Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 60526 |
|---|---|
| ensemblid | ENSG00000118961.15 |
| hgncid | 26145 |
| symbol | LDAH |
| name | lipid droplet associated hydrolase |
| refseq_nuc | NM_021925.4 |
| refseq_prot | NP_068744.1 |
| ensembl_nuc | ENST00000237822.8 |
| ensembl_prot | ENSP00000237822.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 20684031 |
| end | 20823101 |
| strand | - |
| ver | v1.2 |
| region | chr2:20684031-20823101 |
| region5000 | chr2:20679031-20828101 |
| regionname0 | LDAH_chr2_20684031_20823101 |
| regionname5000 | LDAH_chr2_20679031_20828101 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 325 | 250 | 74 | 54 | 76 | 14 | 30 | 53 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0002 | 0/0 | 325 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0003 | 0/0 | 325 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0004 | 0/0 | 325 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0005 | 0/0 | 19 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 978 | 244 | 73 | 54 | 76 | 14 | 25 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| c0002 | 0/0 | 978 | 5 | 0 | 0 | 0 | 0 | 5 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| c0003 | 0/0 | 978 | 4 | 4 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| c0004 | 0/0 | 978 | 2 | 0 | 0 | 2 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| c0005 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| c0006 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| c0007 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| 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 | 1/0 | 2940 | 85 | 33 | 15 | 25 | 3 | 8 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| t0002 | 0/0 | 2934 | 44 | 3 | 8 | 27 | 2 | 4 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| t0003 | 0/0 | 2940 | 40 | 13 | 10 | 7 | 2 | 8 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| t0004 | 0/1 | 2940 | 39 | 10 | 12 | 4 | 5 | 7 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| t0005 | 0/0 | 2940 | 30 | 9 | 6 | 11 | 2 | 2 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| t0006 | 0/0 | 2940 | 6 | 6 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| t0007 | 0/0 | 2940 | 3 | 1 | 2 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| t0008 | 0/0 | 2940 | 2 | 0 | 0 | 2 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| t0009 | 0/0 | 2940 | 2 | 2 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| t0010 | 0/0 | 2940 | 2 | 1 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| t0011 | 0/0 | 2934 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| t0012 | 0/0 | 2940 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| t0013 | 0/0 | 2940 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| t0014 | 0/0 | 2940 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| t0015 | 0/0 | 2940 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| 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 | 1 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0009 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 978 | 244 | 73 | 54 | 76 | 14 | 25 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0001c0002 | 0/0 | 978 | 5 | 0 | 0 | 0 | 0 | 5 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0001c0006 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0002c0003 | 0/0 | 978 | 4 | 4 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0003c0004 | 0/0 | 978 | 2 | 0 | 0 | 2 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0004c0005 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0005c0007 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3917 | 77 | 30 | 15 | 25 | 3 | 3 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0001c0001t0002 | 0/0 | 3911 | 42 | 3 | 8 | 25 | 2 | 4 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0001c0001t0003 | 0/0 | 3917 | 40 | 13 | 10 | 7 | 2 | 8 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0001c0001t0004 | 0/1 | 3917 | 36 | 7 | 12 | 4 | 5 | 7 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0001c0001t0005 | 0/0 | 3917 | 30 | 9 | 6 | 11 | 2 | 2 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0001c0001t0006 | 0/0 | 3917 | 6 | 6 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0001c0001t0007 | 0/0 | 3917 | 3 | 1 | 2 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0001c0001t0008 | 0/0 | 3917 | 2 | 0 | 0 | 2 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0001c0001t0009 | 0/0 | 3917 | 2 | 2 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0001c0001t0010 | 0/0 | 3917 | 2 | 1 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0001c0001t0011 | 0/0 | 3911 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0001c0001t0012 | 0/0 | 3917 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0001c0001t0014 | 0/0 | 3917 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0001c0001t0015 | 0/0 | 3917 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0001c0002t0001 | 0/0 | 3917 | 5 | 0 | 0 | 0 | 0 | 5 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0001c0006t0001 | 0/0 | 3917 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0002c0003t0001 | 0/0 | 3917 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0002c0003t0004 | 0/0 | 3917 | 3 | 3 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0003c0004t0002 | 0/0 | 3911 | 2 | 0 | 0 | 2 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0004c0005t0013 | 0/0 | 3917 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| a0005c0007t0001 | 0/0 | 3917 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | copy fasta | chr2 | 20679031 | 20828101 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0009 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0114 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0004g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0007g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0007g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0008g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0008g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0009g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0009g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0010g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0010g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0011g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0012g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0014g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0001t0015g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0001c0006t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0002c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0002c0003t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0002c0003t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0002c0003t0004g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0003c0004t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0003c0004t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0004c0005t0013g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| a0005c0007t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0005 | g0045 | EUR | GBR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0075 | EUR | GBR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0116 | EUR | GBR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0186 | EUR | GBR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0025 | EUR | FIN | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0135 | EUR | FIN | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG00639 | hp1 | a0001 | c0001 | t0004 | g0026 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0205 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG00642 | hp2 | a0001 | c0001 | t0005 | g0047 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | CHS | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG00735 | hp1 | a0001 | c0001 | t0004 | g0044 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01070 | hp1 | a0001 | c0001 | t0007 | g0085 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0216 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0086 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01081 | hp2 | a0001 | c0001 | t0004 | g0078 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01106 | hp1 | a0001 | c0001 | t0005 | g0048 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0083 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01175 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01175 | hp2 | a0001 | c0001 | t0004 | g0185 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0031 | AMR | PUR | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0079 | AMR | CLM | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0073 | AMR | CLM | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0157 | AMR | CLM | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0201 | AMR | CLM | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | CLM | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0112 | AMR | CLM | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01361 | hp2 | a0001 | c0001 | t0005 | g0163 | AMR | CLM | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0097 | AMR | CLM | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0080 | AMR | CLM | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01496 | hp2 | a0001 | c0001 | t0010 | g0115 | AMR | CLM | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0043 | EUR | IBS | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0124 | EUR | IBS | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0184 | EUR | IBS | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01516 | hp2 | a0001 | c0001 | t0004 | g0001 | EUR | IBS | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01517 | hp1 | a0001 | c0001 | t0004 | g0074 | EUR | IBS | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0125 | EUR | IBS | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01884 | hp1 | a0001 | c0001 | t0005 | g0226 | AFR | ACB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PEL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01952 | hp2 | a0001 | c0001 | t0005 | g0051 | AMR | PEL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0211 | AMR | PEL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0212 | AMR | PEL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PEL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0217 | EAS | KHV | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02040 | hp1 | a0001 | c0001 | t0005 | g0107 | EAS | KHV | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | KHV | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02071 | hp1 | a0001 | c0001 | t0005 | g0119 | EAS | KHV | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02071 | hp2 | a0001 | c0001 | t0005 | g0059 | EAS | KHV | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02080 | hp1 | a0001 | c0001 | t0008 | g0093 | EAS | KHV | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02129 | hp1 | a0001 | c0001 | t0008 | g0061 | EAS | KHV | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02132 | hp1 | a0001 | c0001 | t0015 | g0256 | EAS | KHV | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | KHV | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | KHV | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02135 | hp2 | a0001 | c0001 | t0005 | g0123 | EAS | KHV | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | ACB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0067 | AFR | ACB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CDX | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | CDX | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0099 | AFR | ACB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0065 | AFR | ACB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0224 | AFR | ACB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02523 | hp2 | a0003 | c0004 | t0002 | g0128 | EAS | KHV | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0206 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02615 | hp1 | a0001 | c0001 | t0006 | g0144 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0118 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02622 | hp2 | a0001 | c0001 | t0005 | g0252 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0176 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02647 | hp2 | a0002 | c0003 | t0004 | g0235 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0197 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02723 | hp2 | a0001 | c0001 | t0010 | g0039 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02809 | hp1 | a0002 | c0003 | t0004 | g0234 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0207 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0101 | AFR | ESN | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02922 | hp2 | a0001 | c0001 | t0006 | g0199 | AFR | ESN | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | ESN | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | ESN | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03017 | hp1 | a0001 | c0001 | t0004 | g0210 | SAS | PJL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03041 | hp1 | a0002 | c0003 | t0004 | g0238 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0246 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0198 | AFR | MSL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0180 | AFR | ESN | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | ESN | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | ESN | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03139 | hp2 | a0001 | c0001 | t0007 | g0203 | AFR | ESN | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03209 | hp1 | a0002 | c0003 | t0001 | g0237 | AFR | MSL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03209 | hp2 | a0001 | c0001 | t0014 | g0255 | AFR | MSL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03225 | hp1 | a0001 | c0006 | t0001 | g0240 | AFR | MSL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0214 | SAS | PJL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0142 | SAS | PJL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0145 | AFR | MSL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0227 | AFR | MSL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0164 | SAS | PJL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03492 | hp2 | a0001 | c0001 | t0012 | g0007 | SAS | PJL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0225 | AFR | ESN | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | ESN | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0136 | AFR | GWD | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0170 | SAS | PJL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0188 | SAS | PJL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03688 | hp1 | a0001 | c0002 | t0001 | g0191 | SAS | STU | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | STU | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0015 | SAS | PJL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0192 | SAS | PJL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | BEB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0173 | SAS | BEB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0193 | SAS | BEB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0130 | SAS | BEB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | BEB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0195 | SAS | BEB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0014 | SAS | BEB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0161 | SAS | BEB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0016 | SAS | BEB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0156 | SAS | STU | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0172 | SAS | STU | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0194 | SAS | STU | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | STU | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0250 | AFR | YRI | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | YRI | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | YRI | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18939 | hp1 | a0003 | c0004 | t0002 | g0127 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18939 | hp2 | a0001 | c0001 | t0005 | g0103 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18945 | hp1 | a0001 | c0001 | t0005 | g0166 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18960 | hp1 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18978 | hp1 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19001 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19011 | hp1 | a0001 | c0001 | t0005 | g0165 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19011 | hp2 | a0001 | c0001 | t0011 | g0081 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | LWK | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19043 | hp2 | a0005 | c0007 | t0001 | g0062 | AFR | LWK | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19060 | hp1 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | YRI | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | YRI | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0046 | EUR | TSI | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA20905 | hp1 | a0001 | c0001 | t0005 | g0035 | SAS | GIH | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0017 | SAS | GIH | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0120 | AMR | CLM | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | CLM | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02486 | hp1 | a0004 | c0005 | t0013 | g0243 | AFR | ACB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0204 | AFR | ACB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0253 | AFR | ACB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0239 | AFR | ACB | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0254 | AFR | MSL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0242 | AFR | MSL | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | USA | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0070 | AFR | USA | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0098 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | JPT | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | USA | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | USA | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0114 | REF | REF | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0009 | REF | REF | LDAH_chr2_20679031_20828101 | LDAH | chr2 | 20679031 | 20828101 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:20686946
