 | HG00558.hp2 HG00639.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.293-558C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241740475 | |||||||
chr2:241740517 | G | A | 2 | a0001c0001t0042g0183 a0021c0033t0008g0321 |
2 | HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.293-516G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241740517 | |||||||
chr2:241740566 | C | G | 1 | a0002c0002t0001g0014 | 2 | HG02738.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.293-467C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241740566 | |||||||
chr2:241740604 | T | C | 224 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(221): Show |
237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.293-429T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241740604 | |||||||
chr2:241740605 | G | A | 2 | a0002c0002t0033g0180 a0002c0002t0033g0181 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.293-428G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241740605 | |||||||
chr2:241740615 | A | G | 222 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(219): Show |
235 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.293-418A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241740615 | |||||||
chr2:241740684 | T | C | 7 | a0001c0001t0002g0059 a0001c0001t0002g0062 a0001c0001t0029g0015 others(4): Show |
8 | HG01109.hp1 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-349T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241740684 | |||||||
chr2:241740717 | T | C | 210 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(207): Show |
225 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.293-316T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241740717 | |||||||
chr2:241740773 | T | C | 2 | a0003c0003t0005g0360 a0004c0005t0005g0072 |
2 | HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.293-260T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241740773 | |||||||
chr2:241740814 | G | A | 63 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(60): Show |
69 | HG00140.hp1 HG00639.hp2 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.293-219G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241740814 | |||||||
chr2:241740949 | A | T | 1 | a0002c0002t0025g0169 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.293-84A>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241740949 | |||||||
chr2:241740951 | A | G | 221 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(218): Show |
235 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.293-82A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241740951 | |||||||
chr2:241740960 | C | T | 51 | a0002c0002t0001g0014 a0002c0002t0001g0016 a0002c0002t0001g0141 others(48): Show |
54 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.293-73C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241740960 | |||||||
chr2:241741010 | A | T | 1 | a0003c0003t0002g0342 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.293-23A>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241741010 | |||||||
chr2:241741015 | A | G | 220 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(217): Show |
234 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.293-18A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 2/9 | chr2 | 241741015 | |||||||
chr2:241741112 | C | G | 4 | a0001c0001t0001g0129 a0001c0001t0003g0258 a0001c0001t0003g0259 others(1): Show |
4 | HG00673.hp1 NA18943.hp2 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.350+22C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | chr2 | 241741112 | |||||||
chr2:241741117 | A | G | 4 | a0002c0002t0007g0076 a0002c0002t0007g0168 a0007c0007t0007g0347 others(1): Show |
4 | HG02486.hp2 HG02630.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.350+27A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | chr2 | 241741117 | |||||||
chr2:241741314 | C | G | 1 | a0001c0001t0042g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.350+224C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | chr2 | 241741314 | |||||||
chr2:241741385 | C | A | 37 | a0002c0002t0001g0006 a0002c0002t0001g0048 a0002c0002t0001g0052 others(34): Show |
39 | HG00558.hp2 HG00639.hp1 HG02027.hp1 others(36): Show |
intron_variant | MODIFIER | c.350+295C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | chr2 | 241741385 | |||||||
chr2:241741498 | G | GCTTGCTG others(61): Show |
1 | a0001c0001t0002g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.350+449_350+450ins others(68): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 241741498 | ||||||
chr2:241741527 | GTGGGGCT others(95): Show |
G | 222 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(219): Show |
236 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.350+450_350+551del | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 241741527 | ||||||
chr2:241741532 | G | GCTTGCTG others(95): Show |
1 | a0005c0004t0001g0315 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.350+449_350+450ins others(102): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 241741532 | ||||||
chr2:241741540 | C | T | 1 | a0005c0004t0001g0315 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.350+450C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | chr2 | 241741540 | |||||||
chr2:241741629 | A | ATGGGGCT others(27): Show |
1 | a0001c0001t0006g0229 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.350+573_350+606dup others(34): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 241741629 | ||||||
chr2:241741629 | A | G | 2 | a0001c0001t0028g0171 a0001c0001t0038g0253 |
2 | HG02004.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.350+539A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | chr2 | 241741629 | |||||||
chr2:241741663 | G | A | 220 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(217): Show |
234 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.350+573G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | chr2 | 241741663 | |||||||
chr2:241741663 | G | GTGGGGCT others(27): Show |
1 | a0001c0001t0003g0282 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.350+641_351-671dup others(34): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 241741663 | ||||||
chr2:241741663 | GTGGGGCT others(27): Show |
G | 2 | a0001c0001t0002g0101 a0001c0001t0002g0128 |
2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.350+641_351-671del others(34): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr2 | 241741663 | ||||||
chr2:241741664 | T | G | 1 | a0001c0001t0004g0108 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.350+574T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | chr2 | 241741664 | |||||||
chr2:241741697 | A | G | 1 | a0001c0001t0004g0094 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.350+607A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | chr2 | 241741697 | |||||||
chr2:241741731 | A | G | 223 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(220): Show |
237 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.350+641A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | chr2 | 241741731 | |||||||
chr2:241741736 | G | A | 221 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(218): Show |
235 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.350+646G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | chr2 | 241741736 | |||||||
chr2:241741770 | A | G | 222 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(219): Show |
236 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.351-665A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | chr2 | 241741770 | |||||||
chr2:241741795 | A | G | 1 | a0001c0001t0036g0290 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.351-640A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | chr2 | 241741795 | |||||||
chr2:241741842 | G | T | 5 | a0001c0001t0052g0160 a0004c0005t0007g0063 a0004c0005t0007g0064 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.351-593G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | chr2 | 241741842 | |||||||
chr2:241742029 | C | T | 1 | a0001c0001t0042g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.351-406C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | chr2 | 241742029 | |||||||
chr2:241742098 | C | T | 1 | a0002c0002t0009g0291 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.351-337C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | chr2 | 241742098 | |||||||
chr2:241742173 | G | A | 219 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(216): Show |
233 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.351-262G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 3/9 | chr2 | 241742173 | |||||||
chr2:241742595 | G | A | 1 | a0002c0002t0025g0169 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.490+21G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241742595 | |||||||
chr2:241742614 | T | C | 76 | a0001c0001t0002g0062 a0001c0001t0008g0068 a0001c0001t0008g0166 others(73): Show |
81 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.490+40T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241742614 | |||||||
chr2:241742736 | T | C | 1 | a0001c0001t0006g0265 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.490+162T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241742736 | |||||||
chr2:241742755 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.490+181A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241742755 | |||||||
chr2:241742782 | T | A | 1 | a0001c0026t0002g0088 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.490+208T>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241742782 | |||||||
chr2:241742792 | C | T | 1 | a0001c0012t0030g0312 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.490+218C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241742792 | |||||||
chr2:241742860 | T | C | 19 | a0001c0001t0003g0233 a0001c0001t0004g0155 a0001c0001t0006g0234 others(16): Show |
19 | HG00408.hp2 HG02083.hp2 HG04204.hp2 others(16): Show |
intron_variant | MODIFIER | c.490+286T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241742860 | |||||||
chr2:241742869 | G | A | 26 | a0001c0001t0002g0011 a0001c0001t0002g0109 a0001c0001t0002g0112 others(23): Show |
29 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.490+295G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241742869 | |||||||
chr2:241742876 | G | T | 1 | a0021c0033t0008g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.490+302G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241742876 | |||||||
chr2:241742878 | A | ATGAGGGG others(73): Show |
1 | a0003c0003t0005g0363 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.490+332_490+411dup others(80): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 241742878 | ||||||
chr2:241742878 | A | G | 3 | a0001c0001t0008g0068 a0001c0001t0008g0166 a0004c0023t0002g0172 |
3 | HG02280.hp1 HG02647.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.490+304A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241742878 | |||||||
chr2:241742908 | C | CGTGGCAG others(33): Show |
1 | a0021c0033t0008g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.490+373_490+374ins others(40): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 241742908 | ||||||
chr2:241742918 | G | A | 1 | a0001c0001t0002g0116 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.490+344G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241742918 | |||||||
chr2:241742918 | GTGAGGGG others(73): Show |
G | 70 | a0001c0001t0003g0233 a0001c0001t0004g0155 a0001c0001t0006g0234 others(67): Show |
74 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.490+412_490+491del others(80): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 241742918 | ||||||
chr2:241742958 | G | T | 1 | a0021c0033t0008g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.490+384G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241742958 | |||||||
chr2:241742958 | GTGAGGGG others(33): Show |
G | 1 | a0001c0001t0002g0116 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.490+412_490+451del others(40): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 241742958 | ||||||
chr2:241742980 | C | T | 2 | a0001c0001t0028g0087 a0001c0001t0028g0171 |
2 | HG01261.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.490+406C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241742980 | |||||||
chr2:241742986 | A | G | 171 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(168): Show |
181 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.490+412A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241742986 | |||||||
chr2:241742998 | A | G | 176 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(173): Show |
186 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.490+424A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241742998 | |||||||
chr2:241743020 | C | T | 51 | a0002c0002t0001g0006 a0002c0002t0001g0048 a0002c0002t0001g0052 others(48): Show |
55 | HG00558.hp2 HG00639.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.490+446C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241743020 | |||||||
chr2:241743063 | C | G | 1 | a0002c0002t0004g0055 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.490+489C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241743063 | |||||||
chr2:241743068 | C | T | 1 | a0001c0001t0002g0126 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.490+494C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241743068 | |||||||
chr2:241743077 | C | T | 52 | a0002c0002t0001g0006 a0002c0002t0001g0048 a0002c0002t0001g0052 others(49): Show |
56 | HG00558.hp2 HG00639.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.490+503C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241743077 | |||||||
chr2:241743100 | T | C | 168 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(165): Show |
178 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.491-522T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241743100 | |||||||
chr2:241743109 | G | A | 1 | a0021c0033t0008g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.491-513G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241743109 | |||||||
chr2:241743118 | A | G | 222 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(219): Show |
236 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.491-504A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241743118 | |||||||
chr2:241743140 | C | CGCCAGGG others(113): Show |
7 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0001c0001t0031g0162 others(4): Show |
8 | HG01243.hp1 HG02572.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.491-475_491-474ins others(120): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 241743140 | ||||||
chr2:241743140 | C | CGCCAGGG others(73): Show |
155 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(152): Show |
164 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.491-475_491-474ins others(80): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 241743140 | ||||||
chr2:241743140 | C | CGCCAGGG others(33): Show |
3 | a0002c0002t0033g0180 a0002c0002t0033g0181 a0004c0023t0002g0172 |
3 | HG02647.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.491-475_491-474ins others(40): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 241743140 | ||||||
chr2:241743140 | C | T | 3 | a0003c0003t0005g0363 a0003c0003t0043g0357 a0007c0007t0005g0348 |
3 | HG03486.hp2 HG03579.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.491-482C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241743140 | |||||||
chr2:241743146 | G | GGCGTGGC others(73): Show |
1 | a0001c0001t0042g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.491-475_491-474ins others(80): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr2 | 241743146 | ||||||
chr2:241743174 | C | T | 1 | a0002c0002t0004g0054 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.491-448C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241743174 | |||||||
chr2:241743175 | G | A | 1 | a0003c0008t0001g0028 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.491-447G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241743175 | |||||||
chr2:241743212 | G | A | 9 | a0001c0001t0001g0089 a0001c0001t0001g0117 a0001c0001t0001g0118 others(6): Show |
9 | HG00609.hp2 HG00673.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.491-410G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241743212 | |||||||
chr2:241743414 | T | G | 1 | a0001c0001t0003g0219 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.491-208T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241743414 | |||||||
chr2:241743429 | T | C | 242 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(239): Show |
256 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.491-193T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241743429 | |||||||
chr2:241743460 | G | A | 2 | a0001c0001t0003g0266 a0001c0001t0006g0265 |
2 | HG02080.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.491-162G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241743460 | |||||||
chr2:241743477 | G | T | 3 | a0002c0002t0007g0076 a0002c0002t0007g0168 a0007c0007t0007g0347 |
3 | HG02486.hp2 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.491-145G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241743477 | |||||||
chr2:241743594 | G | A | 1 | a0001c0001t0052g0160 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.491-28G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241743594 | |||||||
chr2:241743604 | C | T | 2 | a0002c0002t0033g0180 a0002c0002t0033g0181 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.491-18C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 4/9 | chr2 | 241743604 | |||||||
chr2:241743913 | G | C | 2 | a0001c0001t0008g0068 a0001c0001t0008g0166 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.684+98G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 5/9 | chr2 | 241743913 | |||||||
chr2:241743952 | G | A | 1 | a0005c0004t0001g0375 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.684+137G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 5/9 | chr2 | 241743952 | |||||||
chr2:241743959 | T | C | 222 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(219): Show |
236 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.684+144T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 5/9 | chr2 | 241743959 | |||||||
chr2:241743975 | C | T | 1 | a0004c0005t0002g0105 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.684+160C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 5/9 | chr2 | 241743975 | |||||||
chr2:241744056 | A | G | 221 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(218): Show |
235 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.684+241A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 5/9 | chr2 | 241744056 | |||||||
chr2:241744107 | C | T | 219 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(216): Show |
232 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(229): Show |
intron_variant | MODIFIER | c.684+292C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 5/9 | chr2 | 241744107 | |||||||
chr2:241744317 | G | A | 1 | a0003c0003t0011g0338 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.685-392G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 5/9 | chr2 | 241744317 | |||||||
chr2:241744379 | C | T | 2 | a0001c0001t0002g0034 a0001c0001t0002g0125 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.685-330C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 5/9 | chr2 | 241744379 | |||||||
chr2:241744460 | G | A | 1 | a0001c0001t0004g0155 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.685-249G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 5/9 | chr2 | 241744460 | |||||||
chr2:241744518 | C | T | 2 | a0001c0001t0008g0068 a0001c0001t0008g0166 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.685-191C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 5/9 | chr2 | 241744518 | |||||||
chr2:241744524 | C | T | 1 | a0002c0002t0001g0080 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.685-185C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 5/9 | chr2 | 241744524 | |||||||
chr2:241744525 | G | A | 1 | a0003c0003t0011g0374 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.685-184G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 5/9 | chr2 | 241744525 | |||||||
chr2:241744576 | C | T | 3 | a0002c0002t0007g0005 a0004c0021t0008g0030 a0004c0023t0002g0172 |
4 | HG02647.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-133C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 5/9 | chr2 | 241744576 | |||||||
chr2:241744577 | A | G | 222 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(219): Show |
236 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.685-132A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 5/9 | chr2 | 241744577 | |||||||
chr2:241744636 | C | T | 2 | a0002c0002t0033g0180 a0002c0002t0033g0181 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.685-73C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 5/9 | chr2 | 241744636 | |||||||
chr2:241744700 | T | C | 222 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(219): Show |
236 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.685-9T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 5/9 | chr2 | 241744700 | |||||||
chr2:241744972 | A | AC | 56 | a0001c0001t0003g0233 a0001c0001t0004g0155 a0001c0001t0006g0234 others(53): Show |
58 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.853+101dupC | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 241744972 | ||||||
chr2:241744972 | A | ACC | 13 | a0002c0002t0007g0002 a0002c0002t0007g0136 a0002c0002t0007g0137 others(10): Show |
15 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.853+100_853+101dup others(2): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 241744972 | ||||||
chr2:241744972 | A | ACCC | 24 | a0001c0001t0001g0070 a0001c0001t0001g0167 a0001c0001t0002g0031 others(21): Show |
25 | HG00642.hp1 HG01099.hp2 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.853+99_853+101dupC others(2): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 241744972 | ||||||
chr2:241744975 | C | A | 2 | a0001c0001t0008g0068 a0001c0001t0008g0166 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.853+98C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241744975 | |||||||
chr2:241744979 | G | C | 373 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0070 others(370): Show |
400 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(397): Show |
intron_variant | MODIFIER | c.853+102G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241744979 | |||||||
chr2:241744992 | G | A | 1 | a0021c0033t0008g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.853+115G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241744992 | |||||||
chr2:241744992 | G | T | 1 | a0001c0001t0001g0167 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.853+115G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241744992 | |||||||
chr2:241744999 | G | A | 5 | a0001c0001t0052g0160 a0004c0005t0007g0063 a0004c0005t0007g0064 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.853+122G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241744999 | |||||||
chr2:241745159 | C | A | 222 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(219): Show |
236 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.853+282C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241745159 | |||||||
chr2:241745385 | C | T | 1 | a0002c0002t0007g0098 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.853+508C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241745385 | |||||||
chr2:241745458 | C | T | 3 | a0003c0003t0013g0366 a0003c0003t0013g0367 a0003c0003t0013g0368 |
3 | HG00733.hp2 HG01123.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.853+581C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241745458 | |||||||
chr2:241745477 | C | T | 1 | a0002c0002t0015g0146 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.853+600C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241745477 | |||||||
chr2:241745529 | C | T | 2 | a0001c0001t0002g0062 a0001c0001t0029g0015 |
