Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79944 |
| ensemblid | ENSG00000087299.12 |
| hgncid | 20499 |
| symbol | L2HGDH |
| name | L-2-hydroxyglutarate dehydrogenase |
| refseq_nuc | NM_024884.3 |
| refseq_prot | NP_079160.1 |
| ensembl_nuc | ENST00000267436.9 |
| ensembl_prot | ENSP00000267436.4 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 50242434 |
| end | 50312229 |
| strand | - |
| ver | v1.2 |
| region | chr14:50242434-50312229 |
| region5000 | chr14:50237434-50317229 |
| regionname0 | L2HGDH_chr14_50242434_50312229 |
| regionname5000 | L2HGDH_chr14_50237434_50317229 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 463 | 209 | 56 | 40 | 87 | 5 | 20 | 61 | L2HGDH_chr14_50237434_50317229 | L2HGDH | MVPAL others(458): Show |
chr14 | 50237434 | 50317229 |
| a0002 | 1/0 | 463 | 145 | 32 | 30 | 53 | 7 | 22 | 39 | L2HGDH_chr14_50237434_50317229 | L2HGDH | MVPAL others(458): Show |
chr14 | 50237434 | 50317229 |
| a0003 | 0/0 | 463 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | MVPAL others(458): Show |
chr14 | 50237434 | 50317229 |
| a0004 | 0/0 | 463 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | MVPAL others(458): Show |
chr14 | 50237434 | 50317229 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1389 | 202 | 55 | 36 | 86 | 5 | 19 | L2HGDH_chr14_50237434_50317229 | L2HGDH | ATGGT others(1384): Show |
chr14 | 50237434 | 50317229 | ||
| a0001c0004 | 0/0 | 1389 | 5 | 1 | 4 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | ATGGT others(1384): Show |
chr14 | 50237434 | 50317229 | ||
| a0001c0007 | 0/0 | 1389 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | ATGGT others(1384): Show |
chr14 | 50237434 | 50317229 | ||
| a0001c0008 | 0/0 | 1389 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | ATGGT others(1384): Show |
chr14 | 50237434 | 50317229 | ||
| a0002c0002 | 1/0 | 1389 | 128 | 25 | 27 | 48 | 7 | 20 | L2HGDH_chr14_50237434_50317229 | L2HGDH | ATGGT others(1384): Show |
chr14 | 50237434 | 50317229 | ||
| a0002c0003 | 0/0 | 1389 | 16 | 6 | 3 | 5 | 0 | 2 | L2HGDH_chr14_50237434_50317229 | L2HGDH | ATGGT others(1384): Show |
chr14 | 50237434 | 50317229 | ||
| a0002c0009 | 0/0 | 1389 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | ATGGT others(1384): Show |
chr14 | 50237434 | 50317229 | ||
| a0003c0005 | 0/0 | 1389 | 4 | 4 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | ATGGT others(1384): Show |
chr14 | 50237434 | 50317229 | ||
| a0004c0006 | 0/0 | 1389 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | ATGGT others(1384): Show |
chr14 | 50237434 | 50317229 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6090 | 64 | 8 | 14 | 35 | 1 | 6 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6085): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0002 | 0/0 | 6088 | 2 | 0 | 0 | 1 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6083): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0003 | 0/0 | 6101 | 33 | 4 | 7 | 13 | 2 | 7 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6096): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0004 | 0/0 | 6095 | 4 | 4 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6090): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0005 | 0/0 | 6088 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6083): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0006 | 0/0 | 6094 | 7 | 7 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6089): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0007 | 0/0 | 6102 | 9 | 1 | 1 | 6 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6097): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0008 | 0/0 | 6103 | 6 | 0 | 0 | 5 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6098): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0009 | 0/0 | 6091 | 5 | 1 | 2 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6086): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0012 | 0/0 | 6090 | 5 | 0 | 0 | 4 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6085): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0013 | 0/0 | 6090 | 5 | 5 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6085): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0014 | 0/0 | 6095 | 3 | 3 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6090): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0017 | 0/0 | 6095 | 3 | 0 | 3 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6090): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0018 | 0/0 | 6089 | 3 | 3 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6084): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0019 | 0/0 | 6099 | 3 | 0 | 3 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6094): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0020 | 0/0 | 6101 | 3 | 3 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6096): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0021 | 0/0 | 6093 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6088): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0025 | 0/0 | 6090 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6085): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0027 | 0/0 | 6103 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6098): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0029 | 0/0 | 6091 | 2 | 0 | 0 | 1 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6086): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0030 | 0/0 | 6093 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6088): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0031 | 0/0 | 6091 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6086): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0032 | 0/0 | 6092 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6087): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0033 | 0/0 | 6102 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6097): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0034 | 0/0 | 6105 | 2 | 0 | 0 | 1 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6100): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0035 | 0/0 | 6105 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6100): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0038 | 0/0 | 6090 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6085): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0042 | 0/0 | 6100 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6095): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0043 | 0/0 | 6104 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6099): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0044 | 0/0 | 6102 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6097): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0045 | 0/0 | 6106 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6101): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0047 | 0/0 | 6101 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6096): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0048 | 0/0 | 6091 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6086): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0049 | 0/0 | 6091 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6086): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0051 | 0/0 | 6101 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6096): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0052 | 0/0 | 6101 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6096): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0054 | 0/0 | 6103 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6098): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0055 | 0/0 | 6101 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6096): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0056 | 0/0 | 6090 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6085): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0057 | 0/0 | 6092 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6087): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0058 | 0/0 | 6090 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6085): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0059 | 0/0 | 6090 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6085): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0060 | 0/0 | 6090 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6085): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0061 | 0/0 | 6092 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6087): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0063 | 0/0 | 6090 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6085): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0064 | 0/0 | 6090 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6085): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0069 | 0/0 | 6088 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6083): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0070 | 0/0 | 6092 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6087): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0071 | 0/0 | 6092 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6087): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0072 | 0/0 | 6089 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6084): Show |
chr14 | 50237434 | 50317229 |
| a0001c0001t0073 | 0/1 | 6101 | 1 | 0 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6096): Show |
chr14 | 50237434 | 50317229 |
| a0001c0004t0002 | 0/0 | 6088 | 4 | 0 | 4 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6083): Show |
chr14 | 50237434 | 50317229 |
| a0001c0004t0005 | 0/0 | 6088 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6083): Show |
chr14 | 50237434 | 50317229 |
| a0001c0007t0001 | 0/0 | 6090 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6085): Show |
chr14 | 50237434 | 50317229 |
| a0001c0008t0008 | 0/0 | 6103 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6098): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0001 | 0/0 | 6090 | 5 | 0 | 1 | 3 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6085): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0002 | 0/0 | 6088 | 47 | 2 | 12 | 25 | 1 | 7 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6083): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0004 | 1/0 | 6095 | 21 | 0 | 3 | 6 | 2 | 9 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6090): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0005 | 0/0 | 6088 | 14 | 7 | 5 | 0 | 2 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6083): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0010 | 0/0 | 6089 | 6 | 0 | 2 | 4 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6084): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0011 | 0/0 | 6087 | 6 | 6 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6082): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0015 | 0/0 | 6093 | 3 | 0 | 0 | 0 | 1 | 2 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6088): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0016 | 0/0 | 6097 | 3 | 0 | 0 | 3 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6092): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0022 | 0/0 | 6088 | 3 | 0 | 0 | 3 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6083): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0023 | 0/0 | 6087 | 3 | 3 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6082): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0024 | 0/0 | 6087 | 3 | 0 | 3 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6082): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0026 | 0/0 | 6096 | 2 | 0 | 0 | 0 | 0 | 2 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6091): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0036 | 0/0 | 6089 | 2 | 1 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6084): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0037 | 0/0 | 6089 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6084): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0039 | 0/0 | 6088 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6083): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0040 | 0/0 | 6094 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6089): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0041 | 0/0 | 6089 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6084): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0046 | 0/0 | 6090 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6085): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0067 | 0/0 | 6088 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6083): Show |
chr14 | 50237434 | 50317229 |
| a0002c0002t0068 | 0/0 | 6088 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6083): Show |
chr14 | 50237434 | 50317229 |
| a0002c0003t0001 | 0/0 | 6090 | 6 | 1 | 0 | 3 | 0 | 2 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6085): Show |
chr14 | 50237434 | 50317229 |
| a0002c0003t0002 | 0/0 | 6088 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6083): Show |
chr14 | 50237434 | 50317229 |
| a0002c0003t0003 | 0/0 | 6101 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6096): Show |
chr14 | 50237434 | 50317229 |
| a0002c0003t0009 | 0/0 | 6091 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6086): Show |
chr14 | 50237434 | 50317229 |
| a0002c0003t0021 | 0/0 | 6093 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6088): Show |
chr14 | 50237434 | 50317229 |
| a0002c0003t0028 | 0/0 | 6094 | 2 | 1 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6089): Show |
chr14 | 50237434 | 50317229 |
| a0002c0003t0050 | 0/0 | 6093 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6088): Show |
chr14 | 50237434 | 50317229 |
| a0002c0003t0053 | 0/0 | 6093 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6088): Show |
chr14 | 50237434 | 50317229 |
| a0002c0003t0062 | 0/0 | 6090 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6085): Show |
chr14 | 50237434 | 50317229 |
| a0002c0003t0065 | 0/0 | 6092 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6087): Show |
chr14 | 50237434 | 50317229 |
| a0002c0009t0066 | 0/0 | 6090 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6085): Show |
chr14 | 50237434 | 50317229 |
| a0003c0005t0006 | 0/0 | 6094 | 3 | 3 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6089): Show |
chr14 | 50237434 | 50317229 |
| a0003c0005t0014 | 0/0 | 6095 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6090): Show |
chr14 | 50237434 | 50317229 |
| a0004c0006t0001 | 0/0 | 6090 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | GCTAA others(6085): Show |
chr14 | 50237434 | 50317229 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0006g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0006g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0006g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0006g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0006g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0006g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0007g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0007g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0007g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0007g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0007g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0007g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0008g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0008g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0008g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0008g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0008g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0008g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0009g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0009g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0009g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0009g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0012g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0012g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0012g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0012g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0012g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0013g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0013g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0013g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0013g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0013g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0014g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0014g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0014g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0017g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0017g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0017g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0018g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0018g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0018g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0019g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0019g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0019g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0020g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0020g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0020g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0021g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0021g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0025g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0025g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0027g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0027g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0029g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0029g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0030g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0030g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0031g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0031g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0032g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0032g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0033g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0034g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0034g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0035g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0035g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0038g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0038g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0042g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0043g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0044g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0045g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0047g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0048g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0049g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0051g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0052g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0054g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0055g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0056g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0057g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0058g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0059g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0060g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0061g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0063g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0064g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0069g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0070g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0071g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0072g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0073g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0004t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0004t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0004t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0004t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0004t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0007t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0008t0008g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0270 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0277 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0010g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0010g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0010g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0010g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0010g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0010g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0011g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0011g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0011g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0011g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0011g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0011g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0015g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0015g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0015g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0016g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0016g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0016g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0022g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0022g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0023g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0023g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0023g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0024g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0024g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0024g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0026g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0026g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0036g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0036g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0037g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0037g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0039g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0039g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0040g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0040g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0041g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0046g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0067g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0068g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0003g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0009g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0021g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0028g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0028g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0050g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0053g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0062g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0065g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0009t0066g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0003c0005t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0003c0005t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0003c0005t0006g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0003c0005t0014g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0004c0006t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0004c0006t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0005 | g0237 | EUR | GBR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00140 | hp1 | a0001 | c0001 | t0034 | g0066 | EUR | GBR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00140 | hp2 | a0002 | c0002 | t0015 | g0276 | EUR | GBR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0305 | EUR | FIN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0047 | EUR | FIN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0326 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0308 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00544 | hp2 | a0001 | c0001 | t0055 | g0069 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00597 | hp1 | a0002 | c0002 | t0004 | g0285 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00609 | hp1 | a0001 | c0001 | t0058 | g0051 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00609 | hp2 | a0002 | c0002 | t0004 | g0217 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0318 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00639 | hp1 | a0001 | c0001 | t0052 | g0045 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00673 | hp1 | a0001 | c0001 | t0008 | g0105 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0295 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00733 | hp1 | a0001 | c0001 | t0017 | g0204 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00733 | hp2 | a0002 | c0002 | t0010 | g0309 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00735 | hp1 | a0001 | c0001 | t0069 | g0056 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00735 | hp2 | a0002 | c0002 | t0004 | g0266 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00738 | hp2 | a0001 | c0001 | t0019 | g0057 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0261 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00741 | hp2 | a0001 | c0001 | t0009 | g0136 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01069 | hp1 | a0002 | c0002 | t0024 | g0292 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01069 | hp2 | a0002 | c0003 | t0003 | g0352 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01070 | hp1 | a0001 | c0004 | t0002 | g0041 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01070 | hp2 | a0002 | c0002 | t0005 | g0244 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01071 | hp1 | a0002 | c0002 | t0024 | g0291 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01071 | hp2 | a0001 | c0004 | t0002 | g0042 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01074 | hp1 | a0002 | c0002 | t0005 | g0238 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0302 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01099 | hp2 | a0002 | c0002 | t0005 | g0241 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0354 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0089 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01109 | hp1 | a0001 | c0001 | t0044 | g0014 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01109 | hp2 | a0002 | c0002 | t0004 | g0271 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0339 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01167 | hp2 | a0002 | c0002 | t0005 | g0223 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01169 | hp1 | a0002 | c0002 | t0005 | g0224 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0307 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0324 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01192 | hp1 | a0002 | c0002 | t0024 | g0290 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01192 | hp2 | a0001 | c0001 | t0019 | g0083 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01255 | hp2 | a0001 | c0001 | t0019 | g0099 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01256 | hp1 | a0001 | c0001 | t0072 | g0142 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01256 | hp2 | a0001 | c0001 | t0017 | g0206 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0293 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01258 | hp1 | a0001 | c0001 | t0017 | g0205 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0294 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01261 | hp1 | a0001 | c0001 | t0071 | g0188 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0077 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0310 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0073 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01358 | hp1 | a0002 | c0002 | t0036 | g0245 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01358 | hp2 | a0002 | c0003 | t0028 | g0349 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0175 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01517 | hp1 | a0002 | c0002 | t0005 | g0233 | EUR | IBS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01517 | hp2 | a0002 | c0002 | t0004 | g0278 | EUR | IBS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01884 | hp1 | a0002 | c0002 | t0011 | g0229 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01884 | hp2 | a0001 | c0001 | t0038 | g0199 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01891 | hp1 | a0001 | c0001 | t0014 | g0108 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0353 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0316 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01934 | hp1 | a0002 | c0003 | t0002 | g0253 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0084 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01981 | hp2 | a0002 | c0002 | t0004 | g0265 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0330 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0299 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02027 | hp1 | a0001 | c0001 | t0007 | g0081 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02027 | hp2 | a0002 | c0002 | t0010 | g0323 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0017 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02055 | hp2 | a0002 | c0002 | t0041 | g0007 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02056 | hp1 | a0001 | c0001 | t0008 | g0067 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02071 | hp1 | a0002 | c0002 | t0004 | g0263 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02074 | hp1 | a0002 | c0003 | t0001 | g0255 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02074 | hp2 | a0001 | c0001 | t0027 | g0076 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0301 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02129 | hp1 | a0002 | c0002 | t0004 | g0246 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02132 | hp1 | a0001 | c0001 | t0008 | g0070 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02132 | hp2 | a0001 | c0001 | t0060 | g0174 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02145 | hp1 | a0002 | c0002 | t0046 | g0321 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02145 | hp2 | a0001 | c0001 | t0043 | g0049 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | CDX | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02155 | hp2 | a0001 | c0001 | t0009 | g0173 | EAS | CDX | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02165 | hp1 | a0002 | c0002 | t0022 | g0005 | EAS | CDX | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02257 | hp1 | a0004 | c0006 | t0001 | g0171 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02257 | hp2 | a0002 | c0002 | t0023 | g0225 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02258 | hp2 | a0001 | c0001 | t0038 | g0198 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02273 | hp2 | a0001 | c0004 | t0002 | g0039 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02280 | hp1 | a0002 | c0003 | t0053 | g0347 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02280 | hp2 | a0002 | c0002 | t0011 | g0228 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02293 | hp1 | a0001 | c0001 | t0009 | g0193 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0247 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02300 | hp1 | a0002 | c0002 | t0010 | g0332 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02451 | hp1 | a0001 | c0001 | t0020 | g0037 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02451 | hp2 | a0001 | c0001 | t0006 | g0092 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0054 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02572 | hp1 | a0001 | c0004 | t0005 | g0200 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02572 | hp2 | a0001 | c0001 | t0049 | g0091 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02602 | hp2 | a0002 | c0002 | t0004 | g0280 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0016 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02622 | hp1 | a0001 | c0001 | t0054 | g0018 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02622 | hp2 | a0002 | c0002 | t0005 | g0235 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02630 | hp2 | a0001 | c0001 | t0020 | g0031 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0202 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02647 | hp2 | a0002 | c0003 | t0028 | g0350 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02683 | hp1 | a0002 | c0002 | t0004 | g0282 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02683 | hp2 | a0001 | c0001 | t0007 | g0065 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02698 | hp1 | a0002 | c0002 | t0004 | g0268 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0059 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02717 | hp1 | a0002 | c0002 | t0023 | g0240 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0093 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02723 | hp2 | a0002 | c0002 | t0005 | g0227 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02735 | hp1 | a0002 | c0002 | t0004 | g0283 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0090 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02809 | hp2 | a0003 | c0005 | t0006 | g0213 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02818 | hp1 | a0002 | c0002 | t0011 | g0243 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02818 | hp2 | a0002 | c0002 | t0039 | g0348 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02886 | hp1 | a0001 | c0001 | t0006 | g0034 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02886 | hp2 | a0001 | c0001 | t0057 | g0029 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02895 | hp1 | a0002 | c0002 | t0011 | g0234 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02922 | hp1 | a0001 | c0001 | t0070 | g0189 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02922 | hp2 | a0004 | c0006 | t0001 | g0144 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02965 | hp1 | a0001 | c0001 | t0013 | g0035 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02965 | hp2 | a0001 | c0001 | t0064 | g0196 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02970 | hp1 | a0002 | c0002 | t0039 | g0286 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0097 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02976 | hp1 | a0001 | c0001 | t0006 | g0096 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02976 | hp2 | a0001 | c0001 | t0020 | g0048 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03017 | hp1 | a0001 | c0008 | t0008 | g0072 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03017 | hp2 | a0002 | c0002 | t0004 | g0272 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0075 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0106 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03098 | hp1 | a0002 | c0002 | t0005 | g0222 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03098 | hp2 | a0002 | c0003 | t0065 | g0215 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03130 | hp1 | a0002 | c0002 | t0067 | g0219 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0203 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03139 | hp1 | a0001 | c0001 | t0030 | g0209 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0208 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03195 | hp2 | a0001 | c0001 | t0018 | g0012 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03209 | hp1 | a0002 | c0002 | t0011 | g0242 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03209 | hp2 | a0001 | c0001 | t0031 | g0187 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03225 | hp1 | a0002 | c0002 | t0005 | g0231 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03225 | hp2 | a0002 | c0003 | t0021 | g0351 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0322 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03453 | hp1 | a0003 | c0005 | t0006 | g0212 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03453 | hp2 | a0001 | c0001 | t0013 | g0036 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03486 | hp1 | a0003 | c0005 | t0014 | g0211 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03486 | hp2 | a0001 | c0001 | t0014 | g0107 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0311 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0061 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03491 | hp1 | a0002 | c0002 | t0015 | g0273 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0060 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0319 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0062 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03516 | hp1 | a0001 | c0001 | t0013 | g0032 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03516 | hp2 | a0003 | c0005 | t0006 | g0214 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0095 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03540 | hp2 | a0002 | c0002 | t0068 | g0230 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03579 | hp1 | a0001 | c0001 | t0013 | g0033 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0306 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03669 | hp1 | a0002 | c0003 | t0001 | g0254 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03669 | hp2 | a0002 | c0002 | t0004 | g0281 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0027 | SAS | STU | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03688 | hp2 | a0002 | c0002 | t0004 | g0269 | SAS | STU | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03704 | hp1 | a0002 | c0002 | t0004 | g0279 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03831 | hp1 | a0002 | c0002 | t0026 | g0274 | SAS | BEB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03831 | hp2 | a0001 | c0001 | t0047 | g0100 | SAS | BEB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0298 | SAS | BEB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0002 | SAS | BEB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0317 | SAS | BEB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03942 | hp2 | a0002 | c0002 | t0004 | g0284 | SAS | BEB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG04115 | hp1 | a0001 | c0001 | t0029 | g0182 | SAS | STU | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG04115 | hp2 | a0001 | c0001 | t0008 | g0023 | SAS | STU | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG04184 | hp2 | a0002 | c0002 | t0026 | g0267 | SAS | BEB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0063 | SAS | STU | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | STU | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0315 | SAS | STU | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG04228 | hp2 | a0001 | c0001 | t0042 | g0181 | SAS | STU | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18522 | hp1 | a0002 | c0002 | t0005 | g0232 | AFR | YRI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18522 | hp2 | a0002 | c0002 | t0005 | g0221 | AFR | YRI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18747 | hp1 | a0002 | c0003 | t0001 | g0259 | EAS | CHB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18747 | hp2 | a0002 | c0002 | t0022 | g0005 | EAS | CHB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18906 | hp1 | a0001 | c0001 | t0021 | g0184 | AFR | YRI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18906 | hp2 | a0002 | c0002 | t0011 | g0239 | AFR | YRI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18939 | hp2 | a0002 | c0002 | t0010 | g0325 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18940 | hp2 | a0002 | c0002 | t0010 | g0340 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18942 | hp2 | a0002 | c0002 | t0040 | g0303 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18946 | hp2 | a0002 | c0002 | t0004 | g0218 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18947 | hp1 | a0002 | c0003 | t0001 | g0257 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18947 | hp2 | a0002 | c0002 | t0037 | g0327 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18949 | hp1 | a0002 | c0002 | t0010 | g0345 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18949 | hp2 | a0002 | c0003 | t0062 | g0260 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18951 | hp1 | a0001 | c0001 | t0035 | g0064 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18952 | hp1 | a0001 | c0001 | t0008 | g0079 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0336 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0314 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18953 | hp2 | a0001 | c0001 | t0007 | g0078 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18957 | hp1 | a0001 | c0001 | t0032 | g0158 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18957 | hp2 | a0002 | c0002 | t0022 | g0333 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18964 | hp2 | a0001 | c0001 | t0012 | g0120 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18971 | hp1 | a0002 | c0002 | t0016 | g0264 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0313 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18973 | hp1 | a0001 | c0001 | t0012 | g0161 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0300 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18977 | hp2 | a0001 | c0001 | t0008 | g0098 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0329 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18979 | hp2 | a0001 | c0001 | t0059 | g0164 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18982 | hp2 | a0001 | c0001 | t0051 | g0103 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18983 | hp2 | a0001 | c0001 | t0033 | g0001 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0296 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0304 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0249 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18994 | hp1 | a0002 | c0002 | t0037 | g0334 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0342 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18995 | hp2 | a0001 | c0001 | t0007 | g0010 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0289 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19000 | hp2 | a0001 | c0001 | t0045 | g0087 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0331 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19002 | hp2 | a0001 | c0007 | t0001 | g0130 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0320 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19009 | hp1 | a0002 | c0002 | t0040 | g0312 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19009 | hp2 | a0002 | c0003 | t0009 | g0258 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0335 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19011 | hp2 | a0001 | c0001 | t0007 | g0135 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19012 | hp2 | a0001 | c0001 | t0027 | g0038 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19030 | hp1 | a0002 | c0002 | t0036 | g0226 | AFR | LWK | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | LWK | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19043 | hp2 | a0002 | c0003 | t0050 | g0346 | AFR | LWK | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19054 | hp1 | a0002 | c0002 | t0016 | g0262 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19054 | hp2 | a0001 | c0001 | t0025 | g0111 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0338 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19065 | hp2 | a0001 | c0001 | t0012 | g0121 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19066 | hp1 | a0001 | c0001 | t0007 | g0102 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19066 | hp2 | a0001 | c0001 | t0012 | g0119 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0248 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19068 | hp2 | a0002 | c0002 | t0016 | g0343 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19070 | hp1 | a0001 | c0001 | t0063 | g0157 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19070 | hp2 | a0001 | c0001 | t0007 | g0053 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19074 | hp2 | a0001 | c0001 | t0009 | g0149 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19081 | hp2 | a0002 | c0002 | t0004 | g0216 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19082 | hp1 | a0001 | c0001 | t0048 | g0133 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19084 | hp2 | a0001 | c0001 | t0034 | g0116 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0337 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19085 | hp2 | a0001 | c0001 | t0035 | g0085 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0328 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19087 | hp2 | a0001 | c0001 | t0032 | g0028 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19088 | hp1 | a0001 | c0001 | t0033 | g0001 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19088 | hp2 | a0001 | c0001 | t0029 | g0162 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19090 | hp1 | a0001 | c0001 | t0025 | g0159 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19240 | hp1 | a0001 | c0001 | t0018 | g0011 | AFR | YRI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19240 | hp2 | a0002 | c0009 | t0066 | g0256 | AFR | YRI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0341 | AFR | ASW | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20129 | hp2 | a0002 | c0002 | t0005 | g0220 | AFR | ASW | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20752 | hp1 | a0002 | c0002 | t0004 | g0270 | EUR | TSI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | TSI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20805 | hp1 | a0001 | c0001 | t0012 | g0129 | EUR | TSI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0344 | EUR | TSI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20905 | hp1 | a0002 | c0002 | t0015 | g0275 | SAS | GIH | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20905 | hp2 | a0002 | c0003 | t0001 | g0252 | SAS | GIH | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01123 | hp1 | a0001 | c0004 | t0002 | g0040 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01123 | hp2 | a0001 | c0001 | t0056 | g0190 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02109 | hp1 | a0001 | c0001 | t0031 | g0186 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0046 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02559 | hp1 | a0001 | c0001 | t0018 | g0013 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02559 | hp2 | a0002 | c0002 | t0023 | g0236 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03471 | hp1 | a0001 | c0001 | t0009 | g0154 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03471 | hp2 | a0001 | c0001 | t0061 | g0015 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0207 | AFR | USA | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG06807 | hp2 | a0001 | c0001 | t0030 | g0210 | AFR | USA | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0297 | AFR | USA | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20300 | hp2 | a0001 | c0001 | t0021 | g0183 | AFR | USA | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0094 | AFR | LWK | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | LWK | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0073 | g0050 | REF | REF | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0004 | g0277 | REF | REF | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50265454 | T | C | 1 | a0004 | 2 | HG02257.hp1 HG02922.hp2 |
missense_variant | MODERATE | c.1100A>G | p.Tyr367Cys | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/10 | 1179/6095 | 1100/1392 | 367/463 | chr14 | 50265454 | |||
| chr14:50312052 | C | A | 1 | a0003 | 4 | HG02809.hp2 HG03453.hp1 HG03486.hp1 others(1): Show |
missense_variant | MODERATE | c.99G>T | p.Arg33Ser | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/10 | 178/6095 | 99/1392 | 33/463 | chr14 | 50312052 | |||
| chr14:50312098 | A | C | 3 | a0001 a0003 a0004 |
214 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(211): Show |
missense_variant | MODERATE | c.53T>G | p.Leu18Arg | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/10 | 132/6095 | 53/1392 | 18/463 | chr14 | 50312098 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50269229 | T | C | 1 | a0001c0008 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.840A>G | p.Pro280Pro | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 7/10 | 919/6095 | 840/1392 | 280/463 | chr14 | 50269229 | |||
| chr14:50302089 | T | C | 1 | a0002c0009 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.336A>G | p.Leu112Leu | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/10 | 415/6095 | 336/1392 | 112/463 | chr14 | 50302089 | |||
| chr14:50302951 | C | G | 1 | a0001c0007 | 1 | NA19002.hp2 | synonymous_variant | LOW | c.207G>C | p.Leu69Leu | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 2/10 | 286/6095 | 207/1392 | 69/463 | chr14 | 50302951 | |||
| chr14:50302999 | G | A | 7 | a0001c0001 a0001c0007 a0001c0008 others(4): Show |
226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
synonymous_variant | LOW | c.159C>T | p.Ile53Ile | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 2/10 | 238/6095 | 159/1392 | 53/463 | chr14 | 50302999 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50242449 | T | G | 1 | a0001c0001t0060 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4609A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 4609 | chr14 | 50242449 | ||||||
| chr14:50242504 | A | G | 1 | a0001c0001t0069 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4554T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 4554 | chr14 | 50242504 | ||||||
| chr14:50242600 | T | C | 1 | a0001c0001t0030 | 2 | HG03139.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4458A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 4458 | chr14 | 50242600 | ||||||
| chr14:50242672 | A | G | 1 | a0002c0003t0065 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4386T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 4386 | chr14 | 50242672 | ||||||
| chr14:50242738 | G | GT | 3 | a0001c0001t0027 a0001c0001t0032 a0001c0001t0033 |
6 | HG02074.hp2 NA18957.hp1 NA18983.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4319dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 4319 | chr14 | 50242738 | ||||||
| chr14:50242848 | T | C | 1 | a0002c0002t0068 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4210A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 4210 | chr14 | 50242848 | ||||||
| chr14:50242858 | T | A | 1 | a0001c0001t0071 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4200A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 4200 | chr14 | 50242858 | ||||||
| chr14:50243002 | G | A | 1 | a0002c0002t0023 | 3 | HG02257.hp2 HG02559.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4056C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 4056 | chr14 | 50243002 | ||||||
| chr14:50243105 | G | A | 2 | a0002c0002t0022 a0002c0002t0037 |
5 | HG02165.hp1 NA18747.hp2 NA18947.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3953C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3953 | chr14 | 50243105 | ||||||
| chr14:50243292 | G | T | 1 | a0001c0001t0059 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3766C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3766 | chr14 | 50243292 | ||||||
| chr14:50243293 | C | T | 1 | a0001c0001t0048 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3765G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3765 | chr14 | 50243293 | ||||||
| chr14:50243435 | T | C | 3 | a0001c0001t0020 a0001c0001t0043 a0001c0001t0054 |
5 | HG02145.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3623A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3623 | chr14 | 50243435 | ||||||
| chr14:50243459 | A | C | 1 | a0001c0001t0058 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3599T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3599 | chr14 | 50243459 | ||||||
| chr14:50243663 | T | TTA | 1 | a0002c0002t0016 | 3 | NA18971.hp1 NA19054.hp1 NA19068.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3393_*3394dupTA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3394 | chr14 | 50243663 | ||||||
| chr14:50243663 | T | TTATA | 2 | a0001c0001t0019 a0001c0001t0042 |
4 | HG00738.hp2 HG01192.hp2 HG01255.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3391_*3394dupTATA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3394 | chr14 | 50243663 | ||||||
| chr14:50243663 | T | TTATATA | 11 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0020 others(8): Show |
55 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*3389_*3394dupTATA others(2): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3394 | chr14 | 50243663 | ||||||
| chr14:50243663 | T | TTATATAT others(1): Show |
4 | a0001c0001t0008 a0001c0001t0043 a0001c0001t0054 others(1): Show |
9 | HG00673.hp1 HG02056.hp1 HG02132.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3387_*3394dupTATA others(4): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3394 | chr14 | 50243663 | ||||||
| chr14:50243663 | T | TTATATAT others(3): Show |
3 | a0001c0001t0034 a0001c0001t0035 a0001c0001t0045 |
5 | HG00140.hp1 NA18951.hp1 NA19000.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3385_*3394dupTATA others(6): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3394 | chr14 | 50243663 | ||||||
| chr14:50243663 | TTA | T | 12 | a0001c0001t0021 a0001c0001t0030 a0001c0001t0057 others(9): Show |
17 | HG00140.hp2 HG01261.hp1 HG01358.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*3393_*3394delTA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3393 | chr14 | 50243663 | ||||||
| chr14:50243663 | TTATA | T | 25 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0012 others(22): Show |
115 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(112): Show |
3_prime_UTR_variant | MODIFIER | c.*3391_*3394delTATA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3391 | chr14 | 50243663 | ||||||
| chr14:50243663 | TTATATA | T | 21 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0018 others(18): Show |
105 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*3389_*3394delTATA others(2): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3389 | chr14 | 50243663 | ||||||
| chr14:50243665 | A | T | 6 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0014 others(3): Show |
20 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*3393T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3393 | chr14 | 50243665 | ||||||
| chr14:50243667 | A | T | 8 | a0001c0001t0021 a0001c0001t0057 a0001c0001t0061 others(5): Show |
10 | HG01261.hp1 HG01358.hp2 HG02647.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3391T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3391 | chr14 | 50243667 | ||||||
| chr14:50243669 | A | T | 2 | a0001c0001t0031 a0001c0001t0038 |
4 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3389T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3389 | chr14 | 50243669 | ||||||
| chr14:50243671 | A | T | 12 | a0001c0001t0005 a0001c0001t0018 a0001c0004t0005 others(9): Show |
38 | HG00099.hp1 HG01069.hp1 HG01070.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*3387T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3387 | chr14 | 50243671 | ||||||
| chr14:50243694 | T | C | 1 | a0001c0001t0044 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3364A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3364 | chr14 | 50243694 | ||||||
| chr14:50243736 | G | A | 2 | a0001c0001t0035 a0001c0001t0045 |
3 | NA18951.hp1 NA19000.hp2 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3322C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3322 | chr14 | 50243736 | ||||||
| chr14:50243762 | G | A | 1 | a0001c0001t0013 | 5 | HG02615.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3296C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3296 | chr14 | 50243762 | ||||||
| chr14:50243764 | G | C | 1 | a0001c0001t0013 | 5 | HG02615.hp2 HG02965.hp1 HG03453.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3294C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3294 | chr14 | 50243764 | ||||||
| chr14:50243780 | C | A | 1 | a0001c0001t0061 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3278G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3278 | chr14 | 50243780 | ||||||
| chr14:50243833 | T | C | 1 | a0002c0003t0062 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3225A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3225 | chr14 | 50243833 | ||||||
| chr14:50243839 | C | G | 9 | a0001c0001t0005 a0001c0004t0005 a0002c0002t0005 others(6): Show |
30 | HG00099.hp1 HG01070.hp2 HG01074.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*3219G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3219 | chr14 | 50243839 | ||||||
| chr14:50243906 | C | A | 22 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0008 others(19): Show |
75 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*3152G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 3152 | chr14 | 50243906 | ||||||
| chr14:50244144 | C | T | 1 | a0001c0001t0052 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2914G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 2914 | chr14 | 50244144 | ||||||
| chr14:50244387 | G | A | 1 | a0001c0001t0055 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2671C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 2671 | chr14 | 50244387 | ||||||
| chr14:50244630 | T | C | 1 | a0001c0001t0063 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2428A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 2428 | chr14 | 50244630 | ||||||
| chr14:50244645 | C | T | 2 | a0001c0001t0012 a0001c0001t0029 |
7 | HG04115.hp1 NA18964.hp2 NA18973.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2413G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 2413 | chr14 | 50244645 | ||||||
| chr14:50244667 | A | G | 1 | a0001c0001t0051 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2391T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 2391 | chr14 | 50244667 | ||||||
| chr14:50244694 | T | C | 2 | a0001c0001t0049 a0001c0001t0064 |
2 | HG02572.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2364A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 2364 | chr14 | 50244694 | ||||||
| chr14:50244814 | C | T | 1 | a0002c0002t0067 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2244G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 2244 | chr14 | 50244814 | ||||||
| chr14:50244991 | C | T | 1 | a0002c0003t0050 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2067G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 2067 | chr14 | 50244991 | ||||||
| chr14:50245190 | A | G | 1 | a0001c0001t0018 | 3 | HG02559.hp1 HG03195.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1868T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 1868 | chr14 | 50245190 | ||||||
| chr14:50245347 | T | C | 3 | a0001c0001t0021 a0002c0003t0021 a0002c0003t0028 |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1711A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 1711 | chr14 | 50245347 | ||||||
| chr14:50245438 | A | G | 6 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0070 others(3): Show |
16 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1620T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 1620 | chr14 | 50245438 | ||||||
| chr14:50245559 | T | A | 1 | a0001c0001t0017 | 3 | HG00733.hp1 HG01256.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1499A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 1499 | chr14 | 50245559 | ||||||
| chr14:50245573 | C | T | 1 | a0001c0001t0056 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1485G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 1485 | chr14 | 50245573 | ||||||
| chr14:50245705 | G | C | 2 | a0001c0001t0031 a0001c0001t0038 |
4 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1353C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 1353 | chr14 | 50245705 | ||||||
| chr14:50245851 | A | G | 73 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(70): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*1207T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 1207 | chr14 | 50245851 | ||||||
| chr14:50246079 | T | C | 82 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(79): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*979A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 979 | chr14 | 50246079 | ||||||
| chr14:50246134 | T | A | 73 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(70): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
3_prime_UTR_variant | MODIFIER | c.*924A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 924 | chr14 | 50246134 | ||||||
| chr14:50246224 | G | A | 21 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0069 others(18): Show |
104 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*834C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 834 | chr14 | 50246224 | ||||||
| chr14:50246262 | A | G | 26 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0012 others(23): Show |
116 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*796T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 796 | chr14 | 50246262 | ||||||
| chr14:50246312 | G | A | 6 | a0001c0001t0006 a0001c0001t0014 a0001c0001t0070 others(3): Show |