|
T | C | 1 | a0004 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.935A>G | p.Asp312Gly | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 1002/3917 | 935/978 | 312/325 | chr2 | 20686946 | ||
| chr2:20790362
|
G | A | 1 | a0002 | 4 | HG02647.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
missense_variant | MODERATE | c.191C>T | p.Ala64Val | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/7 | 258/3917 | 191/978 | 64/325 | chr2 | 20790362 | ||
| chr2:20801400
|
C | T | 1 | a0003 | 2 | HG02523.hp2 NA18939.hp1 |
missense_variant | MODERATE | c.64G>A | p.Glu22Lys | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/7 | 131/3917 | 64/978 | 22/325 | chr2 | 20801400 | ||
| chr2:20801406
|
C | A | 1 | a0005 | 1 | NA19043.hp2 | stop_gained | HIGH | c.58G>T | p.Gly20* | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/7 | 125/3917 | 58/978 | 20/325 | chr2 | 20801406 | ||
| chr2:20801432
|
A | G | 1 | a0004 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.32T>C | p.Val11Ala | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/7 | 99/3917 | 32/978 | 11/325 | chr2 | 20801432 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:20740179
|
T | A | 1 | a0001c0006 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.495A>T | p.Pro165Pro | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/7 | 562/3917 | 495/978 | 165/325 | chr2 | 20740179 | ||
| chr2:20801377
|
C | T | 1 | a0001c0002 | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
synonymous_variant | LOW | c.87G>A | p.Gly29Gly | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/7 | 154/3917 | 87/978 | 29/325 | chr2 | 20801377 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:20684156
|
C | G | 1 | a0001c0001t0008 | 2 | HG02080.hp1 HG02129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2747G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 2747 | chr2 | 20684156 | |||||
| chr2:20684193
|
C | T | 1 | a0001c0001t0005 | 30 | HG00099.hp1 HG00642.hp2 HG01070.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2710G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 2710 | chr2 | 20684193 | |||||
| chr2:20684375
|
TTTAATC | T | 3 | a0001c0001t0002a0001c0001t0011a0003c0004t0002 | 45 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2522_*2527delGATT others(2): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 2522 | chr2 | 20684375 | |||||
| chr2:20684502
|
G | A | 6 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(3): Show | 89 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*2401C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 2401 | chr2 | 20684502 | |||||
| chr2:20684509
|
G | C | 1 | a0001c0001t0006 | 6 | HG02559.hp2 HG02615.hp1 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2394C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 2394 | chr2 | 20684509 | |||||
| chr2:20684516
|
A | T | 1 | a0001c0001t0012 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2387T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 2387 | chr2 | 20684516 | |||||
| chr2:20684608
|
T | C | 3 | a0001c0001t0004a0001c0001t0010a0002c0003t0004 | 41 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2295A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 2295 | chr2 | 20684608 | |||||
| chr2:20684621
|
C | T | 1 | a0001c0001t0005 | 30 | HG00099.hp1 HG00642.hp2 HG01070.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2282G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 2282 | chr2 | 20684621 | |||||
| chr2:20684786
|
A | C | 3 | a0001c0001t0002a0001c0001t0011a0003c0004t0002 | 45 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2117T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 2117 | chr2 | 20684786 | |||||
| chr2:20684790
|
C | A | 3 | a0001c0001t0004a0001c0001t0010a0002c0003t0004 | 41 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2113G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 2113 | chr2 | 20684790 | |||||
| chr2:20684826
|
G | C | 3 | a0001c0001t0002a0001c0001t0011a0003c0004t0002 | 45 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2077C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 2077 | chr2 | 20684826 | |||||
| chr2:20685000
|
T | A | 1 | a0001c0001t0009 | 2 | HG02615.hp2 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1903A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 1903 | chr2 | 20685000 | |||||
| chr2:20685193
|
A | G | 1 | a0001c0001t0011 | 1 | NA19011.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1710T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 1710 | chr2 | 20685193 | |||||
| chr2:20685213
|
A | C | 6 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(3): Show | 89 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*1690T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 1690 | chr2 | 20685213 | |||||
| chr2:20685387
|
G | A | 1 | a0001c0001t0012 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1516C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 1516 | chr2 | 20685387 | |||||
| chr2:20685561
|
C | A | 2 | a0001c0001t0003a0001c0001t0012 | 41 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1342G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 1342 | chr2 | 20685561 | |||||
| chr2:20685982
|
G | C | 1 | a0004c0005t0013 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*921C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 921 | chr2 | 20685982 | |||||
| chr2:20686638
|
T | C | 1 | a0001c0001t0006 | 6 | HG02559.hp2 HG02615.hp1 HG02717.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*265A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 265 | chr2 | 20686638 | |||||
| chr2:20686724
|
T | G | 1 | a0001c0001t0010 | 2 | HG01496.hp2 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*179A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 7/7 | 179 | chr2 | 20686724 | |||||
| chr2:20823067
|
T | G | 1 | a0001c0001t0014 | 1 | HG03209.hp2 | 5_prime_UTR_variant | MODIFIER | c.-33A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/7 | 21604 | chr2 | 20823067 | |||||
| chr2:20823083
|
G | A | 1 | a0001c0001t0015 | 1 | HG02132.hp1 | 5_prime_UTR_variant | MODIFIER | c.-49C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/7 | 21620 | chr2 | 20823083 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:20687132
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.787-38C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20687132 | ||||||
| chr2:20687312
|
G | T | 17 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(14): Show | 17 | HG00140.hp2 HG00673.hp1 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.787-218C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20687312 | ||||||
| chr2:20687409
|
G | A | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.787-315C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20687409 | ||||||
| chr2:20687457
|
G | A | 1 | a0002c0003t0001g0237 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.787-363C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20687457 | ||||||
| chr2:20687458
|
T | G | 1 | a0002c0003t0001g0237 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.787-364A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20687458 | ||||||
| chr2:20687466
|
T | G | 2 | a0001c0001t0004g0043a0001c0001t0004g0157 | 2 | HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.787-372A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20687466 | ||||||
| chr2:20687506
|
T | C | 6 | a0001c0001t0001g0190a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-412A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20687506 | ||||||
| chr2:20687567
|
T | G | 1 | a0001c0001t0001g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.787-473A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20687567 | ||||||
| chr2:20687609
|
C | A | 91 | a0001c0001t0001g0190a0001c0001t0002g0025a0001c0001t0002g0028others(88): Show | 91 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.787-515G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20687609 | ||||||
| chr2:20687902
|
C | A | 1 | a0001c0001t0003g0212 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.787-808G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20687902 | ||||||
| chr2:20688079
|
T | C | 2 | a0001c0001t0003g0008a0001c0001t0003g0030 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.787-985A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20688079 | ||||||
| chr2:20688132
|
G | T | 35 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0014others(32): Show | 35 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.787-1038C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20688132 | ||||||
| chr2:20688261
|
G | A | 43 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0014others(40): Show | 43 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.787-1167C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20688261 | ||||||
| chr2:20688385
|
G | A | 43 | a0001c0001t0003g0008a0001c0001t0003g0013a0001c0001t0003g0014others(40): Show | 43 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(40): Show |
intron_variant | MODIFIER | c.787-1291C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20688385 | ||||||
| chr2:20688486
|
G | C | 209 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(206): Show | 210 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.787-1392C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20688486 | ||||||
| chr2:20688505
|
A | G | 45 | a0001c0001t0002g0025a0001c0001t0002g0028a0001c0001t0002g0029others(42): Show | 45 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(42): Show |
intron_variant | MODIFIER | c.787-1411T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20688505 | ||||||
| chr2:20688659
|
C | T | 82 | a0001c0001t0002g0025a0001c0001t0002g0028a0001c0001t0002g0029others(79): Show | 82 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.787-1565G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20688659 | ||||||
| chr2:20688828
|
CT | C | 32 | a0001c0001t0001g0006a0001c0001t0001g0052a0001c0001t0001g0092others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.787-1735delA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20688828 | ||||||
| chr2:20688828
|
CTT | C | 14 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0117others(11): Show | 14 | HG01070.hp2 HG01261.hp2 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.787-1736_787-1735d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20688828 | ||||||
| chr2:20688828
|
CTTT | C | 8 | a0001c0001t0004g0187a0001c0001t0006g0144a0001c0001t0006g0197others(5): Show | 8 | HG02145.hp1 HG02486.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.787-1737_787-1735d others(5): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20688828 | ||||||
| chr2:20688828
|
CTTTT | C | 95 | a0001c0001t0001g0033a0001c0001t0001g0041a0001c0001t0001g0068others(92): Show | 96 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.787-1738_787-1735d others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20688828 | ||||||
| chr2:20688828
|
CTTTTT | C | 42 | a0001c0001t0001g0236a0001c0001t0002g0141a0001c0001t0003g0008others(39): Show | 42 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.787-1739_787-1735d others(7): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20688828 | ||||||
| chr2:20689206
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.787-2112C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20689206 | ||||||
| chr2:20689653
|
G | C | 43 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(40): Show | 43 | HG00438.hp2 HG01081.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.787-2559C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20689653 | ||||||
| chr2:20689700
|
G | A | 50 | a0001c0001t0001g0190a0001c0001t0003g0008a0001c0001t0003g0013others(47): Show | 50 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(47): Show |
intron_variant | MODIFIER | c.787-2606C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20689700 | ||||||
| chr2:20689778
|
G | C | 6 | a0001c0001t0001g0190a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-2684C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20689778 | ||||||
| chr2:20689851
|
C | T | 2 | a0001c0001t0005g0165a0001c0001t0005g0166 | 2 | NA18945.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.787-2757G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20689851 | ||||||
| chr2:20689942
|
C | T | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.787-2848G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20689942 | ||||||
| chr2:20689954
|
C | T | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 106 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.787-2860G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20689954 | ||||||
| chr2:20689990
|
T | G | 1 | a0001c0001t0002g0089 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.787-2896A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20689990 | ||||||
| chr2:20689994
|
C | T | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(155): Show | 159 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.787-2900G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20689994 | ||||||
| chr2:20690068
|
T | C | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.787-2974A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20690068 | ||||||
| chr2:20690144
|
G | A | 2 | a0001c0001t0003g0067a0001c0001t0003g0101 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.787-3050C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20690144 | ||||||
| chr2:20690177
|
G | GA | 6 | a0001c0001t0006g0144a0001c0001t0006g0197a0001c0001t0006g0198others(3): Show | 6 | HG02559.hp2 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-3084_787-3083i others(3): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20690177 | ||||||
| chr2:20690203
|
ACACC | A | 4 | a0001c0001t0001g0034a0001c0001t0001g0229a0001c0001t0001g0230others(1): Show | 4 | HG01496.hp1 HG02258.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-3113_787-3110d others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20690203 | ||||||
| chr2:20690208
|
C | G | 6 | a0001c0001t0001g0190a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-3114G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20690208 | ||||||
| chr2:20690208
|
C | T | 4 | a0001c0001t0001g0034a0001c0001t0001g0229a0001c0001t0001g0230others(1): Show | 4 | HG01496.hp1 HG02258.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-3114G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20690208 | ||||||
| chr2:20690343
|
G | A | 1 | a0001c0001t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.787-3249C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20690343 | ||||||
| chr2:20690362
|
T | C | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.787-3268A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20690362 | ||||||
| chr2:20690368
|
G | A | 2 | a0001c0001t0001g0236a0002c0003t0001g0237 | 2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.787-3274C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20690368 | ||||||
| chr2:20690455
|
A | T | 1 | a0001c0001t0001g0148 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.787-3361T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20690455 | ||||||
| chr2:20690457
|
T | A | 6 | a0001c0001t0006g0144a0001c0001t0006g0197a0001c0001t0006g0198others(3): Show | 6 | HG02559.hp2 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-3363A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20690457 | ||||||
| chr2:20690522
|
T | G | 1 | a0001c0001t0001g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.787-3428A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20690522 | ||||||
| chr2:20690626
|
G | A | 28 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(25): Show | 28 | HG00639.hp2 HG01123.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.787-3532C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20690626 | ||||||
| chr2:20690773
|
T | C | 12 | a0001c0001t0001g0021a0001c0001t0001g0236a0001c0001t0001g0248others(9): Show | 12 | HG02257.hp2 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.787-3679A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20690773 | ||||||
| chr2:20690831
|
G | A | 1 | a0001c0001t0005g0227 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.787-3737C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20690831 | ||||||
| chr2:20690882
|
CGTT | C | 11 | a0001c0001t0001g0033a0001c0001t0004g0011a0001c0001t0004g0043others(8): Show | 11 | HG01081.hp2 HG01261.hp1 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.787-3791_787-3789d others(5): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20690882 | ||||||
| chr2:20690971
|
T | A | 1 | a0001c0001t0001g0148 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.787-3877A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20690971 | ||||||