3 | HG01167.hp1 HG01169.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.853+652C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241745529 | |||||||
chr2:241745530 | A | G | 222 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(219): Show |
236 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.853+653A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241745530 | |||||||
chr2:241745538 | G | A | 1 | a0006c0006t0001g0310 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.853+661G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241745538 | |||||||
chr2:241745597 | C | T | 1 | a0001c0001t0007g0213 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.853+720C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241745597 | |||||||
chr2:241745675 | T | C | 4 | a0003c0003t0005g0349 a0003c0003t0007g0351 a0003c0003t0013g0350 others(1): Show |
4 | HG02615.hp2 HG02647.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.853+798T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241745675 | |||||||
chr2:241745694 | T | C | 219 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(216): Show |
233 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.853+817T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241745694 | |||||||
chr2:241745829 | C | T | 1 | a0002c0002t0049g0107 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.853+952C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241745829 | |||||||
chr2:241745883 | C | T | 29 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(26): Show |
31 | HG00642.hp1 HG01099.hp2 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.853+1006C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241745883 | |||||||
chr2:241745899 | C | A | 1 | a0002c0002t0004g0043 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.853+1022C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241745899 | |||||||
chr2:241745954 | C | T | 1 | a0002c0002t0004g0054 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.853+1077C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241745954 | |||||||
chr2:241745966 | C | G | 1 | a0001c0001t0003g0022 | 2 | HG01255.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.853+1089C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241745966 | |||||||
chr2:241746021 | G | A | 1 | a0001c0001t0003g0241 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.853+1144G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241746021 | |||||||
chr2:241746287 | G | A | 1 | a0021c0033t0008g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.853+1410G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241746287 | |||||||
chr2:241746296 | C | T | 2 | a0002c0002t0015g0134 a0002c0002t0015g0146 |
2 | HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.853+1419C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241746296 | |||||||
chr2:241746347 | G | A | 2 | a0002c0002t0002g0139 a0002c0002t0002g0153 |
2 | HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.853+1470G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241746347 | |||||||
chr2:241746421 | T | C | 2 | a0002c0009t0008g0132 a0002c0009t0008g0133 |
2 | HG02886.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.853+1544T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241746421 | |||||||
chr2:241746426 | C | T | 25 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(22): Show |
27 | HG00642.hp1 HG01099.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.853+1549C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241746426 | |||||||
chr2:241746491 | C | T | 1 | a0001c0001t0009g0238 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.853+1614C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241746491 | |||||||
chr2:241746511 | T | G | 1 | a0002c0002t0026g0044 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.853+1634T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241746511 | |||||||
chr2:241746601 | A | G | 5 | a0002c0002t0002g0071 a0002c0002t0013g0150 a0002c0009t0008g0100 others(2): Show |
5 | HG01109.hp1 HG02258.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.853+1724A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241746601 | |||||||
chr2:241746682 | G | A | 1 | a0005c0004t0023g0378 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.853+1805G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241746682 | |||||||
chr2:241746691 | C | T | 13 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(10): Show |
14 | HG01358.hp2 HG02559.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.853+1814C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241746691 | |||||||
chr2:241746744 | C | G | 3 | a0002c0002t0007g0076 a0002c0002t0007g0168 a0007c0007t0007g0347 |
3 | HG02486.hp2 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.853+1867C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241746744 | |||||||
chr2:241746744 | C | T | 2 | a0001c0001t0042g0183 a0002c0002t0004g0053 |
2 | HG02602.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.853+1867C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241746744 | |||||||
chr2:241746756 | T | C | 221 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(218): Show |
235 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.853+1879T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241746756 | |||||||
chr2:241746786 | G | T | 1 | a0001c0001t0001g0377 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.853+1909G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241746786 | |||||||
chr2:241746887 | C | CA | 35 | a0001c0001t0002g0059 a0001c0001t0002g0109 a0001c0001t0002g0116 others(32): Show |
35 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(32): Show |
intron_variant | MODIFIER | c.853+2027dupA | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 241746887 | ||||||
chr2:241746999 | A | G | 4 | a0003c0003t0005g0349 a0003c0003t0007g0351 a0003c0003t0013g0350 others(1): Show |
4 | HG02615.hp2 HG02647.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.853+2122A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241746999 | |||||||
chr2:241747052 | G | A | 2 | a0002c0002t0033g0180 a0002c0002t0033g0181 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.853+2175G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747052 | |||||||
chr2:241747114 | A | T | 183 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(180): Show |
195 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.853+2237A>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747114 | |||||||
chr2:241747159 | G | A | 7 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0001c0001t0031g0162 others(4): Show |
8 | HG01243.hp1 HG02572.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.853+2282G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747159 | |||||||
chr2:241747165 | C | G | 9 | a0003c0003t0005g0349 a0003c0003t0005g0354 a0003c0003t0007g0351 others(6): Show |
9 | HG02615.hp2 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.853+2288C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747165 | |||||||
chr2:241747214 | G | A | 58 | a0002c0002t0001g0014 a0002c0002t0001g0016 a0002c0002t0001g0141 others(55): Show |
62 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.853+2337G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747214 | |||||||
chr2:241747275 | G | A | 3 | a0001c0001t0006g0083 a0001c0001t0006g0084 a0001c0001t0006g0170 |
3 | HG02809.hp1 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.853+2398G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747275 | |||||||
chr2:241747318 | C | T | 1 | a0004c0005t0005g0208 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.853+2441C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747318 | |||||||
chr2:241747370 | G | A | 15 | a0002c0002t0002g0096 a0002c0002t0003g0082 a0002c0002t0007g0002 others(12): Show |
17 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.853+2493G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747370 | |||||||
chr2:241747383 | C | A | 1 | a0001c0001t0042g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.853+2506C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747383 | |||||||
chr2:241747391 | GGTTTGC | G | 17 | a0002c0002t0001g0006 a0002c0002t0001g0048 a0002c0002t0001g0052 others(14): Show |
18 | HG00558.hp2 HG02027.hp2 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.853+2515_853+2520d others(8): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747391 | |||||||
chr2:241747392 | GTTTGCT | G | 204 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(201): Show |
217 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.853+2534_853+2539d others(8): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 241747392 | ||||||
chr2:241747495 | C | T | 1 | a0002c0002t0002g0096 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.853+2618C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747495 | |||||||
chr2:241747512 | G | A | 1 | a0001c0001t0016g0179 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.853+2635G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747512 | |||||||
chr2:241747546 | G | GT | 13 | a0001c0001t0003g0018 a0001c0001t0003g0215 a0001c0001t0003g0216 others(10): Show |
14 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.854-2590dupT | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 241747546 | ||||||
chr2:241747546 | G | GTT | 103 | a0001c0001t0002g0062 a0001c0001t0008g0068 a0001c0001t0008g0166 others(100): Show |
111 | HG00140.hp2 HG00558.hp2 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.854-2591_854-2590d others(4): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 241747546 | ||||||
chr2:241747546 | G | GTTT | 104 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(101): Show |
109 | HG00140.hp1 HG00423.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.854-2592_854-2590d others(5): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 241747546 | ||||||
chr2:241747546 | G | GTTTT | 10 | a0003c0003t0010g0331 a0003c0003t0014g0320 a0003c0008t0001g0028 others(7): Show |
11 | HG00408.hp1 HG01106.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.854-2593_854-2590d others(6): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 241747546 | ||||||
chr2:241747600 | A | G | 241 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(238): Show |
255 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(252): Show |
intron_variant | MODIFIER | c.854-2551A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747600 | |||||||
chr2:241747633 | A | G | 1 | a0001c0001t0003g0219 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.854-2518A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747633 | |||||||
chr2:241747710 | A | C | 1 | a0021c0033t0008g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.854-2441A>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747710 | |||||||
chr2:241747738 | T | C | 1 | a0001c0001t0009g0238 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.854-2413T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747738 | |||||||
chr2:241747739 | T | C | 221 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(218): Show |
235 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.854-2412T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747739 | |||||||
chr2:241747785 | A | G | 29 | a0002c0002t0001g0016 a0002c0002t0001g0144 a0002c0002t0001g0145 others(26): Show |
31 | HG00597.hp2 HG00621.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.854-2366A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747785 | |||||||
chr2:241747800 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.854-2351C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747800 | |||||||
chr2:241747857 | C | T | 2 | a0001c0001t0003g0018 a0001c0001t0003g0216 |
3 | HG01070.hp2 HG01071.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.854-2294C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747857 | |||||||
chr2:241747859 | G | A | 1 | a0003c0003t0011g0339 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.854-2292G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747859 | |||||||
chr2:241747911 | C | T | 1 | a0001c0001t0002g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.854-2240C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747911 | |||||||
chr2:241747969 | G | T | 1 | a0002c0002t0008g0380 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.854-2182G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747969 | |||||||
chr2:241747998 | G | A | 1 | a0002c0002t0004g0206 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.854-2153G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241747998 | |||||||
chr2:241748035 | G | A | 3 | a0001c0001t0007g0157 a0001c0001t0007g0212 a0001c0001t0007g0213 |
3 | HG00642.hp1 HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.854-2116G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241748035 | |||||||
chr2:241748121 | T | TTTTTTG | 221 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(218): Show |
235 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.854-2017_854-2012d others(8): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 241748121 | ||||||
chr2:241748154 | T | C | 1 | a0002c0002t0002g0071 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.854-1997T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241748154 | |||||||
chr2:241748164 | A | C | 221 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(218): Show |
235 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.854-1987A>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241748164 | |||||||
chr2:241748223 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.854-1928C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241748223 | |||||||
chr2:241748372 | C | T | 1 | a0003c0008t0005g0371 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.854-1779C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241748372 | |||||||
chr2:241748429 | G | A | 1 | a0003c0003t0010g0316 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.854-1722G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241748429 | |||||||
chr2:241748434 | C | G | 1 | a0004c0005t0050g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.854-1717C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241748434 | |||||||
chr2:241748578 | A | G | 1 | a0021c0033t0008g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.854-1573A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241748578 | |||||||
chr2:241748587 | A | C | 1 | a0003c0003t0010g0330 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.854-1564A>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241748587 | |||||||
chr2:241748642 | G | A | 1 | a0003c0003t0010g0330 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.854-1509G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241748642 | |||||||
chr2:241748788 | C | T | 221 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(218): Show |
235 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.854-1363C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241748788 | |||||||
chr2:241748877 | C | T | 220 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(217): Show |
234 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.854-1274C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241748877 | |||||||
chr2:241748901 | C | T | 2 | a0002c0002t0033g0180 a0002c0002t0033g0181 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.854-1250C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241748901 | |||||||
chr2:241748912 | C | T | 1 | a0001c0001t0002g0116 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.854-1239C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241748912 | |||||||
chr2:241748919 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.854-1232C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241748919 | |||||||
chr2:241748951 | C | T | 218 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(215): Show |
231 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.854-1200C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241748951 | |||||||
chr2:241749009 | G | A | 2 | a0001c0001t0002g0062 a0001c0001t0029g0015 |
3 | HG01167.hp1 HG01169.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.854-1142G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241749009 | |||||||
chr2:241749019 | T | C | 192 | a0001c0001t0002g0062 a0001c0001t0008g0068 a0001c0001t0008g0166 others(189): Show |
204 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.854-1132T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241749019 | |||||||
chr2:241749027 | T | TC | 192 | a0001c0001t0002g0062 a0001c0001t0008g0068 a0001c0001t0008g0166 others(189): Show |
204 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.854-1121dupC | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 241749027 | ||||||
chr2:241749103 | C | T | 2 | a0002c0002t0007g0005 a0002c0002t0007g0098 |
3 | HG02886.hp2 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.854-1048C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241749103 | |||||||
chr2:241749109 | C | G | 1 | a0006c0006t0001g0301 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.854-1042C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241749109 | |||||||
chr2:241749245 | C | T | 1 | a0012c0031t0004g0184 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.854-906C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241749245 | |||||||
chr2:241749257 | C | T | 220 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(217): Show |
234 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.854-894C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241749257 | |||||||
chr2:241749299 | GTGTCTGC others(19): Show |
G | 1 | a0004c0005t0014g0104 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.854-851_854-826del others(26): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241749299 | |||||||
chr2:241749390 | G | T | 1 | a0001c0001t0003g0289 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.854-761G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241749390 | |||||||
chr2:241749407 | C | T | 2 | a0001c0001t0008g0068 a0001c0001t0008g0166 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.854-744C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241749407 | |||||||
chr2:241749455 | T | C | 221 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(218): Show |
235 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.854-696T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241749455 | |||||||
chr2:241749624 | C | T | 2 | a0004c0005t0005g0152 a0004c0005t0031g0161 |
2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.854-527C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241749624 | |||||||
chr2:241749703 | G | T | 1 | a0001c0001t0042g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.854-448G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241749703 | |||||||
chr2:241749726 | C | CCCCTCCT others(5): Show |
1 | a0021c0033t0008g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.854-424_854-413dup others(12): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr2 | 241749726 | ||||||
chr2:241749770 | T | C | 220 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(217): Show |
234 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.854-381T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241749770 | |||||||
chr2:241749848 | G | A | 220 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(217): Show |
234 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.854-303G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 6/9 | chr2 | 241749848 | |||||||
chr2:241750362 | G | A | 2 | a0002c0002t0033g0180 a0002c0002t0033g0181 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.997+68G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 7/9 | chr2 | 241750362 | |||||||
chr2:241750379 | T | TGGGCGGG others(9): Show |
1 | a0004c0005t0002g0102 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.997+95_997+96insGT others(14): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 241750379 | ||||||
chr2:241750379 | T | TGGGCGGG others(8): Show |
5 | a0003c0003t0002g0334 a0003c0003t0002g0335 a0004c0005t0002g0105 others(2): Show |
5 | HG02109.hp1 HG02723.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.997+93_997+107dupG others(14): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr2 | 241750379 | ||||||
chr2:241750394 | C | T | 28 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(25): Show |
30 | HG00642.hp1 HG01099.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.997+100C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 7/9 | chr2 | 241750394 | |||||||
chr2:241750448 | T | C | 59 | a0002c0002t0001g0014 a0002c0002t0001g0016 a0002c0002t0001g0141 others(56): Show |
63 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.997+154T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 7/9 | chr2 | 241750448 | |||||||
chr2:241750485 | G | C | 2 | a0002c0002t0033g0180 a0002c0002t0033g0181 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.997+191G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 7/9 | chr2 | 241750485 | |||||||
chr2:241750542 | T | C | 222 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(219): Show |
236 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.997+248T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 7/9 | chr2 | 241750542 | |||||||
chr2:241750572 | T | C | 49 | a0002c0002t0001g0014 a0002c0002t0001g0016 a0002c0002t0001g0141 others(46): Show |
53 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.997+278T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 7/9 | chr2 | 241750572 | |||||||
chr2:241750663 | G | T | 2 | a0001c0001t0004g0093 a0001c0001t0018g0254 |
2 | HG01433.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.997+369G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 7/9 | chr2 | 241750663 | |||||||
chr2:241750689 | G | T | 1 | a0021c0033t0008g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.997+395G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 7/9 | chr2 | 241750689 | |||||||
chr2:241750755 | A | C | 1 | a0003c0008t0004g0372 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.997+461A>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 7/9 | chr2 | 241750755 | |||||||
chr2:241750768 | C | T | 2 | a0001c0001t0002g0062 a0001c0001t0029g0015 |
3 | HG01167.hp1 HG01169.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.997+474C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 7/9 | chr2 | 241750768 | |||||||
chr2:241750769 | G | A | 1 | a0003c0008t0004g0372 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.997+475G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 7/9 | chr2 | 241750769 | |||||||
chr2:241750785 | C | T | 2 | a0001c0001t0002g0011 a0001c0001t0002g0115 |
3 | HG00438.hp2 HG00673.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.998-461C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 7/9 | chr2 | 241750785 | |||||||
chr2:241750810 | G | A | 1 | a0015c0030t0003g0281 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.998-436G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 7/9 | chr2 | 241750810 | |||||||
chr2:241750983 | C | T | 1 | a0002c0002t0039g0277 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.998-263C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 7/9 | chr2 | 241750983 | |||||||
chr2:241751113 | C | T | 37 | a0002c0002t0001g0006 a0002c0002t0001g0048 a0002c0002t0001g0052 others(34): Show |
39 | HG00558.hp2 HG00639.hp1 HG02027.hp1 others(36): Show |
intron_variant | MODIFIER | c.998-133C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 7/9 | chr2 | 241751113 | |||||||
chr2:241751461 | C | A | 2 | a0002c0002t0015g0134 a0002c0002t0015g0146 |
2 | HG02615.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1140+73C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241751461 | |||||||
chr2:241751606 | C | G | 105 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(102): Show |
110 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.1140+218C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241751606 | |||||||
