| 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 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 463 | 209 | 56 | 40 | 87 | 5 | 20 | 61 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002 | 1/0 | 463 | 145 | 32 | 30 | 53 | 7 | 22 | 39 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0003 | 0/0 | 463 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0004 | 0/0 | 463 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1392 | 202 | 55 | 36 | 86 | 5 | 19 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| c0002 | 1/0 | 1392 | 128 | 25 | 27 | 48 | 7 | 20 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| c0003 | 0/0 | 1392 | 16 | 6 | 3 | 5 | 0 | 2 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| c0004 | 0/0 | 1392 | 5 | 1 | 4 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| c0005 | 0/0 | 1392 | 4 | 4 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| c0006 | 0/0 | 1392 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| c0007 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| c0008 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| c0009 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 4699 | 77 | 11 | 14 | 42 | 2 | 8 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0002 | 0/0 | 4697 | 54 | 2 | 17 | 26 | 1 | 8 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0003 | 0/1 | 4710 | 35 | 4 | 8 | 13 | 2 | 7 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0004 | 0/0 | 4704 | 20 | 0 | 3 | 6 | 2 | 9 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0005 | 0/0 | 4697 | 15 | 9 | 4 | 0 | 2 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0006 | 0/0 | 4711 | 9 | 1 | 1 | 6 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0007 | 0/0 | 4703 | 9 | 9 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0008 | 0/0 | 4712 | 7 | 0 | 0 | 5 | 0 | 2 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0009 | 0/0 | 4700 | 6 | 1 | 2 | 3 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0010 | 0/0 | 4698 | 6 | 0 | 2 | 4 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0011 | 0/0 | 4696 | 6 | 6 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0012 | 0/0 | 4699 | 5 | 0 | 0 | 4 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0013 | 0/0 | 4699 | 5 | 5 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0014 | 0/0 | 4704 | 4 | 4 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0015 | 0/0 | 4704 | 4 | 4 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0016 | 0/0 | 4702 | 3 | 0 | 0 | 0 | 1 | 2 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0017 | 0/0 | 4706 | 3 | 0 | 0 | 3 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0018 | 0/0 | 4704 | 3 | 0 | 3 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0019 | 0/0 | 4702 | 3 | 3 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0020 | 0/0 | 4698 | 3 | 3 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0021 | 0/0 | 4708 | 3 | 0 | 3 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0022 | 0/0 | 4710 | 3 | 3 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0023 | 0/0 | 4697 | 3 | 0 | 0 | 3 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0024 | 0/0 | 4696 | 3 | 3 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0025 | 0/0 | 4696 | 3 | 0 | 3 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0026 | 0/0 | 4699 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0027 | 0/0 | 4705 | 2 | 0 | 0 | 0 | 0 | 2 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0028 | 0/0 | 4703 | 2 | 1 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0029 | 0/0 | 4712 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0030 | 0/0 | 4700 | 2 | 0 | 0 | 1 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0031 | 0/0 | 4702 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0032 | 0/0 | 4700 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0033 | 0/0 | 4701 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0034 | 0/0 | 4711 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0035 | 0/0 | 4714 | 2 | 0 | 0 | 1 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0036 | 0/0 | 4714 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0037 | 0/0 | 4698 | 2 | 1 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0038 | 0/0 | 4698 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0039 | 0/0 | 4699 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0040 | 0/0 | 4697 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0041 | 0/0 | 4703 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0042 | 0/0 | 4698 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0043 | 1/0 | 4704 | 1 | 0 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0044 | 0/0 | 4709 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0045 | 0/0 | 4713 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0046 | 0/0 | 4711 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0047 | 0/0 | 4715 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0048 | 0/0 | 4699 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0049 | 0/0 | 4710 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0050 | 0/0 | 4700 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0051 | 0/0 | 4700 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0052 | 0/0 | 4702 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0053 | 0/0 | 4710 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0054 | 0/0 | 4710 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0055 | 0/0 | 4702 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0056 | 0/0 | 4712 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0057 | 0/0 | 4710 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0058 | 0/0 | 4699 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0059 | 0/0 | 4699 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0060 | 0/0 | 4701 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0061 | 0/0 | 4699 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0062 | 0/0 | 4699 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0063 | 0/0 | 4699 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0064 | 0/0 | 4701 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0065 | 0/0 | 4699 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0066 | 0/0 | 4699 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0067 | 0/0 | 4699 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0068 | 0/0 | 4701 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0069 | 0/0 | 4699 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0070 | 0/0 | 4697 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0071 | 0/0 | 4697 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0072 | 0/0 | 4697 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0073 | 0/0 | 4697 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0074 | 0/0 | 4701 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0075 | 0/0 | 4701 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0076 | 0/0 | 4703 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| t0077 | 0/0 | 4698 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0176 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0275 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1392 | 202 | 55 | 36 | 86 | 5 | 19 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0004 | 0/0 | 1392 | 5 | 1 | 4 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0007 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0008 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002 | 1/0 | 1392 | 128 | 25 | 27 | 48 | 7 | 20 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0003 | 0/0 | 1392 | 16 | 6 | 3 | 5 | 0 | 2 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0009 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0003c0005 | 0/0 | 1392 | 4 | 4 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0004c0006 | 0/0 | 1392 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | 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 | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0002 | 0/0 | 6088 | 2 | 0 | 0 | 1 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0003 | 0/1 | 6101 | 34 | 4 | 7 | 13 | 2 | 7 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0005 | 0/0 | 6088 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0006 | 0/0 | 6102 | 9 | 1 | 1 | 6 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0007 | 0/0 | 6094 | 6 | 6 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0008 | 0/0 | 6103 | 6 | 0 | 0 | 5 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0009 | 0/0 | 6091 | 5 | 1 | 2 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0012 | 0/0 | 6090 | 5 | 0 | 0 | 4 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0013 | 0/0 | 6090 | 5 | 5 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0014 | 0/0 | 6095 | 4 | 4 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0015 | 0/0 | 6095 | 3 | 3 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0018 | 0/0 | 6095 | 3 | 0 | 3 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0019 | 0/0 | 6093 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0020 | 0/0 | 6089 | 3 | 3 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0021 | 0/0 | 6099 | 3 | 0 | 3 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0022 | 0/0 | 6101 | 3 | 3 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0026 | 0/0 | 6090 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0029 | 0/0 | 6103 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0030 | 0/0 | 6091 | 2 | 0 | 0 | 1 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0031 | 0/0 | 6093 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0032 | 0/0 | 6091 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0033 | 0/0 | 6092 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0034 | 0/0 | 6102 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0035 | 0/0 | 6105 | 2 | 0 | 0 | 1 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0036 | 0/0 | 6105 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0039 | 0/0 | 6090 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0044 | 0/0 | 6100 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0045 | 0/0 | 6104 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0046 | 0/0 | 6102 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0047 | 0/0 | 6106 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0049 | 0/0 | 6101 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0050 | 0/0 | 6091 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0051 | 0/0 | 6091 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0053 | 0/0 | 6101 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0054 | 0/0 | 6101 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0056 | 0/0 | 6103 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0057 | 0/0 | 6101 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0059 | 0/0 | 6090 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0060 | 0/0 | 6092 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0061 | 0/0 | 6090 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0062 | 0/0 | 6090 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0063 | 0/0 | 6090 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0064 | 0/0 | 6092 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0066 | 0/0 | 6090 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0067 | 0/0 | 6090 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0073 | 0/0 | 6088 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0074 | 0/0 | 6092 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0075 | 0/0 | 6092 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0076 | 0/0 | 6094 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0001t0077 | 0/0 | 6089 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0004t0002 | 0/0 | 6088 | 4 | 0 | 4 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0004t0005 | 0/0 | 6088 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0007t0001 | 0/0 | 6090 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0001c0008t0008 | 0/0 | 6103 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0001 | 0/0 | 6090 | 4 | 0 | 0 | 3 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0002 | 0/0 | 6088 | 47 | 2 | 12 | 25 | 1 | 7 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0004 | 0/0 | 6095 | 20 | 0 | 3 | 6 | 2 | 9 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0005 | 0/0 | 6088 | 13 | 7 | 4 | 0 | 2 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0010 | 0/0 | 6089 | 6 | 0 | 2 | 4 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0011 | 0/0 | 6087 | 6 | 6 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0016 | 0/0 | 6093 | 3 | 0 | 0 | 0 | 1 | 2 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0017 | 0/0 | 6097 | 3 | 0 | 0 | 3 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0023 | 0/0 | 6088 | 3 | 0 | 0 | 3 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0024 | 0/0 | 6087 | 3 | 3 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0025 | 0/0 | 6087 | 3 | 0 | 3 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0027 | 0/0 | 6096 | 2 | 0 | 0 | 0 | 0 | 2 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0037 | 0/0 | 6089 | 2 | 1 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0038 | 0/0 | 6089 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0040 | 0/0 | 6088 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0041 | 0/0 | 6094 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0042 | 0/0 | 6089 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0043 | 1/0 | 6095 | 1 | 0 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0048 | 0/0 | 6090 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0058 | 0/0 | 6090 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0070 | 0/0 | 6088 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0071 | 0/0 | 6088 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0002t0072 | 0/0 | 6088 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0003t0001 | 0/0 | 6090 | 6 | 1 | 0 | 3 | 0 | 2 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0003t0002 | 0/0 | 6088 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0003t0003 | 0/0 | 6101 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0003t0009 | 0/0 | 6091 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0003t0019 | 0/0 | 6093 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0003t0028 | 0/0 | 6094 | 2 | 1 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0003t0052 | 0/0 | 6093 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0003t0055 | 0/0 | 6093 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0003t0065 | 0/0 | 6090 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0003t0068 | 0/0 | 6092 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0002c0009t0069 | 0/0 | 6090 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0003c0005t0007 | 0/0 | 6094 | 3 | 3 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0003c0005t0015 | 0/0 | 6095 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| a0004c0006t0001 | 0/0 | 6090 | 2 | 2 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | copy fasta | chr14 | 50237434 | 50317229 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0116 | 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 |
| a0001c0001t0001g0121 | 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 |
| a0001c0001t0001g0126 | 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 |
| a0001c0001t0001g0130 | 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 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0164 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0076 | 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 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0176 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0006g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0006g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0006g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0007g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0007g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0007g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0007g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0007g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0008g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0008g0064 | 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 |
| a0001c0001t0008g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0008g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0008g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0009g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0009g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0009g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0009g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0012g0118 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0012g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0012g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0013g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0013g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0013g0031 | 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 |