| chr2:20690972
|
A | T | 1 | a0001c0001t0001g0148 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.787-3878T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20690972 | ||||||
| chr2:20691214
|
G | A | 2 | a0002c0003t0004g0235a0004c0005t0013g0243 | 2 | HG02486.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.787-4120C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20691214 | ||||||
| chr2:20691348
|
A | AT | 172 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(169): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.787-4255dupA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20691348 | ||||||
| chr2:20691348
|
A | ATT | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-4256_787-4255d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20691348 | ||||||
| chr2:20691382
|
T | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-4288A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20691382 | ||||||
| chr2:20691610
|
T | C | 1 | a0001c0001t0004g0185 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.787-4516A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20691610 | ||||||
| chr2:20691644
|
T | C | 1 | a0001c0002t0001g0194 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.787-4550A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20691644 | ||||||
| chr2:20691687
|
G | A | 1 | a0001c0001t0003g0218 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.787-4593C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20691687 | ||||||
| chr2:20691892
|
T | C | 1 | a0001c0001t0002g0084 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.787-4798A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20691892 | ||||||
| chr2:20692012
|
T | C | 47 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0109others(44): Show | 47 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.787-4918A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20692012 | ||||||
| chr2:20692039
|
A | G | 134 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0021others(131): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.787-4945T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20692039 | ||||||
| chr2:20692074
|
A | T | 1 | a0001c0001t0001g0162 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.787-4980T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20692074 | ||||||
| chr2:20692127
|
A | G | 134 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0021others(131): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.787-5033T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20692127 | ||||||
| chr2:20692175
|
G | A | 29 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(26): Show | 29 | HG00673.hp1 HG01175.hp2 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.787-5081C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20692175 | ||||||
| chr2:20692195
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0228 | 2 | HG01255.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.787-5101C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20692195 | ||||||
| chr2:20692246
|
G | T | 81 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0042others(78): Show | 82 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.787-5152C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20692246 | ||||||
| chr2:20692578
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0228 | 2 | HG01255.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.787-5484A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20692578 | ||||||
| chr2:20692616
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.787-5522A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20692616 | ||||||
| chr2:20692703
|
T | C | 1 | a0001c0001t0002g0087 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.787-5609A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20692703 | ||||||
| chr2:20692712
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.787-5618A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20692712 | ||||||
| chr2:20692723
|
A | G | 66 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0042others(63): Show | 67 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.787-5629T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20692723 | ||||||
| chr2:20692850
|
G | T | 13 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0202others(10): Show | 14 | HG01346.hp2 HG01884.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.787-5756C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20692850 | ||||||
| chr2:20693014
|
C | A | 1 | a0001c0001t0002g0084 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.787-5920G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20693014 | ||||||
| chr2:20693330
|
G | A | 8 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0221others(5): Show | 9 | HG01884.hp2 HG02451.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.787-6236C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20693330 | ||||||
| chr2:20693392
|
A | C | 2 | a0001c0001t0001g0236a0001c0006t0001g0240 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.787-6298T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20693392 | ||||||
| chr2:20693420
|
A | G | 139 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0019others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.787-6326T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20693420 | ||||||
| chr2:20693523
|
G | A | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-6429C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20693523 | ||||||
| chr2:20693897
|
G | A | 1 | a0002c0003t0001g0237 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.787-6803C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20693897 | ||||||
| chr2:20693924
|
A | G | 1 | a0001c0001t0005g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.787-6830T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20693924 | ||||||
| chr2:20693989
|
T | C | 1 | a0001c0001t0001g0033 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.787-6895A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20693989 | ||||||
| chr2:20694027
|
T | C | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-6933A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20694027 | ||||||
| chr2:20694094
|
G | A | 6 | a0001c0001t0001g0060a0001c0001t0001g0182a0001c0001t0002g0089others(3): Show | 6 | HG02080.hp1 HG02129.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-7000C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20694094 | ||||||
| chr2:20694106
|
C | T | 1 | a0001c0001t0003g0167 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.787-7012G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20694106 | ||||||
| chr2:20694159
|
G | GC | 238 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(235): Show | 240 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.787-7066dupG | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20694159 | ||||||
| chr2:20694174
|
T | C | 9 | a0001c0001t0001g0033a0001c0001t0001g0202a0001c0001t0003g0200others(6): Show | 10 | HG01346.hp2 HG02451.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.787-7080A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20694174 | ||||||
| chr2:20694252
|
T | A | 2 | a0001c0001t0006g0239a0001c0001t0006g0242 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.787-7158A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20694252 | ||||||
| chr2:20694409
|
C | T | 25 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(22): Show | 25 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.786+7161G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20694409 | ||||||
| chr2:20694459
|
T | TCTGAGCC others(278): Show |
1 | a0001c0001t0005g0059 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.786+7110_786+7111i others(287): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20694459 | ||||||
| chr2:20694662
|
C | G | 32 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0121others(29): Show | 32 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.786+6908G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20694662 | ||||||
| chr2:20694851
|
T | C | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+6719A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20694851 | ||||||
| chr2:20694960
|
G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.786+6610C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20694960 | ||||||
| chr2:20694991
|
C | T | 2 | a0001c0001t0004g0043a0001c0001t0004g0114 | 2 | HG01515.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.786+6579G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20694991 | ||||||
| chr2:20694992
|
G | C | 1 | a0001c0002t0001g0192 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.786+6578C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20694992 | ||||||
| chr2:20695070
|
T | A | 1 | a0001c0001t0004g0114 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.786+6500A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20695070 | ||||||
| chr2:20695150
|
T | C | 1 | a0001c0001t0002g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.786+6420A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20695150 | ||||||
| chr2:20695425
|
G | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+6145C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20695425 | ||||||
| chr2:20695448
|
CTCTT | C | 4 | a0001c0001t0003g0067a0001c0001t0003g0101a0001c0001t0006g0239others(1): Show | 4 | HG02145.hp2 HG02559.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+6118_786+6121d others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20695448 | ||||||
| chr2:20695450
|
CTTTCT | C | 27 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(24): Show | 27 | HG00140.hp2 HG00673.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.786+6115_786+6119d others(7): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20695450 | ||||||
| chr2:20695454
|
CT | C | 9 | a0001c0001t0001g0006a0001c0001t0001g0148a0001c0001t0001g0233others(6): Show | 9 | HG01168.hp2 HG02451.hp2 HG03688.hp1 others(6): Show |
intron_variant | MODIFIER | c.786+6115delA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20695454 | ||||||
| chr2:20695470
|
T | G | 1 | a0001c0001t0001g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.786+6100A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20695470 | ||||||
| chr2:20695502
|
G | C | 1 | a0001c0001t0004g0114 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.786+6068C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20695502 | ||||||
| chr2:20695521
|
T | C | 6 | a0001c0001t0003g0069a0001c0001t0003g0152a0001c0001t0006g0144others(3): Show | 6 | HG02615.hp1 HG02717.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+6049A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20695521 | ||||||
| chr2:20695611
|
G | A | 2 | a0001c0001t0003g0067a0001c0001t0003g0101 | 2 | HG02145.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.786+5959C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20695611 | ||||||
| chr2:20695737
|
C | T | 25 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(22): Show | 25 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.786+5833G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20695737 | ||||||
| chr2:20695820
|
C | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+5750G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20695820 | ||||||
| chr2:20695903
|
G | T | 27 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(24): Show | 27 | HG00140.hp2 HG00673.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.786+5667C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20695903 | ||||||
| chr2:20695910
|
T | G | 1 | a0001c0001t0001g0179 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.786+5660A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20695910 | ||||||
| chr2:20696076
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.786+5494T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20696076 | ||||||
| chr2:20696140
|
A | G | 2 | a0001c0001t0001g0092a0001c0001t0002g0058 | 2 | NA18999.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.786+5430T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20696140 | ||||||
| chr2:20696289
|
C | T | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+5281G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20696289 | ||||||
| chr2:20696438
|
C | T | 2 | a0001c0001t0004g0214a0001c0001t0004g0217 | 2 | HG02015.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.786+5132G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20696438 | ||||||
| chr2:20696520
|
T | C | 1 | a0001c0001t0003g0254 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.786+5050A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20696520 | ||||||
| chr2:20696612
|
C | T | 2 | a0001c0001t0003g0008a0001c0001t0003g0030 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.786+4958G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20696612 | ||||||
| chr2:20696724
|
T | A | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+4846A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20696724 | ||||||
| chr2:20696820
|
C | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+4750G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20696820 | ||||||
| chr2:20696865
|
C | A | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(61): Show | 64 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.786+4705G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20696865 | ||||||
| chr2:20696947
|
T | C | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+4623A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20696947 | ||||||
| chr2:20696956
|
A | G | 1 | a0001c0001t0011g0081 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.786+4614T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20696956 | ||||||
| chr2:20697033
|
C | T | 1 | a0001c0001t0004g0185 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.786+4537G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20697033 | ||||||
| chr2:20697110
|
C | CACGG | 26 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(23): Show | 26 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.786+4456_786+4459d others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20697110 | ||||||
| chr2:20697122
|
T | TGCATGTC others(6): Show |
1 | a0001c0001t0001g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.786+4435_786+4447d others(15): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20697122 | ||||||
| chr2:20697138
|
A | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+4432T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20697138 | ||||||
| chr2:20697160
|
T | G | 1 | a0001c0001t0006g0242 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.786+4410A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20697160 | ||||||
| chr2:20697322
|
T | C | 27 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(24): Show | 27 | HG00140.hp2 HG00673.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.786+4248A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20697322 | ||||||
| chr2:20697345
|
C | A | 1 | a0001c0001t0001g0018 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.786+4225G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20697345 | ||||||
| chr2:20697345
|
C | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+4225G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20697345 | ||||||
| chr2:20697350
|
G | C | 27 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(24): Show | 27 | HG00140.hp2 HG00673.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.786+4220C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20697350 | ||||||
| chr2:20697585
|
T | C | 140 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 141 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.786+3985A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20697585 | ||||||
| chr2:20697741
|
G | A | 7 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0221others(4): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.786+3829C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20697741 | ||||||
| chr2:20697776
|
T | G | 64 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(61): Show | 64 | HG00140.hp2 HG00438.hp2 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.786+3794A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20697776 | ||||||
| chr2:20697847
|
G | A | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+3723C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20697847 | ||||||
| chr2:20697966
|
A | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+3604T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20697966 | ||||||
| chr2:20697967
|
A | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+3603T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20697967 | ||||||
| chr2:20698268
|
T | C | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+3302A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20698268 | ||||||
| chr2:20698308
|
TACATAGG others(7): Show |
T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+3248_786+3261d others(16): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20698308 | ||||||
| chr2:20698412
|
G | A | 27 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(24): Show | 27 | HG00140.hp2 HG00673.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.786+3158C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20698412 | ||||||
| chr2:20698461
|
C | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+3109G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20698461 | ||||||