chr2:241751648 | G | A | 4 | a0002c0002t0003g0082 a0002c0002t0008g0380 a0002c0032t0015g0077 others(1): Show |
4 | HG01496.hp1 HG02055.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.1140+260G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241751648 | |||||||
chr2:241751669 | C | T | 2 | a0001c0001t0002g0034 a0001c0001t0002g0125 |
2 | HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1140+281C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241751669 | |||||||
chr2:241751679 | G | A | 1 | a0001c0001t0003g0233 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1140+291G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241751679 | |||||||
chr2:241751688 | C | T | 4 | a0002c0002t0003g0082 a0002c0002t0008g0380 a0002c0032t0015g0077 others(1): Show |
4 | HG01496.hp1 HG02055.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.1140+300C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241751688 | |||||||
chr2:241751745 | G | A | 1 | a0001c0001t0002g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1140+357G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241751745 | |||||||
chr2:241751875 | G | T | 1 | a0002c0002t0025g0169 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1140+487G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241751875 | |||||||
chr2:241751878 | A | AGGCCTGG others(30): Show |
5 | a0002c0002t0007g0076 a0002c0002t0007g0168 a0005c0004t0001g0375 others(2): Show |
5 | HG02055.hp1 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1140+572_1140+608d others(39): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 241751878 | ||||||
chr2:241751878 | AGGCCTGG others(30): Show |
A | 20 | a0001c0001t0003g0242 a0001c0001t0003g0243 a0001c0001t0003g0282 others(17): Show |
22 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.1140+572_1140+608d others(39): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 241751878 | ||||||
chr2:241751901 | G | A | 1 | a0004c0005t0012g0217 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1140+513G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241751901 | |||||||
chr2:241751913 | C | T | 1 | a0002c0002t0004g0056 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1140+525C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241751913 | |||||||
chr2:241751927 | G | GGGGAGCC others(30): Show |
38 | a0002c0002t0001g0006 a0002c0002t0001g0048 a0002c0002t0001g0052 others(35): Show |
40 | HG00558.hp2 HG00639.hp1 HG02027.hp1 others(37): Show |
intron_variant | MODIFIER | c.1140+571_1140+572i others(39): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 241751927 | ||||||
chr2:241751928 | G | GGGAGCCC others(141): Show |
1 | a0001c0001t0002g0116 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1140+608_1140+609i others(150): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 241751928 | ||||||
chr2:241751945 | G | A | 1 | a0002c0002t0008g0380 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1140+557G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241751945 | |||||||
chr2:241751960 | G | A | 2 | a0001c0001t0002g0062 a0001c0001t0029g0015 |
3 | HG01167.hp1 HG01169.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1140+572G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241751960 | |||||||
chr2:241751961 | C | T | 2 | a0001c0001t0002g0062 a0001c0001t0029g0015 |
3 | HG01167.hp1 HG01169.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1140+573C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241751961 | |||||||
chr2:241751961 | CAGGGGGA others(30): Show |
C | 33 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(30): Show |
35 | HG00642.hp1 HG01099.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1140+576_1140+612d others(39): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 241751961 | ||||||
chr2:241751964 | G | GGGGAGCC others(104): Show |
1 | a0001c0001t0002g0059 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1140+586_1140+587i others(113): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 241751964 | ||||||
chr2:241751964 | G | GGGGAGCC others(103): Show |
1 | a0004c0005t0014g0104 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1140+602_1140+603i others(112): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 241751964 | ||||||
chr2:241751964 | G | GGGGAGCC others(30): Show |
2 | a0001c0001t0008g0068 a0001c0001t0008g0166 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1140+584_1140+620d others(39): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 241751964 | ||||||
chr2:241751964 | G | GGGGAGCC others(104): Show |
75 | a0003c0003t0002g0334 a0003c0003t0002g0335 a0003c0003t0002g0342 others(72): Show |
78 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.1140+608_1140+609i others(113): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 241751964 | ||||||
chr2:241751964 | G | T | 2 | a0001c0001t0002g0062 a0001c0001t0029g0015 |
3 | HG01167.hp1 HG01169.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1140+576G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241751964 | |||||||
chr2:241751964 | GGGGAGCC others(30): Show |
G | 17 | a0001c0001t0003g0233 a0001c0001t0004g0155 a0001c0001t0006g0234 others(14): Show |
17 | HG00408.hp2 HG02083.hp2 NA18939.hp1 others(14): Show |
intron_variant | MODIFIER | c.1140+584_1140+620d others(39): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 241751964 | ||||||
chr2:241751997 | A | G | 1 | a0001c0001t0002g0116 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1140+609A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241751997 | |||||||
chr2:241751998 | T | C | 1 | a0001c0001t0002g0116 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1140+610T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241751998 | |||||||
chr2:241752001 | T | G | 1 | a0001c0001t0002g0116 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1140+613T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752001 | |||||||
chr2:241752030 | C | T | 33 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(30): Show |
35 | HG00642.hp1 HG01099.hp2 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1140+642C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752030 | |||||||
chr2:241752049 | A | G | 34 | a0001c0001t0002g0116 a0001c0001t0003g0233 a0001c0001t0004g0155 others(31): Show |
36 | HG00408.hp2 HG00735.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.1140+661A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752049 | |||||||
chr2:241752052 | T | C | 66 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(63): Show |
70 | HG00408.hp2 HG00642.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.1140+664T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752052 | |||||||
chr2:241752056 | T | G | 66 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(63): Show |
70 | HG00408.hp2 HG00642.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.1140+668T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752056 | |||||||
chr2:241752060 | C | T | 2 | a0001c0001t0008g0068 a0001c0001t0008g0166 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1140+672C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752060 | |||||||
chr2:241752070 | GGCAGTGG others(33): Show |
G | 49 | a0002c0002t0001g0014 a0002c0002t0001g0016 a0002c0002t0001g0141 others(46): Show |
53 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1140+691_1140+730d others(42): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 241752070 | ||||||
chr2:241752075 | T | G | 39 | a0001c0001t0002g0116 a0002c0002t0001g0006 a0002c0002t0001g0048 others(36): Show |
41 | HG00558.hp2 HG00639.hp1 HG02027.hp1 others(38): Show |
intron_variant | MODIFIER | c.1140+687T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752075 | |||||||
chr2:241752088 | T | C | 50 | a0001c0001t0002g0116 a0001c0001t0003g0233 a0001c0001t0004g0155 others(47): Show |
52 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1140+700T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752088 | |||||||
chr2:241752102 | A | G | 57 | a0001c0001t0002g0116 a0001c0001t0003g0233 a0001c0001t0004g0155 others(54): Show |
59 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.1140+714A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752102 | |||||||
chr2:241752110 | A | G | 40 | a0001c0001t0008g0068 a0001c0001t0008g0166 a0002c0002t0001g0006 others(37): Show |
42 | HG00558.hp2 HG00639.hp1 HG02027.hp1 others(39): Show |
intron_variant | MODIFIER | c.1140+722A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752110 | |||||||
chr2:241752241 | G | A | 3 | a0001c0001t0003g0228 a0002c0002t0025g0169 a0005c0004t0001g0322 |
3 | HG01099.hp1 HG03225.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1140+853G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752241 | |||||||
chr2:241752251 | C | T | 1 | a0001c0001t0042g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1140+863C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752251 | |||||||
chr2:241752267 | C | T | 14 | a0002c0002t0002g0096 a0002c0002t0003g0082 a0002c0002t0007g0002 others(11): Show |
16 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1140+879C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752267 | |||||||
chr2:241752323 | C | T | 1 | a0003c0003t0005g0333 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1140+935C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752323 | |||||||
chr2:241752377 | G | A | 1 | a0006c0015t0001g0305 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1140+989G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752377 | |||||||
chr2:241752384 | C | G | 1 | a0001c0001t0038g0253 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1140+996C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752384 | |||||||
chr2:241752449 | C | G | 4 | a0003c0003t0005g0349 a0003c0003t0007g0351 a0003c0003t0013g0350 others(1): Show |
4 | HG02615.hp2 HG02647.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1140+1061C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752449 | |||||||
chr2:241752573 | C | T | 1 | a0002c0002t0001g0204 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1140+1185C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752573 | |||||||
chr2:241752635 | G | A | 1 | a0004c0005t0024g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1140+1247G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752635 | |||||||
chr2:241752659 | T | C | 71 | a0001c0001t0002g0116 a0001c0001t0003g0233 a0001c0001t0004g0155 others(68): Show |
75 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1140+1271T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752659 | |||||||
chr2:241752677 | G | T | 1 | a0021c0033t0008g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1140+1289G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752677 | |||||||
chr2:241752961 | C | T | 51 | a0003c0003t0002g0334 a0003c0003t0002g0335 a0003c0003t0005g0023 others(48): Show |
54 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.1140+1573C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752961 | |||||||
chr2:241752962 | G | A | 3 | a0001c0001t0007g0157 a0001c0001t0007g0212 a0001c0001t0007g0213 |
3 | HG00642.hp1 HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.1140+1574G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752962 | |||||||
chr2:241752987 | C | T | 1 | a0019c0019t0002g0097 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1140+1599C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241752987 | |||||||
chr2:241753071 | C | A | 49 | a0002c0002t0001g0014 a0002c0002t0001g0016 a0002c0002t0001g0141 others(46): Show |
53 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1140+1683C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753071 | |||||||
chr2:241753075 | T | C | 154 | a0001c0001t0002g0059 a0001c0001t0002g0062 a0001c0001t0002g0116 others(151): Show |
162 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.1140+1687T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753075 | |||||||
chr2:241753133 | A | T | 10 | a0001c0001t0004g0176 a0001c0013t0001g0013 a0001c0013t0001g0123 others(7): Show |
11 | HG01928.hp1 HG01952.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.1140+1745A>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753133 | |||||||
chr2:241753157 | C | T | 2 | a0002c0002t0033g0180 a0002c0002t0033g0181 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1140+1769C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753157 | |||||||
chr2:241753173 | C | T | 13 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(10): Show |
14 | HG01358.hp2 HG02559.hp1 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.1140+1785C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753173 | |||||||
chr2:241753193 | C | T | 1 | a0006c0006t0046g0307 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1140+1805C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753193 | |||||||
chr2:241753304 | C | T | 2 | a0001c0001t0008g0068 a0001c0001t0008g0166 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1140+1916C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753304 | |||||||
chr2:241753443 | C | T | 79 | a0001c0001t0002g0062 a0001c0001t0029g0015 a0001c0001t0042g0183 others(76): Show |
83 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.1140+2055C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753443 | |||||||
chr2:241753578 | C | T | 1 | a0002c0002t0002g0153 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1140+2190C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753578 | |||||||
chr2:241753606 | G | A | 4 | a0002c0002t0003g0082 a0002c0002t0008g0380 a0002c0032t0015g0077 others(1): Show |
4 | HG01496.hp1 HG02055.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.1140+2218G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753606 | |||||||
chr2:241753615 | G | A | 2 | a0001c0001t0003g0244 a0001c0001t0036g0290 |
2 | HG03654.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1140+2227G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753615 | |||||||
chr2:241753618 | G | A | 1 | a0002c0002t0025g0169 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1140+2230G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753618 | |||||||
chr2:241753694 | C | T | 1 | a0001c0001t0003g0259 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1141-2155C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753694 | |||||||
chr2:241753696 | C | G | 1 | a0001c0001t0002g0116 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1141-2153C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753696 | |||||||
chr2:241753698 | G | C | 14 | a0003c0003t0002g0334 a0003c0003t0002g0335 a0004c0005t0002g0102 others(11): Show |
15 | HG01261.hp2 HG01884.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1141-2151G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753698 | |||||||
chr2:241753798 | G | A | 49 | a0002c0002t0001g0014 a0002c0002t0001g0016 a0002c0002t0001g0141 others(46): Show |
53 | HG00140.hp2 HG00597.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.1141-2051G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753798 | |||||||
chr2:241753806 | C | T | 4 | a0002c0002t0003g0082 a0002c0002t0008g0380 a0002c0032t0015g0077 others(1): Show |
4 | HG01496.hp1 HG02055.hp2 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.1141-2043C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753806 | |||||||
chr2:241753909 | G | A | 76 | a0003c0003t0002g0334 a0003c0003t0002g0335 a0003c0003t0002g0342 others(73): Show |
79 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1141-1940G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753909 | |||||||
chr2:241753911 | C | T | 3 | a0001c0001t0006g0083 a0001c0001t0006g0084 a0001c0001t0006g0170 |
3 | HG02809.hp1 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1141-1938C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753911 | |||||||
chr2:241753970 | C | T | 2 | a0001c0001t0003g0252 a0001c0001t0003g0288 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1141-1879C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241753970 | |||||||
chr2:241754006 | C | T | 76 | a0003c0003t0002g0334 a0003c0003t0002g0335 a0003c0003t0002g0342 others(73): Show |
79 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1141-1843C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754006 | |||||||
chr2:241754099 | T | C | 71 | a0001c0001t0002g0116 a0001c0001t0003g0233 a0001c0001t0004g0155 others(68): Show |
75 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(72): Show |
intron_variant | MODIFIER | c.1141-1750T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754099 | |||||||
chr2:241754121 | G | A | 1 | a0001c0001t0035g0245 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1141-1728G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754121 | |||||||
chr2:241754157 | G | A | 70 | a0001c0001t0002g0116 a0001c0001t0003g0233 a0001c0001t0004g0155 others(67): Show |
74 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.1141-1692G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754157 | |||||||
chr2:241754180 | T | A | 76 | a0003c0003t0002g0334 a0003c0003t0002g0335 a0003c0003t0002g0342 others(73): Show |
79 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1141-1669T>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754180 | |||||||
chr2:241754203 | A | G | 77 | a0001c0001t0002g0116 a0001c0001t0003g0233 a0001c0001t0004g0155 others(74): Show |
81 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.1141-1646A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754203 | |||||||
chr2:241754212 | C | T | 17 | a0001c0001t0003g0233 a0001c0001t0004g0155 a0001c0001t0006g0234 others(14): Show |
17 | HG00408.hp2 HG02083.hp2 NA18939.hp1 others(14): Show |
intron_variant | MODIFIER | c.1141-1637C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754212 | |||||||
chr2:241754255 | G | A | 1 | a0001c0026t0002g0088 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1141-1594G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754255 | |||||||
chr2:241754317 | C | G | 1 | a0001c0001t0042g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1141-1532C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754317 | |||||||
chr2:241754409 | T | C | 244 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0089 others(241): Show |
258 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(255): Show |
intron_variant | MODIFIER | c.1141-1440T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754409 | |||||||
chr2:241754462 | C | T | 1 | a0002c0002t0026g0044 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1141-1387C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754462 | |||||||
chr2:241754518 | G | A | 8 | a0002c0002t0002g0071 a0002c0002t0007g0076 a0002c0002t0007g0168 others(5): Show |
8 | HG01109.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1141-1331G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754518 | |||||||
chr2:241754652 | G | A | 12 | a0002c0002t0002g0096 a0002c0002t0003g0082 a0002c0002t0007g0002 others(9): Show |
14 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1141-1197G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754652 | |||||||
chr2:241754728 | C | T | 1 | a0003c0003t0010g0330 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1141-1121C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754728 | |||||||
chr2:241754848 | C | G | 3 | a0001c0001t0020g0085 a0001c0001t0020g0086 a0001c0001t0025g0029 |
3 | HG02257.hp2 HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1141-1001C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754848 | |||||||
chr2:241754860 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1141-989C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754860 | |||||||
chr2:241754930 | T | A | 3 | a0001c0001t0020g0085 a0001c0001t0020g0086 a0001c0001t0025g0029 |
3 | HG02257.hp2 HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1141-919T>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754930 | |||||||
chr2:241754973 | G | A | 9 | a0002c0002t0002g0096 a0002c0002t0007g0002 a0002c0002t0007g0136 others(6): Show |
11 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.1141-876G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754973 | |||||||
chr2:241754984 | C | G | 79 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0167 others(76): Show |
83 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1141-865C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241754984 | |||||||
chr2:241755036 | A | G | 3 | a0001c0001t0020g0085 a0001c0001t0020g0086 a0001c0001t0025g0029 |
3 | HG02257.hp2 HG02280.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.1141-813A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241755036 | |||||||
chr2:241755167 | C | A | 33 | a0002c0002t0001g0006 a0002c0002t0001g0048 a0002c0002t0001g0066 others(30): Show |
35 | HG00558.hp2 HG00639.hp1 HG02027.hp1 others(32): Show |
intron_variant | MODIFIER | c.1141-682C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241755167 | |||||||
chr2:241755192 | C | T | 2 | a0001c0001t0008g0068 a0001c0001t0008g0166 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1141-657C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241755192 | |||||||
chr2:241755217 | C | G | 1 | a0007c0007t0007g0347 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1141-632C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241755217 | |||||||
chr2:241755223 | GTGTCCTT others(24): Show |
G | 8 | a0001c0001t0003g0252 a0001c0001t0003g0286 a0001c0001t0003g0288 others(5): Show |
8 | HG01168.hp2 HG01169.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.1141-610_1141-580d others(33): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 241755223 | ||||||
chr2:241755224 | T | G | 1 | a0001c0001t0003g0250 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1141-625T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241755224 | |||||||
chr2:241755356 | A | G | 3 | a0002c0002t0008g0380 a0003c0003t0002g0335 a0004c0005t0007g0074 |
3 | HG02109.hp1 HG02145.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1141-493A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241755356 | |||||||
chr2:241755482 | G | T | 34 | a0002c0002t0001g0006 a0002c0002t0001g0048 a0002c0002t0001g0066 others(31): Show |
36 | HG00558.hp2 HG00639.hp1 HG02027.hp1 others(33): Show |
intron_variant | MODIFIER | c.1141-367G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241755482 | |||||||
chr2:241755500 | A | G | 1 | a0008c0011t0007g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1141-349A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241755500 | |||||||
chr2:241755509 | C | T | 1 | a0006c0006t0001g0298 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1141-340C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241755509 | |||||||
chr2:241755607 | A | AGGGTTGG others(71): Show |
6 | a0001c0001t0025g0029 a0002c0002t0002g0139 a0002c0002t0007g0130 others(3): Show |
6 | HG02809.hp2 HG02896.hp2 NA19030.hp1 others(3): Show |
intron_variant | MODIFIER | c.1141-211_1141-134d others(80): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 241755607 | ||||||
chr2:241755684 | TGGGGTTG others(32): Show |
T | 2 | a0001c0001t0004g0108 a0001c0001t0004g0111 |
2 | NA19064.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1141-159_1141-121d others(41): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 241755684 | ||||||
chr2:241755697 | ACACCTGG others(32): Show |
A | 15 | a0001c0001t0002g0011 a0001c0001t0002g0109 a0001c0001t0002g0113 others(12): Show |
16 | HG00621.hp2 HG00673.hp2 HG01346.hp2 others(13): Show |
intron_variant | MODIFIER | c.1141-143_1141-105d others(41): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr2 | 241755697 | ||||||
chr2:241755729 | C | T | 1 | a0019c0019t0002g0097 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1141-120C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241755729 | |||||||
chr2:241755736 | T | A | 8 | a0001c0001t0002g0112 a0001c0001t0002g0173 a0001c0001t0002g0174 others(5): Show |
8 | NA18957.hp2 NA18990.hp2 NA19004.hp2 others(5): Show |
intron_variant | MODIFIER | c.1141-113T>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241755736 | |||||||