16 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*746C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 746 | chr14 | 50246312 | ||||||
| chr14:50246392 | A | T | 1 | a0001c0001t0047 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*666T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 666 | chr14 | 50246392 | ||||||
| chr14:50246438 | A | AT | 9 | a0001c0001t0007 a0001c0001t0027 a0001c0001t0042 others(6): Show |
20 | HG01106.hp2 HG01109.hp1 HG01358.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*619dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 619 | chr14 | 50246438 | ||||||
| chr14:50246438 | AT | A | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(34): Show |
195 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(192): Show |
3_prime_UTR_variant | MODIFIER | c.*619delA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 619 | chr14 | 50246438 | ||||||
| chr14:50246438 | ATT | A | 4 | a0001c0001t0072 a0002c0002t0011 a0002c0002t0023 others(1): Show |
13 | HG01069.hp1 HG01071.hp1 HG01192.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*618_*619delAA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 618 | chr14 | 50246438 | ||||||
| chr14:50246571 | C | T | 1 | a0001c0001t0025 | 2 | NA19054.hp2 NA19090.hp1 |
3_prime_UTR_variant | MODIFIER | c.*487G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 487 | chr14 | 50246571 | ||||||
| chr14:50312197 | A | G | 1 | a0002c0002t0041 | 1 | HG02055.hp2 | 5_prime_UTR_variant | MODIFIER | c.-47T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/10 | 47 | chr14 | 50312197 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:50247411 | A | G | 16 | a0001c0001t0006g0034 a0001c0001t0006g0092 a0001c0001t0006g0093 others(13): Show |
16 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1197-158T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50247411 | |||||||
| chr14:50247463 | A | G | 6 | a0001c0001t0001g0024 a0001c0001t0001g0137 a0001c0001t0001g0145 others(3): Show |
6 | HG01978.hp2 HG01993.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.1197-210T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50247463 | |||||||
| chr14:50247476 | C | T | 105 | a0001c0001t0002g0126 a0001c0001t0002g0185 a0001c0001t0005g0090 others(102): Show |
107 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.1197-223G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50247476 | |||||||
| chr14:50247556 | C | T | 190 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(187): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.1197-303G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50247556 | |||||||
| chr14:50247614 | C | A | 105 | a0001c0001t0002g0126 a0001c0001t0002g0185 a0001c0001t0005g0090 others(102): Show |
107 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.1197-361G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50247614 | |||||||
| chr14:50247719 | T | C | 1 | a0001c0001t0003g0077 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1197-466A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50247719 | |||||||
| chr14:50247994 | T | C | 317 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(314): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1197-741A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50247994 | |||||||
| chr14:50248115 | C | T | 1 | a0002c0009t0066g0256 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1197-862G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50248115 | |||||||
| chr14:50248267 | T | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(187): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.1197-1014A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50248267 | |||||||
| chr14:50248275 | A | C | 16 | a0001c0001t0006g0034 a0001c0001t0006g0092 a0001c0001t0006g0093 others(13): Show |
16 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1197-1022T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50248275 | |||||||
| chr14:50248312 | A | C | 1 | a0001c0001t0007g0135 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1197-1059T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50248312 | |||||||
| chr14:50248501 | A | G | 117 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(114): Show |
119 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.1197-1248T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50248501 | |||||||
| chr14:50248539 | G | A | 1 | a0001c0001t0061g0015 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1197-1286C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50248539 | |||||||
| chr14:50248557 | C | A | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1197-1304G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50248557 | |||||||
| chr14:50248776 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1197-1523G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50248776 | |||||||
| chr14:50248824 | G | A | 4 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0049g0091 others(1): Show |
4 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197-1571C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50248824 | |||||||
| chr14:50248828 | C | T | 4 | a0002c0002t0005g0235 a0002c0002t0023g0225 a0002c0002t0023g0236 others(1): Show |
4 | HG02257.hp2 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197-1575G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50248828 | |||||||
| chr14:50248846 | T | C | 106 | a0001c0001t0002g0126 a0001c0001t0002g0185 a0001c0001t0005g0090 others(103): Show |
108 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1197-1593A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50248846 | |||||||
| chr14:50248924 | C | T | 100 | a0001c0001t0002g0126 a0001c0001t0002g0185 a0001c0001t0005g0090 others(97): Show |
102 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1197-1671G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50248924 | |||||||
| chr14:50249439 | G | A | 1 | a0001c0001t0007g0017 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1197-2186C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249439 | |||||||
| chr14:50249548 | C | T | 106 | a0001c0001t0002g0126 a0001c0001t0002g0185 a0001c0001t0005g0090 others(103): Show |
108 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.1197-2295G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249548 | |||||||
| chr14:50249549 | G | A | 1 | a0002c0003t0053g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1197-2296C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249549 | |||||||
| chr14:50249570 | C | T | 105 | a0001c0001t0002g0126 a0001c0001t0002g0185 a0001c0001t0005g0090 others(102): Show |
107 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.1197-2317G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249570 | |||||||
| chr14:50249776 | G | C | 1 | a0001c0001t0007g0135 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1197-2523C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249776 | |||||||
| chr14:50249814 | C | A | 1 | a0002c0002t0002g0306 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1197-2561G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249814 | |||||||
| chr14:50249827 | A | T | 1 | a0002c0002t0002g0315 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1197-2574T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249827 | |||||||
| chr14:50249832 | G | A | 1 | a0001c0001t0003g0073 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1197-2579C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249832 | |||||||
| chr14:50249860 | C | T | 116 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(113): Show |
118 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.1197-2607G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249860 | |||||||
| chr14:50249882 | C | CT | 19 | a0001c0001t0001g0118 a0001c0001t0001g0166 a0001c0001t0004g0207 others(16): Show |
19 | HG00438.hp1 HG00597.hp1 HG00609.hp2 others(16): Show |
intron_variant | MODIFIER | c.1197-2630dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249882 | |||||||
| chr14:50249882 | CT | C | 17 | a0001c0001t0001g0021 a0001c0001t0001g0114 a0001c0001t0001g0117 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1197-2630delA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249882 | |||||||
| chr14:50249882 | CTT | C | 35 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0115 others(32): Show |
36 | HG00438.hp2 HG00741.hp2 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.1197-2631_1197-263 others(6): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249882 | |||||||
| chr14:50249882 | CTTT | C | 54 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0022 others(51): Show |
55 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.1197-2632_1197-263 others(7): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249882 | |||||||
| chr14:50249882 | CTTTT | C | 7 | a0001c0001t0013g0016 a0001c0001t0013g0032 a0001c0001t0013g0033 others(4): Show |
7 | HG01256.hp1 HG02615.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1197-2633_1197-263 others(8): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249882 | |||||||
| chr14:50249882 | CTTTTTT | C | 19 | a0001c0001t0003g0027 a0001c0001t0003g0043 a0001c0001t0003g0046 others(16): Show |
19 | HG00597.hp2 HG00673.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.1197-2635_1197-263 others(10): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249882 | |||||||
| chr14:50249882 | CTTTTTTT | C | 54 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0019 others(51): Show |
56 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.1197-2636_1197-263 others(11): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249882 | |||||||
| chr14:50249882 | CTTTTTTT others(4): Show |
C | 13 | a0001c0001t0001g0113 a0001c0001t0002g0185 a0001c0001t0005g0090 others(10): Show |
13 | HG02027.hp2 HG02055.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1197-2640_1197-263 others(15): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249882 | |||||||
| chr14:50249882 | CTTTTTTT others(5): Show |
C | 89 | a0001c0001t0002g0126 a0001c0001t0018g0012 a0001c0001t0021g0183 others(86): Show |
91 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.1197-2641_1197-263 others(16): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249882 | |||||||
| chr14:50249882 | CTTTTTTT others(6): Show |
C | 6 | a0001c0001t0018g0011 a0001c0001t0018g0013 a0002c0002t0002g0338 others(3): Show |
6 | HG01069.hp1 HG01099.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1197-2642_1197-263 others(17): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249882 | |||||||
| chr14:50249882 | CTTTTTTT others(11): Show |
C | 4 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(1): Show |
4 | HG02451.hp2 HG02723.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197-2647_1197-263 others(22): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249882 | |||||||
| chr14:50249882 | CTTTTTTT others(16): Show |
C | 4 | a0001c0001t0031g0186 a0001c0001t0031g0187 a0001c0001t0038g0198 others(1): Show |
4 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197-2652_1197-263 others(27): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249882 | |||||||
| chr14:50249932 | C | T | 71 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0019 others(68): Show |
73 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1197-2679G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249932 | |||||||
| chr14:50249992 | C | T | 1 | a0002c0002t0004g0279 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1197-2739G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50249992 | |||||||
| chr14:50250045 | G | A | 1 | a0001c0001t0019g0057 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1197-2792C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50250045 | |||||||
| chr14:50250182 | A | T | 1 | a0002c0002t0004g0217 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1197-2929T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50250182 | |||||||
| chr14:50250200 | C | T | 1 | a0001c0001t0058g0051 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1197-2947G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50250200 | |||||||
| chr14:50250266 | G | A | 1 | a0001c0001t0061g0015 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1197-3013C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50250266 | |||||||
| chr14:50250324 | C | CT | 3 | a0001c0001t0018g0011 a0001c0001t0018g0012 a0001c0001t0018g0013 |
3 | HG02559.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1197-3072dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50250324 | |||||||
| chr14:50250389 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1197-3136C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50250389 | |||||||
| chr14:50250504 | T | C | 1 | a0001c0001t0006g0094 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1197-3251A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50250504 | |||||||
| chr14:50250542 | C | T | 5 | a0001c0001t0005g0090 a0002c0002t0005g0220 a0002c0002t0005g0221 others(2): Show |
5 | HG02809.hp1 HG03098.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1197-3289G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50250542 | |||||||
| chr14:50250676 | C | G | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1197-3423G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50250676 | |||||||
| chr14:50250730 | G | C | 180 | a0001c0001t0002g0126 a0001c0001t0002g0185 a0001c0001t0003g0002 others(177): Show |
184 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1197-3477C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50250730 | |||||||
| chr14:50250784 | G | A | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1197-3531C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50250784 | |||||||
| chr14:50250849 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1197-3596G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50250849 | |||||||
| chr14:50251080 | G | T | 2 | a0001c0001t0012g0129 a0001c0001t0029g0182 |
2 | HG04115.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1197-3827C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50251080 | |||||||
| chr14:50251458 | C | G | 1 | a0002c0002t0004g0282 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1197-4205G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50251458 | |||||||
| chr14:50251611 | T | C | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1197-4358A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50251611 | |||||||
| chr14:50251741 | A | G | 1 | a0001c0001t0001g0197 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1197-4488T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50251741 | |||||||
| chr14:50251817 | A | C | 1 | a0002c0003t0001g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1197-4564T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50251817 | |||||||
| chr14:50251936 | C | T | 2 | a0002c0002t0004g0265 a0002c0002t0004g0266 |
2 | HG00735.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1197-4683G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50251936 | |||||||
| chr14:50252003 | T | C | 16 | a0001c0001t0006g0034 a0001c0001t0006g0092 a0001c0001t0006g0093 others(13): Show |
16 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1197-4750A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50252003 | |||||||
| chr14:50252027 | A | G | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1197-4774T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50252027 | |||||||
| chr14:50252056 | A | C | 3 | a0001c0001t0001g0137 a0001c0001t0001g0145 a0001c0001t0001g0147 |
3 | HG01978.hp2 HG01993.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1197-4803T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50252056 | |||||||
| chr14:50252098 | GA | G | 35 | a0001c0001t0005g0090 a0001c0001t0019g0057 a0001c0001t0031g0186 others(32): Show |
35 | HG00099.hp1 HG00738.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.1197-4846delT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50252098 | |||||||
| chr14:50252284 | C | T | 296 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(293): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1197-5031G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50252284 | |||||||
| chr14:50252357 | A | C | 5 | a0002c0002t0002g0293 a0002c0002t0002g0294 a0002c0002t0002g0299 others(2): Show |
5 | HG01257.hp1 HG01258.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1197-5104T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50252357 | |||||||
| chr14:50252445 | T | G | 1 | a0001c0001t0001g0178 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1197-5192A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50252445 | |||||||
| chr14:50252481 | G | A | 1 | a0002c0003t0050g0346 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1197-5228C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50252481 | |||||||
| chr14:50252495 | GA | G | 102 | a0001c0001t0002g0126 a0001c0001t0002g0185 a0001c0001t0005g0090 others(99): Show |
104 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.1197-5243delT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50252495 | |||||||
| chr14:50252542 | C | T | 73 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0019 others(70): Show |
75 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1197-5289G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50252542 | |||||||
| chr14:50252544 | T | C | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1197-5291A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50252544 | |||||||
| chr14:50252897 | G | A | 105 | a0001c0001t0002g0126 a0001c0001t0002g0185 a0001c0001t0005g0090 others(102): Show |
107 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.1197-5644C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50252897 | |||||||
| chr14:50253016 | G | C | 1 | a0002c0002t0010g0345 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1197-5763C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50253016 | |||||||
| chr14:50253083 | A | G | 1 | a0002c0003t0003g0352 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1197-5830T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50253083 | |||||||
| chr14:50253092 | G | A | 1 | a0001c0001t0038g0198 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1197-5839C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50253092 | |||||||
| chr14:50253110 | C | T | 73 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0019 others(70): Show |
75 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1197-5857G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50253110 | |||||||
| chr14:50253344 | T | A | 105 | a0001c0001t0002g0126 a0001c0001t0002g0185 a0001c0001t0005g0090 others(102): Show |
107 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.1197-6091A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50253344 | |||||||
| chr14:50253487 | C | T | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(313): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1197-6234G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50253487 | |||||||
| chr14:50253567 | A | C | 345 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(342): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1197-6314T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50253567 | |||||||
| chr14:50253577 | C | A | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(111): Show |
116 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1197-6324G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50253577 | |||||||
| chr14:50253690 | C | G | 1 | a0002c0002t0036g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1197-6437G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50253690 | |||||||
| chr14:50254079 | C | T | 1 | a0001c0001t0047g0100 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1197-6826G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50254079 | |||||||
| chr14:50254194 | T | C | 73 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0019 others(70): Show |
75 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.1197-6941A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50254194 | |||||||
| chr14:50254428 | C | T | 3 | a0001c0001t0018g0011 a0001c0001t0018g0012 a0001c0001t0018g0013 |
3 | HG02559.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1197-7175G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50254428 | |||||||
| chr14:50254440 | T | A | 3 | a0001c0001t0001g0169 a0001c0001t0025g0111 a0001c0001t0025g0159 |
3 | NA18994.hp2 NA19054.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1197-7187A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50254440 | |||||||
| chr14:50254450 | T | C | 3 | a0001c0001t0001g0137 a0001c0001t0001g0145 a0001c0001t0001g0147 |
3 | HG01978.hp2 HG01993.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1197-7197A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50254450 | |||||||
| chr14:50254548 | A | G | 3 | a0002c0002t0002g0261 a0002c0002t0002g0339 a0002c0002t0002g0354 |
3 | HG00741.hp1 HG01106.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.1197-7295T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50254548 | |||||||
| chr14:50254671 | A | T | 3 | a0001c0001t0003g0019 a0001c0001t0003g0058 a0001c0001t0003g0068 |
3 | NA18940.hp1 NA18984.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1197-7418T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50254671 | |||||||
| chr14:50254976 | G | A | 16 | a0001c0001t0006g0034 a0001c0001t0006g0092 a0001c0001t0006g0093 others(13): Show |
16 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1197-7723C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50254976 | |||||||
| chr14:50255229 | A | G | 1 | a0001c0001t0061g0015 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1197-7976T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50255229 | |||||||
| chr14:50255292 | C | T | 30 | a0001c0001t0005g0090 a0001c0004t0005g0200 a0002c0002t0005g0220 others(27): Show |
30 | HG00099.hp1 HG01070.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1197-8039G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50255292 | |||||||
| chr14:50255433 | G | A | 8 | a0002c0002t0002g0247 a0002c0002t0002g0295 a0002c0002t0002g0297 others(5): Show |
8 | HG00544.hp1 HG00621.hp1 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.1197-8180C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50255433 | |||||||
| chr14:50255497 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1197-8244A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50255497 | |||||||
| chr14:50255537 | C | CA | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(220): Show |
227 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.1197-8285dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50255537 | |||||||
| chr14:50255537 | C | CAA | 81 | a0001c0001t0001g0132 a0001c0001t0001g0168 a0001c0001t0003g0002 others(78): Show |
83 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1197-8286_1197-828 others(6): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50255537 | |||||||
| chr14:50255576 | C | T | 1 | a0001c0001t0061g0015 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1197-8323G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50255576 | |||||||
| chr14:50255641 | A | C | 190 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(187): Show |
194 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.1197-8388T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50255641 | |||||||
| chr14:50255647 | C | T | 1 | a0001c0001t0020g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1197-8394G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50255647 | |||||||
| chr14:50255685 | C | A | 1 | a0002c0002t0005g0241 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1197-8432G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50255685 | |||||||
| chr14:50255946 | T | C | 100 | a0001c0001t0002g0126 a0001c0001t0002g0185 a0001c0001t0005g0090 others(97): Show |
102 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.1197-8693A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50255946 | |||||||
| chr14:50255974 | G | C | 1 | a0001c0001t0061g0015 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1197-8721C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50255974 | |||||||
| chr14:50256019 | A | G | 1 | a0002c0002t0036g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1197-8766T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50256019 | |||||||
| chr14:50256046 | T | G | 1 | a0001c0001t0001g0197 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1197-8793A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50256046 | |||||||
| chr14:50256136 | C | T | 4 | a0003c0005t0006g0212 a0003c0005t0006g0213 a0003c0005t0006g0214 others(1): Show |
4 | HG02809.hp2 HG03453.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197-8883G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50256136 | |||||||
| chr14:50256137 | G | A | 2 | a0002c0003t0050g0346 a0002c0003t0053g0347 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1197-8884C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50256137 | |||||||
| chr14:50256187 | C | T | 1 | a0003c0005t0006g0213 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1197-8934G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50256187 | |||||||
| chr14:50256210 | G | A | 2 | a0001c0001t0025g0111 a0001c0001t0025g0159 |
2 | NA19054.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1197-8957C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50256210 | |||||||
| chr14:50256220 | A | G | 5 | a0001c0004t0002g0039 a0001c0004t0002g0040 a0001c0004t0002g0041 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1197-8967T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50256220 | |||||||
| chr14:50256349 | T | TAGG | 296 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(293): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1196+9008_1196+900 others(7): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50256349 | |||||||
| chr14:50256567 | T | A | 296 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(293): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1196+8791A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50256567 | |||||||
| chr14:50256913 | T | C | 30 | a0001c0001t0005g0090 a0001c0004t0005g0200 a0002c0002t0005g0220 others(27): Show |
30 | HG00099.hp1 HG01070.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1196+8445A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50256913 | |||||||
| chr14:50257242 | T | C | 296 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(293): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1196+8116A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50257242 | |||||||
| chr14:50257373 | A | AT | 104 | a0001c0001t0001g0180 a0001c0001t0002g0126 a0001c0001t0002g0185 others(101): Show |
106 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.1196+7984dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50257373 | |||||||
| chr14:50257392 | C | G | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1196+7966G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50257392 | |||||||
| chr14:50257620 | G | C | 317 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(314): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1196+7738C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50257620 | |||||||
| chr14:50257705 | C | T | 2 | a0002c0002t0039g0286 a0002c0002t0039g0348 |
2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1196+7653G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50257705 | |||||||
| chr14:50257760 | G | T | 1 | a0001c0001t0031g0186 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1196+7598C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50257760 | |||||||
| chr14:50257795 | G | C | 1 | a0002c0009t0066g0256 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1196+7563C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50257795 | |||||||
| chr14:50257855 | A | G | 6 | a0001c0001t0001g0150 a0001c0001t0001g0163 a0001c0001t0001g0201 others(3): Show |
6 | HG01433.hp1 HG02257.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1196+7503T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50257855 | |||||||
| chr14:50258010 | G | T | 1 | a0001c0001t0038g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1196+7348C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50258010 | |||||||
| chr14:50258073 | TA | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(216): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.1196+7284delT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50258073 | |||||||
| chr14:50258073 | TAA | T | 98 | a0001c0001t0001g0145 a0001c0001t0001g0155 a0001c0001t0003g0002 others(95): Show |
100 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.1196+7283_1196+728 others(6): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50258073 | |||||||
| chr14:50258226 | T | C | 1 | a0001c0001t0013g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1196+7132A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50258226 | |||||||
| chr14:50258368 | A | T | 105 | a0001c0001t0002g0126 a0001c0001t0002g0185 a0001c0001t0005g0090 others(102): Show |
107 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(104): Show |
intron_variant | MODIFIER | c.1196+6990T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50258368 | |||||||
| chr14:50258604 | C | T | 1 | a0001c0001t0003g0047 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1196+6754G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50258604 | |||||||
| chr14:50258649 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1196+6709C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50258649 | |||||||
| chr14:50258695 | G | A | 1 | a0002c0003t0001g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1196+6663C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50258695 | |||||||
| chr14:50258792 | C | T | 1 | a0002c0003t0001g0252 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1196+6566G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50258792 | |||||||
| chr14:50258921 | T | C | 2 | a0002c0002t0039g0286 a0002c0002t0039g0348 |
2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1196+6437A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50258921 | |||||||
| chr14:50258995 | C | G | 1 | a0001c0001t0007g0017 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1196+6363G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50258995 | |||||||
| chr14:50259010 | C | CT | 7 | a0001c0001t0006g0106 a0001c0001t0007g0081 a0001c0001t0031g0187 others(4): Show |
7 | HG02027.hp1 HG02071.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1196+6347dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259010 | |||||||