| a0001c0001t0013g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0014g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0014g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0014g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0014g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0015g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0015g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0015g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0018g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0018g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0018g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0019g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0019g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0020g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0020g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0020g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0021g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0021g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0021g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0022g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0022g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0022g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0026g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0026g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0029g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0029g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0030g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0030g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0031g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0031g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0032g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0032g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0033g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0033g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0034g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0034g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0035g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0035g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0036g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0036g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0039g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0039g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0044g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0045g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0046g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0047g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0049g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0050g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0051g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0053g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0054g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0056g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0057g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0059g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0060g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0061g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0062g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0063g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0064g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0066g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0067g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0073g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0074g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0075g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0076g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0001t0077g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0004t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0004t0002g0038 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0004t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0007t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0001c0008t0008g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0002c0002t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0002c0002t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0002c0002t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0002c0002t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0002g0356 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0002c0002t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| 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 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0004g0287 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0005g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0010g0314 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0002c0002t0010g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0010g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0010g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0010g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0011g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0011g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0011g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0011g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0011g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0011g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0016g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0016g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0016g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0017g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0017g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0017g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0023g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0023g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0024g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0024g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0024g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0025g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0025g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0025g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0027g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0027g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0037g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0037g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0038g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0038g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0040g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0040g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0041g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0041g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0042g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0043g0275 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0048g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0058g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0070g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0071g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0002t0072g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0002c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0002c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0003g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0009g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0019g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0028g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0028g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0052g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0055g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0065g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0003t0068g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0002c0009t0069g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0003c0005t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0003c0005t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0003c0005t0007g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0003c0005t0015g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0004c0006t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| a0004c0006t0001g0172 | 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 | g0239 | EUR | GBR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | GBR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00140 | hp1 | a0001 | c0001 | t0035 | g0063 | EUR | GBR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00140 | hp2 | a0002 | c0002 | t0016 | g0277 | EUR | GBR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0321 | EUR | FIN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0045 | EUR | FIN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0328 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0313 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00544 | hp2 | a0001 | c0001 | t0057 | g0066 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00597 | hp1 | a0002 | c0002 | t0004 | g0287 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00609 | hp1 | a0001 | c0001 | t0061 | g0048 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00609 | hp2 | a0002 | c0002 | t0004 | g0219 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0319 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00639 | hp1 | a0001 | c0001 | t0054 | g0043 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00673 | hp1 | a0001 | c0001 | t0008 | g0104 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0297 | EAS | CHS | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00733 | hp1 | a0001 | c0001 | t0018 | g0206 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00733 | hp2 | a0002 | c0002 | t0010 | g0314 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00735 | hp1 | a0001 | c0001 | t0073 | g0053 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00735 | hp2 | a0002 | c0002 | t0004 | g0268 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00738 | hp2 | a0001 | c0001 | t0021 | g0054 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0263 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG00741 | hp2 | a0001 | c0001 | t0009 | g0135 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01069 | hp1 | a0002 | c0002 | t0025 | g0294 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01069 | hp2 | a0002 | c0003 | t0003 | g0354 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01070 | hp1 | a0001 | c0004 | t0002 | g0039 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01070 | hp2 | a0002 | c0002 | t0005 | g0246 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01071 | hp1 | a0002 | c0002 | t0025 | g0293 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01071 | hp2 | a0001 | c0004 | t0002 | g0040 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01074 | hp1 | a0002 | c0002 | t0070 | g0240 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0306 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01099 | hp2 | a0002 | c0002 | t0005 | g0243 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01106 | hp1 | a0002 | c0002 | t0002 | g0356 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01106 | hp2 | a0001 | c0001 | t0006 | g0088 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01109 | hp1 | a0001 | c0001 | t0046 | g0012 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01109 | hp2 | a0002 | c0002 | t0004 | g0273 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0341 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01167 | hp2 | a0002 | c0002 | t0005 | g0225 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01169 | hp1 | a0002 | c0002 | t0005 | g0226 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0308 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01175 | hp1 | a0002 | c0002 | t0058 | g0326 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01192 | hp1 | a0002 | c0002 | t0025 | g0292 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01192 | hp2 | a0001 | c0001 | t0021 | g0081 | AMR | PUR | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01255 | hp2 | a0001 | c0001 | t0021 | g0098 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01256 | hp1 | a0001 | c0001 | t0077 | g0143 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01256 | hp2 | a0001 | c0001 | t0018 | g0208 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0295 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0087 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01258 | hp1 | a0001 | c0001 | t0018 | g0207 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01258 | hp2 | a0002 | c0002 | t0002 | g0296 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01261 | hp1 | a0001 | c0001 | t0075 | g0191 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0076 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0309 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0072 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01358 | hp1 | a0002 | c0002 | t0037 | g0247 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01358 | hp2 | a0002 | c0003 | t0028 | g0351 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0177 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01517 | hp1 | a0002 | c0002 | t0005 | g0235 | 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 | g0231 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01884 | hp2 | a0001 | c0001 | t0039 | g0201 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01891 | hp1 | a0001 | c0001 | t0015 | g0107 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0355 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0317 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01934 | hp1 | a0002 | c0003 | t0002 | g0255 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01981 | hp2 | a0002 | c0002 | t0004 | g0267 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0332 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0300 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02027 | hp1 | a0001 | c0001 | t0006 | g0080 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02027 | hp2 | a0002 | c0002 | t0010 | g0325 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0100 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02055 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02055 | hp2 | a0002 | c0002 | t0042 | g0005 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02056 | hp1 | a0001 | c0001 | t0008 | g0064 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02071 | hp1 | a0002 | c0002 | t0004 | g0265 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02074 | hp1 | a0002 | c0003 | t0001 | g0257 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02074 | hp2 | a0001 | c0001 | t0029 | g0075 | 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 | g0304 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02129 | hp1 | a0002 | c0002 | t0004 | g0248 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0124 | 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 | t0063 | g0175 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02145 | hp1 | a0002 | c0002 | t0048 | g0323 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02145 | hp2 | a0001 | c0001 | t0045 | g0047 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0067 | EAS | CDX | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02155 | hp2 | a0001 | c0001 | t0009 | g0174 | EAS | CDX | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02165 | hp1 | a0002 | c0002 | t0023 | g0003 | EAS | CDX | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CDX | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02257 | hp1 | a0004 | c0006 | t0001 | g0172 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02257 | hp2 | a0002 | c0002 | t0024 | g0227 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0178 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02258 | hp2 | a0001 | c0001 | t0039 | g0200 | 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 | g0037 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02280 | hp1 | a0002 | c0003 | t0055 | g0349 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02280 | hp2 | a0002 | c0002 | t0011 | g0230 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02293 | hp1 | a0001 | c0001 | t0009 | g0195 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0249 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02300 | hp1 | a0002 | c0002 | t0010 | g0334 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02451 | hp1 | a0001 | c0001 | t0022 | g0035 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02451 | hp2 | a0001 | c0001 | t0007 | g0091 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0051 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02572 | hp1 | a0001 | c0004 | t0005 | g0202 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02572 | hp2 | a0001 | c0001 | t0051 | g0090 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02602 | hp2 | a0002 | c0002 | t0004 | g0282 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02615 | hp2 | a0001 | c0001 | t0013 | g0014 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02622 | hp1 | a0001 | c0001 | t0056 | g0016 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02622 | hp2 | a0002 | c0002 | t0005 | g0237 