chr2:241755812 | A | G | 3 | a0001c0001t0007g0157 a0004c0022t0048g0210 a0010c0010t0002g0359 |
3 | HG02145.hp2 HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1141-37A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 8/9 | chr2 | 241755812 | |||||||
chr2:241756020 | C | T | 1 | a0001c0013t0001g0123 | 1 | NA18998.hp1 | splice_region_variant&intron_variant | LOW | c.1306+6C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241756020 | |||||||
chr2:241756024 | G | A | 1 | a0014c0036t0001g0304 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1306+10G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241756024 | |||||||
chr2:241756082 | T | C | 131 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0059 others(128): Show |
138 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.1306+68T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241756082 | |||||||
chr2:241756138 | G | A | 1 | a0001c0001t0006g0276 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1306+124G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241756138 | |||||||
chr2:241756326 | C | T | 15 | a0001c0001t0002g0059 a0001c0001t0002g0062 a0002c0002t0008g0380 others(12): Show |
15 | HG01099.hp2 HG02145.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.1306+312C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241756326 | |||||||
chr2:241756371 | G | T | 1 | a0001c0001t0009g0237 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1306+357G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241756371 | |||||||
chr2:241756403 | C | T | 1 | a0001c0001t0002g0175 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1306+389C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241756403 | |||||||
chr2:241756447 | A | G | 2 | a0007c0007t0005g0348 a0010c0010t0005g0026 |
3 | HG02965.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1306+433A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241756447 | |||||||
chr2:241756472 | A | G | 3 | a0001c0001t0003g0019 a0001c0001t0003g0244 a0005c0004t0001g0352 |
4 | HG00323.hp2 HG03017.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306+458A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241756472 | |||||||
chr2:241756485 | T | C | 254 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(251): Show |
271 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(268): Show |
intron_variant | MODIFIER | c.1306+471T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241756485 | |||||||
chr2:241756667 | G | A | 2 | a0005c0004t0023g0378 a0005c0004t0023g0379 |
2 | HG01099.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1306+653G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241756667 | |||||||
chr2:241756674 | A | G | 1 | a0001c0001t0003g0219 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1306+660A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241756674 | |||||||
chr2:241756796 | A | T | 1 | a0001c0001t0003g0244 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1306+782A>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241756796 | |||||||
chr2:241756797 | C | T | 1 | a0021c0033t0008g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1306+783C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241756797 | |||||||
chr2:241756914 | A | G | 257 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(254): Show |
275 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(272): Show |
intron_variant | MODIFIER | c.1306+900A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241756914 | |||||||
chr2:241756936 | A | G | 1 | a0003c0003t0002g0342 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1306+922A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241756936 | |||||||
chr2:241757252 | G | T | 1 | a0002c0002t0004g0051 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1306+1238G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241757252 | |||||||
chr2:241757279 | G | A | 3 | a0002c0002t0007g0130 a0003c0003t0021g0356 a0008c0011t0021g0036 |
3 | HG01884.hp2 HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1306+1265G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241757279 | |||||||
chr2:241757383 | GTATTTCA others(70): Show |
G | 44 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0001c0001t0031g0162 others(41): Show |
47 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.1306+1392_1306+146 others(81): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241757383 | ||||||
chr2:241757406 | G | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0062 |
2 | HG02451.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1306+1392G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241757406 | |||||||
chr2:241757410 | G | A | 1 | a0002c0009t0008g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1306+1396G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241757410 | |||||||
chr2:241757460 | A | G | 1 | a0021c0033t0008g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1306+1446A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241757460 | |||||||
chr2:241757480 | G | A | 1 | a0002c0002t0001g0080 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1306+1466G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241757480 | |||||||
chr2:241757691 | T | C | 46 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0001c0001t0031g0162 others(43): Show |
49 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1306+1677T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241757691 | |||||||
chr2:241757774 | A | G | 210 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(207): Show |
226 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.1306+1760A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241757774 | |||||||
chr2:241757852 | G | A | 68 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0081 others(65): Show |
75 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.1306+1838G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241757852 | |||||||
chr2:241757892 | G | T | 2 | a0002c0009t0008g0095 a0005c0018t0008g0325 |
2 | HG01884.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1306+1878G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241757892 | |||||||
chr2:241757900 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1306+1886A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241757900 | |||||||
chr2:241757959 | C | CA | 10 | a0001c0001t0002g0119 a0001c0001t0003g0019 a0001c0001t0019g0246 others(7): Show |
11 | HG00323.hp2 HG00597.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.1306+1961dupA | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241757959 | ||||||
chr2:241757967 | A | G | 1 | a0002c0002t0002g0140 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1306+1953A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241757967 | |||||||
chr2:241758195 | G | A | 4 | a0001c0001t0008g0068 a0001c0001t0008g0166 a0001c0001t0042g0183 others(1): Show |
4 | HG02280.hp1 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306+2181G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241758195 | |||||||
chr2:241758370 | C | T | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+2356C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241758370 | |||||||
chr2:241758474 | G | GC | 31 | a0001c0001t0003g0258 a0001c0001t0004g0108 a0001c0001t0004g0111 others(28): Show |
32 | HG00558.hp2 HG00639.hp1 HG01928.hp2 others(29): Show |
intron_variant | MODIFIER | c.1306+2465dupC | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758474 | ||||||
chr2:241758575 | C | T | 1 | a0003c0003t0005g0023 | 2 | HG00423.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1306+2561C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241758575 | |||||||
chr2:241758583 | C | G | 236 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0081 others(233): Show |
253 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.1306+2569C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241758583 | |||||||
chr2:241758604 | C | T | 1 | a0001c0001t0006g0239 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1306+2590C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241758604 | |||||||
chr2:241758634 | G | A | 7 | a0001c0001t0020g0085 a0001c0001t0020g0086 a0001c0001t0029g0015 others(4): Show |
8 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.1306+2620G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241758634 | |||||||
chr2:241758636 | T | G | 33 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0059 others(30): Show |
34 | HG01261.hp2 HG01496.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.1306+2622T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241758636 | |||||||
chr2:241758722 | G | A | 2 | a0004c0005t0007g0063 a0004c0005t0007g0064 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1306+2708G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241758722 | |||||||
chr2:241758752 | C | A | 113 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(110): Show |
123 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.1306+2738C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241758752 | |||||||
chr2:241758757 | G | A | 6 | a0001c0001t0007g0157 a0001c0001t0007g0212 a0001c0001t0007g0213 others(3): Show |
7 | HG00642.hp1 HG01891.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1306+2743G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241758757 | |||||||
chr2:241758765 | A | G | 1 | a0003c0003t0043g0357 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1306+2751A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241758765 | |||||||
chr2:241758767 | A | ATG | 10 | a0001c0001t0002g0173 a0001c0001t0006g0234 a0001c0001t0007g0212 others(7): Show |
10 | HG01884.hp2 HG02572.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.1306+2754_1306+275 others(6): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758767 | ||||||
chr2:241758767 | A | ATGTG | 19 | a0001c0001t0002g0122 a0001c0001t0006g0276 a0001c0001t0006g0280 others(16): Show |
19 | HG01109.hp1 HG01123.hp2 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.1306+2754_1306+275 others(8): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758767 | ||||||
chr2:241758767 | A | ATGTGTG | 40 | a0001c0001t0002g0011 a0001c0001t0002g0059 a0001c0001t0002g0109 others(37): Show |
47 | HG00438.hp2 HG00673.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.1306+2754_1306+275 others(10): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758767 | ||||||
chr2:241758767 | A | ATGTGTGT others(1): Show |
22 | a0001c0001t0002g0113 a0001c0001t0002g0114 a0001c0001t0002g0121 others(19): Show |
24 | HG00408.hp2 HG00423.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1306+2754_1306+275 others(12): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758767 | ||||||
chr2:241758767 | A | ATGTGTGT others(3): Show |
5 | a0001c0001t0002g0012 a0001c0001t0002g0062 a0001c0001t0002g0119 others(2): Show |
5 | HG00597.hp1 HG01496.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.1306+2754_1306+275 others(14): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758767 | ||||||
chr2:241758767 | A | ATGTGTGT others(7): Show |
2 | a0002c0002t0015g0134 a0007c0007t0001g0358 |
2 | HG02055.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.1306+2754_1306+275 others(18): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758767 | ||||||
chr2:241758767 | ATATGTGT others(3): Show |
A | 1 | a0002c0009t0008g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1306+2755_1306+276 others(14): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758767 | ||||||
chr2:241758769 | A | ATG | 46 | a0001c0001t0001g0089 a0001c0001t0001g0117 a0001c0001t0001g0118 others(43): Show |
48 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1306+2797_1306+279 others(6): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758769 | ||||||
chr2:241758769 | A | ATGTG | 27 | a0001c0001t0001g0092 a0001c0001t0003g0220 a0001c0001t0003g0224 others(24): Show |
29 | HG00621.hp2 HG01069.hp2 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.1306+2795_1306+279 others(8): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758769 | ||||||
chr2:241758769 | A | ATGTGTG | 52 | a0001c0001t0001g0067 a0001c0001t0003g0018 a0001c0001t0003g0019 others(49): Show |
59 | HG00323.hp2 HG00558.hp2 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.1306+2793_1306+279 others(10): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758769 | ||||||
chr2:241758769 | A | ATGTGTGT others(1): Show |
54 | a0001c0001t0001g0070 a0001c0001t0001g0127 a0001c0001t0001g0167 others(51): Show |
57 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1306+2791_1306+279 others(12): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758769 | ||||||
chr2:241758769 | A | ATGTGTGT others(3): Show |
26 | a0001c0001t0001g0196 a0001c0001t0003g0004 a0001c0001t0003g0243 others(23): Show |
29 | HG00140.hp2 HG00544.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.1306+2789_1306+279 others(14): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758769 | ||||||
chr2:241758769 | A | ATGTGTGT others(5): Show |
11 | a0001c0001t0003g0233 a0001c0001t0003g0258 a0002c0002t0001g0188 others(8): Show |
11 | HG01081.hp1 HG01934.hp2 HG01943.hp1 others(8): Show |
intron_variant | MODIFIER | c.1306+2787_1306+279 others(16): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758769 | ||||||
chr2:241758769 | A | ATGTGTGT others(7): Show |
3 | a0001c0001t0003g0282 a0001c0001t0003g0284 a0007c0017t0008g0373 |
3 | HG00558.hp1 NA18977.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1306+2785_1306+279 others(18): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758769 | ||||||
chr2:241758769 | A | ATGTGTGT others(9): Show |
5 | a0002c0002t0001g0190 a0002c0002t0001g0203 a0002c0002t0004g0195 others(2): Show |
5 | HG01123.hp1 HG01175.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.1306+2783_1306+279 others(20): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758769 | ||||||
chr2:241758769 | A | ATGTGTGT others(11): Show |
1 | a0002c0009t0008g0151 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1306+2781_1306+279 others(22): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758769 | ||||||
chr2:241758769 | A | G | 102 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0059 others(99): Show |
111 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.1306+2755A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241758769 | |||||||
chr2:241758769 | ATG | A | 3 | a0001c0001t0001g0129 a0001c0001t0028g0171 a0002c0002t0002g0139 |
3 | HG00673.hp1 HG02004.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1306+2797_1306+279 others(6): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758769 | ||||||
chr2:241758769 | ATGTGTGT others(5): Show |
A | 1 | a0001c0001t0038g0253 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1306+2787_1306+279 others(16): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241758769 | ||||||
chr2:241758864 | C | T | 7 | a0001c0001t0006g0083 a0001c0001t0006g0084 a0001c0001t0006g0170 others(4): Show |
7 | HG01261.hp2 HG02451.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1306+2850C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241758864 | |||||||
chr2:241758973 | C | G | 1 | a0003c0008t0001g0361 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1306+2959C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241758973 | |||||||
chr2:241759008 | C | T | 168 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(165): Show |
181 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.1306+2994C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241759008 | |||||||
chr2:241759040 | T | G | 1 | a0004c0005t0007g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1306+3026T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241759040 | |||||||
chr2:241759066 | T | A | 1 | a0006c0015t0001g0309 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1306+3052T>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241759066 | |||||||
chr2:241759067 | A | T | 1 | a0006c0015t0001g0309 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1306+3053A>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241759067 | |||||||
chr2:241759068 | C | A | 1 | a0006c0015t0001g0309 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1306+3054C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241759068 | |||||||
chr2:241759138 | G | A | 1 | a0001c0001t0002g0122 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1306+3124G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241759138 | |||||||
chr2:241759225 | G | A | 81 | a0001c0001t0005g0007 a0001c0001t0008g0068 a0001c0001t0008g0166 others(78): Show |
84 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.1306+3211G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241759225 | |||||||
chr2:241759270 | G | T | 51 | a0001c0001t0004g0001 a0001c0001t0004g0008 a0001c0001t0004g0093 others(48): Show |
55 | HG00558.hp2 HG00621.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1306+3256G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241759270 | |||||||
chr2:241759385 | G | A | 1 | a0002c0002t0001g0188 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1306+3371G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241759385 | |||||||
chr2:241759389 | C | T | 51 | a0001c0001t0004g0001 a0001c0001t0004g0008 a0001c0001t0004g0093 others(48): Show |
55 | HG00558.hp2 HG00621.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1306+3375C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241759389 | |||||||
chr2:241759430 | C | T | 2 | a0006c0006t0002g0294 a0006c0006t0002g0296 |
2 | NA19003.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1306+3416C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241759430 | |||||||
chr2:241759617 | G | A | 53 | a0001c0001t0002g0031 a0001c0001t0002g0034 a0001c0001t0002g0101 others(50): Show |
54 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1306+3603G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241759617 | |||||||
chr2:241759676 | CTT | C | 8 | a0001c0001t0020g0085 a0001c0001t0020g0086 a0001c0001t0025g0029 others(5): Show |
9 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1306+3664_1306+366 others(6): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241759676 | ||||||
chr2:241759777 | C | A | 1 | a0001c0001t0002g0081 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1306+3763C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241759777 | |||||||
chr2:241759875 | C | T | 157 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(154): Show |
165 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.1306+3861C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241759875 | |||||||
chr2:241759917 | C | A | 2 | a0001c0001t0028g0087 a0001c0001t0028g0171 |
2 | HG01261.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1306+3903C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241759917 | |||||||
chr2:241759949 | A | G | 2 | a0001c0029t0002g0156 a0004c0023t0002g0172 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1306+3935A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241759949 | |||||||
chr2:241759978 | G | A | 14 | a0001c0001t0003g0258 a0001c0001t0004g0001 a0001c0001t0004g0155 others(11): Show |
16 | HG00558.hp2 HG02056.hp2 NA18939.hp1 others(13): Show |
intron_variant | MODIFIER | c.1306+3964G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241759978 | |||||||
chr2:241760025 | A | G | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4011A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760025 | |||||||
chr2:241760065 | C | CCAAT | 52 | a0001c0001t0005g0007 a0001c0001t0008g0068 a0001c0001t0008g0166 others(49): Show |
55 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1306+4053_1306+405 others(8): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241760065 | ||||||
chr2:241760065 | C | CCAATCAG others(40): Show |
105 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(102): Show |
110 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1306+4053_1306+405 others(51): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241760065 | ||||||
chr2:241760076 | C | A | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4062C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760076 | |||||||
chr2:241760080 | C | T | 4 | a0001c0001t0008g0068 a0001c0001t0008g0166 a0001c0001t0042g0183 others(1): Show |
4 | HG02280.hp1 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306+4066C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760080 | |||||||
chr2:241760083 | C | T | 4 | a0001c0001t0008g0068 a0001c0001t0008g0166 a0001c0001t0042g0183 others(1): Show |
4 | HG02280.hp1 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306+4069C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760083 | |||||||
chr2:241760085 | C | T | 1 | a0001c0001t0002g0148 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1306+4071C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760085 | |||||||
chr2:241760088 | C | T | 4 | a0001c0001t0008g0068 a0001c0001t0008g0166 a0001c0001t0042g0183 others(1): Show |
4 | HG02280.hp1 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306+4074C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760088 | |||||||
chr2:241760089 | A | G | 157 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(154): Show |
165 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.1306+4075A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760089 | |||||||
chr2:241760089 | ATGGGTGG others(79): Show |
A | 3 | a0002c0002t0007g0130 a0003c0003t0021g0356 a0008c0011t0021g0036 |
3 | HG01884.hp2 HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1306+4277_1306+436 others(90): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241760089 | ||||||
chr2:241760119 | A | C | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4105A>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760119 | |||||||
chr2:241760123 | C | A | 1 | a0003c0008t0005g0336 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1306+4109C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760123 | |||||||
chr2:241760123 | C | T | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4109C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760123 | |||||||
chr2:241760126 | C | T | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4112C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760126 | |||||||
chr2:241760131 | C | T | 4 | a0001c0001t0002g0090 a0001c0001t0006g0223 a0001c0001t0012g0293 others(1): Show |
4 | HG01256.hp1 HG01496.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306+4117C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760131 | |||||||
chr2:241760135 | G | C | 5 | a0002c0002t0003g0082 a0002c0002t0015g0134 a0002c0002t0015g0146 others(2): Show |
5 | HG01496.hp1 HG02055.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1306+4121G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760135 | |||||||
chr2:241760148 | C | T | 4 | a0001c0001t0008g0068 a0001c0001t0008g0166 a0001c0001t0042g0183 others(1): Show |
4 | HG02280.hp1 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306+4134C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760148 | |||||||
chr2:241760162 | C | A | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4148C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760162 | |||||||
chr2:241760166 | T | C | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4152T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760166 | |||||||
chr2:241760169 | T | C | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4155T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760169 | |||||||
chr2:241760174 | T | C | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4160T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760174 | |||||||
chr2:241760190 | CCAAT | C | 46 | a0001c0001t0005g0007 a0002c0002t0005g0138 a0002c0002t0012g0225 others(43): Show |
49 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1306+4179_1306+418 others(8): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241760190 | ||||||
chr2:241760191 | C | T | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4177C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760191 | |||||||