| chr2:20698531
|
T | C | 3 | a0001c0001t0002g0131a0001c0001t0003g0049a0001c0001t0003g0050 | 3 | HG02135.hp1 NA18955.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.786+3039A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20698531 | ||||||
| chr2:20698659
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.786+2911C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20698659 | ||||||
| chr2:20698775
|
G | C | 1 | a0001c0001t0004g0114 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.786+2795C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20698775 | ||||||
| chr2:20698948
|
T | C | 1 | a0001c0001t0004g0043 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.786+2622A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20698948 | ||||||
| chr2:20698993
|
T | C | 7 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(4): Show | 7 | HG02647.hp2 HG03688.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.786+2577A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20698993 | ||||||
| chr2:20699024
|
T | C | 253 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(250): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.786+2546A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20699024 | ||||||
| chr2:20699074
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.786+2496A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20699074 | ||||||
| chr2:20699117
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.786+2453T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20699117 | ||||||
| chr2:20699173
|
T | C | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+2397A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20699173 | ||||||
| chr2:20699294
|
G | A | 1 | a0001c0001t0004g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.786+2276C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20699294 | ||||||
| chr2:20699322
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.786+2248G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20699322 | ||||||
| chr2:20699323
|
G | A | 20 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(17): Show | 20 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.786+2247C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20699323 | ||||||
| chr2:20699376
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0027 | 3 | HG02572.hp1 HG02717.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.786+2194G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20699376 | ||||||
| chr2:20699526
|
G | T | 1 | a0001c0001t0002g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.786+2044C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20699526 | ||||||
| chr2:20699531
|
T | C | 6 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(3): Show | 6 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+2039A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20699531 | ||||||
| chr2:20699550
|
T | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0228 | 2 | HG01255.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.786+2020A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20699550 | ||||||
| chr2:20699638
|
C | T | 1 | a0001c0001t0002g0134 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.786+1932G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20699638 | ||||||
| chr2:20699828
|
T | C | 2 | a0001c0001t0003g0253a0001c0001t0003g0254 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.786+1742A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20699828 | ||||||
| chr2:20700005
|
G | T | 1 | a0002c0003t0004g0235 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.786+1565C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20700005 | ||||||
| chr2:20700088
|
C | T | 27 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(24): Show | 27 | HG00140.hp2 HG00673.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.786+1482G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20700088 | ||||||
| chr2:20700129
|
C | T | 32 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0121others(29): Show | 32 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.786+1441G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20700129 | ||||||
| chr2:20700141
|
A | C | 1 | a0001c0001t0006g0197 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.786+1429T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20700141 | ||||||
| chr2:20700388
|
TA | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+1181delT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20700388 | ||||||
| chr2:20700490
|
T | C | 1 | a0001c0001t0005g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.786+1080A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20700490 | ||||||
| chr2:20700526
|
G | GATAAA | 27 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(24): Show | 27 | HG00140.hp2 HG00673.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.786+1043_786+1044i others(7): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20700526 | ||||||
| chr2:20700623
|
T | C | 27 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(24): Show | 27 | HG00140.hp2 HG00673.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.786+947A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20700623 | ||||||
| chr2:20700686
|
G | T | 1 | a0001c0001t0004g0130 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.786+884C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20700686 | ||||||
| chr2:20700714
|
T | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+856A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20700714 | ||||||
| chr2:20700871
|
T | C | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+699A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20700871 | ||||||
| chr2:20700933
|
T | G | 1 | a0001c0001t0005g0119 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.786+637A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20700933 | ||||||
| chr2:20701072
|
T | C | 26 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(23): Show | 26 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.786+498A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20701072 | ||||||
| chr2:20701073
|
G | A | 20 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(17): Show | 20 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.786+497C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20701073 | ||||||
| chr2:20701153
|
C | A | 1 | a0001c0001t0001g0033 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.786+417G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20701153 | ||||||
| chr2:20701187
|
G | T | 27 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(24): Show | 27 | HG00140.hp2 HG00673.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.786+383C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20701187 | ||||||
| chr2:20701219
|
T | C | 41 | a0001c0001t0001g0042a0001c0001t0001g0100a0001c0001t0001g0109others(38): Show | 41 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.786+351A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20701219 | ||||||
| chr2:20701220
|
G | A | 1 | a0001c0001t0005g0119 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.786+350C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20701220 | ||||||
| chr2:20701516
|
G | A | 3 | a0001c0001t0001g0169a0001c0001t0004g0246a0002c0003t0004g0238 | 3 | HG01255.hp2 HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.786+54C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 6/6 | chr2 | 20701516 | ||||||
| chr2:20701731
|
A | G | 1 | a0002c0003t0001g0237 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.704-79T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20701731 | ||||||
| chr2:20701762
|
T | C | 1 | a0001c0001t0001g0221 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.704-110A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20701762 | ||||||
| chr2:20701900
|
G | T | 30 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0121others(27): Show | 30 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.704-248C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20701900 | ||||||
| chr2:20702057
|
C | CT | 7 | a0001c0001t0001g0006a0001c0001t0004g0160a0001c0002t0001g0191others(4): Show | 7 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(4): Show |
intron_variant | MODIFIER | c.704-406dupA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20702057 | ||||||
| chr2:20702301
|
A | G | 1 | a0001c0001t0009g0118 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.704-649T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20702301 | ||||||
| chr2:20702312
|
T | G | 1 | a0001c0001t0005g0017 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.704-660A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20702312 | ||||||
| chr2:20702513
|
C | T | 140 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 141 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.704-861G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20702513 | ||||||
| chr2:20702622
|
T | C | 1 | a0001c0001t0001g0041 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.704-970A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20702622 | ||||||
| chr2:20702667
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0233 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.704-1015C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20702667 | ||||||
| chr2:20702671
|
A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0006g0239others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-1019T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20702671 | ||||||
| chr2:20702875
|
C | T | 1 | a0001c0001t0004g0175 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.704-1223G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20702875 | ||||||
| chr2:20702876
|
G | A | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-1224C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20702876 | ||||||
| chr2:20702893
|
C | G | 1 | a0001c0001t0001g0244 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.704-1241G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20702893 | ||||||
| chr2:20702895
|
C | T | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-1243G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20702895 | ||||||
| chr2:20702915
|
C | T | 1 | a0001c0001t0001g0209 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.704-1263G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20702915 | ||||||
| chr2:20702988
|
C | A | 36 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(33): Show | 36 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.704-1336G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20702988 | ||||||
| chr2:20703136
|
T | G | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-1484A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20703136 | ||||||
| chr2:20703255
|
T | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(33): Show | 36 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.704-1603A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20703255 | ||||||
| chr2:20703293
|
G | A | 30 | a0001c0001t0001g0018a0001c0001t0001g0041a0001c0001t0001g0121others(27): Show | 30 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.704-1641C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20703293 | ||||||
| chr2:20703566
|
G | C | 1 | a0001c0001t0001g0208 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.704-1914C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20703566 | ||||||
| chr2:20703688
|
T | C | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-2036A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20703688 | ||||||
| chr2:20703697
|
C | T | 1 | a0001c0001t0003g0067 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.704-2045G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20703697 | ||||||
| chr2:20703712
|
G | A | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-2060C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20703712 | ||||||
| chr2:20703751
|
A | C | 19 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(16): Show | 19 | HG00673.hp1 HG02074.hp2 HG02080.hp1 others(16): Show |
intron_variant | MODIFIER | c.704-2099T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20703751 | ||||||
| chr2:20703873
|
T | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-2221A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20703873 | ||||||
| chr2:20703880
|
C | T | 2 | a0001c0001t0004g0099a0002c0003t0004g0234 | 2 | HG02257.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.704-2228G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20703880 | ||||||
| chr2:20704239
|
A | G | 1 | a0001c0001t0003g0140 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.704-2587T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20704239 | ||||||
| chr2:20704258
|
A | C | 104 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(101): Show | 105 | HG00099.hp1 HG00140.hp2 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.704-2606T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20704258 | ||||||
| chr2:20704318
|
T | C | 36 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(33): Show | 36 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.704-2666A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20704318 | ||||||
| chr2:20704351
|
C | T | 26 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(23): Show | 26 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.704-2699G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20704351 | ||||||
| chr2:20704506
|
T | A | 2 | a0001c0001t0001g0236a0002c0003t0001g0237 | 2 | HG02257.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.704-2854A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20704506 | ||||||
| chr2:20704938
|
C | T | 26 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(23): Show | 26 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.704-3286G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20704938 | ||||||
| chr2:20704979
|
ACTTCCCT others(23): Show |
A | 1 | a0001c0001t0005g0017 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.704-3357_704-3328d others(32): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20704979 | ||||||
| chr2:20705225
|
C | T | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.704-3573G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20705225 | ||||||
| chr2:20705237
|
G | A | 26 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(23): Show | 26 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.704-3585C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20705237 | ||||||
| chr2:20705285
|
T | C | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.704-3633A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20705285 | ||||||
| chr2:20705435
|
C | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-3783G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20705435 | ||||||
| chr2:20705638
|
G | C | 1 | a0001c0001t0005g0065 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.704-3986C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20705638 | ||||||
| chr2:20705862
|
T | A | 1 | a0001c0001t0002g0096 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.704-4210A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20705862 | ||||||
| chr2:20705869
|
G | A | 1 | a0001c0001t0003g0067 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.704-4217C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20705869 | ||||||
| chr2:20706109
|
G | C | 1 | a0001c0001t0002g0131 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.704-4457C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20706109 | ||||||
| chr2:20706138
|
C | T | 1 | a0001c0001t0003g0067 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.704-4486G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20706138 | ||||||
| chr2:20706197
|
G | T | 1 | a0001c0001t0005g0224 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.704-4545C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20706197 | ||||||
| chr2:20706209
|
G | C | 67 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.704-4557C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20706209 | ||||||
| chr2:20706232
|
G | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0006g0239others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-4580C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20706232 | ||||||
| chr2:20706334
|
T | C | 3 | a0001c0001t0004g0120a0001c0001t0010g0039a0001c0001t0010g0115 | 3 | HG01123.hp1 HG01496.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.704-4682A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20706334 | ||||||
| chr2:20706462
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.704-4810G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20706462 | ||||||
| chr2:20706547
|
C | T | 1 | a0001c0001t0002g0106 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.704-4895G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20706547 | ||||||
| chr2:20706704
|
TA | T | 67 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.704-5053delT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20706704 | ||||||
| chr2:20706731
|
T | C | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-5079A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20706731 | ||||||
| chr2:20706839
|
T | C | 77 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(74): Show | 77 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.704-5187A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20706839 | ||||||
| chr2:20707056
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.704-5404A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20707056 | ||||||