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02630 | hp2 | a0001 | c0001 | t0022 | g0029 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02647 | hp1 | a0001 | c0001 | t0014 | g0204 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02647 | hp2 | a0002 | c0003 | t0028 | g0352 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02683 | hp1 | a0002 | c0002 | t0004 | g0284 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0062 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02698 | hp1 | a0002 | c0002 | t0004 | g0270 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0056 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02717 | hp1 | a0002 | c0002 | t0024 | g0242 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0092 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02723 | hp2 | a0002 | c0002 | t0005 | g0229 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02735 | hp1 | a0002 | c0002 | t0004 | g0285 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0089 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02809 | hp2 | a0003 | c0005 | t0007 | g0215 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02818 | hp1 | a0002 | c0002 | t0011 | g0245 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02818 | hp2 | a0002 | c0002 | t0040 | g0350 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02886 | hp1 | a0001 | c0001 | t0007 | g0032 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02886 | hp2 | a0001 | c0001 | t0060 | g0027 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02895 | hp1 | a0002 | c0002 | t0011 | g0236 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02922 | hp1 | a0001 | c0001 | t0074 | g0190 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02922 | hp2 | a0004 | c0006 | t0001 | g0146 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02965 | hp1 | a0001 | c0001 | t0013 | g0033 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02965 | hp2 | a0001 | c0001 | t0067 | g0198 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02970 | hp1 | a0002 | c0002 | t0040 | g0288 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02970 | hp2 | a0001 | c0001 | t0015 | g0096 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02976 | hp1 | a0001 | c0001 | t0007 | g0095 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02976 | hp2 | a0001 | c0001 | t0022 | g0046 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03017 | hp1 | a0001 | c0008 | t0008 | g0071 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03017 | hp2 | a0002 | c0002 | t0004 | g0274 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03041 | hp2 | a0001 | c0001 | t0076 | g0105 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03098 | hp1 | a0002 | c0002 | t0005 | g0224 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03098 | hp2 | a0002 | c0003 | t0068 | g0217 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03130 | hp1 | a0002 | c0002 | t0071 | g0221 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03130 | hp2 | a0001 | c0001 | t0014 | g0205 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03139 | hp1 | a0001 | c0001 | t0031 | g0211 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03195 | hp1 | a0001 | c0001 | t0014 | g0210 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03195 | hp2 | a0001 | c0001 | t0020 | g0010 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03209 | hp1 | a0002 | c0002 | t0011 | g0244 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03209 | hp2 | a0001 | c0001 | t0032 | g0189 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03225 | hp1 | a0002 | c0002 | t0005 | g0233 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03225 | hp2 | a0002 | c0003 | t0019 | g0353 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0324 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03453 | hp1 | a0003 | c0005 | t0007 | g0214 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03453 | hp2 | a0001 | c0001 | t0013 | g0034 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03486 | hp1 | a0003 | c0005 | t0015 | g0213 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03486 | hp2 | a0001 | c0001 | t0015 | g0106 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0315 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0058 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03491 | hp1 | a0002 | c0002 | t0016 | g0279 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0057 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0320 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0059 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03516 | hp1 | a0001 | c0001 | t0013 | g0030 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03516 | hp2 | a0003 | c0005 | t0007 | g0216 | AFR | ESN | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03540 | hp1 | a0001 | c0001 | t0007 | g0094 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03540 | hp2 | a0002 | c0002 | t0072 | g0232 | AFR | GWD | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03579 | hp1 | a0001 | c0001 | t0013 | g0031 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0307 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03669 | hp1 | a0002 | c0003 | t0001 | g0256 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03669 | hp2 | a0002 | c0002 | t0004 | g0283 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0025 | SAS | STU | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03688 | hp2 | a0002 | c0002 | t0004 | g0271 | SAS | STU | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03704 | hp1 | a0002 | c0002 | t0004 | g0281 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03831 | hp1 | a0002 | c0002 | t0027 | g0280 | SAS | BEB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03831 | hp2 | a0001 | c0001 | t0049 | g0099 | SAS | BEB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0303 | SAS | BEB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | BEB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0318 | SAS | BEB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03942 | hp2 | a0002 | c0002 | t0004 | g0286 | SAS | BEB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG04115 | hp1 | a0001 | c0001 | t0030 | g0184 | SAS | STU | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG04115 | hp2 | a0001 | c0001 | t0008 | g0020 | SAS | STU | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0187 | SAS | BEB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG04184 | hp2 | a0002 | c0002 | t0027 | g0269 | SAS | BEB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0060 | SAS | STU | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | STU | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0316 | SAS | STU | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG04228 | hp2 | a0001 | c0001 | t0044 | g0183 | SAS | STU | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18522 | hp1 | a0002 | c0002 | t0005 | g0234 | AFR | YRI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18522 | hp2 | a0002 | c0002 | t0005 | g0223 | AFR | YRI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18747 | hp1 | a0002 | c0003 | t0001 | g0261 | EAS | CHB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18747 | hp2 | a0002 | c0002 | t0023 | g0003 | EAS | CHB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18906 | hp1 | a0001 | c0001 | t0019 | g0186 | AFR | YRI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18906 | hp2 | a0002 | c0002 | t0011 | g0241 | AFR | YRI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18939 | hp2 | a0002 | c0002 | t0010 | g0327 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18940 | hp2 | a0002 | c0002 | t0010 | g0342 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18942 | hp2 | a0002 | c0002 | t0041 | g0301 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0289 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18946 | hp2 | a0002 | c0002 | t0004 | g0220 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18947 | hp1 | a0002 | c0003 | t0001 | g0259 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18947 | hp2 | a0002 | c0002 | t0038 | g0329 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18949 | hp1 | a0002 | c0002 | t0010 | g0347 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18949 | hp2 | a0002 | c0003 | t0065 | g0262 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18951 | hp1 | a0001 | c0001 | t0036 | g0061 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18952 | hp1 | a0001 | c0001 | t0008 | g0078 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18952 | hp2 | a0002 | c0002 | t0001 | g0338 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18953 | hp1 | a0002 | c0002 | t0002 | g0312 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18953 | hp2 | a0001 | c0001 | t0006 | g0077 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18957 | hp1 | a0001 | c0001 | t0033 | g0156 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18957 | hp2 | a0002 | c0002 | t0023 | g0335 | 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 | g0052 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18964 | hp2 | a0001 | c0001 | t0012 | g0119 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18971 | hp1 | a0002 | c0002 | t0017 | g0266 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0311 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18973 | hp1 | a0001 | c0001 | t0012 | g0162 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0305 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18977 | hp2 | a0001 | c0001 | t0008 | g0097 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0331 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18979 | hp2 | a0001 | c0001 | t0062 | g0165 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0253 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0252 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18982 | hp2 | a0001 | c0001 | t0053 | g0102 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18983 | hp2 | a0001 | c0001 | t0034 | g0065 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0298 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0302 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18994 | hp1 | a0002 | c0002 | t0038 | g0336 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0344 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18995 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0291 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19000 | hp2 | a0001 | c0001 | t0047 | g0086 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0333 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19002 | hp2 | a0001 | c0007 | t0001 | g0129 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0322 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19009 | hp1 | a0002 | c0002 | t0041 | g0310 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19009 | hp2 | a0002 | c0003 | t0009 | g0260 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0337 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19011 | hp2 | a0001 | c0001 | t0006 | g0134 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19012 | hp2 | a0001 | c0001 | t0029 | g0036 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19030 | hp1 | a0002 | c0002 | t0037 | g0228 | AFR | LWK | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | LWK | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | LWK | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19043 | hp2 | a0002 | c0003 | t0052 | g0348 | AFR | LWK | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19054 | hp1 | a0002 | c0002 | t0017 | g0264 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19054 | hp2 | a0001 | c0001 | t0026 | g0110 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0340 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19065 | hp2 | a0001 | c0001 | t0012 | g0120 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19066 | hp1 | a0001 | c0001 | t0006 | g0101 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19066 | hp2 | a0001 | c0001 | t0012 | g0118 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0250 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19068 | hp2 | a0002 | c0002 | t0017 | g0345 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19070 | hp1 | a0001 | c0001 | t0066 | g0159 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19070 | hp2 | a0001 | c0001 | t0006 | g0050 | 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 | g0150 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19081 | hp2 | a0002 | c0002 | t0004 | g0218 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19082 | hp1 | a0001 | c0001 | t0050 | g0132 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19084 | hp2 | a0001 | c0001 | t0035 | g0115 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0339 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19085 | hp2 | a0001 | c0001 | t0036 | g0084 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0330 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0290 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19087 | hp2 | a0001 | c0001 | t0033 | g0026 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19088 | hp1 | a0001 | c0001 | t0034 | g0069 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19088 | hp2 | a0001 | c0001 | t0030 | g0163 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19090 | hp1 | a0001 | c0001 | t0026 | g0160 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19240 | hp1 | a0001 | c0001 | t0020 | g0009 | AFR | YRI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA19240 | hp2 | a0002 | c0009 | t0069 | g0258 | AFR | YRI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0343 | AFR | ASW | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20129 | hp2 | a0002 | c0002 | t0005 | g0222 | AFR | ASW | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20752 | hp1 | a0002 | c0002 | t0004 | g0272 | EUR | TSI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0001 | EUR | TSI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20805 | hp1 | a0001 | c0001 | t0012 | g0128 | EUR | TSI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0346 | EUR | TSI | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20905 | hp1 | a0002 | c0002 | t0016 | g0276 | SAS | GIH | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20905 | hp2 | a0002 | c0003 | t0001 | g0254 | SAS | GIH | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01123 | hp1 | a0001 | c0004 | t0002 | g0038 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG01123 | hp2 | a0001 | c0001 | t0059 | g0194 | AMR | CLM | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02109 | hp1 | a0001 | c0001 | t0032 | g0188 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02559 | hp1 | a0001 | c0001 | t0020 | g0011 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG02559 | hp2 | a0002 | c0002 | t0024 | g0238 | AFR | ACB | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03471 | hp1 | a0001 | c0001 | t0009 | g0155 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG03471 | hp2 | a0001 | c0001 | t0064 | g0013 | AFR | MSL | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG06807 | hp1 | a0001 | c0001 | t0014 | g0209 | AFR | USA | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| HG06807 | hp2 | a0001 | c0001 | t0031 | g0212 | AFR | USA | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0299 | AFR | USA | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA20300 | hp2 | a0001 | c0001 | t0019 | g0185 | AFR | USA | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0093 | AFR | LWK | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0108 | AFR | LWK | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0003 | g0176 | REF | REF | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| homoSapiens_grch38 | hp1 | a0002 | c0002 | t0043 | g0275 | REF | REF | L2HGDH_chr14_50237434_50317229 | L2HGDH | chr14 | 50237434 | 50317229 |
| 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 | a0001a0003a0004 | 215 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(212): 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 |
| 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 | a0001c0001a0001c0007a0001c0008others(4): Show | 227 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(224): 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 |