chr2:241760199 | C | T | 1 | a0002c0032t0015g0077 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1306+4185C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760199 | |||||||
chr2:241760205 | A | C | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4191A>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760205 | |||||||
chr2:241760209 | C | T | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4195C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760209 | |||||||
chr2:241760210 | G | A | 1 | a0002c0002t0004g0054 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1306+4196G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760210 | |||||||
chr2:241760212 | C | T | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4198C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760212 | |||||||
chr2:241760217 | C | T | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4203C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760217 | |||||||
chr2:241760234 | C | T | 151 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(148): Show |
159 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1306+4220C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760234 | |||||||
chr2:241760236 | A | G | 8 | a0001c0001t0020g0085 a0001c0001t0020g0086 a0001c0001t0025g0029 others(5): Show |
9 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1306+4222A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760236 | |||||||
chr2:241760248 | C | A | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4234C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760248 | |||||||
chr2:241760252 | T | C | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4238T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760252 | |||||||
chr2:241760255 | T | C | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4241T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760255 | |||||||
chr2:241760260 | T | C | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4246T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760260 | |||||||
chr2:241760261 | G | A | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4247G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760261 | |||||||
chr2:241760271 | C | A | 4 | a0001c0001t0008g0068 a0001c0001t0008g0166 a0001c0001t0042g0183 others(1): Show |
4 | HG02280.hp1 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1306+4257C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760271 | |||||||
chr2:241760291 | A | C | 6 | a0001c0001t0008g0068 a0001c0001t0008g0166 a0001c0001t0012g0293 others(3): Show |
6 | HG02280.hp1 HG02738.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306+4277A>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760291 | |||||||
chr2:241760295 | C | T | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4281C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760295 | |||||||
chr2:241760298 | C | T | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4284C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760298 | |||||||
chr2:241760303 | C | T | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4289C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760303 | |||||||
chr2:241760303 | CGTGGGTG others(36): Show |
C | 6 | a0001c0001t0008g0068 a0001c0001t0008g0166 a0001c0001t0042g0183 others(3): Show |
6 | HG02280.hp1 HG02572.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306+4327_1306+436 others(47): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241760303 | ||||||
chr2:241760304 | G | A | 46 | a0001c0001t0005g0007 a0002c0002t0005g0138 a0002c0002t0012g0225 others(43): Show |
49 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1306+4290G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760304 | |||||||
chr2:241760305 | T | G | 2 | a0002c0002t0001g0066 a0002c0002t0001g0080 |
2 | HG02027.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.1306+4291T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760305 | |||||||
chr2:241760314 | C | A | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4300C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760314 | |||||||
chr2:241760335 | C | T | 10 | a0001c0012t0008g0032 a0001c0012t0030g0163 a0001c0012t0030g0312 others(7): Show |
10 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1306+4321C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760335 | |||||||
chr2:241760338 | T | C | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4324T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760338 | |||||||
chr2:241760341 | T | C | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4327T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760341 | |||||||
chr2:241760343 | C | T | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4329C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760343 | |||||||
chr2:241760346 | T | C | 2 | a0001c0001t0012g0293 a0001c0001t0031g0162 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1306+4332T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760346 | |||||||
chr2:241760350 | G | A | 6 | a0001c0001t0008g0068 a0001c0001t0008g0166 a0001c0001t0012g0293 others(3): Show |
6 | HG02280.hp1 HG02738.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1306+4336G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760350 | |||||||
chr2:241760350 | G | GGTGGGCA others(36): Show |
98 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(95): Show |
103 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1306+4342_1306+434 others(47): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241760350 | ||||||
chr2:241760357 | C | A | 46 | a0001c0001t0005g0007 a0002c0002t0005g0138 a0002c0002t0012g0225 others(43): Show |
49 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1306+4343C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760357 | |||||||
chr2:241760357 | C | ATTACCCA others(36): Show |
7 | a0001c0001t0002g0062 a0002c0002t0002g0140 a0002c0002t0002g0153 others(4): Show |
7 | HG03041.hp2 HG03453.hp1 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.1306+4342_1306+434 others(47): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760357 | |||||||
chr2:241760363 | C | T | 2 | a0001c0029t0002g0156 a0004c0023t0002g0172 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1306+4349C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760363 | |||||||
chr2:241760366 | T | TCAGTCGA others(32): Show |
45 | a0001c0001t0005g0007 a0002c0002t0005g0138 a0002c0002t0012g0225 others(42): Show |
48 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.1306+4366_1306+436 others(43): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241760366 | ||||||
chr2:241760378 | C | CTTCGCCA others(33): Show |
1 | a0003c0003t0005g0362 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1306+4366_1306+436 others(44): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241760378 | ||||||
chr2:241760381 | T | A | 1 | a0004c0022t0048g0210 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1306+4367T>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760381 | |||||||
chr2:241760381 | T | G | 1 | a0003c0003t0005g0362 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1306+4367T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760381 | |||||||
chr2:241760405 | C | G | 1 | a0008c0011t0007g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1306+4391C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760405 | |||||||
chr2:241760414 | C | T | 1 | a0008c0011t0007g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1306+4400C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760414 | |||||||
chr2:241760427 | C | T | 1 | a0001c0012t0030g0312 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1306+4413C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760427 | |||||||
chr2:241760510 | C | CCACAGCG others(165): Show |
4 | a0001c0001t0020g0085 a0001c0001t0020g0086 a0001c0001t0025g0029 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.1306+4622_1306+462 others(176): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241760510 | ||||||
chr2:241760511 | C | G | 53 | a0001c0001t0003g0258 a0001c0001t0004g0001 a0001c0001t0004g0008 others(50): Show |
57 | HG00558.hp2 HG00621.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1306+4497C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760511 | |||||||
chr2:241760637 | T | C | 244 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(241): Show |
260 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(257): Show |
intron_variant | MODIFIER | c.1306+4623T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760637 | |||||||
chr2:241760642 | C | T | 1 | a0004c0022t0048g0210 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1306+4628C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760642 | |||||||
chr2:241760674 | G | T | 1 | a0004c0022t0048g0210 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1306+4660G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760674 | |||||||
chr2:241760731 | A | C | 1 | a0009c0014t0003g0274 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1306+4717A>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760731 | |||||||
chr2:241760782 | A | T | 1 | a0003c0003t0005g0362 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1306+4768A>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241760782 | |||||||
chr2:241761033 | A | G | 1 | a0001c0001t0022g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1306+5019A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241761033 | |||||||
chr2:241761171 | G | A | 1 | a0005c0004t0001g0315 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1306+5157G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241761171 | |||||||
chr2:241761205 | G | A | 2 | a0004c0005t0007g0063 a0004c0005t0007g0064 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1306+5191G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241761205 | |||||||
chr2:241761208 | G | A | 1 | a0002c0002t0008g0380 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1306+5194G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241761208 | |||||||
chr2:241761260 | C | T | 3 | a0001c0001t0006g0083 a0001c0001t0006g0084 a0001c0001t0006g0170 |
3 | HG02809.hp1 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1306+5246C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241761260 | |||||||
chr2:241761261 | G | A | 1 | a0003c0008t0005g0336 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1306+5247G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241761261 | |||||||
chr2:241761355 | A | G | 48 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0001c0001t0031g0162 others(45): Show |
51 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1306+5341A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241761355 | |||||||
chr2:241761525 | C | T | 1 | a0002c0002t0004g0192 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1306+5511C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241761525 | |||||||
chr2:241761545 | G | A | 241 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(238): Show |
257 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(254): Show |
intron_variant | MODIFIER | c.1306+5531G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241761545 | |||||||
chr2:241761611 | G | C | 1 | a0004c0005t0002g0102 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1306+5597G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241761611 | |||||||
chr2:241761657 | C | T | 3 | a0002c0002t0001g0006 a0002c0002t0001g0048 a0002c0002t0001g0052 |
4 | HG02027.hp2 NA18959.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.1306+5643C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241761657 | |||||||
chr2:241761740 | A | G | 2 | a0002c0009t0008g0095 a0005c0018t0008g0325 |
2 | HG01884.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1306+5726A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241761740 | |||||||
chr2:241761910 | C | T | 2 | a0001c0001t0003g0256 a0001c0001t0003g0257 |
2 | HG01934.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.1307-5800C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241761910 | |||||||
chr2:241762000 | T | G | 243 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(240): Show |
259 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.1307-5710T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241762000 | |||||||
chr2:241762006 | C | A | 7 | a0001c0001t0002g0034 a0001c0001t0002g0101 a0001c0001t0002g0125 others(4): Show |
8 | HG02486.hp1 HG02559.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1307-5704C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241762006 | |||||||
chr2:241762048 | A | AT | 5 | a0001c0001t0002g0081 a0001c0001t0016g0179 a0001c0001t0016g0182 others(2): Show |
5 | HG02258.hp2 HG02717.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.1307-5662_1307-566 others(5): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241762048 | |||||||
chr2:241762069 | C | CT | 17 | a0001c0001t0001g0070 a0001c0001t0003g0282 a0001c0001t0031g0162 others(14): Show |
17 | HG00597.hp2 HG00735.hp1 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.1307-5621dupT | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241762069 | ||||||
chr2:241762069 | CT | C | 101 | a0001c0001t0003g0256 a0001c0001t0004g0001 a0001c0001t0004g0008 others(98): Show |
109 | HG00558.hp2 HG00621.hp2 HG00639.hp1 others(106): Show |
intron_variant | MODIFIER | c.1307-5621delT | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241762069 | ||||||
chr2:241762069 | CTT | C | 91 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(88): Show |
96 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1307-5622_1307-562 others(6): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241762069 | ||||||
chr2:241762081 | T | C | 1 | a0001c0001t0003g0248 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1307-5629T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241762081 | |||||||
chr2:241762232 | C | T | 48 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0001c0001t0031g0162 others(45): Show |
51 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1307-5478C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241762232 | |||||||
chr2:241762357 | A | G | 23 | a0001c0001t0007g0157 a0001c0001t0007g0212 a0001c0001t0007g0213 others(20): Show |
26 | HG00642.hp1 HG00735.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.1307-5353A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241762357 | |||||||
chr2:241762377 | T | C | 1 | a0001c0001t0017g0010 | 2 | NA18943.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1307-5333T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241762377 | |||||||
chr2:241762399 | C | T | 2 | a0001c0001t0022g0069 a0001c0001t0022g0073 |
2 | HG01358.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.1307-5311C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241762399 | |||||||
chr2:241762450 | G | A | 1 | a0008c0011t0007g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1307-5260G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241762450 | |||||||
chr2:241762485 | G | A | 1 | a0001c0001t0005g0007 | 2 | HG01243.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1307-5225G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241762485 | |||||||
chr2:241762531 | C | A | 1 | a0001c0001t0003g0231 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1307-5179C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241762531 | |||||||
chr2:241762574 | C | T | 109 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(106): Show |
114 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.1307-5136C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241762574 | |||||||
chr2:241762598 | C | T | 157 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(154): Show |
165 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.1307-5112C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241762598 | |||||||
chr2:241762622 | C | T | 2 | a0002c0002t0003g0082 a0007c0007t0001g0358 |
2 | HG02055.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1307-5088C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241762622 | |||||||
chr2:241762673 | A | G | 1 | a0021c0033t0008g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1307-5037A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241762673 | |||||||
chr2:241762773 | G | A | 1 | a0002c0002t0001g0189 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1307-4937G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241762773 | |||||||
chr2:241762928 | G | A | 31 | a0001c0001t0008g0068 a0001c0001t0008g0166 a0001c0001t0042g0183 others(28): Show |
31 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.1307-4782G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241762928 | |||||||
chr2:241763123 | C | G | 48 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0001c0001t0031g0162 others(45): Show |
51 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1307-4587C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241763123 | |||||||
chr2:241763212 | C | A | 1 | a0002c0002t0007g0076 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1307-4498C>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241763212 | |||||||
chr2:241763397 | G | A | 48 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0001c0001t0031g0162 others(45): Show |
51 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1307-4313G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241763397 | |||||||
chr2:241763400 | C | T | 1 | a0003c0003t0005g0349 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1307-4310C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241763400 | |||||||
chr2:241763487 | G | T | 1 | a0008c0011t0007g0033 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1307-4223G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241763487 | |||||||
chr2:241763505 | C | T | 1 | a0007c0007t0007g0346 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1307-4205C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241763505 | |||||||
chr2:241763596 | C | G | 1 | a0001c0001t0006g0283 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1307-4114C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241763596 | |||||||
chr2:241763602 | A | G | 1 | a0002c0002t0004g0045 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1307-4108A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241763602 | |||||||
chr2:241763750 | G | A | 1 | a0021c0033t0008g0321 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1307-3960G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241763750 | |||||||
chr2:241763768 | A | G | 243 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(240): Show |
259 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.1307-3942A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241763768 | |||||||
chr2:241763849 | G | A | 8 | a0001c0001t0020g0085 a0001c0001t0020g0086 a0001c0001t0025g0029 others(5): Show |
9 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1307-3861G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241763849 | |||||||
chr2:241763856 | C | T | 2 | a0001c0029t0002g0156 a0004c0023t0002g0172 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1307-3854C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241763856 | |||||||
chr2:241763902 | C | T | 47 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0001c0001t0031g0162 others(44): Show |
50 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1307-3808C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241763902 | |||||||
chr2:241763948 | G | A | 49 | a0001c0001t0002g0059 a0001c0001t0002g0062 a0001c0001t0005g0007 others(46): Show |
52 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1307-3762G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241763948 | |||||||
chr2:241763963 | C | G | 1 | a0012c0031t0004g0184 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1307-3747C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241763963 | |||||||
chr2:241763974 | C | G | 10 | a0003c0003t0010g0316 a0003c0003t0010g0326 a0003c0003t0010g0327 others(7): Show |
10 | HG00438.hp1 HG02040.hp1 NA18946.hp2 others(7): Show |
intron_variant | MODIFIER | c.1307-3736C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241763974 | |||||||
chr2:241764015 | C | T | 40 | a0001c0001t0004g0008 a0001c0001t0004g0093 a0001c0001t0004g0094 others(37): Show |
42 | HG00621.hp2 HG00639.hp1 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.1307-3695C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241764015 | |||||||
chr2:241764046 | A | C | 1 | a0002c0002t0001g0144 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1307-3664A>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241764046 | |||||||
chr2:241764170 | G | A | 112 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(109): Show |
116 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1307-3540G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241764170 | |||||||
chr2:241764203 | C | G | 160 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(157): Show |
168 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.1307-3507C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241764203 | |||||||
chr2:241764231 | T | C | 65 | a0001c0001t0003g0258 a0001c0001t0004g0001 a0001c0001t0004g0008 others(62): Show |
72 | HG00558.hp2 HG00621.hp2 HG00639.hp1 others(69): Show |
intron_variant | MODIFIER | c.1307-3479T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241764231 | |||||||
chr2:241764318 | G | GCAGCTAC others(43): Show |
1 | a0001c0001t0022g0073 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1307-3391_1307-334 others(54): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241764318 | ||||||
chr2:241764450 | CAACA | C | 3 | a0001c0001t0004g0155 a0007c0007t0004g0038 a0007c0007t0026g0047 |
3 | HG02056.hp2 NA18977.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1307-3255_1307-325 others(8): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241764450 | ||||||
chr2:241764467 | T | A | 1 | a0001c0001t0001g0127 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1307-3243T>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241764467 | |||||||
chr2:241764497 | A | G | 1 | a0004c0005t0007g0074 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1307-3213A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241764497 | |||||||
chr2:241764522 | G | A | 49 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0001c0001t0031g0162 others(46): Show |
53 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1307-3188G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241764522 | |||||||
chr2:241764624 | C | T | 40 | a0001c0001t0004g0008 a0001c0001t0004g0093 a0001c0001t0004g0094 others(37): Show |
42 | HG00621.hp2 HG00639.hp1 HG01175.hp2 others(39): Show |
intron_variant | MODIFIER | c.1307-3086C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241764624 | |||||||
chr2:241764646 | T | C | 243 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(240): Show |
259 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(256): Show |
intron_variant | MODIFIER | c.1307-3064T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241764646 | |||||||
chr2:241764647 | G | C | 1 | a0004c0005t0010g0041 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1307-3063G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241764647 | |||||||
chr2:241764778 | C | T | 2 | a0005c0004t0023g0378 a0005c0004t0023g0379 |
2 | HG01099.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1307-2932C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241764778 | |||||||
chr2:241764779 | G | A | 10 | a0001c0012t0008g0032 a0001c0012t0030g0163 a0001c0012t0030g0312 others(7): Show |
10 | HG02622.hp2 HG02723.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1307-2931G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241764779 | |||||||
chr2:241764838 | G | C | 1 | a0002c0002t0004g0045 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1307-2872G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241764838 | |||||||