| chr14:50259010 | C | CTT | 14 | a0001c0001t0006g0034 a0001c0001t0006g0092 a0001c0001t0006g0093 others(11): Show |
14 | HG01891.hp1 HG02451.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.1196+6346_1196+634 others(6): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259010 | |||||||
| chr14:50259010 | CT | C | 20 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0125 others(17): Show |
20 | HG00099.hp2 HG00323.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1196+6347delA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259010 | |||||||
| chr14:50259055 | A | G | 298 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(295): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.1196+6303T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259055 | |||||||
| chr14:50259219 | C | T | 1 | a0002c0002t0005g0231 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1196+6139G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259219 | |||||||
| chr14:50259262 | C | A | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1196+6096G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259262 | |||||||
| chr14:50259364 | C | G | 1 | a0002c0002t0067g0219 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1196+5994G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259364 | |||||||
| chr14:50259364 | C | T | 294 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(291): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1196+5994G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259364 | |||||||
| chr14:50259366 | G | GGT | 29 | a0001c0001t0005g0090 a0001c0004t0005g0200 a0002c0002t0002g0307 others(26): Show |
29 | HG00099.hp1 HG01074.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.1196+5991_1196+599 others(6): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259366 | |||||||
| chr14:50259366 | G | GGTT | 57 | a0001c0001t0002g0126 a0001c0001t0002g0185 a0001c0001t0069g0056 others(54): Show |
59 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.1196+5991_1196+599 others(7): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259366 | |||||||
| chr14:50259366 | G | GGTTT | 18 | a0001c0001t0018g0011 a0001c0001t0018g0012 a0001c0001t0018g0013 others(15): Show |
18 | HG00621.hp1 HG00741.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.1196+5991_1196+599 others(8): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259366 | |||||||
| chr14:50259366 | G | GT | 11 | a0001c0001t0004g0202 a0002c0002t0004g0216 a0002c0002t0004g0263 others(8): Show |
11 | HG00735.hp2 HG01358.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.1196+5991dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259366 | |||||||
| chr14:50259366 | GT | G | 6 | a0001c0001t0001g0127 a0001c0001t0001g0152 a0001c0001t0003g0043 others(3): Show |
6 | HG01175.hp2 HG03471.hp2 NA18977.hp1 others(3): Show |
intron_variant | MODIFIER | c.1196+5991delA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259366 | |||||||
| chr14:50259366 | GTT | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(175): Show |
182 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.1196+5990_1196+599 others(6): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259366 | |||||||
| chr14:50259384 | T | C | 7 | a0001c0001t0003g0009 a0001c0001t0003g0082 a0001c0001t0007g0010 others(4): Show |
7 | HG01884.hp2 HG02083.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1196+5974A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259384 | |||||||
| chr14:50259501 | C | T | 5 | a0001c0001t0018g0011 a0001c0001t0018g0012 a0001c0001t0018g0013 others(2): Show |
5 | HG02559.hp1 HG02818.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1196+5857G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259501 | |||||||
| chr14:50259517 | G | A | 104 | a0001c0001t0002g0126 a0001c0001t0002g0185 a0001c0001t0005g0090 others(101): Show |
106 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.1196+5841C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259517 | |||||||
| chr14:50259561 | G | A | 1 | a0002c0003t0003g0352 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1196+5797C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259561 | |||||||
| chr14:50259586 | T | C | 193 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(190): Show |
197 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1196+5772A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259586 | |||||||
| chr14:50259600 | G | A | 2 | a0001c0001t0031g0186 a0001c0001t0031g0187 |
2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1196+5758C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259600 | |||||||
| chr14:50259633 | G | C | 1 | a0002c0002t0001g0324 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1196+5725C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259633 | |||||||
| chr14:50259675 | G | A | 316 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(313): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1196+5683C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259675 | |||||||
| chr14:50259791 | G | A | 4 | a0001c0001t0001g0163 a0001c0001t0009g0154 a0004c0006t0001g0144 others(1): Show |
4 | HG02257.hp1 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1196+5567C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259791 | |||||||
| chr14:50259933 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1196+5425T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259933 | |||||||
| chr14:50259971 | G | T | 1 | a0001c0001t0001g0080 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1196+5387C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259971 | |||||||
| chr14:50259985 | C | CAG | 78 | a0001c0001t0001g0145 a0001c0001t0002g0126 a0001c0001t0005g0090 others(75): Show |
80 | HG00423.hp2 HG00544.hp1 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.1196+5371_1196+537 others(6): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259985 | |||||||
| chr14:50259985 | CAG | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(134): Show |
140 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1196+5371_1196+537 others(6): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259985 | |||||||
| chr14:50259985 | CAGAG | C | 20 | a0001c0001t0001g0122 a0001c0001t0001g0137 a0001c0001t0001g0146 others(17): Show |
20 | HG01891.hp1 HG01978.hp2 HG02165.hp2 others(17): Show |
intron_variant | MODIFIER | c.1196+5369_1196+537 others(8): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259985 | |||||||
| chr14:50259985 | CAGAGAGA others(3): Show |
C | 1 | a0001c0001t0001g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1196+5363_1196+537 others(14): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259985 | |||||||
| chr14:50260101 | G | A | 1 | a0002c0002t0005g0237 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1196+5257C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260101 | |||||||
| chr14:50260149 | C | T | 1 | a0001c0001t0003g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1196+5209G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260149 | |||||||
| chr14:50260205 | G | A | 2 | a0002c0002t0039g0286 a0002c0002t0039g0348 |
2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1196+5153C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260205 | |||||||
| chr14:50260254 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(93): Show |
98 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1196+5104G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260254 | |||||||
| chr14:50260262 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1196+5096C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260262 | |||||||
| chr14:50260292 | G | C | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(220): Show |
227 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.1196+5066C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260292 | |||||||
| chr14:50260391 | C | G | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(212): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.1196+4967G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260391 | |||||||
| chr14:50260476 | C | A | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(249): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1196+4882G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260476 | |||||||
| chr14:50260498 | G | C | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1196+4860C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260498 | |||||||
| chr14:50260501 | A | T | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(194): Show |
201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.1196+4857T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260501 | |||||||
| chr14:50260510 | A | G | 21 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(18): Show |
21 | HG01261.hp1 HG01358.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.1196+4848T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260510 | |||||||
| chr14:50260525 | C | A | 6 | a0001c0001t0030g0209 a0001c0001t0030g0210 a0001c0001t0031g0186 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1196+4833G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260525 | |||||||
| chr14:50260534 | G | A | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1196+4824C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260534 | |||||||
| chr14:50260631 | G | A | 7 | a0001c0001t0030g0209 a0001c0001t0030g0210 a0001c0001t0031g0186 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1196+4727C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260631 | |||||||
| chr14:50260684 | G | A | 1 | a0001c0001t0057g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1196+4674C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260684 | |||||||
| chr14:50260765 | G | A | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(177): Show |
184 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1196+4593C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260765 | |||||||
| chr14:50260805 | G | A | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(93): Show |
98 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1196+4553C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260805 | |||||||
| chr14:50261115 | T | TA | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1196+4242dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50261115 | |||||||
| chr14:50261395 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1196+3963C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50261395 | |||||||
| chr14:50261623 | T | C | 2 | a0002c0002t0039g0286 a0002c0002t0039g0348 |
2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1196+3735A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50261623 | |||||||
| chr14:50261628 | G | A | 8 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(5): Show |
8 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1196+3730C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50261628 | |||||||
| chr14:50261887 | A | T | 14 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0095 others(11): Show |
14 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1196+3471T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50261887 | |||||||
| chr14:50262018 | A | C | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(220): Show |
227 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.1196+3340T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50262018 | |||||||
| chr14:50262068 | A | C | 2 | a0001c0001t0027g0038 a0001c0001t0033g0001 |
3 | NA18983.hp2 NA19012.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1196+3290T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50262068 | |||||||
| chr14:50262415 | C | T | 96 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(93): Show |
98 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1196+2943G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50262415 | |||||||
| chr14:50262424 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1196+2934C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50262424 | |||||||
| chr14:50262428 | CA | C | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(188): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.1196+2929delT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50262428 | |||||||
| chr14:50262532 | A | G | 173 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(170): Show |
177 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.1196+2826T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50262532 | |||||||
| chr14:50262576 | G | GTA | 3 | a0001c0001t0001g0169 a0001c0001t0025g0111 a0001c0001t0025g0159 |
3 | NA18994.hp2 NA19054.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1196+2780_1196+278 others(6): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50262576 | |||||||
| chr14:50262611 | A | G | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1196+2747T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50262611 | |||||||
| chr14:50262639 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1196+2719A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50262639 | |||||||
| chr14:50262680 | A | G | 252 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(249): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.1196+2678T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50262680 | |||||||
| chr14:50262707 | C | T | 20 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(17): Show |
20 | HG01261.hp1 HG01358.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1196+2651G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50262707 | |||||||
| chr14:50262998 | C | A | 1 | a0002c0002t0039g0286 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1196+2360G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50262998 | |||||||
| chr14:50263319 | A | G | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1196+2039T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50263319 | |||||||
| chr14:50263359 | T | C | 8 | a0001c0001t0006g0034 a0001c0001t0013g0016 a0001c0001t0013g0032 others(5): Show |
8 | HG02615.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1196+1999A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50263359 | |||||||
| chr14:50263469 | A | G | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1196+1889T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50263469 | |||||||
| chr14:50263637 | T | C | 3 | a0001c0001t0018g0011 a0001c0001t0018g0012 a0001c0001t0018g0013 |
3 | HG02559.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1196+1721A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50263637 | |||||||
| chr14:50263726 | G | C | 1 | a0002c0002t0002g0317 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1196+1632C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50263726 | |||||||
| chr14:50263766 | C | A | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1196+1592G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50263766 | |||||||
| chr14:50263766 | C | T | 1 | a0001c0001t0008g0098 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1196+1592G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50263766 | |||||||
| chr14:50263774 | C | CT | 202 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(199): Show |
206 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(203): Show |
intron_variant | MODIFIER | c.1196+1583dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50263774 | |||||||
| chr14:50263797 | C | T | 8 | a0001c0001t0006g0034 a0001c0001t0013g0016 a0001c0001t0013g0032 others(5): Show |
8 | HG02615.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1196+1561G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50263797 | |||||||
| chr14:50263888 | G | A | 2 | a0002c0002t0005g0223 a0002c0002t0005g0224 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1196+1470C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50263888 | |||||||
| chr14:50263943 | T | C | 10 | a0001c0001t0006g0034 a0001c0001t0013g0016 a0001c0001t0013g0032 others(7): Show |
10 | HG02280.hp1 HG02615.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1196+1415A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50263943 | |||||||
| chr14:50264100 | C | T | 12 | a0001c0001t0006g0034 a0001c0001t0013g0016 a0001c0001t0013g0032 others(9): Show |
12 | HG02074.hp1 HG02280.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.1196+1258G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50264100 | |||||||
| chr14:50264118 | G | A | 1 | a0002c0002t0002g0287 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1196+1240C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50264118 | |||||||
| chr14:50264121 | T | A | 10 | a0001c0001t0006g0034 a0001c0001t0013g0016 a0001c0001t0013g0032 others(7): Show |
10 | HG02074.hp1 HG02615.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1196+1237A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50264121 | |||||||
| chr14:50264160 | G | A | 1 | a0002c0002t0002g0289 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1196+1198C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50264160 | |||||||
| chr14:50264289 | A | T | 1 | a0001c0001t0003g0077 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1196+1069T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50264289 | |||||||
| chr14:50264296 | T | A | 2 | a0001c0001t0021g0183 a0001c0001t0021g0184 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1196+1062A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50264296 | |||||||
| chr14:50264331 | T | C | 7 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(4): Show |
7 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1196+1027A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50264331 | |||||||
| chr14:50264429 | C | A | 1 | a0002c0002t0002g0344 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1196+929G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50264429 | |||||||
| chr14:50264438 | C | A | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1196+920G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50264438 | |||||||
| chr14:50264578 | A | G | 1 | a0001c0001t0007g0089 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1196+780T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50264578 | |||||||
| chr14:50264641 | A | G | 13 | a0001c0001t0006g0034 a0001c0001t0013g0016 a0001c0001t0013g0032 others(10): Show |
13 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1196+717T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50264641 | |||||||
| chr14:50264782 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG00099.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.1196+576C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50264782 | |||||||
| chr14:50264800 | T | C | 1 | a0001c0001t0061g0015 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1196+558A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50264800 | |||||||
| chr14:50264829 | CAT | C | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1196+527_1196+528d others(4): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50264829 | |||||||
| chr14:50264882 | T | C | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1196+476A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50264882 | |||||||
| chr14:50264907 | AAT | A | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1196+449_1196+450d others(4): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50264907 | |||||||
| chr14:50265324 | G | A | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(154): Show |
161 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1196+34C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50265324 | |||||||
| chr14:50265688 | C | A | 1 | a0001c0001t0009g0149 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1065-199G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50265688 | |||||||
| chr14:50265770 | C | T | 3 | a0001c0001t0031g0186 a0001c0001t0031g0187 a0001c0001t0038g0199 |
3 | HG01884.hp2 HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1065-281G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50265770 | |||||||
| chr14:50265906 | C | T | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1065-417G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50265906 | |||||||
| chr14:50265979 | T | C | 1 | a0001c0001t0001g0160 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1065-490A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50265979 | |||||||
| chr14:50266007 | A | C | 1 | a0002c0002t0002g0339 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1065-518T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50266007 | |||||||
| chr14:50266143 | C | CA | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(181): Show |
188 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1065-655dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50266143 | |||||||
| chr14:50266229 | C | T | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(181): Show |
188 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.1065-740G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50266229 | |||||||
| chr14:50266289 | G | C | 2 | a0001c0001t0031g0186 a0001c0001t0031g0187 |
2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1065-800C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50266289 | |||||||
| chr14:50266475 | T | C | 4 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1065-986A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50266475 | |||||||
| chr14:50266509 | A | G | 2 | a0001c0001t0021g0183 a0001c0001t0021g0184 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1065-1020T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50266509 | |||||||
| chr14:50266515 | T | G | 7 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(4): Show |
7 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1065-1026A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50266515 | |||||||
| chr14:50266530 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0059g0164 |
2 | NA18979.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1065-1041G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50266530 | |||||||
| chr14:50266541 | C | G | 1 | a0001c0001t0014g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1065-1052G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50266541 | |||||||
| chr14:50266641 | T | C | 1 | a0001c0001t0020g0037 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1064+1112A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50266641 | |||||||
| chr14:50266841 | A | G | 1 | a0001c0001t0014g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1064+912T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50266841 | |||||||
| chr14:50266867 | C | T | 3 | a0002c0002t0024g0290 a0002c0002t0024g0291 a0002c0002t0024g0292 |
3 | HG01069.hp1 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1064+886G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50266867 | |||||||
| chr14:50266904 | T | A | 1 | a0001c0001t0001g0024 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1064+849A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50266904 | |||||||
| chr14:50267107 | A | C | 8 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 others(5): Show |
8 | HG01106.hp2 HG01257.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1064+646T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267107 | |||||||
| chr14:50267138 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1064+615A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267138 | |||||||
| chr14:50267145 | T | TTTTA | 12 | a0001c0001t0001g0022 a0001c0001t0001g0086 a0001c0001t0001g0128 others(9): Show |
12 | HG00408.hp2 HG00639.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1064+604_1064+607d others(6): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267145 | |||||||
| chr14:50267145 | TTTTA | T | 59 | a0001c0001t0001g0122 a0001c0001t0001g0139 a0001c0001t0001g0151 others(56): Show |
59 | HG00323.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1064+604_1064+607d others(6): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267145 | |||||||
| chr14:50267145 | TTTTATTT others(1): Show |
T | 68 | a0001c0001t0001g0152 a0001c0001t0002g0185 a0001c0001t0003g0002 others(65): Show |
70 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.1064+600_1064+607d others(10): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267145 | |||||||
| chr14:50267145 | TTTTATTT others(5): Show |
T | 4 | a0001c0001t0002g0126 a0001c0001t0021g0183 a0001c0001t0021g0184 others(1): Show |
4 | HG02145.hp2 NA18906.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.1064+596_1064+607d others(14): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267145 | |||||||
| chr14:50267145 | TTTTATTT others(9): Show |
T | 7 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(4): Show |
7 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1064+592_1064+607d others(18): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267145 | |||||||
| chr14:50267145 | TTTTATTT others(13): Show |
T | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1064+588_1064+607d others(22): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267145 | |||||||
| chr14:50267188 | T | C | 6 | a0001c0001t0008g0023 a0001c0001t0012g0129 a0001c0001t0029g0182 others(3): Show |
6 | HG00735.hp1 HG04115.hp1 HG04115.hp2 others(3): Show |
intron_variant | MODIFIER | c.1064+565A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267188 | |||||||
| chr14:50267188 | T | TATTC | 5 | a0002c0002t0001g0305 a0002c0002t0001g0324 a0002c0002t0002g0247 others(2): Show |
5 | HG00323.hp1 HG01099.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1064+561_1064+564d others(6): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267188 | |||||||
| chr14:50267239 | T | G | 1 | a0001c0001t0044g0014 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1064+514A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267239 | |||||||
| chr14:50267245 | C | T | 12 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0046 others(9): Show |
12 | HG00323.hp2 HG00639.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1064+508G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267245 | |||||||
| chr14:50267346 | C | T | 1 | a0002c0002t0002g0314 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1064+407G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267346 | |||||||
| chr14:50267382 | T | C | 224 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(221): Show |
228 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.1064+371A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267382 | |||||||
| chr14:50267471 | T | C | 22 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(19): Show |
22 | HG01261.hp1 HG01891.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.1064+282A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267471 | |||||||
| chr14:50267556 | AT | A | 10 | a0002c0002t0001g0305 a0002c0002t0002g0294 a0002c0002t0002g0306 others(7): Show |
10 | HG00323.hp1 HG00597.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1064+196delA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267556 | |||||||
| chr14:50267556 | ATTTT | A | 6 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0002t0036g0245 others(3): Show |
6 | HG01358.hp1 HG01358.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1064+193_1064+196d others(6): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267556 | |||||||
| chr14:50267557 | T | C | 5 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(2): Show |
5 | HG01934.hp1 HG02074.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1064+196A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267557 | |||||||
| chr14:50267560 | T | G | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(154): Show |
161 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1064+193A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267560 | |||||||
| chr14:50267564 | T | G | 250 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(247): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.1064+189A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267564 | |||||||
| chr14:50267567 | TG | T | 3 | a0002c0002t0024g0290 a0002c0002t0024g0291 a0002c0002t0024g0292 |
3 | HG01069.hp1 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1064+185delC | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267567 | |||||||
| chr14:50268239 | C | T | 16 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(13): Show |
16 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.907-329G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 7/9 | chr14 | 50268239 | |||||||
| chr14:50268372 | C | G | 1 | a0002c0002t0005g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.907-462G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 7/9 | chr14 | 50268372 | |||||||
| chr14:50268381 | G | GA | 29 | a0001c0001t0001g0112 a0001c0001t0001g0139 a0001c0001t0001g0160 others(26): Show |
29 | HG00408.hp2 HG00438.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.907-472dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 7/9 | chr14 | 50268381 | |||||||
| chr14:50268398 | A | G | 1 | a0002c0002t0004g0218 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.907-488T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 7/9 | chr14 | 50268398 | |||||||
| chr14:50268463 | A | G | 3 | a0001c0001t0003g0101 a0001c0001t0008g0105 a0001c0001t0047g0100 |
3 | HG00673.hp1 HG02040.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.907-553T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 7/9 | chr14 | 50268463 | |||||||
| chr14:50268482 | T | A | 5 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(2): Show |
5 | HG01934.hp1 HG02074.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.907-572A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 7/9 | chr14 | 50268482 | |||||||
| chr14:50268499 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0172 |
2 | NA18960.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.907-589G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 7/9 | chr14 | 50268499 | |||||||
| chr14:50268610 | G | A | 13 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(10): Show |
13 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.906+553C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 7/9 | chr14 | 50268610 | |||||||
| chr14:50268787 | T | C | 22 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(19): Show |
22 | HG01261.hp1 HG01891.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.906+376A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 7/9 | chr14 | 50268787 | |||||||
| chr14:50268884 | C | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG00099.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.906+279G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 7/9 | chr14 | 50268884 | |||||||
| chr14:50268893 | G | A | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.906+270C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 7/9 | chr14 | 50268893 | |||||||