| 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 | a0001c0001t0063 | 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 | a0001c0001t0073 | 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 | a0001c0001t0031 | 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 | a0002c0003t0068 | 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 | a0001c0001t0029a0001c0001t0033a0001c0001t0034 | 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 | a0002c0002t0072 | 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 | a0001c0001t0075 | 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 | a0002c0002t0024 | 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 | a0002c0002t0023a0002c0002t0038 | 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 | a0001c0001t0062 | 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 | a0001c0001t0050 | 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 | a0001c0001t0022a0001c0001t0045a0001c0001t0056 | 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 | a0001c0001t0061 | 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 | a0002c0002t0017 | 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 | a0001c0001t0021a0001c0001t0044 | 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 | a0001c0001t0003a0001c0001t0006a0001c0001t0022others(8): Show | 56 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(53): 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 | a0001c0001t0008a0001c0001t0045a0001c0001t0056others(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 | a0001c0001t0035a0001c0001t0036a0001c0001t0047 | 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 | a0001c0001t0019a0001c0001t0031a0001c0001t0060others(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 | 26 | a0001c0001t0001a0001c0001t0009a0001c0001t0012others(23): 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 | 22 | a0001c0001t0002a0001c0001t0005a0001c0001t0020others(19): 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 | a0001c0001t0007a0001c0001t0014a0001c0001t0015others(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 | a0001c0001t0019a0001c0001t0060a0001c0001t0064others(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 | a0001c0001t0032a0001c0001t0039 | 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 | 13 | a0001c0001t0005a0001c0001t0020a0001c0004t0005others(10): 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 | a0001c0001t0046 | 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 | a0001c0001t0036a0001c0001t0047 | 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 | a0001c0001t0064 | 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 | a0002c0003t0065 | 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 | 10 | a0001c0001t0005a0001c0004t0005a0002c0002t0005others(7): 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 | a0001c0001t0003a0001c0001t0006a0001c0001t0008others(19): Show | 76 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(73): 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 | a0001c0001t0054 | 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 | a0001c0001t0057 | 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 | a0001c0001t0066 | 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 | a0001c0001t0012a0001c0001t0030 | 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 | a0001c0001t0053 | 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 | a0001c0001t0051a0001c0001t0067 | 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 | a0002c0002t0071 | 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 | a0002c0003t0052 | 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 | a0001c0001t0020 | 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 | a0001c0001t0019a0002c0003t0019a0002c0003t0028 | 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 | 7 | a0001c0001t0007a0001c0001t0015a0001c0001t0074others(4): 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 | a0001c0001t0018 | 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 | a0001c0001t0059 | 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 | a0001c0001t0032a0001c0001t0039 | 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 | 75 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(72): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): 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 | 85 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(82): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): 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 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(70): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): 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 | 22 | a0001c0001t0002a0001c0001t0005a0001c0001t0073others(19): 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 | 27 | a0001c0001t0001a0001c0001t0009a0001c0001t0012others(24): 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 | 7 | a0001c0001t0007a0001c0001t0015a0001c0001t0074others(4): 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 | a0001c0001t0049 | 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 | a0001c0001t0006a0001c0001t0029a0001c0001t0044others(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 | 40 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(37): 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 | a0001c0001t0077a0002c0002t0011a0002c0002t0024others(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 | a0001c0001t0026 | 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 | |||||
| chr14:50246961
|
T | G | 91 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(88): Show | 359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
3_prime_UTR_variant | MODIFIER | c.*97A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 10/10 | 97 | chr14 | 50246961 | |||||
| chr14:50312197
|
A | G | 1 | a0002c0002t0042 | 1 | HG02055.hp2 | 5_prime_UTR_variant | MODIFIER | c.-47T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/10 | 47 | chr14 | 50312197 |
| 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 | a0001c0001t0007g0032a0001c0001t0007g0091a0001c0001t0007g0092others(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 | a0001c0001t0001g0022a0001c0001t0001g0136a0001c0001t0001g0144others(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 | a0001c0001t0002g0125a0001c0001t0002g0187a0001c0001t0005g0089others(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 | 193 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(190): Show | 195 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(192): 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 | a0001c0001t0002g0125a0001c0001t0002g0187a0001c0001t0005g0089others(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 | a0001c0001t0003g0076 | 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 | 320 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(317): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): 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 | a0002c0009t0069g0258 | 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 | 193 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(190): Show | 195 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(192): 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 | a0001c0001t0007g0032a0001c0001t0007g0091a0001c0001t0007g0092others(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 | a0001c0001t0006g0134 | 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 | 118 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(115): 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 | a0001c0001t0064g0013 | 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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0001c0001t0001g0117 | 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 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0051g0090others(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 | a0002c0002t0005g0237a0002c0002t0024g0227a0002c0002t0024g0238others(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 | a0001c0001t0002g0125a0001c0001t0002g0187a0001c0001t0005g0089others(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 | a0001c0001t0002g0125a0001c0001t0002g0187a0001c0001t0005g0089others(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 | a0001c0001t0006g0015 | 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 | a0001c0001t0002g0125a0001c0001t0002g0187a0001c0001t0005g0089others(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 | a0002c0003t0055g0349 | 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 | a0001c0001t0002g0125a0001c0001t0002g0187a0001c0001t0005g0089others(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 | a0001c0001t0006g0134 | 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 | a0002c0002t0002g0307 | 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 | a0002c0002t0002g0316 | 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 | a0001c0001t0003g0072 | 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 | 117 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(114): 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 | a0001c0001t0001g0117a0001c0001t0001g0167a0001c0001t0014g0209others(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 | a0001c0001t0001g0019a0001c0001t0001g0113a0001c0001t0001g0116others(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 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0114others(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 | 55 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0022others(52): 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 | a0001c0001t0013g0014a0001c0001t0013g0030a0001c0001t0013g0031others(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 | a0001c0001t0003g0025a0001c0001t0003g0041a0001c0001t0003g0044others(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 | 56 | a0001c0001t0003g0001a0001c0001t0003g0007a0001c0001t0003g0017others(53): Show | 57 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(54): 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 | a0001c0001t0001g0112a0001c0001t0002g0187a0001c0001t0005g0089others(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 | a0001c0001t0002g0125a0001c0001t0019g0185a0001c0001t0019g0186others(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 | a0001c0001t0020g0009a0001c0001t0020g0011a0002c0002t0002g0340others(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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0032g0188a0001c0001t0032g0189a0001c0001t0039g0200others(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 | 73 | a0001c0001t0003g0001a0001c0001t0003g0007a0001c0001t0003g0017others(70): Show | 74 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(71): 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 | a0002c0002t0004g0281 | 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 | a0001c0001t0021g0054 | 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 | a0002c0002t0004g0219 | 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 | a0001c0001t0061g0048 | 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 | a0001c0001t0064g0013 | 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 | a0001c0001t0020g0009a0001c0001t0020g0010a0001c0001t0020g0011 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0007g0093 | 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 | a0001c0001t0005g0089a0002c0002t0005g0222a0002c0002t0005g0223others(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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | 182 | a0001c0001t0002g0125a0001c0001t0002g0187a0001c0001t0003g0001others(179): Show | 185 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(182): 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 | a0002c0003t0068g0217 | 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 | a0001c0001t0001g0109 | 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 | a0001c0001t0012g0128a0001c0001t0030g0184 | 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 | a0002c0002t0004g0284 | 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 | a0002c0003t0068g0217 | 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 | a0001c0001t0001g0199 | 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 | a0002c0003t0001g0355 | 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 | a0002c0002t0004g0267a0002c0002t0004g0268 | 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 | a0001c0001t0007g0032a0001c0001t0007g0091a0001c0001t0007g0092others(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 | a0002c0003t0068g0217 | 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 | a0001c0001t0001g0136a0001c0001t0001g0144a0001c0001t0001g0145 | 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 | a0001c0001t0005g0089a0001c0001t0021g0054a0001c0001t0032g0188others(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 | 299 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(296): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): 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 | a0002c0002t0002g0295a0002c0002t0002g0296a0002c0002t0002g0300others(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 | a0001c0001t0001g0180 | 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 | a0002c0003t0052g0348 | 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 | a0001c0001t0002g0125a0001c0001t0002g0187a0001c0001t0005g0089others(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 | 75 | a0001c0001t0003g0001a0001c0001t0003g0007a0001c0001t0003g0017others(72): Show | 76 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(73): 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 | a0002c0003t0068g0217 | 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 | a0001c0001t0002g0125a0001c0001t0002g0187a0001c0001t0005g0089others(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 | a0002c0002t0010g0347 | 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 | a0002c0003t0003g0354 | 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 | a0001c0001t0039g0200 | 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 | 75 | a0001c0001t0003g0001a0001c0001t0003g0007a0001c0001t0003g0017others(72): Show | 76 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(73): 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 | a0001c0001t0002g0125a0001c0001t0002g0187a0001c0001t0005g0089others(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 | 319 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(316): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1197-6234G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50253487 | ||||||
| chr14:50253567
|
A | C | 348 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(345): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.1197-6314T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50253567 | ||||||
| chr14:50253577
|
C | A | 115 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(112): 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 | a0002c0002t0037g0228 | 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 | a0001c0001t0049g0099 | 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 | 75 | a0001c0001t0003g0001a0001c0001t0003g0007a0001c0001t0003g0017others(72): Show | 76 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(73): 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 | a0001c0001t0020g0009a0001c0001t0020g0010a0001c0001t0020g0011 | 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 | a0001c0001t0001g0170a0001c0001t0026g0110a0001c0001t0026g0160 | 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 | a0001c0001t0001g0136a0001c0001t0001g0144a0001c0001t0001g0145 | 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 | a0002c0002t0002g0263a0002c0002t0002g0341a0002c0002t0002g0356 | 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 | a0001c0001t0003g0017a0001c0001t0003g0055a0001c0001t0003g0068 | 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 | a0001c0001t0007g0032a0001c0001t0007g0091a0001c0001t0007g0092others(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 | a0001c0001t0064g0013 | 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 | a0001c0001t0005g0089a0001c0004t0005g0202a0002c0002t0005g0222others(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 | a0002c0002t0002g0249a0002c0002t0002g0297a0002c0002t0002g0299others(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 | 224 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(221): 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 | 83 | a0001c0001t0001g0131a0001c0001t0001g0169a0001c0001t0003g0001others(80): Show | 84 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(81): 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 | a0001c0001t0064g0013 | 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 | 193 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(190): Show | 195 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(192): 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 | a0001c0001t0022g0029 | 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 | a0002c0002t0005g0243 | 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 | a0001c0001t0002g0125a0001c0001t0002g0187a0001c0001t0005g0089others(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 | a0001c0001t0064g0013 | 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 | a0002c0002t0037g0228 | 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 | a0001c0001t0001g0199 | 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 | a0003c0005t0007g0214a0003c0005t0007g0215a0003c0005t0007g0216others(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 | a0002c0003t0052g0348a0002c0003t0055g0349 | 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 | a0003c0005t0007g0215 | 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 | a0001c0001t0026g0110a0001c0001t0026g0160 | 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 | a0001c0004t0002g0037a0001c0004t0002g0038a0001c0004t0002g0039others(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 | 299 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(296): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): 