chr2:241764844 | C | G | 24 | a0001c0001t0007g0157 a0001c0001t0007g0212 a0001c0001t0007g0213 others(21): Show |
27 | HG00642.hp1 HG00735.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.1307-2866C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241764844 | |||||||
chr2:241764922 | C | T | 3 | a0002c0002t0007g0130 a0003c0003t0021g0356 a0008c0011t0021g0036 |
3 | HG01884.hp2 HG02976.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1307-2788C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241764922 | |||||||
chr2:241764950 | G | A | 1 | a0007c0007t0007g0347 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1307-2760G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241764950 | |||||||
chr2:241764951 | T | A | 1 | a0016c0020t0005g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1307-2759T>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241764951 | |||||||
chr2:241765041 | G | T | 1 | a0005c0004t0001g0315 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1307-2669G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765041 | |||||||
chr2:241765082 | A | G | 1 | a0002c0002t0034g0262 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1307-2628A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765082 | |||||||
chr2:241765098 | G | A | 1 | a0001c0001t0003g0256 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1307-2612G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765098 | |||||||
chr2:241765101 | G | A | 1 | a0004c0022t0048g0210 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1307-2609G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765101 | |||||||
chr2:241765159 | G | C | 4 | a0001c0001t0008g0068 a0001c0001t0008g0166 a0001c0001t0042g0183 others(1): Show |
4 | HG02280.hp1 HG02897.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1307-2551G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765159 | |||||||
chr2:241765213 | G | A | 1 | a0002c0002t0002g0153 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1307-2497G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765213 | |||||||
chr2:241765256 | CTGGGGAG others(1443): Show |
C | 3 | a0004c0022t0048g0210 a0005c0004t0023g0378 a0005c0004t0023g0379 |
3 | HG01099.hp2 HG02922.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1307-2255_1307-806 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765256 | ||||||
chr2:241765274 | C | T | 15 | a0002c0002t0013g0150 a0002c0002t0034g0262 a0003c0003t0011g0338 others(12): Show |
15 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.1307-2436C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765274 | |||||||
chr2:241765305 | C | G | 3 | a0001c0029t0002g0156 a0003c0003t0010g0328 a0004c0023t0002g0172 |
3 | HG00438.hp1 HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1307-2405C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765305 | |||||||
chr2:241765305 | CTTGGGGA others(1393): Show |
C | 79 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(76): Show |
83 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1307-2224_1307-825 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765305 | ||||||
chr2:241765320 | G | GCCCCGGG others(245): Show |
1 | a0004c0005t0050g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1307-2376_1307-237 others(256): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765320 | ||||||
chr2:241765324 | C | T | 2 | a0004c0005t0005g0152 a0004c0005t0031g0161 |
2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1307-2386C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765324 | |||||||
chr2:241765333 | GGAGTAGG others(1093): Show |
G | 1 | a0001c0029t0002g0156 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1307-2305_1307-120 others(4): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765333 | ||||||
chr2:241765345 | G | GGGGGAGA others(240): Show |
1 | a0003c0003t0010g0327 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1307-2361_1307-236 others(251): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765345 | ||||||
chr2:241765348 | G | T | 60 | a0001c0001t0002g0113 a0001c0001t0006g0083 a0001c0001t0006g0084 others(57): Show |
63 | HG00642.hp1 HG00735.hp2 HG01069.hp1 others(60): Show |
intron_variant | MODIFIER | c.1307-2362G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765348 | |||||||
chr2:241765355 | C | CTTGGGGA others(393): Show |
2 | a0007c0007t0005g0348 a0010c0010t0005g0026 |
3 | HG02965.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1307-2337_1307-233 others(404): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765355 | ||||||
chr2:241765355 | C | G | 1 | a0006c0006t0001g0298 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1307-2355C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765355 | |||||||
chr2:241765355 | CTTGGGGA others(1143): Show |
C | 1 | a0004c0023t0002g0172 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1307-2305_1307-115 others(4): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765355 | ||||||
chr2:241765355 | CTTGGGGA others(1343): Show |
C | 5 | a0002c0002t0002g0079 a0002c0002t0002g0139 a0002c0002t0002g0153 others(2): Show |
5 | HG01074.hp2 HG01261.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1307-2224_1307-875 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765355 | ||||||
chr2:241765366 | G | A | 2 | a0003c0003t0010g0327 a0004c0005t0050g0075 |
2 | NA18984.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1307-2344G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765366 | |||||||
chr2:241765374 | C | T | 42 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0001c0001t0031g0162 others(39): Show |
45 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.1307-2336C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765374 | |||||||
chr2:241765375 | G | GGGCTGAG others(343): Show |
1 | a0003c0003t0014g0318 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1307-2313_1307-231 others(354): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765375 | ||||||
chr2:241765398 | G | T | 85 | a0001c0001t0002g0113 a0001c0001t0005g0007 a0001c0001t0006g0083 others(82): Show |
91 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.1307-2312G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765398 | |||||||
chr2:241765401 | A | T | 4 | a0002c0002t0007g0076 a0002c0002t0007g0168 a0003c0003t0007g0351 others(1): Show |
4 | HG02486.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307-2309A>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765401 | |||||||
chr2:241765405 | C | G | 11 | a0001c0001t0008g0068 a0001c0001t0008g0166 a0001c0001t0042g0183 others(8): Show |
12 | HG02280.hp1 HG02717.hp2 HG02897.hp2 others(9): Show |
intron_variant | MODIFIER | c.1307-2305C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765405 | |||||||
chr2:241765405 | CTTGGGGA others(1243): Show |
C | 3 | a0002c0002t0013g0150 a0003c0003t0013g0350 a0004c0005t0013g0147 |
3 | HG01109.hp1 HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1307-2255_1307-100 others(4): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765405 | ||||||
chr2:241765405 | CTTGGGGA others(1493): Show |
C | 12 | a0001c0012t0008g0032 a0001c0012t0030g0163 a0001c0012t0030g0312 others(9): Show |
12 | HG00558.hp2 HG02622.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1307-2255_1307-756 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765405 | ||||||
chr2:241765405 | CTTGGGGA others(1543): Show |
C | 11 | a0001c0001t0004g0001 a0001c0001t0004g0155 a0001c0001t0009g0221 others(8): Show |
13 | HG02056.hp2 NA18939.hp1 NA18953.hp1 others(10): Show |
intron_variant | MODIFIER | c.1307-2255_1307-706 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765405 | ||||||
chr2:241765405 | CTTGGGGA others(1693): Show |
C | 7 | a0001c0001t0004g0093 a0001c0001t0018g0254 a0001c0001t0020g0085 others(4): Show |
8 | HG01167.hp1 HG01169.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1307-2255_1307-556 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765405 | ||||||
chr2:241765405 | CTTGGGGA others(1893): Show |
C | 4 | a0002c0002t0007g0076 a0002c0002t0007g0168 a0003c0003t0007g0351 others(1): Show |
4 | HG02486.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307-2255_1307-356 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765405 | ||||||
chr2:241765405 | CTTGGGGA others(1943): Show |
C | 1 | a0001c0001t0022g0073 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1307-2255_1307-306 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765405 | ||||||
chr2:241765417 | G | GGAGCCCC others(142): Show |
1 | a0003c0008t0005g0371 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1307-2256_1307-225 others(153): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765417 | ||||||
chr2:241765417 | G | GGAGCCCC others(143): Show |
5 | a0004c0005t0005g0211 a0004c0005t0024g0037 a0004c0016t0012g0275 others(2): Show |
6 | HG01106.hp2 HG02559.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1307-2256_1307-225 others(154): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765417 | ||||||
chr2:241765425 | G | GGGCTGAG others(293): Show |
3 | a0003c0003t0005g0332 a0003c0003t0014g0320 a0004c0005t0012g0218 |
3 | HG03239.hp1 NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1307-2256_1307-225 others(304): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765425 | ||||||
chr2:241765436 | GTAGGAAG others(43): Show |
G | 2 | a0002c0009t0008g0095 a0005c0018t0008g0325 |
2 | HG01884.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1307-2255_1307-220 others(54): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765436 | ||||||
chr2:241765445 | GGGGGGAG others(1542): Show |
G | 1 | a0007c0007t0026g0047 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1307-2259_1307-711 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765445 | ||||||
chr2:241765455 | C | CTTGGGGA others(43): Show |
1 | a0004c0005t0024g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1307-2225_1307-222 others(54): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765455 | ||||||
chr2:241765455 | C | G | 52 | a0001c0001t0002g0113 a0001c0001t0005g0007 a0001c0001t0006g0083 others(49): Show |
55 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(52): Show |
intron_variant | MODIFIER | c.1307-2255C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765455 | |||||||
chr2:241765455 | CTTGGGGA others(1493): Show |
C | 2 | a0004c0005t0007g0063 a0004c0005t0007g0064 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1307-2224_1307-725 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765455 | ||||||
chr2:241765455 | CTTGGGGA others(1543): Show |
C | 1 | a0002c0002t0039g0277 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1307-2224_1307-675 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765455 | ||||||
chr2:241765455 | CTTGGGGA others(1593): Show |
C | 35 | a0001c0001t0004g0008 a0001c0001t0004g0094 a0001c0001t0004g0108 others(32): Show |
37 | HG00639.hp1 HG01175.hp2 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.1307-2224_1307-625 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765455 | ||||||
chr2:241765455 | CTTGGGGA others(1643): Show |
C | 2 | a0002c0002t0004g0043 a0011c0028t0004g0110 |
2 | HG00621.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.1307-2224_1307-575 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765455 | ||||||
chr2:241765455 | CTTGGGGA others(1893): Show |
C | 15 | a0001c0001t0007g0157 a0001c0001t0007g0212 a0001c0001t0007g0213 others(12): Show |
17 | HG00642.hp1 HG00735.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1307-2224_1307-325 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765455 | ||||||
chr2:241765457 | TGGGGAGA others(1394): Show |
T | 1 | a0001c0001t0002g0113 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1307-2249_1307-849 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765457 | ||||||
chr2:241765466 | G | A | 9 | a0003c0003t0010g0327 a0003c0008t0005g0371 a0004c0005t0005g0152 others(6): Show |
10 | HG01106.hp2 HG01257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1307-2244G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765466 | |||||||
chr2:241765466 | G | GGAGCCCC others(242): Show |
1 | a0004c0005t0010g0041 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1307-2243_1307-224 others(253): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765466 | ||||||
chr2:241765474 | CGGGCTGA others(1894): Show |
C | 1 | a0002c0002t0007g0002 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1307-2233_1307-333 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765474 | ||||||
chr2:241765475 | G | A | 5 | a0003c0003t0010g0327 a0004c0005t0005g0152 a0004c0005t0010g0041 others(2): Show |
5 | HG02717.hp2 HG02976.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.1307-2235G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765475 | |||||||
chr2:241765475 | G | GGGCTGAG others(243): Show |
28 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0002c0002t0005g0138 others(25): Show |
30 | HG00423.hp1 HG00438.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1307-2225_1307-222 others(254): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765475 | ||||||
chr2:241765475 | G | GGGCTGAG others(245): Show |
1 | a0001c0001t0031g0162 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1307-2225_1307-222 others(256): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765475 | ||||||
chr2:241765486 | T | G | 63 | a0001c0001t0005g0007 a0001c0001t0006g0083 a0001c0001t0006g0084 others(60): Show |
67 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.1307-2224T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765486 | |||||||
chr2:241765486 | TTAGGAAG others(1493): Show |
T | 116 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0070 others(113): Show |
130 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.1307-1904_1307-405 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765486 | ||||||
chr2:241765486 | TTAGGAAG others(1543): Show |
T | 4 | a0001c0001t0001g0089 a0001c0001t0003g0244 a0002c0002t0001g0193 others(1): Show |
4 | HG00735.hp1 HG01981.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1307-1904_1307-355 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765486 | ||||||
chr2:241765486 | TTAGGAAG others(1593): Show |
T | 1 | a0005c0004t0001g0375 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1307-1904_1307-305 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765486 | ||||||
chr2:241765486 | TTAGGAAG others(1693): Show |
T | 1 | a0008c0024t0001g0035 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1307-1905_1307-206 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765486 | ||||||
chr2:241765505 | G | C | 7 | a0001c0001t0006g0083 a0001c0001t0006g0084 a0001c0001t0006g0170 others(4): Show |
7 | HG00408.hp1 HG02145.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1307-2205G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765505 | |||||||
chr2:241765516 | G | A | 3 | a0003c0003t0005g0354 a0003c0003t0043g0357 a0003c0008t0005g0336 |
3 | HG00408.hp1 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1307-2194G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765516 | |||||||
chr2:241765517 | G | C | 2 | a0004c0005t0005g0152 a0004c0005t0031g0161 |
2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1307-2193G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765517 | |||||||
chr2:241765525 | G | A | 3 | a0003c0003t0005g0354 a0003c0003t0043g0357 a0003c0008t0005g0336 |
3 | HG00408.hp1 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1307-2185G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765525 | |||||||
chr2:241765543 | GAGGGGGG others(1894): Show |
G | 1 | a0001c0001t0022g0069 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1307-2166_1307-266 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765543 | |||||||
chr2:241765544 | A | AGGGGGGA others(44): Show |
1 | a0001c0001t0031g0162 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1307-2160_1307-211 others(55): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765544 | ||||||
chr2:241765555 | G | C | 6 | a0001c0001t0042g0183 a0002c0002t0008g0078 a0002c0009t0008g0095 others(3): Show |
6 | HG01884.hp1 HG02717.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1307-2155G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765555 | |||||||
chr2:241765555 | GTTGGGGA others(1293): Show |
G | 1 | a0001c0001t0003g0243 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1307-1904_1307-605 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765555 | ||||||
chr2:241765556 | T | G | 2 | a0001c0001t0008g0068 a0001c0001t0008g0166 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1307-2154T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765556 | |||||||
chr2:241765566 | G | A | 7 | a0003c0008t0005g0371 a0004c0005t0005g0152 a0004c0005t0005g0211 others(4): Show |
8 | HG01106.hp2 HG01257.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1307-2144G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765566 | |||||||
chr2:241765567 | G | C | 3 | a0003c0003t0005g0354 a0003c0003t0043g0357 a0003c0008t0005g0336 |
3 | HG00408.hp1 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1307-2143G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765567 | |||||||
chr2:241765569 | AGCCCCGG others(1504): Show |
A | 1 | a0001c0001t0037g0230 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1307-2140_1307-630 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765569 | |||||||
chr2:241765575 | G | A | 4 | a0003c0008t0005g0371 a0004c0005t0005g0211 a0004c0016t0012g0275 others(1): Show |
5 | HG01106.hp2 HG01257.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.1307-2135G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765575 | |||||||
chr2:241765595 | G | C | 1 | a0003c0003t0014g0319 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1307-2115G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765595 | |||||||
chr2:241765605 | G | C | 3 | a0003c0003t0005g0354 a0003c0003t0043g0357 a0003c0008t0005g0336 |
3 | HG00408.hp1 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1307-2105G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765605 | |||||||
chr2:241765606 | T | G | 1 | a0002c0002t0015g0146 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1307-2104T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765606 | |||||||
chr2:241765616 | G | A | 3 | a0003c0003t0005g0354 a0003c0003t0043g0357 a0003c0008t0005g0336 |
3 | HG00408.hp1 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1307-2094G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765616 | |||||||
chr2:241765655 | G | C | 2 | a0007c0007t0005g0348 a0010c0010t0005g0026 |
3 | HG02965.hp1 HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1307-2055G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765655 | |||||||
chr2:241765656 | T | G | 4 | a0002c0002t0003g0082 a0002c0002t0015g0134 a0002c0032t0015g0077 others(1): Show |
4 | HG01496.hp1 HG02055.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307-2054T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765656 | |||||||
chr2:241765666 | G | A | 2 | a0004c0005t0005g0152 a0004c0005t0031g0161 |
2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1307-2044G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765666 | |||||||
chr2:241765675 | G | A | 2 | a0004c0005t0005g0152 a0004c0005t0031g0161 |
2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1307-2035G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765675 | |||||||
chr2:241765705 | G | C | 1 | a0003c0003t0014g0318 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1307-2005G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765705 | |||||||
chr2:241765705 | G | GTTGGGGA others(43): Show |
3 | a0001c0001t0031g0162 a0003c0003t0014g0320 a0004c0005t0012g0218 |
3 | HG02738.hp1 HG03239.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1307-1956_1307-195 others(54): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765705 | ||||||
chr2:241765706 | T | G | 7 | a0001c0001t0001g0118 a0001c0001t0001g0127 a0001c0001t0001g0377 others(4): Show |
7 | HG03130.hp2 HG03540.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.1307-2004T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765706 | |||||||
chr2:241765706 | TTGGGGAG others(93): Show |
T | 2 | a0002c0009t0008g0095 a0005c0018t0008g0325 |
2 | HG01884.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1307-1904_1307-180 others(104): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765706 | ||||||
chr2:241765716 | G | A | 3 | a0003c0003t0005g0354 a0003c0003t0043g0357 a0003c0008t0005g0336 |
3 | HG00408.hp1 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1307-1994G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765716 | |||||||
chr2:241765724 | CGGGCTGA others(1494): Show |
C | 1 | a0001c0001t0001g0377 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1307-1983_1307-483 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765724 | ||||||
chr2:241765724 | CGGGCTGA others(1644): Show |
C | 1 | a0001c0001t0001g0127 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1307-1983_1307-333 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765724 | ||||||
chr2:241765725 | G | A | 3 | a0003c0003t0005g0354 a0003c0003t0043g0357 a0003c0008t0005g0336 |
3 | HG00408.hp1 HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1307-1985G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765725 | |||||||
chr2:241765745 | GGGGGGAG others(1492): Show |
G | 1 | a0001c0001t0001g0118 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1307-1959_1307-461 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765745 | ||||||
chr2:241765756 | T | G | 11 | a0001c0001t0006g0083 a0001c0001t0006g0084 a0001c0001t0006g0170 others(8): Show |
11 | HG00621.hp1 HG01496.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1307-1954T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765756 | |||||||
chr2:241765805 | G | C | 27 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0002c0002t0005g0138 others(24): Show |
29 | HG00423.hp1 HG00438.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1307-1905G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765805 | |||||||
chr2:241765805 | G | CTTGGGGA others(43): Show |
2 | a0003c0003t0005g0360 a0004c0005t0005g0072 |
2 | HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1307-1906_1307-190 others(54): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765805 | |||||||
chr2:241765805 | G | CTTGGGGA others(143): Show |
1 | a0003c0003t0014g0319 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1307-1906_1307-190 others(154): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765805 | |||||||
chr2:241765806 | G | T | 51 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0001c0001t0031g0162 others(48): Show |
55 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1307-1904G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765806 | |||||||
chr2:241765806 | GTGGGGAG others(643): Show |
G | 1 | a0001c0001t0008g0068 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1307-1655_1307-100 others(4): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765806 | ||||||
chr2:241765806 | GTGGGGAG others(1343): Show |
G | 1 | a0002c0002t0015g0146 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1307-1655_1307-306 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765806 | ||||||
chr2:241765806 | GTGGGGAG others(1443): Show |
G | 2 | a0002c0002t0001g0199 a0009c0014t0003g0292 |
2 | HG00621.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.1307-1645_1307-196 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765806 | ||||||
chr2:241765855 | G | GTTGGGGA others(42): Show |
1 | a0003c0008t0005g0371 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1307-1821_1307-182 others(53): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765855 | ||||||
chr2:241765855 | G | GTTGGGGA others(43): Show |
4 | a0004c0005t0005g0211 a0004c0016t0012g0275 a0004c0016t0012g0279 others(1): Show |
5 | HG01106.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1307-1806_1307-180 others(54): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765855 | ||||||