| chr14:50268895 | T | C | 1 | a0002c0002t0010g0340 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.906+268A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 7/9 | chr14 | 50268895 | |||||||
| chr14:50268927 | A | C | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.906+236T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 7/9 | chr14 | 50268927 | |||||||
| chr14:50269053 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.906+110G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 7/9 | chr14 | 50269053 | |||||||
| chr14:50269128 | G | GA | 8 | a0001c0001t0001g0178 a0001c0001t0003g0043 a0001c0001t0003g0044 others(5): Show |
8 | HG00323.hp2 HG00408.hp2 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.906+34dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 7/9 | chr14 | 50269128 | |||||||
| chr14:50269136 | T | A | 7 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(4): Show |
7 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.906+27A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 7/9 | chr14 | 50269136 | |||||||
| chr14:50269403 | T | C | 2 | a0001c0001t0006g0034 a0001c0001t0013g0016 |
2 | HG02615.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.739-73A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50269403 | |||||||
| chr14:50269569 | T | C | 5 | a0001c0001t0031g0186 a0001c0001t0031g0187 a0001c0001t0038g0198 others(2): Show |
5 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.739-239A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50269569 | |||||||
| chr14:50269624 | T | A | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.739-294A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50269624 | |||||||
| chr14:50269624 | T | C | 1 | a0001c0001t0008g0070 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.739-294A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50269624 | |||||||
| chr14:50269763 | A | T | 1 | a0001c0001t0061g0015 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.739-433T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50269763 | |||||||
| chr14:50270007 | C | T | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(175): Show |
182 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.739-677G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50270007 | |||||||
| chr14:50270009 | G | T | 1 | a0001c0001t0007g0053 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.739-679C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50270009 | |||||||
| chr14:50270067 | C | T | 1 | a0002c0009t0066g0256 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.739-737G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50270067 | |||||||
| chr14:50270084 | C | T | 1 | a0001c0001t0057g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.739-754G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50270084 | |||||||
| chr14:50270153 | A | C | 2 | a0001c0001t0003g0058 a0001c0001t0003g0068 |
2 | NA18984.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.739-823T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50270153 | |||||||
| chr14:50270257 | C | A | 1 | a0002c0009t0066g0256 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.739-927G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50270257 | |||||||
| chr14:50270492 | T | TTTG | 13 | a0001c0001t0001g0201 a0001c0001t0070g0189 a0002c0002t0002g0249 others(10): Show |
13 | HG01167.hp2 HG01169.hp1 HG02922.hp1 others(10): Show |
intron_variant | MODIFIER | c.739-1165_739-1163d others(5): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50270492 | |||||||
| chr14:50270492 | T | TTTGTTG | 5 | a0002c0002t0001g0335 a0002c0002t0001g0336 a0002c0002t0001g0337 others(2): Show |
5 | HG03098.hp2 NA18952.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.739-1168_739-1163d others(8): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50270492 | |||||||
| chr14:50270492 | TTTG | T | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.739-1165_739-1163d others(5): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50270492 | |||||||
| chr14:50270492 | TTTGTTGT others(2): Show |
T | 12 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0046 others(9): Show |
12 | HG00323.hp2 HG00639.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.739-1171_739-1163d others(11): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50270492 | |||||||
| chr14:50270581 | A | T | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.739-1251T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50270581 | |||||||
| chr14:50270601 | G | A | 15 | a0002c0002t0005g0233 a0002c0002t0005g0235 a0002c0002t0005g0237 others(12): Show |
15 | HG00099.hp1 HG01070.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.739-1271C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50270601 | |||||||
| chr14:50270951 | A | G | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(154): Show |
161 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.739-1621T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50270951 | |||||||
| chr14:50271053 | C | T | 3 | a0001c0001t0018g0011 a0001c0001t0018g0012 a0001c0001t0018g0013 |
3 | HG02559.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.739-1723G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50271053 | |||||||
| chr14:50271143 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.739-1813C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50271143 | |||||||
| chr14:50271268 | C | A | 1 | a0002c0002t0046g0321 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.739-1938G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50271268 | |||||||
| chr14:50271355 | G | C | 3 | a0001c0001t0018g0011 a0001c0001t0018g0012 a0001c0001t0018g0013 |
3 | HG02559.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.739-2025C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50271355 | |||||||
| chr14:50271356 | C | T | 4 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(1): Show |
4 | HG02451.hp2 HG02723.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.739-2026G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50271356 | |||||||
| chr14:50271828 | C | A | 1 | a0002c0002t0005g0221 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.739-2498G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50271828 | |||||||
| chr14:50271874 | C | T | 3 | a0002c0002t0024g0290 a0002c0002t0024g0291 a0002c0002t0024g0292 |
3 | HG01069.hp1 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.739-2544G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50271874 | |||||||
| chr14:50272067 | G | C | 1 | a0001c0001t0019g0057 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.739-2737C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50272067 | |||||||
| chr14:50272198 | C | T | 1 | a0001c0001t0003g0044 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.739-2868G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50272198 | |||||||
| chr14:50272320 | T | C | 1 | a0002c0002t0004g0283 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.739-2990A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50272320 | |||||||
| chr14:50272424 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | HG00099.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.739-3094G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50272424 | |||||||
| chr14:50272444 | G | A | 1 | a0001c0001t0003g0063 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.739-3114C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50272444 | |||||||
| chr14:50272534 | G | A | 1 | a0001c0001t0019g0099 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.739-3204C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50272534 | |||||||
| chr14:50272663 | T | C | 1 | a0001c0001t0043g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.739-3333A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50272663 | |||||||
| chr14:50272767 | A | C | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(215): Show |
222 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.739-3437T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50272767 | |||||||
| chr14:50272829 | A | T | 2 | a0001c0001t0027g0038 a0001c0001t0033g0001 |
3 | NA18983.hp2 NA19012.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.739-3499T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50272829 | |||||||
| chr14:50273028 | C | T | 1 | a0002c0003t0001g0255 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.739-3698G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50273028 | |||||||
| chr14:50273310 | C | T | 2 | a0001c0001t0021g0183 a0001c0001t0021g0184 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.739-3980G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50273310 | |||||||
| chr14:50273329 | C | T | 7 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(4): Show |
7 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.739-3999G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50273329 | |||||||
| chr14:50273382 | G | A | 1 | a0001c0001t0007g0135 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.739-4052C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50273382 | |||||||
| chr14:50273473 | A | C | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(181): Show |
188 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.739-4143T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50273473 | |||||||
| chr14:50273560 | T | A | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.739-4230A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50273560 | |||||||
| chr14:50273622 | A | C | 2 | a0001c0001t0003g0088 a0001c0001t0007g0089 |
2 | HG01106.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.739-4292T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50273622 | |||||||
| chr14:50273732 | A | T | 8 | a0001c0001t0006g0034 a0001c0001t0013g0016 a0001c0001t0013g0032 others(5): Show |
8 | HG02615.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.739-4402T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50273732 | |||||||
| chr14:50273746 | T | C | 3 | a0002c0003t0021g0351 a0002c0003t0028g0349 a0002c0003t0028g0350 |
3 | HG01358.hp2 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.739-4416A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50273746 | |||||||
| chr14:50273806 | C | A | 1 | a0001c0001t0019g0099 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.739-4476G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50273806 | |||||||
| chr14:50273808 | C | T | 1 | a0001c0001t0003g0068 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.739-4478G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50273808 | |||||||
| chr14:50273887 | C | T | 222 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(219): Show |
226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.739-4557G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50273887 | |||||||
| chr14:50273910 | C | T | 12 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0046 others(9): Show |
12 | HG00323.hp2 HG00639.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.739-4580G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50273910 | |||||||
| chr14:50273982 | C | A | 222 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(219): Show |
226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.738+4538G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50273982 | |||||||
| chr14:50274032 | C | T | 1 | a0001c0001t0006g0034 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.738+4488G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50274032 | |||||||
| chr14:50274245 | C | T | 1 | a0001c0001t0003g0175 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.738+4275G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50274245 | |||||||
| chr14:50274274 | C | CA | 24 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(21): Show |
24 | HG01261.hp1 HG01358.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.738+4245dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50274274 | |||||||
| chr14:50274286 | A | G | 7 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(4): Show |
7 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.738+4234T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50274286 | |||||||
| chr14:50274313 | A | G | 8 | a0001c0001t0006g0034 a0001c0001t0013g0016 a0001c0001t0013g0032 others(5): Show |
8 | HG02615.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.738+4207T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50274313 | |||||||
| chr14:50274663 | T | C | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.738+3857A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50274663 | |||||||
| chr14:50274787 | G | T | 1 | a0001c0001t0061g0015 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.738+3733C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50274787 | |||||||
| chr14:50274797 | G | C | 1 | a0002c0002t0016g0343 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.738+3723C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50274797 | |||||||
| chr14:50274842 | T | C | 1 | a0001c0001t0019g0083 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.738+3678A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50274842 | |||||||
| chr14:50274920 | T | C | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.738+3600A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50274920 | |||||||
| chr14:50274950 | T | C | 1 | a0001c0001t0006g0093 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.738+3570A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50274950 | |||||||
| chr14:50274970 | G | C | 1 | a0001c0001t0032g0158 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.738+3550C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50274970 | |||||||
| chr14:50274989 | A | G | 6 | a0001c0001t0031g0186 a0001c0001t0031g0187 a0001c0001t0038g0198 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.738+3531T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50274989 | |||||||
| chr14:50275180 | T | TA | 12 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0046 others(9): Show |
12 | HG00323.hp2 HG00639.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.738+3339dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50275180 | |||||||
| chr14:50275318 | T | A | 1 | a0001c0001t0019g0057 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.738+3202A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50275318 | |||||||
| chr14:50275531 | T | C | 253 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(250): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.738+2989A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50275531 | |||||||
| chr14:50275623 | A | C | 8 | a0001c0001t0001g0150 a0001c0001t0001g0163 a0001c0001t0001g0179 others(5): Show |
8 | HG00099.hp2 HG01433.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.738+2897T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50275623 | |||||||
| chr14:50275674 | C | T | 8 | a0001c0001t0006g0034 a0001c0001t0013g0016 a0001c0001t0013g0032 others(5): Show |
8 | HG02615.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.738+2846G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50275674 | |||||||
| chr14:50275758 | G | A | 3 | a0002c0002t0023g0225 a0002c0002t0023g0236 a0002c0002t0023g0240 |
3 | HG02257.hp2 HG02559.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.738+2762C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50275758 | |||||||
| chr14:50275829 | T | C | 22 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(19): Show |
22 | HG01261.hp1 HG01891.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.738+2691A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50275829 | |||||||
| chr14:50275909 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.738+2611C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50275909 | |||||||
| chr14:50275973 | T | C | 2 | a0001c0001t0021g0183 a0001c0001t0021g0184 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.738+2547A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50275973 | |||||||
| chr14:50275979 | C | G | 1 | a0001c0001t0025g0159 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.738+2541G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50275979 | |||||||
| chr14:50276051 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.738+2469T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50276051 | |||||||
| chr14:50276193 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.738+2327C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50276193 | |||||||
| chr14:50276462 | G | C | 1 | a0002c0002t0004g0284 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.738+2058C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50276462 | |||||||
| chr14:50276462 | G | GC | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(192): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.738+2057dupG | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50276462 | |||||||
| chr14:50276470 | C | CA | 3 | a0001c0001t0001g0169 a0001c0001t0025g0111 a0001c0001t0025g0159 |
3 | NA18994.hp2 NA19054.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.738+2049dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50276470 | |||||||
| chr14:50276626 | T | C | 7 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(4): Show |
7 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.738+1894A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50276626 | |||||||
| chr14:50277014 | T | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(216): Show |
223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.738+1506A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50277014 | |||||||
| chr14:50277181 | T | A | 3 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0017g0206 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.738+1339A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50277181 | |||||||
| chr14:50277190 | T | C | 1 | a0002c0002t0002g0287 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.738+1330A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50277190 | |||||||
| chr14:50277194 | CTGTTTTT others(4): Show |
C | 3 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0017g0206 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.738+1315_738+1325d others(13): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50277194 | |||||||
| chr14:50277207 | G | GT | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(129): Show |
135 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.738+1312dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50277207 | |||||||
| chr14:50277207 | G | GTT | 30 | a0001c0001t0001g0080 a0001c0001t0001g0123 a0001c0001t0001g0141 others(27): Show |
31 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.738+1311_738+1312d others(4): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50277207 | |||||||
| chr14:50277698 | G | A | 1 | a0001c0001t0061g0015 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.738+822C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50277698 | |||||||
| chr14:50277744 | G | A | 6 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(3): Show |
6 | HG01358.hp2 HG02647.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.738+776C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50277744 | |||||||
| chr14:50277774 | AAAT | A | 126 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0024 others(123): Show |
127 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.738+743_738+745del others(3): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50277774 | |||||||
| chr14:50277774 | AAATAAT | A | 61 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0021 others(58): Show |
62 | HG00140.hp1 HG00438.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.738+740_738+745del others(6): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50277774 | |||||||
| chr14:50277774 | AAATAATA others(2): Show |
A | 77 | a0001c0001t0001g0004 a0001c0001t0001g0118 a0001c0001t0001g0143 others(74): Show |
79 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.738+737_738+745del others(9): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50277774 | |||||||
| chr14:50277774 | AAATAATA others(5): Show |
A | 56 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0004g0202 others(53): Show |
56 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.738+734_738+745del others(12): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50277774 | |||||||
| chr14:50277774 | AAATAATA others(8): Show |
A | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0001c0001t0030g0210 others(2): Show |
5 | HG02280.hp1 HG06807.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.738+731_738+745del others(15): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50277774 | |||||||
| chr14:50277774 | AAATAATA others(11): Show |
A | 2 | a0002c0002t0002g0311 a0002c0002t0002g0319 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.738+728_738+745del others(18): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50277774 | |||||||
| chr14:50277820 | A | C | 1 | a0002c0002t0068g0230 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.738+700T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50277820 | |||||||
| chr14:50277823 | A | C | 3 | a0001c0004t0005g0200 a0002c0002t0005g0238 a0002c0002t0068g0230 |
3 | HG01074.hp1 HG02572.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.738+697T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50277823 | |||||||
| chr14:50277826 | A | C | 29 | a0001c0004t0005g0200 a0002c0002t0005g0220 a0002c0002t0005g0221 others(26): Show |
29 | HG00099.hp1 HG01070.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.738+694T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50277826 | |||||||
| chr14:50278405 | A | ATTACTT | 219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(216): Show |
223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.738+114_738+115ins others(6): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50278405 | |||||||
| chr14:50278505 | C | T | 3 | a0001c0001t0018g0011 a0001c0001t0018g0012 a0001c0001t0018g0013 |
3 | HG02559.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.738+15G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50278505 | |||||||
| chr14:50278807 | C | G | 6 | a0001c0001t0031g0186 a0001c0001t0031g0187 a0001c0001t0038g0198 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-253G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50278807 | |||||||
| chr14:50279074 | C | A | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.704-520G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50279074 | |||||||
| chr14:50279076 | T | A | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-522A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50279076 | |||||||
| chr14:50279116 | T | C | 1 | a0002c0002t0005g0238 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.704-562A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50279116 | |||||||
| chr14:50279249 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.704-695C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50279249 | |||||||
| chr14:50279378 | TG | T | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(188): Show |
195 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.704-825delC | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50279378 | |||||||
| chr14:50279456 | A | G | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.704-902T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50279456 | |||||||
| chr14:50279473 | A | G | 1 | a0001c0001t0038g0199 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.704-919T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50279473 | |||||||
| chr14:50279534 | G | A | 1 | a0001c0001t0043g0049 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.704-980C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50279534 | |||||||
| chr14:50279710 | G | A | 1 | a0002c0002t0036g0226 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.704-1156C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50279710 | |||||||
| chr14:50279897 | C | T | 1 | a0001c0001t0009g0149 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.704-1343G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50279897 | |||||||
| chr14:50280064 | G | GA | 13 | a0001c0001t0004g0207 a0001c0001t0004g0208 a0001c0001t0017g0204 others(10): Show |
13 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.704-1511dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50280064 | |||||||
| chr14:50280064 | GA | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(180): Show |
187 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.704-1511delT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50280064 | |||||||
| chr14:50280165 | C | CT | 9 | a0001c0001t0001g0117 a0001c0001t0008g0067 a0001c0001t0009g0154 others(6): Show |
9 | HG00597.hp1 HG02056.hp1 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.704-1612dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50280165 | |||||||
| chr14:50280325 | C | T | 1 | a0002c0003t0050g0346 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.704-1771G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50280325 | |||||||
| chr14:50280380 | G | C | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-1826C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50280380 | |||||||
| chr14:50280394 | G | C | 8 | a0002c0002t0011g0239 a0002c0003t0001g0252 a0002c0003t0001g0254 others(5): Show |
8 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.704-1840C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50280394 | |||||||
| chr14:50280400 | A | G | 3 | a0002c0002t0024g0290 a0002c0002t0024g0291 a0002c0002t0024g0292 |
3 | HG01069.hp1 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.704-1846T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50280400 | |||||||
| chr14:50280408 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.704-1854G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50280408 | |||||||
| chr14:50280619 | T | G | 212 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(209): Show |
216 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.704-2065A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50280619 | |||||||
| chr14:50280684 | T | G | 2 | a0002c0002t0002g0330 a0002c0002t0010g0332 |
2 | HG01993.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.704-2130A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50280684 | |||||||
| chr14:50280752 | G | A | 8 | a0001c0001t0006g0034 a0001c0001t0013g0016 a0001c0001t0013g0032 others(5): Show |
8 | HG02615.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.704-2198C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50280752 | |||||||
| chr14:50280783 | G | A | 1 | a0002c0002t0004g0246 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.704-2229C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50280783 | |||||||
| chr14:50280825 | A | T | 3 | a0002c0003t0021g0351 a0002c0003t0028g0349 a0002c0003t0028g0350 |
3 | HG01358.hp2 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.704-2271T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50280825 | |||||||
| chr14:50280854 | G | A | 3 | a0002c0002t0024g0290 a0002c0002t0024g0291 a0002c0002t0024g0292 |
3 | HG01069.hp1 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.704-2300C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50280854 | |||||||
| chr14:50280854 | G | C | 1 | a0002c0003t0001g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.704-2300C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50280854 | |||||||
| chr14:50281001 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.704-2447C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50281001 | |||||||
| chr14:50281113 | T | G | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-2559A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50281113 | |||||||
| chr14:50281128 | C | G | 1 | a0001c0001t0012g0120 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.704-2574G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50281128 | |||||||
| chr14:50281132 | G | C | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-2578C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50281132 | |||||||
| chr14:50281155 | A | G | 1 | a0001c0001t0069g0056 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.704-2601T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50281155 | |||||||
| chr14:50281408 | C | A | 5 | a0001c0001t0031g0186 a0001c0001t0031g0187 a0001c0001t0038g0198 others(2): Show |
5 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+2463G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50281408 | |||||||
| chr14:50281408 | C | G | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.703+2463G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50281408 | |||||||
| chr14:50281456 | G | A | 3 | a0001c0001t0001g0169 a0001c0001t0025g0111 a0001c0001t0025g0159 |
3 | NA18994.hp2 NA19054.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.703+2415C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50281456 | |||||||
| chr14:50281489 | G | A | 1 | a0002c0003t0001g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.703+2382C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50281489 | |||||||
| chr14:50281705 | G | A | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.703+2166C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50281705 | |||||||
| chr14:50281707 | C | A | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.703+2164G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50281707 | |||||||
| chr14:50281708 | T | G | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.703+2163A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50281708 | |||||||
| chr14:50281709 | A | AG | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.703+2161_703+2162i others(3): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50281709 | |||||||
| chr14:50281847 | T | G | 1 | a0001c0001t0061g0015 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.703+2024A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50281847 | |||||||
| chr14:50282016 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0114 others(3): Show |
7 | HG00408.hp1 NA19012.hp1 NA19062.hp1 others(4): Show |
intron_variant | MODIFIER | c.703+1855T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50282016 | |||||||
| chr14:50282087 | G | A | 1 | a0002c0003t0001g0252 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.703+1784C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50282087 | |||||||
| chr14:50282118 | G | A | 1 | a0001c0001t0007g0081 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.703+1753C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50282118 | |||||||
| chr14:50282135 | T | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(216): Show |