| chr2:20707151
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0233 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.704-5499G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20707151 | ||||||
| chr2:20707411
|
C | G | 36 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(33): Show | 36 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.704-5759G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20707411 | ||||||
| chr2:20707750
|
C | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-6098G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20707750 | ||||||
| chr2:20707921
|
C | T | 67 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.704-6269G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20707921 | ||||||
| chr2:20708231
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.704-6579C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20708231 | ||||||
| chr2:20708377
|
C | T | 16 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(13): Show | 16 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.704-6725G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20708377 | ||||||
| chr2:20708775
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0006g0239others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-7123C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20708775 | ||||||
| chr2:20708956
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.704-7304T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20708956 | ||||||
| chr2:20709007
|
A | G | 77 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(74): Show | 77 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.704-7355T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20709007 | ||||||
| chr2:20709055
|
T | C | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-7403A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20709055 | ||||||
| chr2:20709084
|
C | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-7432G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20709084 | ||||||
| chr2:20709125
|
G | A | 1 | a0001c0001t0003g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.704-7473C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20709125 | ||||||
| chr2:20709208
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0006g0239others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-7556G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20709208 | ||||||
| chr2:20709221
|
G | A | 5 | a0001c0001t0003g0008a0001c0001t0003g0030a0001c0001t0003g0101others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-7569C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20709221 | ||||||
| chr2:20709230
|
G | A | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-7578C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20709230 | ||||||
| chr2:20709374
|
T | G | 2 | a0001c0001t0006g0239a0001c0001t0006g0242 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.704-7722A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20709374 | ||||||
| chr2:20709487
|
TA | T | 77 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(74): Show | 77 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.704-7836delT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20709487 | ||||||
| chr2:20709629
|
A | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-7977T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20709629 | ||||||
| chr2:20709905
|
G | C | 77 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(74): Show | 77 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.704-8253C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20709905 | ||||||
| chr2:20710063
|
C | T | 2 | a0003c0004t0002g0127a0003c0004t0002g0128 | 2 | HG02523.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.704-8411G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710063 | ||||||
| chr2:20710075
|
G | A | 10 | a0001c0001t0001g0072a0001c0001t0001g0196a0001c0001t0001g0219others(7): Show | 10 | HG01069.hp1 HG01071.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.704-8423C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710075 | ||||||
| chr2:20710171
|
T | C | 1 | a0001c0001t0002g0095 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.704-8519A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710171 | ||||||
| chr2:20710241
|
G | C | 2 | a0001c0001t0003g0049a0001c0001t0003g0050 | 2 | NA18955.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.704-8589C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710241 | ||||||
| chr2:20710254
|
T | G | 6 | a0001c0001t0003g0069a0001c0001t0003g0152a0001c0001t0006g0144others(3): Show | 6 | HG02615.hp1 HG02717.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-8602A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710254 | ||||||
| chr2:20710302
|
A | C | 77 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(74): Show | 77 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.704-8650T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710302 | ||||||
| chr2:20710516
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.704-8864A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710516 | ||||||
| chr2:20710567
|
G | A | 11 | a0001c0001t0001g0006a0001c0001t0001g0202a0001c0001t0003g0200others(8): Show | 11 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.704-8915C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710567 | ||||||
| chr2:20710585
|
G | GGT | 45 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0033others(42): Show | 46 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.704-8935_704-8934d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710585 | ||||||
| chr2:20710585
|
G | GGTGT | 45 | a0001c0001t0001g0042a0001c0001t0001g0100a0001c0001t0001g0109others(42): Show | 45 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.704-8937_704-8934d others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710585 | ||||||
| chr2:20710585
|
G | GGTGTGT | 6 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(3): Show | 6 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-8939_704-8934d others(8): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710585 | ||||||
| chr2:20710587
|
T | G | 2 | a0001c0001t0004g0214a0001c0001t0004g0217 | 2 | HG02015.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.704-8935A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710587 | ||||||
| chr2:20710596
|
G | GTGTGTGT others(3): Show |
2 | a0001c0002t0001g0191a0001c0002t0001g0194 | 2 | HG03688.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.704-8945_704-8944i others(12): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710596 | ||||||
| chr2:20710604
|
G | GTATGTGT others(11): Show |
1 | a0001c0001t0001g0006 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.704-8953_704-8952i others(20): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710604 | ||||||
| chr2:20710606
|
G | A | 1 | a0001c0001t0001g0006 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.704-8954C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710606 | ||||||
| chr2:20710606
|
G | GTGTGTAT others(3): Show |
17 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(14): Show | 17 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.704-8955_704-8954i others(12): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710606 | ||||||
| chr2:20710606
|
G | GTGTGTAT others(33): Show |
1 | a0001c0001t0006g0242 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.704-8955_704-8954i others(42): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710606 | ||||||
| chr2:20710606
|
G | GTGTGTGT others(31): Show |
1 | a0001c0001t0006g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.704-8955_704-8954i others(40): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710606 | ||||||
| chr2:20710607
|
TATATATA others(7): Show |
T | 1 | a0001c0001t0006g0198 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.704-8969_704-8956d others(16): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710607 | ||||||
| chr2:20710608
|
A | G | 8 | a0001c0001t0003g0082a0001c0001t0003g0173a0001c0001t0004g0188others(5): Show | 8 | HG03654.hp2 HG03688.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-8956T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710608 | ||||||
| chr2:20710609
|
T | G | 2 | a0001c0001t0006g0239a0001c0001t0006g0242 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.704-8957A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710609 | ||||||
| chr2:20710610
|
A | G | 3 | a0001c0002t0001g0192a0001c0002t0001g0193a0001c0002t0001g0195 | 3 | HG03710.hp2 HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.704-8958T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710610 | ||||||
| chr2:20710612
|
A | C | 17 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(14): Show | 17 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.704-8960T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710612 | ||||||
| chr2:20710612
|
A | G | 1 | a0001c0002t0001g0193 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.704-8960T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710612 | ||||||
| chr2:20710615
|
T | C | 2 | a0001c0001t0004g0246a0002c0003t0004g0238 | 2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.704-8963A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710615 | ||||||
| chr2:20710615
|
T | G | 2 | a0001c0001t0006g0239a0001c0001t0006g0242 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.704-8963A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710615 | ||||||
| chr2:20710615
|
T | TATATATA others(59): Show |
2 | a0001c0001t0001g0041a0001c0001t0001g0233 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.704-8964_704-8963i others(68): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710615 | ||||||
| chr2:20710618
|
A | C | 50 | a0001c0001t0001g0042a0001c0001t0001g0100a0001c0001t0001g0109others(47): Show | 50 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.704-8966T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710618 | ||||||
| chr2:20710621
|
G | T | 73 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0042others(70): Show | 73 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.704-8969C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710621 | ||||||
| chr2:20710627
|
T | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0006g0239others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-8975A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710627 | ||||||
| chr2:20710629
|
T | G | 17 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(14): Show | 17 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.704-8977A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710629 | ||||||
| chr2:20710635
|
G | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0202a0001c0001t0003g0200others(8): Show | 11 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.704-8983C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710635 | ||||||
| chr2:20710637
|
T | G | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-8985A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710637 | ||||||
| chr2:20710640
|
ATAG | A | 45 | a0001c0001t0001g0042a0001c0001t0001g0100a0001c0001t0001g0109others(42): Show | 45 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.704-8991_704-8989d others(5): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710640 | ||||||
| chr2:20710643
|
G | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-8991C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710643 | ||||||
| chr2:20710643
|
GT | G | 22 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(19): Show | 22 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.704-8992delA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710643 | ||||||
| chr2:20710644
|
T | G | 45 | a0001c0001t0001g0042a0001c0001t0001g0100a0001c0001t0001g0109others(42): Show | 45 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.704-8992A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710644 | ||||||
| chr2:20710648
|
C | T | 67 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.704-8996G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710648 | ||||||
| chr2:20710648
|
CAT | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0006g0239others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-8998_704-8997d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710648 | ||||||
| chr2:20710652
|
T | G | 67 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.704-9000A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710652 | ||||||
| chr2:20710658
|
C | T | 67 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.704-9006G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710658 | ||||||
| chr2:20710660
|
C | G | 67 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.704-9008G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710660 | ||||||
| chr2:20710668
|
T | G | 67 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.704-9016A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710668 | ||||||
| chr2:20710673
|
CAT | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0006g0239others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-9023_704-9022d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710673 | ||||||
| chr2:20710714
|
T | TTATACAT others(24): Show |
1 | a0001c0001t0003g0067 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.704-9093_704-9063d others(33): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710714 | ||||||
| chr2:20710740
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.704-9088A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710740 | ||||||
| chr2:20710744
|
C | T | 77 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(74): Show | 77 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.704-9092G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20710744 | ||||||
| chr2:20711046
|
A | G | 10 | a0001c0001t0001g0023a0001c0001t0001g0034a0001c0001t0001g0229others(7): Show | 10 | HG01261.hp2 HG01496.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.704-9394T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711046 | ||||||
| chr2:20711125
|
A | G | 1 | a0001c0001t0002g0029 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.704-9473T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711125 | ||||||
| chr2:20711146
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0233 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.704-9494A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711146 | ||||||
| chr2:20711159
|
C | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-9507G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711159 | ||||||
| chr2:20711163
|
C | T | 67 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.704-9511G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711163 | ||||||
| chr2:20711184
|
C | T | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.704-9532G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711184 | ||||||
| chr2:20711196
|
G | A | 1 | a0001c0001t0005g0166 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.704-9544C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711196 | ||||||
| chr2:20711223
|
C | T | 1 | a0001c0001t0003g0013 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.704-9571G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711223 | ||||||
| chr2:20711280
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0233 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.704-9628G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711280 | ||||||
| chr2:20711363
|
C | T | 1 | a0001c0001t0005g0097 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.704-9711G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711363 | ||||||
| chr2:20711371
|
C | T | 2 | a0001c0001t0003g0049a0001c0001t0003g0050 | 2 | NA18955.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.704-9719G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711371 | ||||||
| chr2:20711384
|
C | CA | 9 | a0001c0001t0001g0041a0001c0001t0001g0109a0001c0001t0001g0233others(6): Show | 9 | HG02080.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.704-9733dupT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711384 | ||||||
| chr2:20711447
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.704-9795C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711447 | ||||||
| chr2:20711468
|
T | C | 1 | a0001c0001t0001g0052 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.704-9816A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711468 | ||||||
| chr2:20711523
|
C | T | 39 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(36): Show | 40 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.704-9871G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711523 | ||||||
| chr2:20711525
|
T | C | 1 | a0001c0001t0011g0081 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.704-9873A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711525 | ||||||
| chr2:20711752
|
C | G | 2 | a0001c0001t0001g0236a0001c0006t0001g0240 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.704-10100G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711752 | ||||||
| chr2:20711752
|
C | T | 1 | a0001c0001t0004g0185 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.704-10100G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711752 | ||||||
| chr2:20711824
|
C | T | 1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.704-10172G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711824 | ||||||
| chr2:20711829
|
G | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0233 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.704-10177C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711829 | ||||||