chr2:241765856 | T | G | 7 | a0001c0001t0008g0166 a0001c0001t0042g0183 a0002c0002t0003g0082 others(4): Show |
7 | HG01496.hp1 HG02055.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1307-1854T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765856 | |||||||
chr2:241765874 | C | G | 1 | a0004c0005t0050g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1307-1836C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765874 | |||||||
chr2:241765905 | G | GTTGGGGA others(143): Show |
1 | a0004c0005t0005g0042 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1307-1777_1307-162 others(154): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765905 | ||||||
chr2:241765906 | T | G | 3 | a0001c0001t0006g0083 a0001c0001t0006g0084 a0001c0001t0006g0170 |
3 | HG02809.hp1 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1307-1804T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241765906 | |||||||
chr2:241765955 | G | GTTGGGGA others(94): Show |
1 | a0002c0002t0005g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1307-1660_1307-165 others(105): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765955 | ||||||
chr2:241765955 | GTTGGGGA others(143): Show |
G | 1 | a0001c0001t0042g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1307-1655_1307-150 others(4): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765955 | ||||||
chr2:241765955 | GTTGGGGA others(893): Show |
G | 1 | a0002c0002t0008g0380 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1307-1655_1307-756 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765955 | ||||||
chr2:241765995 | GGGGGGAG others(1292): Show |
G | 1 | a0007c0007t0001g0358 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1307-1709_1307-411 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241765995 | ||||||
chr2:241766005 | G | C | 6 | a0002c0002t0003g0082 a0002c0002t0015g0134 a0002c0032t0015g0077 others(3): Show |
6 | HG01496.hp1 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1307-1705G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766005 | |||||||
chr2:241766005 | G | GTTGGGGA others(243): Show |
1 | a0003c0003t0005g0362 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1307-1628_1307-162 others(254): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766005 | ||||||
chr2:241766005 | GTTGGGGA others(793): Show |
G | 1 | a0001c0001t0008g0166 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1307-1627_1307-828 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766005 | ||||||
chr2:241766018 | G | A | 1 | a0005c0004t0027g0369 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1307-1692G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766018 | |||||||
chr2:241766021 | CCCCGGGC others(1479): Show |
C | 1 | a0005c0004t0027g0369 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1307-1688_1307-203 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766021 | |||||||
chr2:241766033 | GGAGTAGG others(43): Show |
G | 1 | a0003c0003t0043g0357 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1307-1627_1307-157 others(54): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766033 | ||||||
chr2:241766055 | C | CTTGGGGA others(95): Show |
1 | a0004c0005t0050g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1307-1628_1307-162 others(106): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766055 | ||||||
chr2:241766055 | C | CTTGGGGA others(43): Show |
1 | a0003c0003t0010g0316 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1307-1628_1307-162 others(54): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766055 | ||||||
chr2:241766055 | C | CTTGGGGA others(93): Show |
15 | a0001c0001t0005g0007 a0002c0002t0012g0225 a0003c0003t0005g0023 others(12): Show |
16 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.1307-1628_1307-162 others(104): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766055 | ||||||
chr2:241766055 | C | G | 20 | a0001c0001t0012g0293 a0001c0001t0031g0162 a0002c0002t0005g0138 others(17): Show |
22 | HG01106.hp2 HG01257.hp1 HG02559.hp1 others(19): Show |
intron_variant | MODIFIER | c.1307-1655C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766055 | |||||||
chr2:241766055 | CTTGGGGA others(143): Show |
C | 1 | a0003c0003t0005g0354 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1307-1627_1307-147 others(4): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766055 | ||||||
chr2:241766055 | CTTGGGGA others(1293): Show |
C | 3 | a0002c0002t0003g0082 a0002c0002t0015g0134 a0002c0032t0015g0077 |
3 | HG01496.hp1 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1307-1627_1307-328 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766055 | ||||||
chr2:241766058 | G | GGGAGATG others(88): Show |
1 | a0004c0005t0010g0041 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1307-1650_1307-164 others(99): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766058 | ||||||
chr2:241766074 | C | CGGGCTGA others(94): Show |
1 | a0005c0004t0045g0355 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1307-1628_1307-162 others(105): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766074 | ||||||
chr2:241766075 | G | GGGCTGAG others(91): Show |
1 | a0003c0003t0010g0327 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1307-1628_1307-162 others(102): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766075 | ||||||
chr2:241766083 | T | G | 53 | a0001c0001t0005g0007 a0001c0001t0006g0083 a0001c0001t0006g0084 others(50): Show |
57 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.1307-1627T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766083 | |||||||
chr2:241766105 | C | G | 14 | a0001c0001t0012g0293 a0002c0002t0008g0078 a0003c0003t0005g0023 others(11): Show |
14 | HG00408.hp1 HG00438.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.1307-1605C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766105 | |||||||
chr2:241766105 | CTTGGGGA others(793): Show |
C | 2 | a0002c0009t0008g0095 a0005c0018t0008g0325 |
2 | HG01884.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1307-1354_1307-555 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766105 | ||||||
chr2:241766125 | G | GGGCTGAG others(42): Show |
1 | a0003c0003t0010g0327 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1307-1582_1307-153 others(53): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766125 | ||||||
chr2:241766155 | G | C | 1 | a0003c0003t0010g0316 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1307-1555G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766155 | |||||||
chr2:241766155 | G | GTTGGGGA others(193): Show |
1 | a0003c0003t0005g0023 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1307-1506_1307-150 others(204): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766155 | ||||||
chr2:241766155 | GTTGGGGA others(1343): Show |
G | 3 | a0001c0001t0006g0083 a0001c0001t0006g0084 a0001c0001t0006g0170 |
3 | HG02809.hp1 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1307-1545_1307-196 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766155 | ||||||
chr2:241766156 | T | G | 1 | a0002c0002t0008g0078 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1307-1554T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766156 | |||||||
chr2:241766205 | G | C | 12 | a0001c0001t0012g0293 a0003c0003t0005g0023 a0003c0003t0005g0349 others(9): Show |
12 | HG00438.hp1 HG01243.hp2 HG02135.hp1 others(9): Show |
intron_variant | MODIFIER | c.1307-1505G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766205 | |||||||
chr2:241766205 | G | GTTGGGGA others(43): Show |
18 | a0001c0001t0005g0007 a0001c0001t0031g0162 a0002c0002t0005g0138 others(15): Show |
19 | HG00423.hp1 HG01070.hp1 HG01243.hp1 others(16): Show |
intron_variant | MODIFIER | c.1307-1456_1307-145 others(54): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766205 | ||||||
chr2:241766205 | G | GTTGGGGA others(93): Show |
1 | a0004c0005t0005g0072 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1307-1456_1307-145 others(104): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766205 | ||||||
chr2:241766205 | G | GTTGGGGA others(293): Show |
1 | a0004c0005t0012g0218 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1307-1456_1307-145 others(304): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766205 | ||||||
chr2:241766225 | G | GGGCTGAG others(92): Show |
1 | a0004c0005t0010g0041 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1307-1465_1307-146 others(103): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766225 | ||||||
chr2:241766244 | A | AGGGGGGA others(44): Show |
1 | a0004c0005t0014g0104 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1307-1456_1307-145 others(55): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766244 | ||||||
chr2:241766255 | G | C | 31 | a0001c0001t0005g0007 a0001c0001t0031g0162 a0002c0002t0005g0138 others(28): Show |
33 | HG00423.hp1 HG01070.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.1307-1455G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766255 | |||||||
chr2:241766255 | G | GTTGGGGA others(43): Show |
2 | a0003c0003t0005g0363 a0003c0008t0005g0336 |
2 | HG00408.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1307-1406_1307-140 others(54): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766255 | ||||||
chr2:241766255 | G | GTTGGGGA others(93): Show |
1 | a0003c0003t0010g0316 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1307-1406_1307-140 others(104): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766255 | ||||||
chr2:241766255 | G | GTTGGGGA others(143): Show |
4 | a0003c0003t0005g0349 a0003c0003t0010g0328 a0003c0003t0024g0317 others(1): Show |
4 | HG00438.hp1 HG02523.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307-1356_1307-135 others(154): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766255 | ||||||
chr2:241766282 | G | GGGAGTAG others(43): Show |
1 | a0004c0005t0050g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1307-1405_1307-140 others(54): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766282 | ||||||
chr2:241766296 | G | GGTGGAGA others(371): Show |
1 | a0004c0005t0010g0041 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1307-1413_1307-141 others(382): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766296 | ||||||
chr2:241766297 | G | T | 1 | a0004c0005t0012g0218 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1307-1413G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766297 | |||||||
chr2:241766298 | G | T | 2 | a0003c0003t0005g0023 a0004c0005t0005g0072 |
2 | HG02135.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1307-1412G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766298 | |||||||
chr2:241766305 | G | C | 4 | a0003c0003t0005g0023 a0003c0003t0005g0332 a0003c0003t0014g0320 others(1): Show |
4 | HG02135.hp1 HG03942.hp1 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307-1405G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766305 | |||||||
chr2:241766306 | T | G | 1 | a0002c0002t0008g0078 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1307-1404T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766306 | |||||||
chr2:241766348 | G | T | 27 | a0001c0001t0005g0007 a0001c0001t0031g0162 a0002c0002t0005g0138 others(24): Show |
28 | HG00423.hp1 HG00438.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.1307-1362G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766348 | |||||||
chr2:241766351 | A | G | 1 | a0003c0003t0043g0357 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1307-1359A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766351 | |||||||
chr2:241766355 | G | C | 32 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0001c0001t0031g0162 others(29): Show |
34 | HG00423.hp1 HG00438.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.1307-1355G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766355 | |||||||
chr2:241766355 | G | GTTGGGGA others(43): Show |
2 | a0003c0003t0005g0332 a0003c0003t0014g0320 |
2 | NA19065.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1307-1355_1307-135 others(54): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766355 | |||||||
chr2:241766356 | G | T | 48 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0001c0001t0031g0162 others(45): Show |
52 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.1307-1354G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766356 | |||||||
chr2:241766356 | GTGGGGAG others(643): Show |
G | 1 | a0001c0001t0042g0183 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1307-1305_1307-656 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766356 | ||||||
chr2:241766356 | GTGGGGAG others(693): Show |
G | 1 | a0002c0002t0008g0078 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1307-1305_1307-606 others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766356 | ||||||
chr2:241766358 | G | T | 1 | a0004c0005t0050g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1307-1352G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766358 | |||||||
chr2:241766398 | G | T | 1 | a0004c0005t0050g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1307-1312G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766398 | |||||||
chr2:241766405 | C | CTTGGGGA others(543): Show |
1 | a0004c0005t0024g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1307-1256_1307-125 others(554): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766405 | ||||||
chr2:241766405 | C | G | 4 | a0003c0003t0005g0354 a0003c0003t0043g0357 a0004c0005t0010g0041 others(1): Show |
4 | HG02630.hp2 HG03239.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1307-1305C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766405 | |||||||
chr2:241766447 | G | GGGGAGAA others(1243): Show |
1 | a0003c0003t0005g0023 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1307-1256_1307-125 others(1254): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766447 | ||||||
chr2:241766448 | G | GGGAGAAG others(43): Show |
1 | a0005c0004t0005g0324 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1307-1256_1307-125 others(54): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766448 | ||||||
chr2:241766451 | A | AGAAGTTG others(442): Show |
1 | a0003c0003t0010g0326 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1307-1256_1307-125 others(453): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766451 | ||||||
chr2:241766451 | A | AGAAGTTG others(693): Show |
1 | a0007c0007t0005g0348 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1307-1256_1307-125 others(704): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766451 | ||||||
chr2:241766451 | A | G | 1 | a0003c0003t0043g0357 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1307-1259A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766451 | |||||||
chr2:241766455 | C | CTTGGGGA others(643): Show |
1 | a0010c0010t0005g0026 | 2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1307-1163_1307-116 others(654): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766455 | ||||||
chr2:241766455 | C | CTTGGGGA others(1293): Show |
1 | a0003c0003t0005g0023 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1307-1164_1307-116 others(1304): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766455 | ||||||
chr2:241766455 | C | CTTGGGGA others(443): Show |
1 | a0003c0003t0005g0363 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1307-1164_1307-116 others(454): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766455 | ||||||
chr2:241766455 | C | CTTGGGGA others(442): Show |
1 | a0003c0003t0010g0327 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1307-1187_1307-118 others(453): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766455 | ||||||
chr2:241766455 | C | G | 12 | a0001c0001t0012g0293 a0003c0003t0005g0023 a0003c0003t0010g0326 others(9): Show |
12 | HG00408.hp1 HG02135.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.1307-1255C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766455 | |||||||
chr2:241766497 | G | GGGGAGAA others(43): Show |
3 | a0003c0003t0014g0318 a0003c0003t0014g0320 a0004c0005t0014g0104 |
3 | NA18972.hp1 NA19005.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1307-1164_1307-116 others(54): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766497 | ||||||
chr2:241766497 | G | T | 1 | a0004c0005t0005g0072 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1307-1213G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766497 | |||||||
chr2:241766501 | A | G | 1 | a0004c0005t0024g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1307-1209A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766501 | |||||||
chr2:241766505 | G | C | 3 | a0001c0001t0012g0293 a0004c0005t0050g0075 a0005c0004t0005g0324 |
3 | HG03209.hp2 HG03834.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1307-1205G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766505 | |||||||
chr2:241766505 | G | GTTGGGGA others(43): Show |
1 | a0003c0008t0005g0336 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1307-1156_1307-115 others(54): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766505 | ||||||
chr2:241766506 | T | G | 1 | a0001c0001t0008g0068 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1307-1204T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766506 | |||||||
chr2:241766547 | G | GGGGAGAA others(43): Show |
1 | a0004c0005t0050g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1307-1114_1307-111 others(54): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766547 | ||||||
chr2:241766547 | G | T | 23 | a0001c0001t0005g0007 a0001c0001t0031g0162 a0002c0002t0005g0138 others(20): Show |
24 | HG00438.hp1 HG01070.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.1307-1163G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766547 | |||||||
chr2:241766548 | G | T | 3 | a0003c0008t0005g0371 a0004c0005t0005g0211 a0005c0004t0005g0025 |
4 | HG01257.hp1 HG02559.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307-1162G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766548 | |||||||
chr2:241766548 | G | TGGAGAAC others(43): Show |
2 | a0004c0016t0012g0275 a0004c0016t0012g0279 |
2 | HG01106.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1307-1163_1307-116 others(54): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766548 | |||||||
chr2:241766551 | A | AGAAGTTG others(93): Show |
1 | a0004c0005t0012g0218 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1307-1060_1307-105 others(104): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766551 | ||||||
chr2:241766551 | A | G | 5 | a0003c0003t0005g0363 a0003c0003t0010g0326 a0003c0003t0010g0327 others(2): Show |
6 | HG02965.hp1 HG04228.hp1 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.1307-1159A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766551 | |||||||
chr2:241766555 | G | C | 11 | a0001c0001t0012g0293 a0001c0029t0002g0156 a0003c0008t0005g0336 others(8): Show |
12 | HG00408.hp1 HG01106.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1307-1155G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766555 | |||||||
chr2:241766601 | A | G | 2 | a0004c0005t0010g0041 a0004c0005t0024g0037 |
2 | NA18939.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1307-1109A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766601 | |||||||
chr2:241766605 | G | C | 9 | a0001c0001t0012g0293 a0003c0003t0005g0354 a0003c0008t0005g0371 others(6): Show |
10 | HG01106.hp2 HG01257.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1307-1105G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766605 | |||||||
chr2:241766617 | G | C | 2 | a0003c0003t0043g0357 a0007c0007t0005g0348 |
2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1307-1093G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766617 | |||||||
chr2:241766647 | G | T | 1 | a0005c0004t0005g0324 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1307-1063G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766647 | |||||||
chr2:241766648 | G | T | 1 | a0003c0008t0005g0336 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1307-1062G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766648 | |||||||
chr2:241766651 | A | G | 1 | a0004c0005t0012g0218 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1307-1059A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766651 | |||||||
chr2:241766655 | G | C | 6 | a0003c0003t0043g0357 a0003c0008t0005g0336 a0003c0008t0005g0371 others(3): Show |
7 | HG00408.hp1 HG01257.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1307-1055G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766655 | |||||||
chr2:241766697 | G | T | 2 | a0004c0016t0012g0275 a0004c0016t0012g0279 |
2 | HG01106.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1307-1013G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766697 | |||||||
chr2:241766698 | G | T | 2 | a0004c0005t0005g0152 a0004c0005t0031g0161 |
2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1307-1012G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766698 | |||||||
chr2:241766705 | G | C | 6 | a0001c0029t0002g0156 a0003c0003t0043g0357 a0003c0008t0005g0336 others(3): Show |
6 | HG00408.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1307-1005G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766705 | |||||||
chr2:241766705 | G | GTTGGGGA others(543): Show |
2 | a0003c0003t0010g0328 a0003c0003t0010g0330 |
2 | HG00438.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1307-965_1307-964i others(552): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766705 | ||||||
chr2:241766707 | T | TGGGGAGA others(45): Show |
1 | a0004c0005t0050g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1307-963_1307-962i others(54): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766707 | ||||||
chr2:241766717 | G | C | 6 | a0003c0003t0005g0363 a0003c0003t0010g0326 a0003c0003t0010g0327 others(3): Show |
7 | HG02965.hp1 HG04228.hp1 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.1307-993G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766717 | |||||||
chr2:241766717 | G | GGAGCCCC others(343): Show |
1 | a0003c0003t0005g0332 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1307-956_1307-955i others(352): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766717 | ||||||
chr2:241766717 | G | GGAGCCCC others(443): Show |
1 | a0003c0003t0005g0349 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1307-956_1307-955i others(452): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766717 | ||||||
chr2:241766717 | G | GGAGCCCC others(343): Show |
1 | a0003c0003t0010g0316 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1307-965_1307-964i others(352): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766717 | ||||||
chr2:241766717 | G | GGAGCCCC others(443): Show |
3 | a0003c0003t0010g0329 a0004c0005t0047g0057 a0005c0004t0045g0355 |
3 | HG02040.hp1 NA18952.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1307-965_1307-964i others(452): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766717 | ||||||
chr2:241766717 | G | GGAGCCCC others(443): Show |
1 | a0003c0003t0010g0331 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1307-965_1307-964i others(452): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766717 | ||||||
chr2:241766747 | G | T | 2 | a0003c0008t0005g0371 a0005c0004t0005g0025 |
3 | HG01257.hp1 HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1307-963G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766747 | |||||||
chr2:241766748 | G | T | 84 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(81): Show |
88 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1307-962G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766748 | |||||||
chr2:241766751 | A | AGAAGTTG others(693): Show |
1 | a0001c0001t0012g0293 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1307-956_1307-955i others(702): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766751 | ||||||
chr2:241766751 | A | AGAAGTTG others(543): Show |
4 | a0001c0001t0031g0162 a0003c0003t0005g0333 a0003c0003t0005g0353 others(1): Show |
4 | HG02622.hp1 HG02738.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307-956_1307-955i others(552): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766751 | ||||||