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 | 299 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(296): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): 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 | a0001c0001t0005g0089a0001c0004t0005g0202a0002c0002t0005g0222others(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 | 299 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(296): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): 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 | a0001c0001t0001g0182a0001c0001t0002g0125a0001c0001t0002g0187others(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 | a0002c0003t0068g0217 | 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 | 320 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(317): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): 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 | a0002c0002t0040g0288a0002c0002t0040g0350 | 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 | a0001c0001t0032g0188 | 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 | a0002c0009t0069g0258 | 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 | a0001c0001t0001g0151a0001c0001t0001g0164a0001c0001t0001g0203others(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 | a0001c0001t0039g0201 | 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 | 220 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(217): 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 | 100 | a0001c0001t0001g0144a0001c0001t0001g0157a0001c0001t0003g0001others(97): Show | 101 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(98): 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 | a0001c0001t0013g0034 | 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 | a0001c0001t0002g0125a0001c0001t0002g0187a0001c0001t0005g0089others(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 | a0001c0001t0003g0045 | 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 | a0001c0001t0001g0151 | 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 | a0002c0003t0001g0355 | 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 | a0002c0003t0001g0254 | 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 | a0002c0002t0040g0288a0002c0002t0040g0350 | 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 | a0001c0001t0006g0015 | 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 | a0001c0001t0006g0080a0001c0001t0032g0189a0001c0001t0076g0105others(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 | a0001c0001t0007g0032a0001c0001t0007g0091a0001c0001t0007g0092others(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 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0124others(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 | 301 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(298): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): 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 | a0002c0002t0005g0233 | 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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0002c0002t0071g0221 | 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 | 297 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(294): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): 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 | a0001c0001t0005g0089a0001c0004t0005g0202a0002c0002t0002g0308others(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 | a0001c0001t0002g0125a0001c0001t0002g0187a0001c0001t0073g0053others(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 | a0001c0001t0020g0009a0001c0001t0020g0010a0001c0001t0020g0011others(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 | a0001c0001t0014g0204a0002c0002t0004g0218a0002c0002t0004g0265others(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 | a0001c0001t0001g0126a0001c0001t0001g0153a0001c0001t0003g0041others(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 | 181 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(178): Show | 183 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(180): 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 | a0001c0001t0003g0007a0001c0001t0003g0082a0001c0001t0006g0008others(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 | a0001c0001t0020g0009a0001c0001t0020g0010a0001c0001t0020g0011others(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 | a0001c0001t0002g0125a0001c0001t0002g0187a0001c0001t0005g0089others(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 | 2 | a0001c0001t0003g0176a0002c0003t0003g0354 | 2 | HG01069.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1196+5797C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50259561 | ||||||
| chr14:50259586
|
T | C | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(193): Show | 198 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(195): 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 | a0001c0001t0032g0188a0001c0001t0032g0189 | 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 | a0002c0002t0058g0326 | 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 | 319 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(316): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): 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 | a0001c0001t0001g0164a0001c0001t0009g0155a0004c0006t0001g0146others(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 | a0001c0001t0001g0171 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0144a0001c0001t0002g0125a0001c0001t0005g0089others(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 | 139 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(136): 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 | a0001c0001t0001g0121a0001c0001t0001g0136a0001c0001t0001g0141others(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 | a0001c0001t0001g0203 | 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 | a0002c0002t0005g0239 | 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 | a0001c0001t0003g0108 | 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 | a0002c0002t0040g0288a0002c0002t0040g0350 | 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 | 97 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(94): 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 | a0001c0001t0001g0154 | 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 | 226 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(223): Show | 228 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.1196+5066C>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260292 | ||||||
| chr14:50260391
|
C | G | 218 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(215): Show | 220 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.1196+4967G>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260391 | ||||||
| chr14:50260476
|
C | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(252): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): 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 | a0002c0003t0068g0217 | 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 | 200 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(197): Show | 202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0031g0211a0001c0001t0031g0212a0001c0001t0032g0188others(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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0001c0001t0031g0211a0001c0001t0031g0212a0001c0001t0032g0188others(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 | a0001c0001t0060g0027 | 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 | 183 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(180): Show | 185 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.1196+4593C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50260765 | ||||||
| chr14:50260805
|
G | A | 97 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(94): 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0001g0199 | 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 | a0002c0002t0040g0288a0002c0002t0040g0350 | 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 | a0001c0001t0007g0032a0001c0001t0014g0204a0001c0001t0014g0205others(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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0094others(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 | 226 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(223): Show | 228 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.1196+3340T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50262018 | ||||||
| chr14:50262068
|
A | C | 3 | a0001c0001t0029g0036a0001c0001t0034g0065a0001c0001t0034g0069 | 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 | 97 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(94): 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 | a0001c0001t0001g0140 | 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 | 194 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(191): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.1196+2929delT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50262428 | ||||||
| chr14:50262532
|
A | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(173): Show | 178 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(175): 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 | a0001c0001t0001g0170a0001c0001t0026g0110a0001c0001t0026g0160 | 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 | a0002c0003t0068g0217 | 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 | a0001c0001t0001g0136 | 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 | 255 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(252): Show | 257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0002c0002t0040g0288 | 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 | a0002c0003t0068g0217 | 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 | a0001c0001t0007g0032a0001c0001t0013g0014a0001c0001t0013g0030others(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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0001c0001t0020g0009a0001c0001t0020g0010a0001c0001t0020g0011 | 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 | a0002c0002t0002g0318 | 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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0001c0001t0008g0097 | 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 | 205 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(202): Show | 207 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.1196+1583dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 9/9 | chr14 | 50263774 | ||||||
| chr14:50263797
|
C | T | 8 | a0001c0001t0007g0032a0001c0001t0013g0014a0001c0001t0013g0030others(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 | a0002c0002t0005g0225a0002c0002t0005g0226 | 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 | a0001c0001t0007g0032a0001c0001t0013g0014a0001c0001t0013g0030others(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 | a0001c0001t0007g0032a0001c0001t0013g0014a0001c0001t0013g0030others(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 | a0002c0002t0002g0289 | 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 | a0001c0001t0007g0032a0001c0001t0013g0014a0001c0001t0013g0030others(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 | a0002c0002t0002g0291 | 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 | a0001c0001t0003g0076 | 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 | a0001c0001t0019g0185a0001c0001t0019g0186 | 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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | a0002c0002t0002g0346 | 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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0001c0001t0006g0088 | 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 | a0001c0001t0007g0032a0001c0001t0013g0014a0001c0001t0013g0030others(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 | a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | a0001c0001t0064g0013 | 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | 160 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(157): Show | 162 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(159): 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 | a0001c0001t0009g0150 | 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 | a0001c0001t0032g0188a0001c0001t0032g0189a0001c0001t0039g0201 | 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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0001c0001t0001g0161 | 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 | a0002c0002t0002g0341 | 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 | 187 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(184): Show | 189 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.1065-655dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50266143 | ||||||
| chr14:50266229
|
C | T | 187 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(184): Show | 189 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(186): 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 | a0001c0001t0032g0188a0001c0001t0032g0189 | 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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | a0001c0001t0019g0185a0001c0001t0019g0186 | 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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0001c0001t0001g0168a0001c0001t0062g0165 | 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 | a0001c0001t0015g0106 | 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 | a0001c0001t0022g0035 | 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 | a0001c0001t0015g0106 | 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 | a0002c0002t0025g0292a0002c0002t0025g0293a0002c0002t0025g0294 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0058others(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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0021a0001c0001t0001g0085a0001c0001t0001g0127others(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 | a0001c0001t0001g0121a0001c0001t0001g0138a0001c0001t0001g0152others(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 | 70 | a0001c0001t0001g0153a0001c0001t0002g0187a0001c0001t0003g0001others(67): Show | 71 | HG00099.hp1 HG00140.hp1 HG00544.hp2 others(68): 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 | a0001c0001t0002g0125a0001c0001t0019g0185a0001c0001t0019g0186others(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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0008g0020a0001c0001t0012g0128a0001c0001t0030g0184others(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 | a0002c0002t0001g0321a0002c0002t0002g0249a0002c0002t0002g0306others(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 | a0001c0001t0046g0012 | 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 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0044others(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 | a0002c0002t0002g0312 | 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 | 227 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(224): Show | 229 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(226): 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0002c0002t0001g0321a0002c0002t0002g0296a0002c0002t0002g0307others(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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0002t0037g0247others(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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | 160 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(157): Show | 162 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.1064+193A>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 8/9 | chr14 | 50267560 | ||||||
| chr14:50267564
|