| chr2:20711893
|
C | G | 62 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(59): Show | 62 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.704-10241G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711893 | ||||||
| chr2:20711899
|
A | G | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 142 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.704-10247T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711899 | ||||||
| chr2:20711900
|
G | C | 1 | a0001c0001t0003g0204 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.704-10248C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20711900 | ||||||
| chr2:20712015
|
G | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0233 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.704-10363C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20712015 | ||||||
| chr2:20712046
|
A | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-10394T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20712046 | ||||||
| chr2:20712049
|
A | G | 78 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(75): Show | 78 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.704-10397T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20712049 | ||||||
| chr2:20712254
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.704-10602A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20712254 | ||||||
| chr2:20712256
|
G | T | 1 | a0001c0001t0005g0065 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.704-10604C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20712256 | ||||||
| chr2:20712305
|
G | C | 2 | a0001c0001t0006g0239a0001c0001t0006g0242 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.704-10653C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20712305 | ||||||
| chr2:20712346
|
A | G | 1 | a0001c0001t0006g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.704-10694T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20712346 | ||||||
| chr2:20712371
|
C | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-10719G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20712371 | ||||||
| chr2:20712437
|
G | C | 1 | a0001c0001t0003g0067 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.704-10785C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20712437 | ||||||
| chr2:20712527
|
A | G | 77 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(74): Show | 77 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.704-10875T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20712527 | ||||||
| chr2:20712545
|
T | C | 62 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(59): Show | 62 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.704-10893A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20712545 | ||||||
| chr2:20712570
|
C | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-10918G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20712570 | ||||||
| chr2:20712570
|
C | T | 63 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(60): Show | 64 | HG00140.hp2 HG00673.hp1 HG01069.hp1 others(61): Show |
intron_variant | MODIFIER | c.704-10918G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20712570 | ||||||
| chr2:20712618
|
A | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-10966T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20712618 | ||||||
| chr2:20712631
|
A | G | 1 | a0001c0001t0002g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.704-10979T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20712631 | ||||||
| chr2:20712660
|
T | G | 1 | a0001c0001t0003g0067 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.704-11008A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20712660 | ||||||
| chr2:20712753
|
A | G | 62 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(59): Show | 62 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.704-11101T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20712753 | ||||||
| chr2:20713025
|
G | A | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-11373C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20713025 | ||||||
| chr2:20713090
|
G | C | 62 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(59): Show | 62 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.704-11438C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20713090 | ||||||
| chr2:20713193
|
A | G | 71 | a0001c0001t0001g0018a0001c0001t0001g0041a0001c0001t0001g0042others(68): Show | 71 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.704-11541T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20713193 | ||||||
| chr2:20713415
|
C | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG01106.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.704-11763G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20713415 | ||||||
| chr2:20713454
|
A | G | 181 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(178): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.704-11802T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20713454 | ||||||
| chr2:20713530
|
C | A | 1 | a0001c0001t0002g0028 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.704-11878G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20713530 | ||||||
| chr2:20713569
|
C | A | 1 | a0001c0001t0001g0190 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.704-11917G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20713569 | ||||||
| chr2:20713845
|
T | C | 2 | a0001c0001t0006g0239a0001c0001t0006g0242 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.704-12193A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20713845 | ||||||
| chr2:20713858
|
C | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-12206G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20713858 | ||||||
| chr2:20714170
|
C | A | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-12518G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20714170 | ||||||
| chr2:20714184
|
T | G | 2 | a0001c0001t0006g0239a0001c0001t0006g0242 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.704-12532A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20714184 | ||||||
| chr2:20714341
|
A | C | 1 | a0001c0001t0001g0022 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.704-12689T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20714341 | ||||||
| chr2:20714351
|
G | A | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-12699C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20714351 | ||||||
| chr2:20714449
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0233 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.704-12797G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20714449 | ||||||
| chr2:20714546
|
A | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-12894T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20714546 | ||||||
| chr2:20714626
|
G | C | 2 | a0001c0001t0007g0085a0001c0001t0007g0086 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.704-12974C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20714626 | ||||||
| chr2:20714682
|
C | A | 1 | a0001c0001t0003g0067 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.704-13030G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20714682 | ||||||
| chr2:20714695
|
G | C | 1 | a0001c0001t0001g0006 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.704-13043C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20714695 | ||||||
| chr2:20715080
|
A | G | 2 | a0001c0001t0001g0184a0001c0001t0001g0186 | 2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.704-13428T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20715080 | ||||||
| chr2:20715116
|
G | A | 140 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(137): Show | 141 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.704-13464C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20715116 | ||||||
| chr2:20715209
|
C | T | 77 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(74): Show | 77 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.704-13557G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20715209 | ||||||
| chr2:20715270
|
C | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-13618G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20715270 | ||||||
| chr2:20715303
|
G | A | 181 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(178): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.704-13651C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20715303 | ||||||
| chr2:20715304
|
GA | G | 4 | a0001c0001t0003g0124a0001c0001t0003g0125a0001c0001t0003g0126others(1): Show | 4 | HG00735.hp2 HG01515.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-13653delT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20715304 | ||||||
| chr2:20715326
|
A | C | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-13674T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20715326 | ||||||
| chr2:20715418
|
A | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-13766T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20715418 | ||||||
| chr2:20715469
|
A | G | 40 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(37): Show | 41 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.704-13817T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20715469 | ||||||
| chr2:20715487
|
A | C | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-13835T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20715487 | ||||||
| chr2:20715488
|
T | C | 40 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(37): Show | 41 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.704-13836A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20715488 | ||||||
| chr2:20715530
|
G | C | 1 | a0001c0001t0011g0081 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.704-13878C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20715530 | ||||||
| chr2:20715714
|
C | A | 78 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(75): Show | 78 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.704-14062G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20715714 | ||||||
| chr2:20715855
|
G | A | 1 | a0001c0001t0005g0059 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.704-14203C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20715855 | ||||||
| chr2:20716192
|
A | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-14540T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716192 | ||||||
| chr2:20716213
|
G | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0006g0239others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-14561C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716213 | ||||||
| chr2:20716278
|
G | A | 2 | a0001c0001t0001g0196a0001c0006t0001g0240 | 2 | HG01167.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.704-14626C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716278 | ||||||
| chr2:20716291
|
A | G | 77 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(74): Show | 77 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.704-14639T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716291 | ||||||
| chr2:20716372
|
C | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0006g0239others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-14720G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716372 | ||||||
| chr2:20716374
|
A | G | 1 | a0002c0003t0001g0237 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.704-14722T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716374 | ||||||
| chr2:20716519
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0233 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.704-14867A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716519 | ||||||
| chr2:20716720
|
G | GTATATAT others(3): Show |
3 | a0001c0001t0003g0170a0001c0001t0005g0103a0001c0001t0005g0108 | 3 | HG03654.hp1 NA18939.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.704-15069_704-1506 others(14): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716720 | ||||||
| chr2:20716720
|
G | GTATATAT others(11): Show |
1 | a0001c0001t0005g0166 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.704-15069_704-1506 others(22): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716720 | ||||||
| chr2:20716720
|
G | GTATATAT others(13): Show |
4 | a0001c0001t0001g0202a0001c0001t0003g0201a0001c0001t0005g0113others(1): Show | 4 | HG01346.hp2 HG02132.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-15069_704-1506 others(24): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716720 | ||||||
| chr2:20716720
|
G | GTATATAT others(15): Show |
5 | a0001c0001t0002g0112a0001c0001t0003g0104a0001c0001t0003g0200others(2): Show | 5 | HG01358.hp2 HG02071.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-15069_704-1506 others(26): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716720 | ||||||
| chr2:20716720
|
G | GTATATAT others(17): Show |
5 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0003g0105others(2): Show | 5 | HG00099.hp1 HG02004.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-15069_704-1506 others(28): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716720 | ||||||
| chr2:20716720
|
G | GTATATAT others(19): Show |
8 | a0001c0001t0001g0111a0001c0001t0001g0233a0001c0001t0002g0037others(5): Show | 8 | HG00735.hp1 HG00741.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-15069_704-1506 others(30): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716720 | ||||||
| chr2:20716720
|
G | GTATATAT others(21): Show |
8 | a0001c0001t0001g0190a0001c0001t0003g0167a0001c0001t0005g0017others(5): Show | 8 | HG01070.hp2 HG02071.hp1 HG03471.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-15069_704-1506 others(32): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716720 | ||||||
| chr2:20716720
|
G | GTATATAT others(23): Show |
6 | a0001c0001t0001g0100a0001c0001t0001g0154a0001c0001t0001g0162others(3): Show | 6 | HG00642.hp2 HG01081.hp1 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.704-15069_704-1506 others(34): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716720 | ||||||
| chr2:20716720
|
G | GTATATAT others(25): Show |
3 | a0001c0001t0003g0082a0001c0001t0005g0051a0001c0001t0006g0239 | 3 | HG01952.hp2 HG02559.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.704-15069_704-1506 others(36): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716720 | ||||||
| chr2:20716720
|
G | GTATATAT others(29): Show |
2 | a0001c0001t0003g0172a0001c0001t0003g0173 | 2 | HG03831.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.704-15069_704-1506 others(40): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716720 | ||||||
| chr2:20716720
|
G | GTATATAT others(33): Show |
1 | a0001c0001t0001g0109 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.704-15069_704-1506 others(44): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716720 | ||||||
| chr2:20716721
|
TATATATA others(1): Show |
T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-15077_704-1507 others(12): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716721 | ||||||
| chr2:20716727
|
TAC | T | 19 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(16): Show | 19 | HG01106.hp2 HG01192.hp1 HG01934.hp2 others(16): Show |
intron_variant | MODIFIER | c.704-15077_704-1507 others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716727 | ||||||
| chr2:20716729
|
C | CAT | 6 | a0001c0001t0003g0067a0001c0001t0004g0246a0001c0001t0009g0118others(3): Show | 6 | HG02145.hp2 HG02486.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-15079_704-1507 others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716729 | ||||||
| chr2:20716729
|
C | T | 52 | a0001c0001t0001g0041a0001c0001t0001g0042a0001c0001t0001g0100others(49): Show | 52 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.704-15077G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716729 | ||||||
| chr2:20716862
|
C | CATACTGT others(24): Show |
67 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.704-15211_704-1521 others(35): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716862 | ||||||
| chr2:20716957
|
T | C | 26 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(23): Show | 26 | HG00140.hp2 HG00673.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.704-15305A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20716957 | ||||||
| chr2:20717003
|
A | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-15351T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20717003 | ||||||
| chr2:20717025
|
T | G | 2 | a0001c0001t0006g0239a0001c0001t0006g0242 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.704-15373A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20717025 | ||||||
| chr2:20717026
|
G | A | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-15374C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20717026 | ||||||
| chr2:20717176
|
A | G | 2 | a0001c0001t0006g0239a0001c0001t0006g0242 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.704-15524T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20717176 | ||||||
| chr2:20717325
|
A | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-15673T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20717325 | ||||||
| chr2:20717351
|
C | T | 1 | a0001c0001t0004g0142 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.704-15699G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20717351 | ||||||
| chr2:20717474
|
A | T | 1 | a0001c0001t0003g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.704-15822T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20717474 | ||||||
| chr2:20717509
|
C | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0241 | 2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.704-15857G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20717509 | ||||||