chr2:241766751 | A | AGAAGTTG others(543): Show |
1 | a0004c0005t0012g0217 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1307-956_1307-955i others(552): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766751 | ||||||
chr2:241766751 | A | AGAAGTTG others(793): Show |
1 | a0001c0001t0005g0007 | 2 | HG01243.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1307-956_1307-955i others(802): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766751 | ||||||
chr2:241766751 | A | G | 4 | a0003c0003t0010g0328 a0003c0003t0010g0330 a0003c0003t0043g0357 others(1): Show |
4 | HG00438.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1307-959A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766751 | |||||||
chr2:241766755 | C | G | 33 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0001c0001t0031g0162 others(30): Show |
36 | HG00423.hp1 HG00438.hp1 HG01070.hp1 others(33): Show |
intron_variant | MODIFIER | c.1307-955C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766755 | |||||||
chr2:241766759 | GGGAGATG others(40): Show |
G | 1 | a0001c0001t0008g0068 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1307-950_1307-904d others(49): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766759 | |||||||
chr2:241766767 | G | C | 1 | a0004c0005t0024g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1307-943G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766767 | |||||||
chr2:241766767 | G | GGAGCCCC others(493): Show |
1 | a0004c0005t0005g0208 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1307-906_1307-905i others(502): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766767 | ||||||
chr2:241766767 | G | GGAGCCCC others(393): Show |
4 | a0002c0002t0012g0225 a0003c0003t0005g0360 a0003c0003t0014g0319 others(1): Show |
4 | HG02735.hp1 HG03710.hp2 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307-906_1307-905i others(402): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766767 | ||||||
chr2:241766767 | G | GGAGCCCC others(343): Show |
1 | a0004c0005t0005g0072 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1307-906_1307-905i others(352): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766767 | ||||||
chr2:241766789 | G | GGAAGAGG others(394): Show |
1 | a0003c0003t0024g0317 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1307-906_1307-905i others(403): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766789 | ||||||
chr2:241766797 | G | GGGGAGAA others(43): Show |
1 | a0003c0008t0005g0336 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1307-906_1307-905i others(52): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766797 | ||||||
chr2:241766798 | G | T | 80 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(77): Show |
84 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1307-912G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766798 | |||||||
chr2:241766801 | A | AGAAGTTG others(43): Show |
1 | a0003c0003t0014g0318 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1307-906_1307-905i others(52): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766801 | ||||||
chr2:241766805 | C | G | 35 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0001c0001t0031g0162 others(32): Show |
38 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.1307-905C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766805 | |||||||
chr2:241766805 | CTTGGGGA others(293): Show |
C | 2 | a0004c0005t0005g0152 a0004c0005t0031g0161 |
2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1307-855_1307-556d others(2): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766805 | ||||||
chr2:241766817 | G | GGAGCCCC others(343): Show |
1 | a0003c0003t0005g0362 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1307-856_1307-855i others(352): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766817 | ||||||
chr2:241766851 | A | AGAAGTTG others(1244): Show |
1 | a0005c0004t0045g0355 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1307-856_1307-855i others(1253): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766851 | ||||||
chr2:241766851 | A | G | 15 | a0003c0003t0005g0023 a0003c0003t0005g0332 a0003c0003t0005g0349 others(12): Show |
17 | HG00423.hp1 HG02040.hp1 HG02135.hp1 others(14): Show |
intron_variant | MODIFIER | c.1307-859A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766851 | |||||||
chr2:241766855 | C | G | 124 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(121): Show |
132 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.1307-855C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766855 | |||||||
chr2:241766855 | CTTGGGGA others(43): Show |
G | 1 | a0001c0029t0002g0156 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1307-855_1307-806d others(52): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766855 | |||||||
chr2:241766856 | T | G | 1 | a0001c0001t0008g0068 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1307-854T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766856 | |||||||
chr2:241766857 | T | TGGGGAGA others(444): Show |
1 | a0002c0002t0005g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1307-810_1307-809i others(453): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766857 | ||||||
chr2:241766875 | G | A | 1 | a0001c0001t0008g0068 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1307-835G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766875 | |||||||
chr2:241766898 | G | T | 6 | a0001c0001t0002g0034 a0001c0001t0002g0101 a0001c0001t0002g0125 others(3): Show |
6 | HG02486.hp1 HG02559.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1307-812G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766898 | |||||||
chr2:241766901 | A | G | 2 | a0003c0003t0005g0023 a0003c0003t0014g0318 |
3 | HG00423.hp1 HG02135.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1307-809A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766901 | |||||||
chr2:241766905 | G | C | 82 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(79): Show |
86 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1307-805G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766905 | |||||||
chr2:241766905 | G | GTTGGGGA others(293): Show |
1 | a0003c0003t0014g0318 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1307-644_1307-643i others(302): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766905 | ||||||
chr2:241766905 | G | GTTGGGGA others(293): Show |
1 | a0004c0005t0014g0104 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1307-760_1307-759i others(302): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766905 | ||||||
chr2:241766905 | G | GTTGGGGA others(343): Show |
1 | a0003c0003t0014g0320 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1307-760_1307-759i others(352): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766905 | ||||||
chr2:241766945 | G | GGGGGGAG others(42): Show |
1 | a0002c0002t0005g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1307-759_1307-711d others(51): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766945 | ||||||
chr2:241766948 | G | T | 2 | a0002c0009t0008g0095 a0005c0018t0008g0325 |
2 | HG01884.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1307-762G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766948 | |||||||
chr2:241766951 | A | AGAAGTTG others(43): Show |
1 | a0005c0004t0005g0324 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1307-710_1307-709i others(52): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241766951 | ||||||
chr2:241766955 | G | C | 3 | a0002c0009t0008g0095 a0003c0003t0005g0354 a0005c0018t0008g0325 |
3 | HG01884.hp1 HG02630.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.1307-755G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766955 | |||||||
chr2:241766966 | G | A | 2 | a0002c0002t0004g0049 a0002c0002t0004g0051 |
2 | HG00558.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1307-744G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766966 | |||||||
chr2:241766995 | G | A | 1 | a0007c0007t0026g0047 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1307-715G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241766995 | |||||||
chr2:241767005 | G | C | 11 | a0001c0012t0008g0032 a0001c0012t0030g0163 a0001c0012t0030g0312 others(8): Show |
11 | HG02622.hp2 HG02630.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1307-705G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767005 | |||||||
chr2:241767006 | T | G | 2 | a0001c0001t0008g0068 a0001c0001t0008g0166 |
2 | HG02280.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1307-704T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767006 | |||||||
chr2:241767016 | G | A | 11 | a0001c0001t0004g0001 a0001c0001t0004g0155 a0001c0001t0009g0221 others(8): Show |
13 | HG02056.hp2 NA18939.hp1 NA18953.hp1 others(10): Show |
intron_variant | MODIFIER | c.1307-694G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767016 | |||||||
chr2:241767051 | A | AGAAGTTG others(93): Show |
1 | a0003c0008t0005g0336 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1307-560_1307-559i others(102): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241767051 | ||||||
chr2:241767051 | A | AGAAGTTG others(43): Show |
1 | a0005c0004t0005g0025 | 2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1307-610_1307-609i others(52): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241767051 | ||||||
chr2:241767051 | A | G | 4 | a0003c0003t0043g0357 a0004c0016t0012g0275 a0004c0016t0012g0279 others(1): Show |
4 | HG01106.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1307-659A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767051 | |||||||
chr2:241767055 | G | C | 4 | a0001c0001t0006g0271 a0002c0002t0039g0277 a0005c0004t0002g0345 others(1): Show |
4 | HG02735.hp2 NA18612.hp2 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307-655G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767055 | |||||||
chr2:241767056 | T | G | 10 | a0001c0001t0002g0034 a0001c0001t0002g0125 a0001c0001t0008g0166 others(7): Show |
10 | HG01099.hp2 HG01884.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1307-654T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767056 | |||||||
chr2:241767071 | C | CCCCGGGC others(91): Show |
1 | a0003c0008t0005g0371 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1307-610_1307-609i others(100): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241767071 | ||||||
chr2:241767096 | G | C | 4 | a0002c0002t0008g0380 a0002c0002t0013g0150 a0003c0003t0013g0350 others(1): Show |
4 | HG01109.hp1 HG02145.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1307-614G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767096 | |||||||
chr2:241767097 | G | T | 1 | a0003c0003t0005g0354 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1307-613G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767097 | |||||||
chr2:241767101 | A | AGAAGTTG others(92): Show |
1 | a0003c0003t0010g0326 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1307-608_1307-510d others(101): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241767101 | ||||||
chr2:241767101 | A | AGAAGTTG others(93): Show |
6 | a0003c0003t0005g0332 a0003c0003t0010g0327 a0003c0003t0010g0329 others(3): Show |
7 | HG02040.hp1 HG02965.hp1 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.1307-510_1307-509i others(102): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241767101 | ||||||
chr2:241767101 | A | AGAAGTTG others(43): Show |
1 | a0002c0002t0005g0138 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1307-560_1307-559i others(52): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241767101 | ||||||
chr2:241767101 | A | G | 23 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0001c0001t0031g0162 others(20): Show |
25 | HG00423.hp1 HG00438.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.1307-609A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767101 | |||||||
chr2:241767105 | G | C | 35 | a0001c0001t0004g0008 a0001c0001t0004g0094 a0001c0001t0004g0108 others(32): Show |
37 | HG00639.hp1 HG01175.hp2 HG01346.hp1 others(34): Show |
intron_variant | MODIFIER | c.1307-605G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767105 | |||||||
chr2:241767106 | T | G | 74 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(71): Show |
78 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1307-604T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767106 | |||||||
chr2:241767116 | G | A | 5 | a0001c0001t0020g0085 a0001c0001t0020g0086 a0001c0001t0025g0029 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1307-594G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767116 | |||||||
chr2:241767125 | G | A | 5 | a0001c0001t0020g0085 a0001c0001t0020g0086 a0001c0001t0025g0029 others(2): Show |
6 | HG01167.hp1 HG01169.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1307-585G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767125 | |||||||
chr2:241767132 | G | GGGAGTAG others(99): Show |
1 | a0004c0005t0010g0041 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1307-510_1307-509i others(108): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241767132 | ||||||
chr2:241767136 | G | A | 11 | a0002c0002t0034g0262 a0003c0003t0011g0338 a0003c0003t0011g0339 others(8): Show |
11 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.1307-574G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767136 | |||||||
chr2:241767146 | G | A | 1 | a0001c0012t0030g0312 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1307-564G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767146 | |||||||
chr2:241767151 | A | AGAAGTTG others(43): Show |
2 | a0003c0003t0010g0316 a0004c0005t0005g0211 |
2 | HG02723.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1307-510_1307-509i others(52): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241767151 | ||||||
chr2:241767151 | A | G | 5 | a0003c0003t0005g0023 a0003c0008t0005g0336 a0004c0016t0012g0275 others(2): Show |
7 | HG00408.hp1 HG00423.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.1307-559A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767151 | |||||||
chr2:241767155 | G | C | 5 | a0002c0002t0004g0043 a0004c0005t0007g0063 a0004c0005t0007g0064 others(2): Show |
5 | HG00621.hp2 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1307-555G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767155 | |||||||
chr2:241767156 | T | G | 3 | a0001c0001t0002g0034 a0001c0001t0002g0125 a0001c0001t0008g0068 |
3 | HG02559.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1307-554T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767156 | |||||||
chr2:241767158 | G | GGGGAGAT others(193): Show |
1 | a0004c0005t0050g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1307-544_1307-543i others(202): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241767158 | ||||||
chr2:241767174 | C | T | 1 | a0006c0006t0002g0295 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1307-536C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767174 | |||||||
chr2:241767194 | A | AC | 3 | a0002c0002t0013g0150 a0003c0003t0013g0350 a0004c0005t0013g0147 |
3 | HG01109.hp1 HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1307-516_1307-515i others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767194 | |||||||
chr2:241767197 | G | GGGGGGAA others(193): Show |
1 | a0003c0003t0005g0349 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1307-510_1307-509i others(202): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241767197 | ||||||
chr2:241767197 | G | T | 2 | a0004c0005t0005g0152 a0004c0005t0031g0161 |
2 | HG02717.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1307-513G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767197 | |||||||
chr2:241767205 | G | C | 2 | a0004c0005t0007g0063 a0004c0005t0007g0064 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1307-505G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767205 | |||||||
chr2:241767206 | T | G | 125 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0070 others(122): Show |
139 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1307-504T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767206 | |||||||
chr2:241767208 | G | T | 1 | a0001c0001t0037g0230 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1307-502G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767208 | |||||||
chr2:241767244 | A | G | 1 | a0001c0001t0037g0230 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1307-466A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767244 | |||||||
chr2:241767246 | G | C | 12 | a0002c0002t0034g0262 a0003c0003t0011g0338 a0003c0003t0011g0339 others(9): Show |
12 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.1307-464G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767246 | |||||||
chr2:241767247 | G | T | 1 | a0001c0001t0037g0230 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1307-463G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767247 | |||||||
chr2:241767255 | G | C | 2 | a0004c0005t0007g0063 a0004c0005t0007g0064 |
2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1307-455G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767255 | |||||||
chr2:241767256 | T | G | 205 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0070 others(202): Show |
223 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.1307-454T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767256 | |||||||
chr2:241767305 | G | C | 8 | a0002c0002t0013g0150 a0002c0002t0015g0146 a0003c0003t0013g0350 others(5): Show |
8 | HG01109.hp1 HG02055.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1307-405G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767305 | |||||||
chr2:241767305 | GTTGGGGA others(193): Show |
G | 1 | a0001c0001t0008g0068 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1307-395_1307-196d others(2): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241767305 | ||||||
chr2:241767306 | T | G | 12 | a0001c0012t0008g0032 a0001c0012t0030g0163 a0001c0012t0030g0312 others(9): Show |
12 | HG02055.hp1 HG02145.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1307-404T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767306 | |||||||
chr2:241767324 | C | T | 65 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(62): Show |
69 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.1307-386C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767324 | |||||||
chr2:241767344 | A | AC | 12 | a0002c0002t0034g0262 a0003c0003t0011g0338 a0003c0003t0011g0339 others(9): Show |
12 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.1307-366_1307-365i others(3): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767344 | |||||||
chr2:241767344 | A | AGGGGGGA others(46): Show |
1 | a0004c0005t0050g0075 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1307-336_1307-335i others(55): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241767344 | ||||||
chr2:241767346 | G | T | 2 | a0001c0029t0002g0156 a0004c0023t0002g0172 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1307-364G>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767346 | |||||||
chr2:241767355 | G | C | 7 | a0001c0001t0002g0034 a0001c0001t0002g0125 a0002c0002t0015g0146 others(4): Show |
7 | HG02055.hp2 HG02559.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1307-355G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767355 | |||||||
chr2:241767356 | T | G | 17 | a0001c0001t0008g0166 a0001c0001t0042g0183 a0002c0002t0008g0078 others(14): Show |
17 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(14): Show |
intron_variant | MODIFIER | c.1307-354T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767356 | |||||||
chr2:241767371 | C | CCCCGGGC others(42): Show |
1 | a0003c0003t0010g0316 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1307-335_1307-287d others(51): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241767371 | ||||||
chr2:241767375 | G | A | 1 | a0001c0001t0002g0115 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1307-335G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767375 | |||||||
chr2:241767405 | G | C | 119 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(116): Show |
125 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.1307-305G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767405 | |||||||
chr2:241767406 | T | G | 2 | a0001c0001t0001g0127 a0021c0033t0008g0321 |
2 | NA18949.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1307-304T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767406 | |||||||
chr2:241767427 | G | C | 2 | a0001c0001t0001g0376 a0001c0001t0001g0377 |
2 | NA18992.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1307-283G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767427 | |||||||
chr2:241767443 | GA | G | 8 | a0001c0001t0020g0085 a0001c0001t0020g0086 a0001c0001t0022g0073 others(5): Show |
9 | HG01099.hp2 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1307-266delA | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767443 | |||||||
chr2:241767455 | G | C | 153 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(150): Show |
162 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.1307-255G>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767455 | |||||||
chr2:241767455 | G | GTTGGGGA others(43): Show |
1 | a0003c0003t0024g0317 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1307-245_1307-196d others(52): Show |
D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr2 | 241767455 | ||||||
chr2:241767496 | G | A | 3 | a0001c0029t0002g0156 a0004c0005t0007g0074 a0004c0023t0002g0172 |
3 | HG02572.hp1 HG02647.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1307-214G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767496 | |||||||
chr2:241767505 | C | G | 141 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(138): Show |
149 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.1307-205C>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767505 | |||||||
chr2:241767506 | T | G | 5 | a0002c0002t0003g0082 a0002c0002t0015g0134 a0002c0002t0015g0146 others(2): Show |
5 | HG01496.hp1 HG02055.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1307-204T>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767506 | |||||||
chr2:241767516 | A | T | 1 | a0001c0001t0006g0269 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1307-194A>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767516 | |||||||
chr2:241767541 | C | T | 49 | a0001c0001t0005g0007 a0001c0001t0012g0293 a0001c0001t0031g0162 others(46): Show |
53 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1307-169C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767541 | |||||||
chr2:241767547 | C | T | 77 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(74): Show |
81 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1307-163C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767547 | |||||||
chr2:241767573 | C | T | 77 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(74): Show |
81 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1307-137C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767573 | |||||||
chr2:241767609 | G | A | 1 | a0005c0004t0045g0355 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1307-101G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767609 | |||||||
chr2:241767636 | G | A | 1 | a0001c0001t0017g0010 | 2 | NA18943.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.1307-74G>A | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767636 | |||||||
chr2:241767686 | A | G | 242 | a0001c0001t0002g0011 a0001c0001t0002g0012 a0001c0001t0002g0031 others(239): Show |
258 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.1307-24A>G | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767686 | |||||||
chr2:241767691 | T | C | 2 | a0001c0029t0002g0156 a0004c0023t0002g0172 |
2 | HG02572.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1307-19T>C | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767691 | |||||||
chr2:241767695 | C | T | 1 | a0004c0022t0048g0210 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1307-15C>T | D2HGDH | ENSG00000180902.18 | transcript | ENST00000321264.9 | protein_coding | 9/9 | chr2 | 241767695 |