T | G | 253 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(250): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): 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 | a0002c0002t0025g0292a0002c0002t0025g0293a0002c0002t0025g0294 | 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0002c0002t0005g0223 | 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 | a0001c0001t0001g0111a0001c0001t0001g0138a0001c0001t0001g0161others(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 | a0002c0002t0004g0220 | 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 | a0001c0001t0003g0100a0001c0001t0008g0104a0001c0001t0049g0099 | 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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0001c0001t0001g0123a0001c0001t0001g0173 | 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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0002c0002t0010g0342 | 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0180a0001c0001t0003g0041a0001c0001t0003g0042others(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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | a0001c0001t0007g0032a0001c0001t0013g0014 | 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 | a0001c0001t0032g0188a0001c0001t0032g0189a0001c0001t0039g0200others(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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0001c0001t0064g0013 | 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 | 181 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(178): Show | 183 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(180): 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 | a0001c0001t0006g0050 | 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 | a0002c0009t0069g0258 | 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 | a0001c0001t0060g0027 | 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 | a0001c0001t0003g0055a0001c0001t0003g0068 | 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 | a0002c0009t0069g0258 | 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 | a0001c0001t0001g0203a0001c0001t0074g0190a0002c0002t0002g0251others(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 | a0002c0002t0001g0337a0002c0002t0001g0338a0002c0002t0001g0339others(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 | 188 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(185): Show | 190 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(187): 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 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0044others(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 | a0002c0003t0068g0217 | 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 | a0002c0002t0005g0235a0002c0002t0005g0237a0002c0002t0005g0239others(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 | 160 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(157): Show | 162 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(159): 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 | a0001c0001t0020g0009a0001c0001t0020g0010a0001c0001t0020g0011 | 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 | a0001c0001t0001g0117 | 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 | a0002c0002t0048g0323 | 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 | a0001c0001t0020g0009a0001c0001t0020g0010a0001c0001t0020g0011 | 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0002c0002t0005g0223 | 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 | a0002c0002t0025g0292a0002c0002t0025g0293a0002c0002t0025g0294 | 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 | a0001c0001t0021g0054 | 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 | a0001c0001t0003g0042 | 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 | a0002c0002t0004g0285 | 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 | a0001c0001t0001g0181a0001c0001t0001g0182 | 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 | a0001c0001t0003g0060 | 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 | a0001c0001t0021g0098 | 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 | a0001c0001t0045g0047 | 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 | 221 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(218): Show | 223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.739-3437T>G | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50272767 | ||||||
| chr14:50272829
|
A | T | 3 | a0001c0001t0029g0036a0001c0001t0034g0065a0001c0001t0034g0069 | 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 | a0002c0003t0001g0257 | 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 | a0001c0001t0019g0185a0001c0001t0019g0186 | 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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0001c0001t0006g0134 | 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 | 187 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(184): Show | 189 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(186): 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0003g0087a0001c0001t0006g0088 | 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 | a0001c0001t0007g0032a0001c0001t0013g0014a0001c0001t0013g0030others(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 | a0002c0003t0019g0353a0002c0003t0028g0351a0002c0003t0028g0352 | 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 | a0001c0001t0021g0098 | 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 | 225 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(222): Show | 227 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(224): 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 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0044others(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 | 225 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(222): Show | 227 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(224): 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 | a0001c0001t0007g0032 | 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 | a0001c0001t0003g0177 | 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | a0001c0001t0007g0032a0001c0001t0013g0014a0001c0001t0013g0030others(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 | a0002c0003t0068g0217 | 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 | a0001c0001t0064g0013 | 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 | a0002c0002t0017g0345 | 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 | a0001c0001t0021g0081 | 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 | a0002c0003t0068g0217 | 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 | a0001c0001t0007g0092 | 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 | a0001c0001t0033g0156 | 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 | a0001c0001t0032g0188a0001c0001t0032g0189a0001c0001t0039g0200others(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 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0044others(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 | a0001c0001t0021g0054 | 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 | 256 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(253): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): 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 | a0001c0001t0001g0151a0001c0001t0001g0164a0001c0001t0001g0181others(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 | a0001c0001t0007g0032a0001c0001t0013g0014a0001c0001t0013g0030others(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 | a0002c0002t0024g0227a0002c0002t0024g0238a0002c0002t0024g0242 | 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0001g0167 | 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 | a0001c0001t0019g0185a0001c0001t0019g0186 | 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 | a0001c0001t0026g0160 | 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0133 | 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 | a0002c0002t0004g0286 | 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 | 197 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(194): 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 | a0001c0001t0001g0170a0001c0001t0026g0110a0001c0001t0026g0160 | 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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | 222 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(219): Show | 224 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(221): 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 | a0001c0001t0018g0206a0001c0001t0018g0207a0001c0001t0018g0208 | 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 | a0002c0002t0002g0289 | 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 | a0001c0001t0018g0206a0001c0001t0018g0207a0001c0001t0018g0208 | 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 | 134 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(131): Show | 136 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.738+1312dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 6/9 | chr14 | 50277207 | ||||||
| chr14:50277207
|
G | GTT | 31 | a0001c0001t0001g0079a0001c0001t0001g0123a0001c0001t0001g0140others(28): 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 | a0001c0001t0064g0013 | 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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0022others(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 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0021others(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 | a0001c0001t0001g0117a0001c0001t0001g0148a0001c0001t0001g0149others(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 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0014g0204others(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 | a0001c0001t0019g0185a0001c0001t0019g0186a0001c0001t0031g0212others(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 | a0002c0002t0002g0315a0002c0002t0002g0320 | 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 | a0002c0002t0072g0232 | 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 | a0001c0004t0005g0202a0002c0002t0070g0240a0002c0002t0072g0232 | 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 | a0001c0004t0005g0202a0002c0002t0005g0222a0002c0002t0005g0223others(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 | 222 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(219): Show | 224 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(221): 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 | a0001c0001t0020g0009a0001c0001t0020g0010a0001c0001t0020g0011 | 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 | a0001c0001t0032g0188a0001c0001t0032g0189a0001c0001t0039g0200others(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 | a0002c0003t0068g0217 | 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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0002c0002t0070g0240 | 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 | a0001c0001t0001g0121 | 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 | 194 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(191): Show | 196 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.704-825delC | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50279378 | ||||||
| chr14:50279456
|
A | G | 15 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0039g0201 | 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 | a0001c0001t0045g0047 | 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 | a0002c0002t0037g0228 | 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 | a0001c0001t0009g0150 | 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 | a0001c0001t0014g0209a0001c0001t0014g0210a0001c0001t0018g0206others(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 | 186 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(183): Show | 188 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.704-1511delT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 5/9 | chr14 | 50280064 | ||||||
| chr14:50280165
|
C | CT | 9 | a0001c0001t0001g0116a0001c0001t0008g0064a0001c0001t0009g0155others(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 | a0002c0003t0052g0348 | 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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0002c0002t0011g0241a0002c0003t0001g0254a0002c0003t0001g0256others(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 | a0002c0002t0025g0292a0002c0002t0025g0293a0002c0002t0025g0294 | 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 | a0001c0001t0001g0112 | 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 | 215 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(212): Show | 217 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(214): 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 | a0002c0002t0002g0332a0002c0002t0010g0334 | 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 | a0001c0001t0007g0032a0001c0001t0013g0014a0001c0001t0013g0030others(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 | a0002c0002t0004g0248 | 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 | a0002c0003t0019g0353a0002c0003t0028g0351a0002c0003t0028g0352 | 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 | a0002c0002t0025g0292a0002c0002t0025g0293a0002c0002t0025g0294 | 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 | a0002c0003t0001g0355 | 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 | a0001c0001t0001g0164 | 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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0001c0001t0012g0119 | 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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0001c0001t0073g0053 | 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 | a0001c0001t0032g0188a0001c0001t0032g0189a0001c0001t0039g0200others(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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0001g0170a0001c0001t0026g0110a0001c0001t0026g0160 | 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 | a0002c0003t0001g0355 | 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0064g0013 | 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 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0113others(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 | a0002c0003t0001g0254 | 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 | a0001c0001t0006g0080 | 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 | 222 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(219): Show | 224 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(221): 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 | a0002c0002t0002g0316 | 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 | a0002c0002t0040g0288 | 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 | a0001c0001t0064g0013 | 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 | a0002c0002t0040g0288a0002c0002t0040g0350 | 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 | a0002c0002t0004g0219 | 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 | a0002c0003t0052g0348a0002c0003t0055g0349 | 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 | a0001c0001t0001g0137 | 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 | a0002c0003t0052g0348a0002c0003t0055g0349 | 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 | a0001c0001t0002g0125 | 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 | a0002c0002t0002g0299 | 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 | a0002c0003t0001g0355 | 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 | a0002c0002t0004g0265a0002c0002t0017g0264a0002c0002t0017g0266others(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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | 210 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(207): Show | 212 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(209): 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 | a0001c0001t0003g0055 | 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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | a0002c0003t0052g0348a0002c0003t0055g0349 | 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 | 214 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(211): Show | 216 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(213): 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 | a0002c0003t0068g0217 | 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 | 187 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(184): Show | 189 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(186): 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 | a0001c0004t0005g0202a0002c0002t0005g0222a0002c0002t0005g0223others(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 | a0002c0002t0025g0292a0002c0002t0025g0293a0002c0002t0025g0294 | 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 | a0001c0001t0001g0109 | 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 | a0002c0003t0019g0353a0002c0003t0028g0351a0002c0003t0028g0352 | 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 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0044others(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 | 187 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(184): Show | 189 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.541-449dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50284481 | ||||||
| chr14:50284536
|