223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.703+1736A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50282135 | |||||||
| chr14:50282236 | G | A | 1 | a0002c0002t0002g0315 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.703+1635C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50282236 | |||||||
| chr14:50282267 | C | T | 1 | a0002c0002t0039g0286 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.703+1604G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50282267 | |||||||
| chr14:50282355 | C | T | 1 | a0001c0001t0061g0015 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.703+1516G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50282355 | |||||||
| chr14:50282758 | T | A | 2 | a0002c0002t0039g0286 a0002c0002t0039g0348 |
2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.703+1113A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50282758 | |||||||
| chr14:50282777 | C | G | 1 | a0002c0002t0004g0217 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.703+1094G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50282777 | |||||||
| chr14:50282780 | G | A | 2 | a0002c0003t0050g0346 a0002c0003t0053g0347 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.703+1091C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50282780 | |||||||
| chr14:50282799 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.703+1072A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50282799 | |||||||
| chr14:50282824 | T | A | 2 | a0002c0003t0050g0346 a0002c0003t0053g0347 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.703+1047A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50282824 | |||||||
| chr14:50282848 | A | C | 1 | a0001c0001t0002g0126 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.703+1023T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50282848 | |||||||
| chr14:50282958 | C | G | 1 | a0002c0002t0002g0297 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.703+913G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50282958 | |||||||
| chr14:50283098 | G | A | 1 | a0002c0003t0001g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.703+773C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50283098 | |||||||
| chr14:50283149 | C | T | 4 | a0002c0002t0004g0263 a0002c0002t0016g0262 a0002c0002t0016g0264 others(1): Show |
4 | HG02071.hp1 NA18971.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+722G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50283149 | |||||||
| chr14:50283198 | C | T | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.703+673G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50283198 | |||||||
| chr14:50283202 | AG | A | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.703+668delC | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50283202 | |||||||
| chr14:50283206 | G | A | 207 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(204): Show |
211 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(208): Show |
intron_variant | MODIFIER | c.703+665C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50283206 | |||||||
| chr14:50283340 | G | A | 1 | a0001c0001t0003g0058 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.703+531C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50283340 | |||||||
| chr14:50283347 | C | T | 7 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(4): Show |
7 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.703+524G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50283347 | |||||||
| chr14:50283439 | A | G | 2 | a0002c0003t0050g0346 a0002c0003t0053g0347 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.703+432T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50283439 | |||||||
| chr14:50283598 | C | T | 211 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(208): Show |
215 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.703+273G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50283598 | |||||||
| chr14:50283770 | T | C | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.703+101A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50283770 | |||||||
| chr14:50283859 | A | G | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(181): Show |
188 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.703+12T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50283859 | |||||||
| chr14:50284061 | G | A | 29 | a0001c0004t0005g0200 a0002c0002t0005g0220 a0002c0002t0005g0221 others(26): Show |
29 | HG00099.hp1 HG01070.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.541-28C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50284061 | |||||||
| chr14:50284184 | A | C | 3 | a0002c0002t0024g0290 a0002c0002t0024g0291 a0002c0002t0024g0292 |
3 | HG01069.hp1 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.541-151T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50284184 | |||||||
| chr14:50284335 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.541-302C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50284335 | |||||||
| chr14:50284430 | G | A | 3 | a0002c0003t0021g0351 a0002c0003t0028g0349 a0002c0003t0028g0350 |
3 | HG01358.hp2 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.541-397C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50284430 | |||||||
| chr14:50284465 | G | T | 12 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0046 others(9): Show |
12 | HG00323.hp2 HG00639.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.541-432C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50284465 | |||||||
| chr14:50284481 | A | AT | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(181): Show |
188 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.541-449dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50284481 | |||||||
| chr14:50284536 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.541-503A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50284536 | |||||||
| chr14:50284728 | A | C | 1 | a0002c0002t0046g0321 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.541-695T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50284728 | |||||||
| chr14:50284847 | G | T | 222 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(219): Show |
226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.541-814C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50284847 | |||||||
| chr14:50284955 | T | C | 1 | a0001c0001t0030g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.541-922A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50284955 | |||||||
| chr14:50284974 | G | A | 2 | a0002c0002t0001g0305 a0002c0002t0001g0324 |
2 | HG00323.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.541-941C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50284974 | |||||||
| chr14:50285044 | G | A | 1 | a0002c0003t0001g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.541-1011C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50285044 | |||||||
| chr14:50285054 | T | C | 1 | a0002c0002t0002g0250 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.541-1021A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50285054 | |||||||
| chr14:50285502 | C | T | 324 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(321): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.541-1469G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50285502 | |||||||
| chr14:50285526 | A | C | 1 | a0001c0001t0001g0086 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.541-1493T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50285526 | |||||||
| chr14:50285632 | C | T | 1 | a0001c0001t0003g0019 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.541-1599G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50285632 | |||||||
| chr14:50285640 | T | C | 4 | a0001c0001t0013g0032 a0001c0001t0013g0033 a0001c0001t0013g0035 others(1): Show |
4 | HG02965.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-1607A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50285640 | |||||||
| chr14:50285866 | T | C | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.541-1833A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50285866 | |||||||
| chr14:50285902 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0128 |
2 | HG02071.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.541-1869A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50285902 | |||||||
| chr14:50285914 | C | A | 1 | a0002c0002t0002g0316 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.541-1881G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50285914 | |||||||
| chr14:50286040 | T | C | 6 | a0001c0001t0031g0186 a0001c0001t0031g0187 a0001c0001t0038g0198 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.541-2007A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50286040 | |||||||
| chr14:50286158 | T | C | 4 | a0001c0001t0003g0075 a0001c0001t0003g0175 a0001c0001t0003g0176 others(1): Show |
4 | HG01069.hp2 HG01433.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.541-2125A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50286158 | |||||||
| chr14:50286297 | C | T | 1 | a0002c0003t0053g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.541-2264G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50286297 | |||||||
| chr14:50286355 | T | TA | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-2323dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50286355 | |||||||
| chr14:50286356 | A | T | 1 | a0002c0002t0005g0227 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.541-2323T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50286356 | |||||||
| chr14:50286524 | C | G | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(215): Show |
222 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.541-2491G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50286524 | |||||||
| chr14:50286553 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.541-2520G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50286553 | |||||||
| chr14:50286634 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.541-2601T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50286634 | |||||||
| chr14:50286687 | C | T | 1 | a0002c0003t0053g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.541-2654G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50286687 | |||||||
| chr14:50286699 | T | C | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.541-2666A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50286699 | |||||||
| chr14:50286845 | C | T | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.541-2812G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50286845 | |||||||
| chr14:50286913 | C | G | 1 | a0001c0001t0004g0207 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.541-2880G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50286913 | |||||||
| chr14:50286985 | A | G | 3 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0017g0206 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.541-2952T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50286985 | |||||||
| chr14:50286989 | T | C | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.541-2956A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50286989 | |||||||
| chr14:50286994 | A | C | 1 | a0001c0001t0003g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.541-2961T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50286994 | |||||||
| chr14:50287100 | C | A | 9 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(6): Show |
9 | HG01891.hp1 HG02451.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.541-3067G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50287100 | |||||||
| chr14:50287109 | G | T | 62 | a0001c0001t0001g0020 a0001c0001t0001g0080 a0001c0001t0002g0185 others(59): Show |
64 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.541-3076C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50287109 | |||||||
| chr14:50287189 | T | C | 1 | a0003c0005t0014g0211 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.541-3156A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50287189 | |||||||
| chr14:50287274 | T | C | 222 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(219): Show |
226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.541-3241A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50287274 | |||||||
| chr14:50287532 | T | C | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.541-3499A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50287532 | |||||||
| chr14:50287636 | A | T | 1 | a0002c0002t0002g0249 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.541-3603T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50287636 | |||||||
| chr14:50287691 | C | CT | 44 | a0001c0001t0001g0021 a0001c0001t0001g0110 a0001c0001t0001g0117 others(41): Show |
44 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.541-3659dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50287691 | |||||||
| chr14:50287691 | CT | C | 10 | a0001c0001t0001g0163 a0001c0001t0009g0149 a0001c0001t0018g0011 others(7): Show |
10 | HG01928.hp1 HG02559.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.541-3659delA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50287691 | |||||||
| chr14:50287691 | CTT | C | 14 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(11): Show |
14 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.541-3660_541-3659d others(4): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50287691 | |||||||
| chr14:50287740 | C | T | 1 | a0002c0002t0002g0339 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.541-3707G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50287740 | |||||||
| chr14:50287963 | A | G | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(181): Show |
188 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.541-3930T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50287963 | |||||||
| chr14:50287992 | C | T | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(152): Show |
159 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.541-3959G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50287992 | |||||||
| chr14:50288251 | A | C | 12 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0046 others(9): Show |
12 | HG00323.hp2 HG00639.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.541-4218T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50288251 | |||||||
| chr14:50288370 | C | T | 12 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(9): Show |
12 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.541-4337G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50288370 | |||||||
| chr14:50288493 | C | T | 1 | a0001c0001t0003g0043 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.541-4460G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50288493 | |||||||
| chr14:50288644 | C | T | 29 | a0001c0004t0005g0200 a0002c0002t0005g0220 a0002c0002t0005g0221 others(26): Show |
29 | HG00099.hp1 HG01070.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.541-4611G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50288644 | |||||||
| chr14:50288656 | C | T | 2 | a0002c0002t0005g0227 a0002c0002t0068g0230 |
2 | HG02723.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.541-4623G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50288656 | |||||||
| chr14:50288668 | T | C | 12 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0046 others(9): Show |
12 | HG00323.hp2 HG00639.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.541-4635A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50288668 | |||||||
| chr14:50288683 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.541-4650C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50288683 | |||||||
| chr14:50288851 | A | C | 2 | a0001c0001t0031g0186 a0001c0001t0031g0187 |
2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.541-4818T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50288851 | |||||||
| chr14:50288942 | C | G | 1 | a0001c0001t0013g0033 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.541-4909G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50288942 | |||||||
| chr14:50288953 | C | T | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(193): Show |
200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.541-4920G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50288953 | |||||||
| chr14:50288985 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.541-4952C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50288985 | |||||||
| chr14:50288988 | A | G | 1 | a0001c0001t0006g0096 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.541-4955T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50288988 | |||||||
| chr14:50288992 | A | T | 1 | a0001c0001t0057g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.541-4959T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50288992 | |||||||
| chr14:50289005 | T | C | 7 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(4): Show |
7 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.541-4972A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289005 | |||||||
| chr14:50289008 | A | G | 1 | a0001c0001t0002g0185 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.541-4975T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289008 | |||||||
| chr14:50289106 | T | C | 1 | a0001c0001t0001g0115 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.540+5009A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289106 | |||||||
| chr14:50289139 | A | G | 7 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(4): Show |
7 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+4976T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289139 | |||||||
| chr14:50289194 | T | C | 1 | a0001c0001t0003g0073 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.540+4921A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289194 | |||||||
| chr14:50289273 | C | T | 222 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(219): Show |
226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.540+4842G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289273 | |||||||
| chr14:50289302 | T | C | 12 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(9): Show |
12 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.540+4813A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289302 | |||||||
| chr14:50289366 | C | G | 1 | a0001c0001t0018g0013 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.540+4749G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289366 | |||||||
| chr14:50289371 | C | T | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(215): Show |
222 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.540+4744G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289371 | |||||||
| chr14:50289405 | A | G | 2 | a0001c0001t0070g0189 a0001c0001t0071g0188 |
2 | HG01261.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.540+4710T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289405 | |||||||
| chr14:50289437 | C | T | 1 | a0002c0002t0002g0295 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.540+4678G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289437 | |||||||
| chr14:50289488 | G | C | 1 | a0001c0001t0029g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.540+4627C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289488 | |||||||
| chr14:50289490 | T | C | 11 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0114 others(8): Show |
12 | HG00408.hp1 HG04204.hp2 NA18951.hp2 others(9): Show |
intron_variant | MODIFIER | c.540+4625A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289490 | |||||||
| chr14:50289527 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.540+4588G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289527 | |||||||
| chr14:50289577 | G | C | 5 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(2): Show |
5 | HG01934.hp1 HG02074.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+4538C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289577 | |||||||
| chr14:50289667 | T | C | 7 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(4): Show |
7 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+4448A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289667 | |||||||
| chr14:50289678 | A | T | 7 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0046 others(4): Show |
7 | HG00323.hp2 HG00639.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+4437T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289678 | |||||||
| chr14:50289976 | C | A | 3 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0017g0206 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.540+4139G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289976 | |||||||
| chr14:50289994 | A | G | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.540+4121T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50289994 | |||||||
| chr14:50290037 | G | A | 6 | a0001c0001t0031g0186 a0001c0001t0031g0187 a0001c0001t0038g0198 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+4078C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50290037 | |||||||
| chr14:50290092 | T | C | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.540+4023A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50290092 | |||||||
| chr14:50290268 | T | TA | 13 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(10): Show |
13 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.540+3846dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50290268 | |||||||
| chr14:50290334 | A | G | 2 | a0001c0001t0006g0092 a0001c0001t0006g0094 |
2 | HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.540+3781T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50290334 | |||||||
| chr14:50290377 | C | T | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(180): Show |
187 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.540+3738G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50290377 | |||||||
| chr14:50290413 | A | C | 222 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(219): Show |
226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.540+3702T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50290413 | |||||||
| chr14:50290548 | G | T | 1 | a0001c0001t0001g0024 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.540+3567C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50290548 | |||||||
| chr14:50290584 | G | A | 1 | a0002c0002t0002g0307 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.540+3531C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50290584 | |||||||
| chr14:50290759 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.540+3356C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50290759 | |||||||
| chr14:50290812 | C | T | 1 | a0001c0001t0013g0035 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.540+3303G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50290812 | |||||||
| chr14:50290813 | G | A | 7 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(4): Show |
7 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+3302C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50290813 | |||||||
| chr14:50290817 | C | T | 1 | a0001c0001t0003g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.540+3298G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50290817 | |||||||
| chr14:50290866 | T | C | 1 | a0002c0002t0002g0331 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.540+3249A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50290866 | |||||||
| chr14:50290868 | T | G | 2 | a0001c0001t0021g0183 a0001c0001t0021g0184 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.540+3247A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50290868 | |||||||
| chr14:50290876 | A | AT | 13 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(10): Show |
13 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.540+3238dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50290876 | |||||||
| chr14:50291064 | G | A | 1 | a0002c0002t0002g0317 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.540+3051C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291064 | |||||||
| chr14:50291087 | A | G | 5 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(2): Show |
5 | HG01934.hp1 HG02074.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+3028T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291087 | |||||||
| chr14:50291119 | C | T | 4 | a0001c0001t0013g0032 a0001c0001t0013g0033 a0001c0001t0013g0035 others(1): Show |
4 | HG02965.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+2996G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291119 | |||||||
| chr14:50291130 | G | A | 12 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0001g0252 others(9): Show |
12 | HG01358.hp2 HG01934.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.540+2985C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291130 | |||||||
| chr14:50291187 | G | T | 1 | a0001c0001t0057g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.540+2928C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291187 | |||||||
| chr14:50291190 | T | C | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.540+2925A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291190 | |||||||
| chr14:50291197 | C | CA | 86 | a0001c0001t0001g0003 a0001c0001t0001g0020 a0001c0001t0001g0026 others(83): Show |
87 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.540+2917dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291197 | |||||||
| chr14:50291197 | C | CAA | 13 | a0001c0001t0001g0021 a0001c0001t0003g0104 a0001c0001t0007g0102 others(10): Show |
13 | HG00621.hp1 HG02071.hp1 HG03453.hp2 others(10): Show |
intron_variant | MODIFIER | c.540+2916_540+2917d others(4): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291197 | |||||||
| chr14:50291197 | CA | C | 34 | a0001c0001t0014g0107 a0001c0001t0034g0066 a0002c0002t0005g0220 others(31): Show |
35 | HG00099.hp1 HG00140.hp1 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.540+2917delT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291197 | |||||||
| chr14:50291197 | CAA | C | 18 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(15): Show |
18 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.540+2916_540+2917d others(4): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291197 | |||||||
| chr14:50291197 | CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(4): Show |
7 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+2909_540+2917d others(11): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291197 | |||||||
| chr14:50291197 | CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+2908_540+2917d others(12): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291197 | |||||||
| chr14:50291197 | CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0002c0003t0001g0353 |
3 | HG00099.hp2 HG01891.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.540+2906_540+2917d others(14): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291197 | |||||||
| chr14:50291211 | A | C | 1 | a0001c0001t0020g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.540+2904T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291211 | |||||||
| chr14:50291224 | AC | A | 9 | a0001c0001t0003g0044 a0001c0001t0003g0046 a0001c0001t0003g0047 others(6): Show |
9 | HG00323.hp2 HG00639.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.540+2890delG | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291224 | |||||||
| chr14:50291225 | C | A | 6 | a0001c0001t0003g0043 a0001c0001t0007g0017 a0001c0001t0044g0014 others(3): Show |
6 | HG00323.hp1 HG01109.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+2890G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291225 | |||||||
| chr14:50291229 | C | A | 1 | a0001c0001t0054g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.540+2886G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291229 | |||||||
| chr14:50291257 | A | T | 5 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(2): Show |
5 | HG01934.hp1 HG02074.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.540+2858T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291257 | |||||||
| chr14:50291424 | T | G | 3 | a0002c0003t0001g0254 a0002c0003t0001g0255 a0002c0003t0002g0253 |
3 | HG01934.hp1 HG02074.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.540+2691A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291424 | |||||||
| chr14:50291482 | A | G | 1 | a0002c0002t0002g0296 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.540+2633T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291482 | |||||||
| chr14:50291489 | T | C | 1 | a0001c0001t0069g0056 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.540+2626A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291489 | |||||||
| chr14:50291500 | G | A | 3 | a0001c0001t0018g0011 a0001c0001t0018g0012 a0001c0001t0018g0013 |
3 | HG02559.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.540+2615C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291500 | |||||||
| chr14:50291501 | A | G | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+2614T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291501 | |||||||
| chr14:50291535 | G | A | 13 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(10): Show |
13 | HG01891.hp1 HG02451.hp2 HG02723.hp1 others(10): Show |
intron_variant | MODIFIER | c.540+2580C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291535 | |||||||
| chr14:50291606 | G | A | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.540+2509C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291606 | |||||||
| chr14:50291847 | T | C | 29 | a0001c0004t0005g0200 a0002c0002t0005g0220 a0002c0002t0005g0221 others(26): Show |
29 | HG00099.hp1 HG01070.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.540+2268A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50291847 | |||||||
| chr14:50292098 | AAATAT | A | 15 | a0002c0002t0005g0233 a0002c0002t0005g0235 a0002c0002t0005g0237 others(12): Show |
15 | HG00099.hp1 HG01070.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.540+2012_540+2016d others(7): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50292098 | |||||||
| chr14:50292292 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.540+1823A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50292292 | |||||||
| chr14:50292405 | T | G | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.540+1710A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50292405 | |||||||
| chr14:50292438 | C | T | 3 | a0001c0001t0012g0119 a0001c0001t0012g0120 a0001c0001t0012g0121 |
3 | NA18964.hp2 NA19065.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.540+1677G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50292438 | |||||||
| chr14:50292445 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.540+1670C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50292445 | |||||||
| chr14:50292485 | T | C | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(154): Show |
161 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.540+1630A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50292485 | |||||||
| chr14:50292523 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.540+1592C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50292523 | |||||||
| chr14:50292543 | C | T | 6 | a0001c0001t0031g0186 a0001c0001t0031g0187 a0001c0001t0038g0198 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+1572G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50292543 | |||||||
| chr14:50292598 | C | T | 1 | a0001c0001t0007g0065 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.540+1517G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50292598 | |||||||
| chr14:50292635 | G | A | 22 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(19): Show |
22 | HG01261.hp1 HG01891.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.540+1480C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50292635 | |||||||
| chr14:50292667 | T | C | 4 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(1): Show |
4 | HG01934.hp1 HG02074.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+1448A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50292667 | |||||||
| chr14:50292745 | T | C | 22 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(19): Show |
22 | HG01261.hp1 HG01891.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.540+1370A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50292745 | |||||||
| chr14:50292785 | C | T | 1 | a0002c0002t0004g0217 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.540+1330G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50292785 | |||||||
| chr14:50292798 | T | A | 1 | a0001c0001t0030g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.540+1317A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50292798 | |||||||
| chr14:50292798 | T | C | 1 | a0001c0001t0001g0128 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.540+1317A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50292798 | |||||||
| chr14:50292884 | C | CA | 16 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(13): Show |
16 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.540+1230dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50292884 | |||||||
| chr14:50292884 | C | CAA | 7 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(4): Show |
7 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+1229_540+1230d others(4): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50292884 | |||||||
| chr14:50292960 | A | G | 222 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(219): Show |
226 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.540+1155T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50292960 | |||||||
| chr14:50293149 | T | C | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.540+966A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50293149 | |||||||
| chr14:50293209 | T | C | 2 | a0001c0001t0070g0189 a0001c0001t0071g0188 |
2 | HG01261.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.540+906A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50293209 | |||||||
| chr14:50293311 | C | A | 5 | a0001c0001t0031g0186 a0001c0001t0031g0187 a0001c0001t0038g0198 others(2): Show |
5 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.540+804G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50293311 | |||||||
| chr14:50293312 | C | T | 62 | a0001c0001t0001g0020 a0001c0001t0001g0080 a0001c0001t0001g0086 others(59): Show |
64 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.540+803G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50293312 | |||||||
| chr14:50293340 | T | A | 4 | a0001c0001t0013g0032 a0001c0001t0013g0033 a0001c0001t0013g0035 others(1): Show |
4 | HG02965.hp1 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.540+775A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50293340 | |||||||
| chr14:50293533 | A | T | 29 | a0001c0004t0005g0200 a0002c0002t0005g0220 a0002c0002t0005g0221 others(26): Show |
29 | HG00099.hp1 HG01070.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.540+582T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50293533 | |||||||
| chr14:50293578 | T | C | 1 | a0002c0002t0005g0241 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.540+537A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50293578 | |||||||
| chr14:50293664 | C | A | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.540+451G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50293664 | |||||||
| chr14:50293666 | G | A | 7 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(4): Show |
7 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+449C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50293666 | |||||||
| chr14:50293672 | C | T | 2 | a0001c0001t0031g0186 a0001c0001t0031g0187 |
2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.540+443G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50293672 | |||||||
| chr14:50293726 | G | A | 1 | a0001c0001t0006g0096 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.540+389C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50293726 | |||||||
| chr14:50293748 | T | C | 7 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(4): Show |
7 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+367A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50293748 | |||||||
| chr14:50293804 | T | C | 3 | a0002c0002t0005g0220 a0002c0002t0005g0221 a0002c0002t0005g0222 |
3 | HG03098.hp1 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.540+311A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50293804 | |||||||
| chr14:50293919 | T | C | 1 | a0002c0002t0005g0241 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.540+196A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50293919 | |||||||
| chr14:50294006 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.540+109C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50294006 | |||||||
| chr14:50294370 | T | C | 8 | a0001c0001t0006g0034 a0001c0001t0013g0016 a0001c0001t0013g0032 others(5): Show |
8 | HG02615.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.409-124A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50294370 | |||||||
| chr14:50294491 | A | G | 1 | a0002c0003t0053g0347 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.409-245T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50294491 | |||||||
| chr14:50294518 | A | G | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.409-272T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50294518 | |||||||
| chr14:50294661 | A | C | 2 | a0002c0003t0050g0346 a0002c0003t0053g0347 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.409-415T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50294661 | |||||||
| chr14:50294674 | G | A | 4 | a0002c0003t0001g0257 a0002c0003t0001g0259 a0002c0003t0009g0258 others(1): Show |
4 | NA18747.hp1 NA18947.hp1 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-428C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50294674 | |||||||
| chr14:50294945 | A | C | 3 | a0001c0001t0018g0011 a0001c0001t0018g0012 a0001c0001t0018g0013 |
3 | HG02559.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.409-699T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50294945 | |||||||
| chr14:50295129 | G | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(196): Show |
203 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.409-883C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50295129 | |||||||
| chr14:50295294 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.409-1048C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50295294 | |||||||
| chr14:50295500 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.409-1254C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50295500 | |||||||
| chr14:50295553 | T | C | 13 | a0002c0002t0004g0216 a0002c0002t0004g0217 a0002c0002t0004g0218 others(10): Show |
13 | HG00597.hp1 HG00609.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.409-1307A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50295553 | |||||||
| chr14:50295572 | A | AT | 48 | a0001c0001t0001g0022 a0001c0001t0001g0110 a0001c0001t0001g0118 others(45): Show |
48 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.409-1327dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50295572 | |||||||
| chr14:50295572 | AT | A | 27 | a0001c0001t0001g0177 a0001c0001t0001g0195 a0001c0001t0001g0197 others(24): Show |
27 | HG00597.hp2 HG00733.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.409-1327delA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50295572 | |||||||
| chr14:50295620 | C | T | 1 | a0001c0001t0013g0016 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.409-1374G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50295620 | |||||||
| chr14:50295745 | CT | C | 25 | a0001c0001t0001g0134 a0001c0001t0001g0163 a0001c0001t0003g0058 others(22): Show |
25 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(22): Show |
intron_variant | MODIFIER | c.409-1500delA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50295745 | |||||||
| chr14:50295814 | C | T | 1 | a0002c0003t0050g0346 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.409-1568G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50295814 | |||||||
| chr14:50295827 | G | A | 1 | a0001c0001t0003g0075 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.409-1581C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50295827 | |||||||
| chr14:50295983 | T | C | 253 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(250): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.409-1737A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50295983 | |||||||
| chr14:50295985 | C | G | 4 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 others(1): Show |
4 | HG02698.hp2 HG03490.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.409-1739G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50295985 | |||||||
| chr14:50296109 | T | A | 3 | a0002c0002t0005g0220 a0002c0002t0005g0221 a0002c0002t0005g0222 |
3 | HG03098.hp1 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.409-1863A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50296109 | |||||||
| chr14:50296111 | C | T | 1 | a0001c0001t0027g0076 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.409-1865G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50296111 | |||||||
| chr14:50296140 | G | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0114 others(3): Show |
7 | HG00408.hp1 NA19012.hp1 NA19062.hp1 others(4): Show |
intron_variant | MODIFIER | c.409-1894C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50296140 | |||||||
| chr14:50296372 | C | CA | 187 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0020 others(184): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.409-2127dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50296372 | |||||||
| chr14:50296372 | C | CAA | 51 | a0001c0001t0001g0003 a0001c0001t0001g0080 a0001c0001t0001g0117 others(48): Show |
52 | HG00733.hp1 HG01106.hp2 HG01175.hp1 others(49): Show |
intron_variant | MODIFIER | c.409-2128_409-2127d others(4): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50296372 | |||||||
| chr14:50296372 | C | CAAA | 10 | a0001c0001t0014g0097 a0001c0001t0014g0107 a0001c0001t0018g0013 others(7): Show |
10 | HG01358.hp2 HG02559.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.409-2129_409-2127d others(5): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50296372 | |||||||
| chr14:50296372 | CAAAAAAA | C | 7 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(4): Show |
7 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.409-2133_409-2127d others(9): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50296372 | |||||||
| chr14:50296477 | C | T | 1 | a0002c0003t0001g0353 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.409-2231G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50296477 | |||||||
| chr14:50296593 | TA | T | 55 | a0001c0001t0001g0195 a0001c0001t0003g0043 a0001c0001t0003g0044 others(52): Show |
55 | HG00639.hp1 HG00733.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.409-2348delT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50296593 | |||||||
| chr14:50297076 | T | C | 1 | a0003c0005t0006g0214 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.409-2830A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50297076 | |||||||
| chr14:50297130 | G | T | 1 | a0001c0001t0012g0119 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.409-2884C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50297130 | |||||||
| chr14:50297371 | G | GAC | 182 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(179): Show |
186 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.409-3127_409-3126d others(4): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50297371 | |||||||
| chr14:50297389 | C | CA | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.409-3144dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50297389 | |||||||
| chr14:50297552 | C | T | 2 | a0002c0002t0002g0293 a0002c0002t0002g0294 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.409-3306G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50297552 | |||||||
| chr14:50297612 | A | G | 1 | a0001c0001t0057g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.409-3366T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50297612 | |||||||
| chr14:50297636 | G | C | 3 | a0002c0002t0005g0220 a0002c0002t0005g0221 a0002c0002t0005g0222 |
3 | HG03098.hp1 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.409-3390C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50297636 | |||||||
| chr14:50297697 | A | T | 2 | a0001c0001t0070g0189 a0001c0001t0071g0188 |
2 | HG01261.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.409-3451T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50297697 | |||||||
| chr14:50297818 | C | A | 3 | a0002c0002t0001g0335 a0002c0002t0001g0336 a0002c0002t0001g0337 |
3 | NA18952.hp2 NA19011.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.409-3572G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50297818 | |||||||
| chr14:50297934 | C | CAA | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.409-3690_409-3689d others(4): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50297934 | |||||||
| chr14:50297934 | CA | C | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(191): Show |
198 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.409-3689delT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50297934 | |||||||
| chr14:50297959 | C | A | 3 | a0002c0002t0001g0335 a0002c0002t0001g0336 a0002c0002t0001g0337 |
3 | NA18952.hp2 NA19011.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.409-3713G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50297959 | |||||||
| chr14:50298157 | T | C | 1 | a0002c0002t0002g0287 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.408+3860A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50298157 | |||||||
| chr14:50298215 | G | A | 3 | a0001c0001t0018g0011 a0001c0001t0018g0012 a0001c0001t0018g0013 |
3 | HG02559.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.408+3802C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50298215 | |||||||
| chr14:50298241 | C | CA | 8 | a0001c0001t0001g0086 a0001c0001t0031g0186 a0001c0001t0031g0187 others(5): Show |
8 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.408+3775dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50298241 | |||||||
| chr14:50298379 | G | C | 16 | a0002c0002t0001g0335 a0002c0002t0001g0336 a0002c0002t0001g0337 others(13): Show |
18 | HG00423.hp2 HG01993.hp1 HG02165.hp1 others(15): Show |
intron_variant | MODIFIER | c.408+3638C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50298379 | |||||||
| chr14:50298489 | A | G | 1 | a0001c0001t0019g0057 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.408+3528T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50298489 | |||||||
| chr14:50298493 | T | G | 22 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(19): Show |
22 | HG01261.hp1 HG01891.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.408+3524A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50298493 | |||||||
| chr14:50298595 | C | T | 4 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0134 others(1): Show |
4 | NA18951.hp2 NA18993.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+3422G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50298595 | |||||||
| chr14:50298733 | T | C | 7 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(4): Show |
7 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.408+3284A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50298733 | |||||||
| chr14:50298784 | A | T | 2 | a0002c0003t0050g0346 a0002c0003t0053g0347 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.408+3233T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50298784 | |||||||
| chr14:50299040 | G | A | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(181): Show |
188 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.408+2977C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50299040 | |||||||
| chr14:50299087 | A | G | 1 | a0001c0001t0054g0018 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.408+2930T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50299087 | |||||||
| chr14:50299206 | A | G | 12 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0046 others(9): Show |
12 | HG00323.hp2 HG00639.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.408+2811T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50299206 | |||||||
| chr14:50299271 | C | T | 1 | a0001c0001t0069g0056 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.408+2746G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50299271 | |||||||
| chr14:50299311 | A | G | 29 | a0001c0004t0005g0200 a0002c0002t0005g0220 a0002c0002t0005g0221 others(26): Show |
29 | HG00099.hp1 HG01070.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.408+2706T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50299311 | |||||||
| chr14:50299532 | A | G | 1 | a0001c0001t0001g0172 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.408+2485T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50299532 | |||||||
| chr14:50299921 | G | A | 1 | a0001c0001t0013g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.408+2096C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50299921 | |||||||
| chr14:50300170 | A | T | 1 | a0001c0001t0003g0019 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.408+1847T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50300170 | |||||||
| chr14:50300225 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.408+1792A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50300225 | |||||||
| chr14:50300456 | G | A | 1 | a0001c0001t0030g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.408+1561C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50300456 | |||||||
| chr14:50300514 | C | T | 1 | a0001c0001t0002g0185 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.408+1503G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50300514 | |||||||
| chr14:50300787 | C | T | 7 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(4): Show |
7 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.408+1230G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50300787 | |||||||
| chr14:50300831 | T | C | 8 | a0001c0001t0006g0034 a0001c0001t0013g0016 a0001c0001t0013g0032 others(5): Show |
8 | HG02615.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.408+1186A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50300831 | |||||||
| chr14:50300893 | T | C | 2 | a0001c0001t0070g0189 a0001c0001t0071g0188 |
2 | HG01261.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.408+1124A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50300893 | |||||||
| chr14:50301005 | T | G | 1 | a0002c0002t0002g0338 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.408+1012A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50301005 | |||||||
| chr14:50301034 | C | T | 7 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(4): Show |
7 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.408+983G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50301034 | |||||||
| chr14:50301035 | G | A | 1 | a0001c0001t0012g0129 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.408+982C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50301035 | |||||||
| chr14:50301096 | C | G | 7 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(4): Show |
7 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.408+921G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50301096 | |||||||
| chr14:50301156 | G | A | 7 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(4): Show |
7 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.408+861C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50301156 | |||||||
| chr14:50301246 | T | C | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.408+771A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50301246 | |||||||
| chr14:50301410 | TG | T | 5 | a0001c0001t0021g0183 a0001c0001t0021g0184 a0002c0003t0021g0351 others(2): Show |
5 | HG01358.hp2 HG02647.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.408+606delC | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50301410 | |||||||
| chr14:50301501 | G | A | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.408+516C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50301501 | |||||||
| chr14:50301672 | A | G | 14 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(11): Show |
14 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.408+345T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50301672 | |||||||
| chr14:50301765 | A | G | 220 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(217): Show |
224 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.408+252T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50301765 | |||||||
| chr14:50301870 | C | T | 3 | a0001c0001t0018g0011 a0001c0001t0018g0012 a0001c0001t0018g0013 |
3 | HG02559.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.408+147G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50301870 | |||||||
| chr14:50301981 | T | C | 4 | a0002c0002t0002g0261 a0002c0002t0002g0339 a0002c0002t0002g0341 others(1): Show |
4 | HG00741.hp1 HG01106.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.408+36A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50301981 | |||||||
| chr14:50302609 | A | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(216): Show |
223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.256+293T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 2/9 | chr14 | 50302609 | |||||||
| chr14:50302638 | C | T | 5 | a0001c0001t0031g0186 a0001c0001t0031g0187 a0001c0001t0038g0198 others(2): Show |
5 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.256+264G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 2/9 | chr14 | 50302638 | |||||||
| chr14:50302667 | C | T | 12 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0046 others(9): Show |
12 | HG00323.hp2 HG00639.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.256+235G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 2/9 | chr14 | 50302667 | |||||||
| chr14:50302733 | A | T | 1 | a0001c0001t0020g0048 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.256+169T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 2/9 | chr14 | 50302733 | |||||||
| chr14:50302737 | G | T | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(215): Show |
222 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.256+165C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 2/9 | chr14 | 50302737 | |||||||
| chr14:50302800 | A | G | 2 | a0001c0001t0070g0189 a0001c0001t0071g0188 |
2 | HG01261.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.256+102T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 2/9 | chr14 | 50302800 | |||||||
| chr14:50303141 | C | T | 8 | a0002c0002t0004g0272 a0002c0003t0001g0252 a0002c0003t0001g0254 others(5): Show |
8 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.141-124G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303141 | |||||||
| chr14:50303150 | G | A | 165 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(162): Show |
169 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.141-133C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303150 | |||||||
| chr14:50303183 | A | G | 219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(216): Show |
223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.141-166T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303183 | |||||||
| chr14:50303205 | C | T | 1 | a0001c0001t0030g0209 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.141-188G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303205 | |||||||
| chr14:50303290 | C | T | 3 | a0002c0002t0024g0290 a0002c0002t0024g0291 a0002c0002t0024g0292 |
3 | HG01069.hp1 HG01071.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.141-273G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303290 | |||||||
| chr14:50303297 | C | T | 186 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(183): Show |
190 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(187): Show |
intron_variant | MODIFIER | c.141-280G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303297 | |||||||
| chr14:50303325 | G | A | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0002c0003t0001g0353 |
3 | HG00099.hp2 HG01891.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.141-308C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303325 | |||||||
| chr14:50303412 | C | T | 3 | a0002c0003t0021g0351 a0002c0003t0028g0349 a0002c0003t0028g0350 |
3 | HG01358.hp2 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.141-395G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303412 | |||||||
| chr14:50303459 | T | TA | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(212): Show |
219 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.141-443dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303459 | |||||||
| chr14:50303555 | T | A | 8 | a0001c0001t0006g0034 a0001c0001t0013g0016 a0001c0001t0013g0032 others(5): Show |
8 | HG02615.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.141-538A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303555 | |||||||
| chr14:50303685 | G | C | 1 | a0003c0005t0006g0213 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.141-668C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303685 | |||||||
| chr14:50303781 | C | CA | 25 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0003g0176 others(22): Show |
25 | HG01261.hp1 HG01891.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.141-765dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303781 | |||||||
| chr14:50303803 | G | T | 219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(216): Show |
223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.141-786C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303803 | |||||||
| chr14:50303810 | T | TA | 204 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(201): Show |
208 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.141-794dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303810 | |||||||
| chr14:50303810 | T | TAA | 20 | a0001c0001t0001g0117 a0001c0001t0001g0179 a0001c0001t0001g0180 others(17): Show |
20 | HG00099.hp2 HG01106.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.141-795_141-794dup others(2): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303810 | |||||||
| chr14:50303844 | G | A | 5 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0005g0090 others(2): Show |
5 | HG02572.hp2 HG02615.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.141-827C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303844 | |||||||
| chr14:50303930 | C | A | 3 | a0002c0003t0021g0351 a0002c0003t0028g0349 a0002c0003t0028g0350 |
3 | HG01358.hp2 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.141-913G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303930 | |||||||
| chr14:50304102 | T | A | 3 | a0001c0001t0001g0172 a0001c0001t0009g0173 a0001c0001t0060g0174 |
3 | HG02132.hp2 HG02155.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.141-1085A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50304102 | |||||||
| chr14:50304116 | C | G | 3 | a0002c0002t0004g0269 a0002c0002t0004g0270 a0002c0002t0004g0271 |
3 | HG01109.hp2 HG03688.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.141-1099G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50304116 | |||||||
| chr14:50304267 | G | A | 15 | a0001c0001t0006g0092 a0001c0001t0006g0093 a0001c0001t0006g0094 others(12): Show |
15 | HG01261.hp1 HG01891.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.141-1250C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50304267 | |||||||
| chr14:50304449 | C | T | 3 | a0001c0001t0012g0119 a0001c0001t0012g0120 a0001c0001t0012g0121 |
3 | NA18964.hp2 NA19065.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.141-1432G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50304449 | |||||||
| chr14:50304488 | A | T | 1 | a0002c0002t0005g0244 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.141-1471T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50304488 | |||||||
| chr14:50304574 | G | A | 1 | a0002c0002t0016g0264 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.141-1557C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50304574 | |||||||
| chr14:50304728 | G | T | 1 | a0002c0002t0004g0268 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.141-1711C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50304728 | |||||||
| chr14:50304884 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.141-1867G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50304884 | |||||||
| chr14:50304995 | G | T | 1 | a0001c0001t0013g0032 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.141-1978C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50304995 | |||||||
| chr14:50305072 | C | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0021 a0001c0001t0001g0114 others(3): Show |
7 | HG00408.hp1 NA19012.hp1 NA19062.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-2055G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50305072 | |||||||
| chr14:50305158 | T | C | 1 | a0001c0001t0008g0105 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.141-2141A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50305158 | |||||||
| chr14:50305164 | G | C | 1 | a0001c0001t0004g0203 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.141-2147C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50305164 | |||||||
| chr14:50305169 | T | C | 3 | a0002c0003t0021g0351 a0002c0003t0028g0349 a0002c0003t0028g0350 |
3 | HG01358.hp2 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.141-2152A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50305169 | |||||||