T | C | 1 | a0001c0001t0001g0196 | 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 | a0002c0002t0048g0323 | 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 | 225 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(222): Show | 227 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(224): 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 | a0001c0001t0031g0211 | 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 | a0002c0002t0001g0321a0002c0002t0058g0326 | 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 | a0002c0003t0001g0355 | 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 | a0002c0002t0002g0252 | 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 | 327 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(324): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): 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 | a0001c0001t0001g0085 | 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 | a0001c0001t0003g0017 | 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 | a0001c0001t0013g0030a0001c0001t0013g0031a0001c0001t0013g0033others(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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0001g0124a0001c0001t0001g0127 | 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 | a0002c0002t0002g0317 | 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 | a0001c0001t0032g0188a0001c0001t0032g0189a0001c0001t0039g0200others(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 | 5 | a0001c0001t0003g0074a0001c0001t0003g0176a0001c0001t0003g0177others(2): Show | 5 | HG01069.hp2 HG01433.hp2 HG02258.hp1 others(2): 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 | a0002c0003t0055g0349 | 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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0002c0002t0005g0229 | 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 | 221 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(218): Show | 223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): 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 | a0001c0001t0001g0151 | 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 | a0001c0001t0001g0109 | 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 | a0002c0003t0055g0349 | 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 | a0002c0003t0068g0217 | 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0014g0209 | 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 | a0001c0001t0018g0206a0001c0001t0018g0207a0001c0001t0018g0208 | 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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0001c0001t0003g0108 | 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | 64 | a0001c0001t0001g0018a0001c0001t0001g0079a0001c0001t0002g0187others(61): Show | 65 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(62): 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 | a0003c0005t0015g0213 | 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 | 225 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(222): Show | 227 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(224): 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0002c0002t0002g0251 | 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 | a0001c0001t0001g0019a0001c0001t0001g0109a0001c0001t0001g0116others(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 | a0001c0001t0001g0164a0001c0001t0009g0150a0001c0001t0020g0009others(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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0002c0002t0002g0341 | 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 | 187 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(184): Show | 189 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(186): Show |
intron_variant | MODIFIER | c.541-3930T>C | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50287963 | ||||||
| chr14:50287992
|
C | T | 158 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(155): Show | 160 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(157): 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 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0044others(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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | a0001c0001t0003g0041 | 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 | a0001c0004t0005g0202a0002c0002t0005g0222a0002c0002t0005g0223others(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 | a0002c0002t0005g0229a0002c0002t0072g0232 | 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 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0044others(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 | a0001c0001t0001g0180 | 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 | a0001c0001t0032g0188a0001c0001t0032g0189 | 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 | a0001c0001t0013g0031 | 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 | 199 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(196): Show | 201 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(198): 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 | a0001c0001t0001g0161 | 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 | a0001c0001t0007g0095 | 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 | a0001c0001t0060g0027 | 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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | a0001c0001t0002g0187 | 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 | a0001c0001t0001g0114 | 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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0001c0001t0003g0072 | 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 | 225 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(222): Show | 227 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(224): 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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | a0001c0001t0020g0011 | 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 | 221 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(218): Show | 223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): 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 | a0001c0001t0074g0190a0001c0001t0075g0191 | 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 | a0002c0002t0002g0297 | 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 | a0001c0001t0030g0184 | 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 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0113others(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 | a0001c0001t0001g0152 | 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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0044others(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 | a0001c0001t0018g0206a0001c0001t0018g0207a0001c0001t0018g0208 | 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0032g0188a0001c0001t0032g0189a0001c0001t0039g0200others(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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | a0001c0001t0007g0091a0001c0001t0007g0093 | 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 | 186 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(183): Show | 188 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.540+3738G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 4/9 | chr14 | 50290377 | ||||||
| chr14:50290413
|
A | C | 225 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(222): Show | 227 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(224): 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 | a0001c0001t0001g0022 | 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 | a0002c0002t0002g0308 | 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 | a0001c0001t0001g0151 | 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 | a0001c0001t0013g0033 | 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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | a0001c0001t0003g0074 | 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 | a0002c0002t0002g0333 | 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 | a0001c0001t0019g0185a0001c0001t0019g0186 | 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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | a0002c0002t0002g0318 | 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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0001c0001t0013g0030a0001c0001t0013g0031a0001c0001t0013g0033others(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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0001g0254others(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 | a0001c0001t0060g0027 | 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 | a0002c0003t0068g0217 | 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 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0024others(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 | a0001c0001t0001g0019a0001c0001t0003g0103a0001c0001t0006g0101others(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 | a0001c0001t0015g0106a0001c0001t0035g0063a0002c0002t0005g0222others(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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0001c0001t0001g0181a0001c0001t0001g0182a0002c0003t0001g0355 | 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 | a0001c0001t0022g0029 | 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 | a0001c0001t0003g0042a0001c0001t0003g0044a0001c0001t0003g0045others(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 | a0001c0001t0003g0041a0001c0001t0006g0015a0001c0001t0046g0012others(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 | a0001c0001t0056g0016 | 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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0002c0003t0001g0256a0002c0003t0001g0257a0002c0003t0002g0255 | 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 | a0002c0002t0002g0298 | 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 | a0001c0001t0073g0053 | 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 | a0001c0001t0020g0009a0001c0001t0020g0010a0001c0001t0020g0011 | 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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0002c0003t0068g0217 | 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 | a0001c0004t0005g0202a0002c0002t0005g0222a0002c0002t0005g0223others(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 | a0002c0002t0005g0235a0002c0002t0005g0237a0002c0002t0005g0239others(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 | a0001c0001t0001g0126 | 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 | a0002c0003t0068g0217 | 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 | a0001c0001t0012g0118a0001c0001t0012g0119a0001c0001t0012g0120 | 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 | a0001c0001t0001g0171 | 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 | 160 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(157): Show | 162 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(159): 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0032g0188a0001c0001t0032g0189a0001c0001t0039g0200others(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 | a0001c0001t0006g0062 | 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0002c0002t0004g0219 | 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 | a0001c0001t0031g0211 | 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 | a0001c0001t0001g0127 | 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | 225 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(222): Show | 227 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(224): 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0074g0190a0001c0001t0075g0191 | 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 | a0001c0001t0032g0188a0001c0001t0032g0189a0001c0001t0039g0200others(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 | 64 | a0001c0001t0001g0018a0001c0001t0001g0079a0001c0001t0001g0085others(61): Show | 65 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(62): 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 | a0001c0001t0013g0030a0001c0001t0013g0031a0001c0001t0013g0033others(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 | a0001c0004t0005g0202a0002c0002t0005g0222a0002c0002t0005g0223others(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 | a0002c0002t0005g0243 | 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0001c0001t0032g0188a0001c0001t0032g0189 | 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 | a0001c0001t0007g0095 | 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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0002c0002t0005g0222a0002c0002t0005g0223a0002c0002t0005g0224 | 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 | a0002c0002t0005g0243 | 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0007g0032a0001c0001t0013g0014a0001c0001t0013g0030others(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 | a0002c0003t0055g0349 | 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 | a0002c0003t0068g0217 | 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 | a0002c0003t0052g0348a0002c0003t0055g0349 | 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 | a0002c0003t0001g0259a0002c0003t0001g0261a0002c0003t0009g0260others(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 | a0001c0001t0020g0009a0001c0001t0020g0010a0001c0001t0020g0011 | 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 | 202 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(199): Show | 204 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(201): 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 | a0001c0001t0001g0171 | 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 | a0001c0001t0001g0171 | 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 | a0002c0002t0004g0218a0002c0002t0004g0219a0002c0002t0004g0220others(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 | a0001c0001t0001g0021a0001c0001t0001g0109a0001c0001t0001g0117others(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 | a0001c0001t0001g0179a0001c0001t0001g0197a0001c0001t0001g0199others(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 | a0001c0001t0013g0014 | 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 | a0001c0001t0001g0133a0001c0001t0001g0164a0001c0001t0003g0055others(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 | a0002c0003t0052g0348 | 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 | a0001c0001t0003g0074 | 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 | 256 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(253): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): 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 | a0001c0001t0003g0056a0001c0001t0003g0057a0001c0001t0003g0058others(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 | a0002c0002t0005g0222a0002c0002t0005g0223a0002c0002t0005g0224 | 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 | a0001c0001t0029g0075 | 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 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0113others(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 | 190 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(187): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.409-2127dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50296372 | ||||||
| chr14:50296372
|
C | CAA | 51 | a0001c0001t0001g0002a0001c0001t0001g0079a0001c0001t0001g0116others(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 | a0001c0001t0015g0096a0001c0001t0015g0106a0001c0001t0019g0186others(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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0002c0003t0001g0355 | 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 | a0001c0001t0001g0197a0001c0001t0003g0041a0001c0001t0003g0042others(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 | a0003c0005t0007g0216 | 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 | a0001c0001t0012g0118 | 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 | 185 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(182): Show | 187 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(184): 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0002c0002t0002g0295a0002c0002t0002g0296 | 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 | a0001c0001t0060g0027 | 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 | a0002c0002t0005g0222a0002c0002t0005g0223a0002c0002t0005g0224 | 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 | a0001c0001t0074g0190a0001c0001t0075g0191 | 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 | a0002c0002t0001g0337a0002c0002t0001g0338a0002c0002t0001g0339 | 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | 197 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(194): Show | 199 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.409-3689delT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 3/9 | chr14 | 50297934 | ||||||
| chr14:50297959
|
C | A | 3 | a0002c0002t0001g0337a0002c0002t0001g0338a0002c0002t0001g0339 | 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 | a0002c0002t0002g0289 | 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 | a0001c0001t0020g0009a0001c0001t0020g0010a0001c0001t0020g0011 | 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 | a0001c0001t0001g0085a0001c0001t0032g0188a0001c0001t0032g0189others(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 | a0002c0002t0001g0337a0002c0002t0001g0338a0002c0002t0001g0339others(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 | a0001c0001t0021g0054 | 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0133others(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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | a0002c0003t0052g0348a0002c0003t0055g0349 | 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 | 187 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(184): Show | 189 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(186): 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 | a0001c0001t0056g0016 | 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 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0044others(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 | a0001c0001t0073g0053 | 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 | a0001c0004t0005g0202a0002c0002t0005g0222a0002c0002t0005g0223others(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 | a0001c0001t0001g0173 | 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 | a0001c0001t0013g0034 | 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 | a0001c0001t0003g0017 | 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 | a0001c0001t0001g0169 | 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 | a0001c0001t0031g0211 | 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 | a0001c0001t0002g0187 | 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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0001c0001t0007g0032a0001c0001t0013g0014a0001c0001t0013g0030others(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 | a0001c0001t0074g0190a0001c0001t0075g0191 | 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 | a0002c0002t0002g0340 | 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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0001c0001t0012g0128 | 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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0002c0003t0068g0217 | 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 | a0001c0001t0019g0185a0001c0001t0019g0186a0002c0003t0019g0353others(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 | a0002c0003t0068g0217 | 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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | 223 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(220): Show | 225 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(222): 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 | a0001c0001t0020g0009a0001c0001t0020g0010a0001c0001t0020g0011 | 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 | a0002c0002t0002g0263a0002c0002t0002g0341a0002c0002t0002g0343others(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 | 222 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(219): Show | 224 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(221): 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 | a0001c0001t0032g0188a0001c0001t0032g0189a0001c0001t0039g0200others(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 | a0001c0001t0003g0041a0001c0001t0003g0042a0001c0001t0003g0044others(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 | a0001c0001t0022g0046 | 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 | 221 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(218): Show | 223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): 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 | a0001c0001t0074g0190a0001c0001t0075g0191 | 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 | a0002c0002t0004g0274a0002c0003t0001g0254a0002c0003t0001g0256others(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 | 168 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(165): Show | 170 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(167): Show |
intron_variant | MODIFIER | c.141-133C>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303150 | ||||||
| chr14:50303183
|
A | G | 222 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(219): Show | 224 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(221): 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 | a0001c0001t0031g0211 | 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 | a0002c0002t0025g0292a0002c0002t0025g0293a0002c0002t0025g0294 | 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 | 189 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(186): Show | 191 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(188): 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 | a0001c0001t0001g0181a0001c0001t0001g0182a0002c0003t0001g0355 | 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 | a0002c0003t0019g0353a0002c0003t0028g0351a0002c0003t0028g0352 | 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 | 218 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(215): Show | 220 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.141-443dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303459 | ||||||
| chr14:50303555
|
T | A | 8 | a0001c0001t0007g0032a0001c0001t0013g0014a0001c0001t0013g0030others(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 | a0003c0005t0007g0215 | 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 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0003g0178others(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 | 222 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(219): Show | 224 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.141-786C>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303803 | ||||||
| chr14:50303810
|
T | TA | 207 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(204): Show | 209 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.141-794dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50303810 | ||||||
| chr14:50303810
|
T | TAA | 20 | a0001c0001t0001g0116a0001c0001t0001g0181a0001c0001t0001g0182others(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 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0005g0089others(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 | a0002c0003t0019g0353a0002c0003t0028g0351a0002c0003t0028g0352 | 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 | a0001c0001t0001g0173a0001c0001t0009g0174a0001c0001t0063g0175 | 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 | a0002c0002t0004g0271a0002c0002t0004g0272a0002c0002t0004g0273 | 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 | a0001c0001t0007g0091a0001c0001t0007g0092a0001c0001t0007g0093others(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 | a0001c0001t0012g0118a0001c0001t0012g0119a0001c0001t0012g0120 | 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 | a0002c0002t0005g0246 | 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 | a0002c0002t0017g0266 | 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 | a0002c0002t0004g0270 | 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 | a0001c0001t0001g0117 | 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 | a0001c0001t0013g0030 | 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 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0113others(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 | a0001c0001t0008g0104 | 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 | a0001c0001t0014g0205 | 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 | a0002c0003t0019g0353a0002c0003t0028g0351a0002c0003t0028g0352 | 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 | a0002c0003t0052g0348a0002c0003t0055g0349 | 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 | a0002c0002t0002g0291 | 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 | a0001c0001t0020g0009a0001c0001t0020g0010a0001c0001t0020g0011 | 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 | a0001c0001t0060g0027 | 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 | a0001c0001t0001g0111a0001c0001t0001g0112 | 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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | 221 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(218): Show | 223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): 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 | a0002c0002t0071g0221 | 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 | a0001c0001t0008g0097 | 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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | a0001c0001t0019g0185a0001c0001t0019g0186 | 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 | 198 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(195): Show | 200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): 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 | a0001c0001t0060g0027a0002c0002t0002g0290a0002c0002t0004g0268others(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 | 188 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(185): Show | 190 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.141-3033delA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306049 | ||||||
| chr14:50306049
|
CTT | C | 12 | a0001c0001t0003g0042a0001c0001t0003g0044a0001c0001t0003g0045others(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 | a0001c0001t0020g0011 | 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 | a0001c0001t0006g0050 | 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 | a0001c0001t0001g0179 | 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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | 220 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(217): Show | 222 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(219): 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 | a0001c0001t0003g0049a0001c0001t0003g0100a0001c0001t0003g0103others(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 | a0001c0001t0015g0106a0001c0001t0015g0107a0001c0001t0076g0105 | 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 | a0001c0001t0020g0009a0001c0001t0020g0010a0001c0001t0020g0011others(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 | 186 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(183): Show | 188 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.141-3584delA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306600 | ||||||
| chr14:50306600
|
GTT | G | 6 | a0001c0001t0003g0108a0001c0001t0022g0029a0001c0001t0022g0035others(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 | a0001c0001t0022g0029a0001c0001t0022g0035a0001c0001t0022g0046others(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 | 92 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0019others(89): 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 | 221 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(218): Show | 223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.141-3805A>T | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50306822 | ||||||
| chr14:50306858
|
T | C | 221 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(218): Show | 223 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(220): 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 | a0002c0002t0040g0288a0002c0002t0040g0350 | 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 | a0001c0004t0002g0037a0001c0004t0002g0038a0001c0004t0002g0039others(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 | a0002c0009t0069g0258 | 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 | a0001c0001t0018g0207a0001c0001t0018g0208 | 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 | a0002c0002t0004g0265a0002c0002t0017g0264a0002c0002t0017g0266others(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 | a0002c0002t0002g0263 | 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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0001c0001t0020g0009a0001c0001t0020g0010a0001c0001t0020g0011 | 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 | a0002c0003t0001g0254a0002c0003t0001g0256a0002c0003t0001g0257others(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 | a0002c0003t0052g0348a0002c0003t0055g0349 | 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 | a0002c0002t0002g0344 | 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 | a0002c0002t0017g0345 | 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 | a0001c0001t0061g0048 | 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 | a0001c0001t0001g0181a0001c0001t0001g0182a0002c0003t0001g0355 | 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 | a0001c0004t0005g0202a0002c0002t0005g0222a0002c0002t0005g0223others(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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0003g0041others(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 | 172 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(169): 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 | a0001c0001t0020g0009a0001c0001t0020g0010a0001c0001t0020g0011 | 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 | a0002c0002t0002g0346 | 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 | 222 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(219): Show | 224 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(221): 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 | a0002c0003t0019g0353a0002c0003t0028g0351a0002c0003t0028g0352 | 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 | 177 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(174): Show | 179 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(176): 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 | a0002c0002t0010g0347 | 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 | a0003c0005t0007g0216 | 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 | 198 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(195): Show | 200 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(197): 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 | a0001c0001t0013g0034 | 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0074g0190a0001c0001t0075g0191a0002c0003t0001g0254others(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 | 228 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(225): Show | 230 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.140+2488G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50309523 | ||||||
| chr14:50309561
|
T | TA | 200 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(197): Show | 202 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.140+2449dupT | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50309561 | ||||||
| chr14:50309561
|
TA | T | 12 | a0001c0001t0032g0188a0001c0001t0039g0200a0001c0001t0039g0201others(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 | a0001c0001t0007g0032a0001c0001t0013g0014a0001c0001t0013g0030others(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 | a0002c0002t0037g0247 | 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 | 208 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(205): Show | 210 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.140+2322dupA | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50309688 | ||||||
| chr14:50309734
|
G | A | 3 | a0001c0001t0002g0187a0001c0001t0030g0184a0001c0001t0044g0183 | 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 | a0001c0001t0020g0009a0001c0001t0020g0010a0001c0001t0020g0011 | 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 | 217 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(214): Show | 219 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(216): 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 | a0001c0001t0032g0188a0001c0001t0032g0189a0001c0001t0039g0200others(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 | a0002c0002t0005g0225a0002c0002t0005g0226 | 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 | a0001c0001t0074g0190a0001c0001t0075g0191a0003c0005t0007g0214others(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 | a0001c0001t0074g0190a0001c0001t0075g0191a0003c0005t0007g0214others(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 | a0001c0001t0022g0029 | 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 | a0001c0001t0018g0206a0001c0001t0018g0207a0001c0001t0018g0208 | 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 | 203 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0018others(200): Show | 205 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(202): 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 | a0001c0001t0001g0028a0001c0001t0001g0192a0001c0001t0001g0193others(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 | a0002c0002t0002g0249a0002c0002t0002g0250a0002c0002t0002g0251others(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 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0021others(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 | 185 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0079others(182): Show | 187 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(184): 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 | a0001c0001t0001g0199a0001c0001t0014g0204a0001c0001t0014g0205others(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 | a0001c0004t0005g0202a0002c0002t0005g0225a0002c0002t0005g0226others(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 | a0001c0001t0001g0203 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0001c0001t0014g0204a0001c0001t0014g0205 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0002c0002t0002g0356 | 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 | a0001c0001t0020g0009a0001c0001t0020g0010a0001c0001t0020g0011others(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 | a0001c0001t0014g0204a0001c0001t0014g0205a0001c0001t0014g0209others(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 | a0001c0001t0003g0007a0001c0001t0006g0008 | 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 | a0002c0002t0004g0218a0002c0002t0004g0219a0002c0002t0004g0220 | 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 | a0001c0001t0031g0211a0001c0001t0031g0212 | 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 | a0002c0003t0068g0217 | 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 | a0001c0001t0001g0006 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.140+187G>A | L2HGDH | ENSG00000087299.12 | transcript | ENST00000267436.9 | protein_coding | 1/9 | chr14 | 50311824 |