| chr14:50305314 | G | A | 2 | a0002c0003t0050g0346 a0002c0003t0053g0347 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.141-2297C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50305314 | |||||||
| chr14:50305409 | A | C | 1 | a0002c0002t0002g0289 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.141-2392T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50305409 | |||||||
| chr14:50305470 | A | G | 3 | a0001c0001t0018g0011 a0001c0001t0018g0012 a0001c0001t0018g0013 |
3 | HG02559.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.141-2453T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50305470 | |||||||
| chr14:50305535 | T | C | 1 | a0001c0001t0057g0029 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.141-2518A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50305535 | |||||||
| chr14:50305629 | G | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02615.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.141-2612C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50305629 | |||||||
| chr14:50305658 | C | T | 7 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(4): Show |
7 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-2641G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50305658 | |||||||
| chr14:50305685 | C | T | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(215): Show |
222 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.141-2668G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50305685 | |||||||
| chr14:50305690 | A | T | 1 | a0002c0002t0067g0219 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.141-2673T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50305690 | |||||||
| chr14:50305816 | T | C | 1 | a0001c0001t0008g0098 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.141-2799A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50305816 | |||||||
| chr14:50305851 | AC | A | 7 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(4): Show |
7 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-2835delG | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50305851 | |||||||
| chr14:50305884 | G | A | 2 | a0001c0001t0021g0183 a0001c0001t0021g0184 |
2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.141-2867C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50305884 | |||||||
| chr14:50306016 | C | T | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(192): Show |
199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.141-2999G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306016 | |||||||
| chr14:50306049 | C | CT | 8 | a0001c0001t0057g0029 a0002c0002t0002g0288 a0002c0002t0004g0266 others(5): Show |
8 | HG00735.hp2 HG01358.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.141-3033dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306049 | |||||||
| chr14:50306049 | CT | C | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(182): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.141-3033delA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306049 | |||||||
| chr14:50306049 | CTT | C | 12 | a0001c0001t0003g0044 a0001c0001t0003g0046 a0001c0001t0003g0047 others(9): Show |
12 | HG00323.hp2 HG00639.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.141-3034_141-3033d others(4): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306049 | |||||||
| chr14:50306091 | G | A | 1 | a0001c0001t0018g0013 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.141-3074C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306091 | |||||||
| chr14:50306284 | C | T | 1 | a0001c0001t0007g0053 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.141-3267G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306284 | |||||||
| chr14:50306338 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.141-3321G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306338 | |||||||
| chr14:50306357 | T | G | 7 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(4): Show |
7 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-3340A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306357 | |||||||
| chr14:50306578 | T | G | 217 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(214): Show |
221 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(218): Show |
intron_variant | MODIFIER | c.141-3561A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306578 | |||||||
| chr14:50306585 | T | G | 8 | a0001c0001t0003g0052 a0001c0001t0003g0101 a0001c0001t0003g0104 others(5): Show |
8 | HG00597.hp2 HG00673.hp1 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.141-3568A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306585 | |||||||
| chr14:50306597 | G | A | 3 | a0001c0001t0006g0106 a0001c0001t0014g0107 a0001c0001t0014g0108 |
3 | HG01891.hp1 HG03041.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.141-3580C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306597 | |||||||
| chr14:50306600 | G | GT | 39 | a0001c0001t0018g0011 a0001c0001t0018g0012 a0001c0001t0018g0013 others(36): Show |
39 | HG00099.hp1 HG01074.hp1 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.141-3584dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306600 | |||||||
| chr14:50306600 | GT | G | 183 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(180): Show |
187 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.141-3584delA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306600 | |||||||
| chr14:50306600 | GTT | G | 6 | a0001c0001t0003g0109 a0001c0001t0020g0031 a0001c0001t0020g0037 others(3): Show |
6 | HG02145.hp2 HG02451.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.141-3585_141-3584d others(4): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306600 | |||||||
| chr14:50306709 | T | C | 5 | a0001c0001t0020g0031 a0001c0001t0020g0037 a0001c0001t0020g0048 others(2): Show |
5 | HG02145.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.141-3692A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306709 | |||||||
| chr14:50306821 | T | A | 91 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(88): Show |
93 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.141-3804A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306821 | |||||||
| chr14:50306822 | T | A | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(215): Show |
222 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.141-3805A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306822 | |||||||
| chr14:50306858 | T | C | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(215): Show |
222 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.141-3841A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306858 | |||||||
| chr14:50306868 | T | G | 2 | a0002c0002t0039g0286 a0002c0002t0039g0348 |
2 | HG02818.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.141-3851A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306868 | |||||||
| chr14:50307152 | T | G | 71 | a0001c0004t0002g0039 a0001c0004t0002g0040 a0001c0004t0002g0041 others(68): Show |
73 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.141-4135A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50307152 | |||||||
| chr14:50307163 | G | C | 1 | a0002c0009t0066g0256 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.141-4146C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50307163 | |||||||
| chr14:50307304 | G | A | 2 | a0001c0001t0017g0205 a0001c0001t0017g0206 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.141-4287C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50307304 | |||||||
| chr14:50307312 | C | T | 4 | a0002c0002t0004g0263 a0002c0002t0016g0262 a0002c0002t0016g0264 others(1): Show |
4 | HG02071.hp1 NA18971.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-4295G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50307312 | |||||||
| chr14:50307340 | A | G | 1 | a0002c0002t0002g0261 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.141-4323T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50307340 | |||||||
| chr14:50307786 | G | C | 7 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(4): Show |
7 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.140+4225C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50307786 | |||||||
| chr14:50308007 | T | C | 3 | a0001c0001t0018g0011 a0001c0001t0018g0012 a0001c0001t0018g0013 |
3 | HG02559.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.140+4004A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50308007 | |||||||
| chr14:50308113 | G | A | 7 | a0002c0003t0001g0252 a0002c0003t0001g0254 a0002c0003t0001g0255 others(4): Show |
7 | HG01934.hp1 HG02074.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.140+3898C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50308113 | |||||||
| chr14:50308128 | C | T | 2 | a0002c0003t0050g0346 a0002c0003t0053g0347 |
2 | HG02280.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.140+3883G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50308128 | |||||||
| chr14:50308147 | T | G | 1 | a0002c0002t0002g0342 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.140+3864A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50308147 | |||||||
| chr14:50308259 | G | A | 1 | a0002c0002t0016g0343 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.140+3752C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50308259 | |||||||
| chr14:50308327 | C | T | 1 | a0001c0001t0058g0051 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.140+3684G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50308327 | |||||||
| chr14:50308336 | G | A | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0002c0003t0001g0353 |
3 | HG00099.hp2 HG01891.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.140+3675C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50308336 | |||||||
| chr14:50308388 | G | GA | 30 | a0001c0004t0005g0200 a0002c0002t0005g0220 a0002c0002t0005g0221 others(27): Show |
30 | HG00099.hp1 HG01070.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.140+3622dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50308388 | |||||||
| chr14:50308388 | GAA | G | 24 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(21): Show |
24 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.140+3621_140+3622d others(4): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50308388 | |||||||
| chr14:50308388 | GAAA | G | 20 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0003g0043 others(17): Show |
20 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.140+3620_140+3622d others(5): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50308388 | |||||||
| chr14:50308388 | GAAAA | G | 170 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(167): Show |
174 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.140+3619_140+3622d others(6): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50308388 | |||||||
| chr14:50308528 | G | T | 3 | a0001c0001t0018g0011 a0001c0001t0018g0012 a0001c0001t0018g0013 |
3 | HG02559.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.140+3483C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50308528 | |||||||
| chr14:50308566 | G | A | 1 | a0002c0002t0002g0344 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.140+3445C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50308566 | |||||||
| chr14:50308601 | C | A | 219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(216): Show |
223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.140+3410G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50308601 | |||||||
| chr14:50308658 | G | T | 3 | a0002c0003t0021g0351 a0002c0003t0028g0349 a0002c0003t0028g0350 |
3 | HG01358.hp2 HG02647.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.140+3353C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50308658 | |||||||
| chr14:50308758 | G | A | 174 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(171): Show |
178 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.140+3253C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50308758 | |||||||
| chr14:50308829 | T | G | 1 | a0002c0002t0010g0345 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.140+3182A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50308829 | |||||||
| chr14:50308877 | G | A | 1 | a0003c0005t0006g0214 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.140+3134C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50308877 | |||||||
| chr14:50309022 | GTTTTGAG others(3): Show |
G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(192): Show |
199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.140+2979_140+2988d others(12): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50309022 | |||||||
| chr14:50309070 | T | C | 1 | a0001c0001t0013g0036 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.140+2941A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50309070 | |||||||
| chr14:50309108 | T | A | 1 | a0001c0001t0001g0178 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.140+2903A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50309108 | |||||||
| chr14:50309288 | T | G | 16 | a0001c0001t0070g0189 a0001c0001t0071g0188 a0002c0003t0001g0252 others(13): Show |
16 | HG01261.hp1 HG01358.hp2 HG01934.hp1 others(13): Show |
intron_variant | MODIFIER | c.140+2723A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50309288 | |||||||
| chr14:50309523 | C | T | 225 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(222): Show |
229 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(226): Show |
intron_variant | MODIFIER | c.140+2488G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50309523 | |||||||
| chr14:50309561 | T | TA | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(194): Show |
201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): Show |
intron_variant | MODIFIER | c.140+2449dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50309561 | |||||||
| chr14:50309561 | TA | T | 12 | a0001c0001t0031g0186 a0001c0001t0038g0198 a0001c0001t0038g0199 others(9): Show |
12 | HG01884.hp2 HG01934.hp1 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.140+2449delT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50309561 | |||||||
| chr14:50309580 | A | C | 8 | a0001c0001t0006g0034 a0001c0001t0013g0016 a0001c0001t0013g0032 others(5): Show |
8 | HG02615.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.140+2431T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50309580 | |||||||
| chr14:50309681 | T | C | 1 | a0002c0002t0036g0245 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.140+2330A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50309681 | |||||||
| chr14:50309688 | C | CT | 205 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(202): Show |
209 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.140+2322dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50309688 | |||||||
| chr14:50309734 | G | A | 3 | a0001c0001t0002g0185 a0001c0001t0029g0182 a0001c0001t0042g0181 |
3 | HG04115.hp1 HG04184.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.140+2277C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50309734 | |||||||
| chr14:50309815 | T | A | 3 | a0001c0001t0018g0011 a0001c0001t0018g0012 a0001c0001t0018g0013 |
3 | HG02559.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.140+2196A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50309815 | |||||||
| chr14:50309827 | A | G | 214 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(211): Show |
218 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.140+2184T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50309827 | |||||||
| chr14:50309869 | T | C | 6 | a0001c0001t0031g0186 a0001c0001t0031g0187 a0001c0001t0038g0198 others(3): Show |
6 | HG01884.hp2 HG02109.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.140+2142A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50309869 | |||||||
| chr14:50309966 | A | C | 2 | a0002c0002t0005g0223 a0002c0002t0005g0224 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.140+2045T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50309966 | |||||||
| chr14:50310146 | T | A | 6 | a0001c0001t0070g0189 a0001c0001t0071g0188 a0003c0005t0006g0212 others(3): Show |
6 | HG01261.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+1865A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50310146 | |||||||
| chr14:50310179 | T | G | 6 | a0001c0001t0070g0189 a0001c0001t0071g0188 a0003c0005t0006g0212 others(3): Show |
6 | HG01261.hp1 HG02809.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+1832A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50310179 | |||||||
| chr14:50310509 | C | G | 1 | a0001c0001t0020g0031 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.140+1502G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50310509 | |||||||
| chr14:50310706 | A | C | 3 | a0001c0001t0017g0204 a0001c0001t0017g0205 a0001c0001t0017g0206 |
3 | HG00733.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.140+1305T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50310706 | |||||||
| chr14:50310712 | T | C | 200 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(197): Show |
204 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(201): Show |
intron_variant | MODIFIER | c.140+1299A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50310712 | |||||||
| chr14:50310916 | T | G | 7 | a0001c0001t0001g0030 a0001c0001t0001g0191 a0001c0001t0001g0192 others(4): Show |
7 | HG01123.hp2 HG01934.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.140+1095A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50310916 | |||||||
| chr14:50310936 | C | CT | 6 | a0002c0002t0002g0247 a0002c0002t0002g0248 a0002c0002t0002g0249 others(3): Show |
6 | HG02129.hp1 HG02293.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+1074dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50310936 | |||||||
| chr14:50310936 | CT | C | 22 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(19): Show |
22 | HG00639.hp2 HG01074.hp2 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.140+1074delA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50310936 | |||||||
| chr14:50310936 | CTT | C | 182 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(179): Show |
186 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.140+1073_140+1074d others(4): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50310936 | |||||||
| chr14:50310936 | CTTT | C | 12 | a0001c0001t0001g0197 a0001c0001t0004g0202 a0001c0001t0004g0203 others(9): Show |
12 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.140+1072_140+1074d others(5): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50310936 | |||||||
| chr14:50310941 | T | C | 25 | a0001c0004t0005g0200 a0002c0002t0005g0223 a0002c0002t0005g0224 others(22): Show |
25 | HG00099.hp1 HG01070.hp2 HG01074.hp1 others(22): Show |
intron_variant | MODIFIER | c.140+1070A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50310941 | |||||||
| chr14:50310945 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.140+1066A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50310945 | |||||||
| chr14:50311302 | G | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+709C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311302 | |||||||
| chr14:50311306 | T | C | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+705A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311306 | |||||||
| chr14:50311308 | C | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+703G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311308 | |||||||
| chr14:50311315 | G | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+696C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311315 | |||||||
| chr14:50311316 | T | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+695A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311316 | |||||||
| chr14:50311317 | C | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+694G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311317 | |||||||
| chr14:50311319 | T | G | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+692A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311319 | |||||||
| chr14:50311322 | C | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+689G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311322 | |||||||
| chr14:50311324 | C | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+687G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311324 | |||||||
| chr14:50311333 | T | G | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+678A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311333 | |||||||
| chr14:50311334 | C | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+677G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311334 | |||||||
| chr14:50311335 | T | G | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+676A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311335 | |||||||
| chr14:50311336 | T | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+675A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311336 | |||||||
| chr14:50311338 | C | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+673G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311338 | |||||||
| chr14:50311339 | A | G | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+672T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311339 | |||||||
| chr14:50311340 | C | T | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+671G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311340 | |||||||
| chr14:50311341 | T | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+670A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311341 | |||||||
| chr14:50311345 | C | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+666G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311345 | |||||||
| chr14:50311346 | T | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+665A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311346 | |||||||
| chr14:50311351 | T | TGATTGAC others(15): Show |
1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+659_140+660ins others(22): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311351 | |||||||
| chr14:50311352 | C | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+659G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311352 | |||||||
| chr14:50311354 | C | T | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+657G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311354 | |||||||
| chr14:50311356 | C | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+655G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311356 | |||||||
| chr14:50311358 | C | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+653G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311358 | |||||||
| chr14:50311362 | T | G | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+649A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311362 | |||||||
| chr14:50311366 | C | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+645G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311366 | |||||||
| chr14:50311367 | C | G | 2 | a0001c0001t0004g0202 a0001c0001t0004g0203 |
2 | HG02647.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.140+644G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311367 | |||||||
| chr14:50311369 | C | G | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+642G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311369 | |||||||
| chr14:50311370 | C | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+641G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311370 | |||||||
| chr14:50311373 | C | T | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+638G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311373 | |||||||
| chr14:50311374 | T | C | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+637A>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311374 | |||||||
| chr14:50311375 | A | T | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+636T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311375 | |||||||
| chr14:50311377 | T | G | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+634A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311377 | |||||||
| chr14:50311378 | C | G | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+633G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311378 | |||||||
| chr14:50311381 | C | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+630G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311381 | |||||||
| chr14:50311382 | A | G | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+629T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311382 | |||||||
| chr14:50311386 | TAGCCAAA others(3): Show |
T | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+615_140+624del others(10): Show |
L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311386 | |||||||
| chr14:50311397 | T | G | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+614A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311397 | |||||||
| chr14:50311410 | C | T | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+601G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311410 | |||||||
| chr14:50311414 | C | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+597G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311414 | |||||||
| chr14:50311422 | A | C | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+589T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311422 | |||||||
| chr14:50311424 | A | T | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+587T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311424 | |||||||
| chr14:50311425 | C | G | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+586G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311425 | |||||||
| chr14:50311428 | T | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+583A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311428 | |||||||
| chr14:50311430 | T | G | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+581A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311430 | |||||||
| chr14:50311433 | T | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+578A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311433 | |||||||
| chr14:50311434 | C | T | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+577G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311434 | |||||||
| chr14:50311435 | T | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+576A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311435 | |||||||
| chr14:50311437 | C | T | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+574G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311437 | |||||||
| chr14:50311438 | A | T | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+573T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311438 | |||||||
| chr14:50311439 | G | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+572C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311439 | |||||||
| chr14:50311444 | C | T | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+567G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311444 | |||||||
| chr14:50311446 | G | C | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+565C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311446 | |||||||
| chr14:50311448 | G | T | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+563C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311448 | |||||||
| chr14:50311449 | A | G | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+562T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311449 | |||||||
| chr14:50311450 | A | T | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+561T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311450 | |||||||
| chr14:50311451 | A | C | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+560T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311451 | |||||||
| chr14:50311452 | G | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+559C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311452 | |||||||
| chr14:50311453 | A | T | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+558T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311453 | |||||||
| chr14:50311456 | A | T | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+555T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311456 | |||||||
| chr14:50311458 | G | C | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+553C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311458 | |||||||
| chr14:50311459 | G | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+552C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311459 | |||||||
| chr14:50311464 | G | T | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+547C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311464 | |||||||
| chr14:50311465 | A | C | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+546T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311465 | |||||||
| chr14:50311470 | G | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+541C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311470 | |||||||
| chr14:50311472 | C | A | 1 | a0002c0002t0002g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.140+539G>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311472 | |||||||
| chr14:50311550 | C | CT | 31 | a0001c0001t0018g0011 a0001c0001t0018g0012 a0001c0001t0018g0013 others(28): Show |
31 | HG00099.hp1 HG01070.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.140+460dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311550 | |||||||
| chr14:50311636 | T | G | 7 | a0001c0001t0004g0202 a0001c0001t0004g0203 a0001c0001t0004g0207 others(4): Show |
7 | HG00733.hp1 HG01256.hp2 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.140+375A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311636 | |||||||
| chr14:50311690 | G | T | 2 | a0001c0001t0003g0009 a0001c0001t0007g0010 |
2 | NA18964.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.140+321C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311690 | |||||||
| chr14:50311707 | A | T | 3 | a0002c0002t0004g0216 a0002c0002t0004g0217 a0002c0002t0004g0218 |
3 | HG00609.hp2 NA18946.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.140+304T>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311707 | |||||||
| chr14:50311731 | G | A | 2 | a0001c0001t0030g0209 a0001c0001t0030g0210 |
2 | HG03139.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.140+280C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311731 | |||||||
| chr14:50311823 | C | T | 1 | a0002c0003t0065g0215 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.140+188G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311823 | |||||||
| chr14:50311824 | C | T | 1 | a0001c0001t0001g0008 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.140+187G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311824 |