| chr2:20717547
|
G | A | 8 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(5): Show | 8 | HG01255.hp1 HG02109.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.704-15895C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20717547 | ||||||
| chr2:20717719
|
T | C | 62 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(59): Show | 62 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.704-16067A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20717719 | ||||||
| chr2:20717762
|
A | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-16110T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20717762 | ||||||
| chr2:20717793
|
C | G | 77 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(74): Show | 77 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.704-16141G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20717793 | ||||||
| chr2:20717983
|
T | C | 1 | a0001c0001t0003g0105 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.704-16331A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20717983 | ||||||
| chr2:20717998
|
T | C | 73 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0042others(70): Show | 73 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.704-16346A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20717998 | ||||||
| chr2:20718362
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0006g0239others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-16710G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20718362 | ||||||
| chr2:20718428
|
ATATAAT | A | 4 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0006g0239others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-16782_704-1677 others(10): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20718428 | ||||||
| chr2:20718621
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.704-16969A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20718621 | ||||||
| chr2:20718663
|
G | A | 2 | a0001c0001t0004g0246a0002c0003t0004g0238 | 2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.704-17011C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20718663 | ||||||
| chr2:20718743
|
C | T | 6 | a0001c0001t0003g0069a0001c0001t0003g0152a0001c0001t0006g0144others(3): Show | 6 | HG02615.hp1 HG02717.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-17091G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20718743 | ||||||
| chr2:20718751
|
G | A | 10 | a0001c0001t0001g0072a0001c0001t0001g0196a0001c0001t0001g0219others(7): Show | 10 | HG01069.hp1 HG01071.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.704-17099C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20718751 | ||||||
| chr2:20718863
|
T | C | 73 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0042others(70): Show | 73 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.704-17211A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20718863 | ||||||
| chr2:20718881
|
C | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0006g0239others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-17229G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20718881 | ||||||
| chr2:20719063
|
T | C | 1 | a0001c0001t0005g0119 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.704-17411A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20719063 | ||||||
| chr2:20719191
|
T | TA | 67 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.704-17540dupT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20719191 | ||||||
| chr2:20719224
|
G | GT | 40 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(37): Show | 41 | HG00639.hp2 HG00735.hp2 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.704-17573dupA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20719224 | ||||||
| chr2:20719224
|
G | GTTTT | 67 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0042others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.704-17576_704-1757 others(8): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20719224 | ||||||
| chr2:20719224
|
GT | G | 5 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0222others(2): Show | 5 | HG01069.hp1 HG01167.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-17573delA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20719224 | ||||||
| chr2:20719466
|
T | TAAG | 77 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(74): Show | 77 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.704-17817_704-1781 others(7): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20719466 | ||||||
| chr2:20719521
|
A | G | 73 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0042others(70): Show | 73 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.704-17869T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20719521 | ||||||
| chr2:20719848
|
A | G | 1 | a0001c0001t0007g0203 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.704-18196T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20719848 | ||||||
| chr2:20720414
|
A | G | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-18762T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20720414 | ||||||
| chr2:20720451
|
C | T | 1 | a0001c0001t0003g0013 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.704-18799G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20720451 | ||||||
| chr2:20720528
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0006g0239others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-18876A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20720528 | ||||||
| chr2:20720649
|
C | T | 2 | a0001c0001t0001g0236a0001c0006t0001g0240 | 2 | HG02257.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.704-18997G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20720649 | ||||||
| chr2:20720651
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0233 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.704-18999G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20720651 | ||||||
| chr2:20720653
|
G | A | 1 | a0001c0001t0002g0112 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.704-19001C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20720653 | ||||||
| chr2:20720737
|
T | C | 67 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.704-19085A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20720737 | ||||||
| chr2:20720825
|
A | C | 1 | a0001c0001t0004g0217 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.703+19146T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20720825 | ||||||
| chr2:20720831
|
T | C | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+19140A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20720831 | ||||||
| chr2:20720912
|
T | C | 1 | a0001c0001t0004g0026 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.703+19059A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20720912 | ||||||
| chr2:20720936
|
A | C | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.703+19035T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20720936 | ||||||
| chr2:20720945
|
C | A | 1 | a0001c0001t0006g0199 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.703+19026G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20720945 | ||||||
| chr2:20720960
|
C | G | 6 | a0001c0001t0003g0069a0001c0001t0003g0152a0001c0001t0006g0144others(3): Show | 6 | HG02615.hp1 HG02717.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+19011G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20720960 | ||||||
| chr2:20721056
|
T | C | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+18915A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20721056 | ||||||
| chr2:20721112
|
C | T | 6 | a0001c0001t0001g0068a0001c0001t0001g0221a0001c0001t0001g0223others(3): Show | 7 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.703+18859G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20721112 | ||||||
| chr2:20721115
|
A | G | 1 | a0001c0001t0002g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.703+18856T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20721115 | ||||||
| chr2:20721411
|
A | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0233 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.703+18560T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20721411 | ||||||
| chr2:20721441
|
A | G | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+18530T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20721441 | ||||||
| chr2:20721486
|
A | G | 2 | a0001c0001t0006g0239a0001c0001t0006g0242 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.703+18485T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20721486 | ||||||
| chr2:20721498
|
G | A | 1 | a0001c0001t0004g0073 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.703+18473C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20721498 | ||||||
| chr2:20721574
|
A | C | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 142 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.703+18397T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20721574 | ||||||
| chr2:20721731
|
T | C | 181 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(178): Show | 183 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.703+18240A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20721731 | ||||||
| chr2:20722146
|
C | T | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(57): Show | 61 | HG00140.hp2 HG00673.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.703+17825G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20722146 | ||||||
| chr2:20722377
|
C | CA | 5 | a0001c0001t0002g0076a0001c0001t0002g0132a0001c0001t0004g0098others(2): Show | 5 | HG02145.hp1 HG03471.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+17593dupT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20722377 | ||||||
| chr2:20722377
|
C | CAA | 12 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0202others(9): Show | 12 | HG01346.hp2 HG02451.hp2 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.703+17592_703+1759 others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20722377 | ||||||
| chr2:20722377
|
C | CAAA | 54 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(51): Show | 54 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.703+17591_703+1759 others(7): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20722377 | ||||||
| chr2:20722377
|
C | CAAAA | 9 | a0001c0001t0001g0147a0001c0001t0001g0162a0001c0001t0001g0248others(6): Show | 9 | HG01934.hp1 HG01934.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.703+17590_703+1759 others(8): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20722377 | ||||||
| chr2:20722377
|
CA | C | 105 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(102): Show | 107 | HG00099.hp2 HG00140.hp2 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.703+17593delT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20722377 | ||||||
| chr2:20722392
|
A | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0004 | 2 | NA18984.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.703+17579T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20722392 | ||||||
| chr2:20722695
|
T | C | 2 | a0001c0001t0005g0225a0001c0001t0005g0226 | 2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.703+17276A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20722695 | ||||||
| chr2:20722780
|
G | C | 8 | a0001c0001t0003g0069a0001c0001t0003g0152a0001c0001t0004g0246others(5): Show | 8 | HG02615.hp1 HG02717.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.703+17191C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20722780 | ||||||
| chr2:20723105
|
T | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+16866A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20723105 | ||||||
| chr2:20723144
|
C | A | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+16827G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20723144 | ||||||
| chr2:20723211
|
G | C | 1 | a0001c0001t0003g0083 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.703+16760C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20723211 | ||||||
| chr2:20723510
|
T | G | 2 | a0001c0001t0006g0239a0001c0001t0006g0242 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.703+16461A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20723510 | ||||||
| chr2:20723540
|
C | T | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(57): Show | 61 | HG00140.hp2 HG00673.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.703+16431G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20723540 | ||||||
| chr2:20723691
|
T | C | 2 | a0001c0001t0005g0002a0001c0001t0005g0224 | 3 | HG02451.hp1 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.703+16280A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20723691 | ||||||
| chr2:20724099
|
T | G | 1 | a0001c0001t0004g0157 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.703+15872A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20724099 | ||||||
| chr2:20724190
|
C | G | 1 | a0001c0001t0004g0078 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.703+15781G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20724190 | ||||||
| chr2:20724191
|
C | T | 5 | a0001c0001t0003g0008a0001c0001t0003g0030a0001c0001t0003g0101others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+15780G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20724191 | ||||||
| chr2:20724304
|
G | A | 6 | a0001c0001t0001g0068a0001c0001t0001g0221a0001c0001t0001g0223others(3): Show | 7 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.703+15667C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20724304 | ||||||
| chr2:20724350
|
T | C | 199 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(196): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(198): Show |
intron_variant | MODIFIER | c.703+15621A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20724350 | ||||||
| chr2:20724429
|
C | G | 3 | a0001c0001t0003g0101a0001c0001t0003g0206a0001c0001t0003g0207 | 3 | HG02572.hp2 HG02809.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.703+15542G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20724429 | ||||||
| chr2:20724484
|
A | G | 3 | a0001c0001t0004g0043a0001c0001t0004g0114a0001c0001t0004g0157 | 3 | HG01261.hp1 HG01515.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.703+15487T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20724484 | ||||||
| chr2:20724526
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.703+15445T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20724526 | ||||||
| chr2:20724557
|
G | C | 2 | a0001c0001t0001g0219a0001c0001t0001g0231 | 2 | HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.703+15414C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20724557 | ||||||
| chr2:20724620
|
A | G | 73 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0042others(70): Show | 73 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.703+15351T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20724620 | ||||||
| chr2:20724646
|
A | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+15325T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20724646 | ||||||
| chr2:20724665
|
C | T | 77 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(74): Show | 77 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.703+15306G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20724665 | ||||||
| chr2:20725309
|
T | C | 42 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(39): Show | 43 | HG00140.hp2 HG00673.hp1 HG01175.hp2 others(40): Show |
intron_variant | MODIFIER | c.703+14662A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20725309 | ||||||
| chr2:20725350
|
G | C | 73 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0042others(70): Show | 73 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.703+14621C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20725350 | ||||||
| chr2:20725414
|
C | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0006g0239others(1): Show | 4 | HG02451.hp2 HG02559.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+14557G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20725414 | ||||||
| chr2:20725443
|
C | T | 1 | a0001c0001t0001g0033 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.703+14528G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20725443 | ||||||
| chr2:20725474
|
C | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+14497G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20725474 | ||||||
| chr2:20725486
|
G | C | 1 | a0001c0001t0004g0185 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.703+14485C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20725486 | ||||||
| chr2:20725544
|
A | G | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(57): Show | 61 | HG00140.hp2 HG00673.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.703+14427T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20725544 | ||||||
| chr2:20725622
|
A | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+14349T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20725622 | ||||||
| chr2:20725715
|
C | T | 1 | a0001c0001t0003g0140 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.703+14256G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20725715 | ||||||
| chr2:20725776
|
G | C | 1 | a0001c0001t0003g0067 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.703+14195C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20725776 | ||||||
| chr2:20725903
|
T | C | 67 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.703+14068A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20725903 | ||||||
| chr2:20725914
|
C | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0233 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.703+14057G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20725914 | ||||||
| chr2:20726076
|
T | C | 1 | a0001c0001t0004g0210 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.703+13895A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20726076 | ||||||
| chr2:20726160
|
C | G | 67 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.703+13811G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20726160 | ||||||
| chr2:20726208
|
A | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+13763T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20726208 | ||||||
| chr2:20726391
|
G | C | 1 | a0002c0003t0004g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.703+13580C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20726391 | ||||||
| chr2:20726536
|
A | G | 1 | a0001c0001t0004g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.703+13435T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20726536 | ||||||
| chr2:20726556
|
C | A | 62 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(59): Show | 62 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.703+13415G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20726556 | ||||||
| chr2:20726557
|
A | G | 67 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(64): Show | 67 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.703+13414T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20726557 | ||||||
| chr2:20726607
|
C | A | 1 | a0001c0001t0005g0113 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.703+13364G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20726607 | ||||||
| chr2:20726656
|
AT | A | 6 | a0001c0001t0001g0068a0001c0001t0001g0221a0001c0001t0001g0223others(3): Show | 7 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.703+13314delA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20726656 | ||||||
| chr2:20726701
|
T | G | 6 | a0001c0001t0001g0068a0001c0001t0001g0221a0001c0001t0001g0223others(3): Show | 7 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.703+13270A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20726701 | ||||||
| chr2:20726702
|
C | T | 39 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0034others(36): Show | 40 | HG00099.hp2 HG00639.hp2 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.703+13269G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20726702 | ||||||
| chr2:20726706
|
G | C | 1 | a0001c0001t0001g0150 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.703+13265C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20726706 | ||||||
| chr2:20726798
|
C | T | 77 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(74): Show | 77 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.703+13173G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20726798 | ||||||
| chr2:20726920
|
T | C | 2 | a0001c0001t0004g0160a0001c0001t0004g0175 | 2 | NA18942.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.703+13051A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20726920 | ||||||
| chr2:20726943
|
A | G | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+13028T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20726943 | ||||||
| chr2:20727147
|
G | A | 1 | a0001c0001t0003g0067 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.703+12824C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20727147 | ||||||
| chr2:20727150
|
G | A | 4 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(1): Show | 4 | HG01934.hp2 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+12821C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20727150 | ||||||
| chr2:20727191
|
AC | A | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+12779delG | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20727191 | ||||||
| chr2:20727207
|
T | C | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(57): Show | 61 | HG00140.hp2 HG00673.hp1 HG01069.hp1 others(58): Show |
intron_variant | MODIFIER | c.703+12764A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20727207 | ||||||
| chr2:20727256
|
T | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+12715A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20727256 | ||||||
| chr2:20727327
|
A | G | 1 | a0001c0001t0003g0206 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.703+12644T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20727327 | ||||||
| chr2:20727468
|
T | A | 8 | a0001c0001t0001g0072a0001c0001t0001g0196a0001c0001t0001g0222others(5): Show | 8 | HG01069.hp1 HG01071.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.703+12503A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20727468 | ||||||
| chr2:20727830
|
T | C | 80 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(77): Show | 80 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.703+12141A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20727830 | ||||||
| chr2:20727833
|
C | T | 1 | a0001c0001t0003g0101 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.703+12138G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20727833 | ||||||
| chr2:20728091
|
T | C | 1 | a0001c0001t0005g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.703+11880A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20728091 | ||||||
| chr2:20728193
|
T | A | 1 | a0001c0001t0001g0248 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.703+11778A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20728193 | ||||||
| chr2:20728229
|
G | A | 1 | a0002c0003t0004g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.703+11742C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20728229 | ||||||
| chr2:20728237
|
T | C | 61 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(58): Show | 62 | HG00140.hp2 HG00673.hp1 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.703+11734A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20728237 | ||||||
| chr2:20728282
|
T | C | 62 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(59): Show | 62 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(59): Show |
intron_variant | MODIFIER | c.703+11689A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20728282 | ||||||
| chr2:20728284
|
T | C | 1 | a0001c0001t0002g0155 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.703+11687A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20728284 | ||||||
| chr2:20728291
|
T | C | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 143 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.703+11680A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20728291 | ||||||
| chr2:20728432
|
C | T | 2 | a0001c0001t0006g0239a0001c0001t0006g0242 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.703+11539G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20728432 | ||||||
| chr2:20728535
|
G | GCT | 142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 143 | HG00099.hp1 HG00140.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.703+11434_703+1143 others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20728535 | ||||||
| chr2:20728608
|
C | T | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.703+11363G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20728608 | ||||||
| chr2:20728614
|
C | T | 4 | a0001c0001t0001g0219a0001c0001t0001g0231a0001c0001t0004g0214others(1): Show | 4 | HG02015.hp2 HG02109.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+11357G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20728614 | ||||||
| chr2:20728722
|
A | C | 1 | a0005c0007t0001g0062 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.703+11249T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20728722 | ||||||
| chr2:20728816
|
GA | G | 11 | a0001c0001t0001g0072a0001c0001t0001g0196a0001c0001t0001g0219others(8): Show | 11 | HG01069.hp1 HG01071.hp2 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.703+11154delT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20728816 | ||||||
| chr2:20728817
|
A | G | 36 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(33): Show | 36 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.703+11154T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20728817 | ||||||
| chr2:20728833
|
G | C | 2 | a0001c0001t0001g0219a0001c0001t0001g0231 | 2 | HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.703+11138C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20728833 | ||||||
| chr2:20729100
|
T | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 5 | HG02572.hp1 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+10871A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20729100 | ||||||
| chr2:20729163
|
C | T | 1 | a0001c0001t0003g0050 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.703+10808G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20729163 | ||||||
| chr2:20729209
|
G | C | 64 | a0001c0001t0001g0018a0001c0001t0001g0042a0001c0001t0001g0100others(61): Show | 64 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.703+10762C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20729209 | ||||||
| chr2:20729212
|
C | CT | 73 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(70): Show | 73 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.703+10758dupA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20729212 | ||||||
| chr2:20729259
|
A | G | 3 | a0001c0001t0001g0071a0001c0001t0001g0181a0001c0001t0003g0180 | 3 | HG02280.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.703+10712T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20729259 | ||||||
| chr2:20729307
|
T | C | 52 | a0001c0001t0001g0012a0001c0001t0001g0133a0001c0001t0001g0139others(49): Show | 52 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.703+10664A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20729307 | ||||||
| chr2:20729364
|
T | C | 79 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0041others(76): Show | 79 | HG00099.hp1 HG00438.hp2 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.703+10607A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20729364 | ||||||
| chr2:20729373
|
T | C | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+10598A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20729373 | ||||||
| chr2:20729377
|
G | A | 6 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(3): Show | 6 | HG01346.hp2 HG02486.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.703+10594C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20729377 | ||||||
| chr2:20729434
|
A | C | 15 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0202others(12): Show | 15 | HG01346.hp2 HG02451.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.703+10537T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20729434 | ||||||
| chr2:20729453
|
G | C | 1 | a0002c0003t0004g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.703+10518C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20729453 | ||||||
| chr2:20729549
|
A | G | 1 | a0001c0001t0003g0014 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.703+10422T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20729549 | ||||||
| chr2:20729675
|
T | C | 1 | a0001c0001t0006g0199 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.703+10296A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20729675 | ||||||
| chr2:20729702
|
C | G | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+10269G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20729702 | ||||||
| chr2:20729794
|
G | A | 1 | a0002c0003t0004g0235 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.703+10177C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20729794 | ||||||
| chr2:20729844
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.703+10127C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20729844 | ||||||
| chr2:20729954
|
C | T | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+10017G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20729954 | ||||||
| chr2:20729997
|
C | T | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+9974G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20729997 | ||||||
| chr2:20730053
|
A | G | 1 | a0001c0001t0005g0097 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.703+9918T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20730053 | ||||||
| chr2:20730113
|
T | C | 8 | a0001c0001t0001g0032a0001c0001t0001g0228a0001c0001t0003g0069others(5): Show | 8 | HG01255.hp1 HG02109.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.703+9858A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20730113 | ||||||
| chr2:20730336
|
GT | G | 17 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0202others(14): Show | 17 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.703+9634delA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20730336 | ||||||
| chr2:20730380
|
C | T | 1 | a0001c0001t0004g0114 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.703+9591G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20730380 | ||||||
| chr2:20730483
|
A | AT | 8 | a0001c0001t0003g0083a0001c0001t0003g0124a0001c0001t0003g0126others(5): Show | 8 | HG00735.hp2 HG01168.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.703+9487dupA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20730483 | ||||||
| chr2:20730516
|
T | C | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.703+9455A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20730516 | ||||||
| chr2:20730719
|
CTCTCCT | C | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+9246_703+9251d others(8): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20730719 | ||||||
| chr2:20730784
|
C | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+9187G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20730784 | ||||||
| chr2:20730854
|
C | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+9117G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20730854 | ||||||
| chr2:20730971
|
C | A | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+9000G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20730971 | ||||||
| chr2:20730981
|
C | T | 3 | a0001c0001t0006g0197a0001c0001t0006g0198a0001c0001t0006g0199 | 3 | HG02717.hp1 HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.703+8990G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20730981 | ||||||
| chr2:20731090
|
C | T | 1 | a0001c0001t0006g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.703+8881G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20731090 | ||||||
| chr2:20731092
|
G | C | 2 | a0001c0001t0002g0153a0001c0001t0002g0174 | 2 | NA18953.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.703+8879C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20731092 | ||||||
| chr2:20731206
|
G | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+8765C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20731206 | ||||||
| chr2:20731269
|
C | T | 3 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0005g0035 | 3 | HG00741.hp2 HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.703+8702G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20731269 | ||||||
| chr2:20731331
|
G | A | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+8640C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20731331 | ||||||
| chr2:20731345
|
T | C | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+8626A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20731345 | ||||||
| chr2:20731390
|
G | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+8581C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20731390 | ||||||
| chr2:20731413
|
A | G | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+8558T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20731413 | ||||||
| chr2:20731433
|
G | A | 1 | a0002c0003t0004g0235 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.703+8538C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20731433 | ||||||
| chr2:20731501
|
T | G | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+8470A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20731501 | ||||||
| chr2:20731603
|
A | G | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+8368T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20731603 | ||||||
| chr2:20731685
|
C | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+8286G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20731685 | ||||||
| chr2:20731691
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0241 | 2 | NA18522.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.703+8280C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20731691 | ||||||
| chr2:20731796
|
T | C | 1 | a0001c0001t0002g0132 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.703+8175A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20731796 | ||||||
| chr2:20731827
|
T | C | 1 | a0001c0001t0003g0167 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.703+8144A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20731827 | ||||||
| chr2:20731841
|
A | AT | 7 | a0001c0001t0001g0006a0001c0001t0006g0242a0001c0002t0001g0191others(4): Show | 7 | HG03471.hp2 HG03688.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+8129dupA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20731841 | ||||||
| chr2:20731855
|
G | GT | 15 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0202others(12): Show | 15 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.703+8115dupA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20731855 | ||||||
| chr2:20731904
|
G | A | 8 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(5): Show | 8 | HG01346.hp2 HG02451.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.703+8067C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20731904 | ||||||
| chr2:20732126
|
C | T | 15 | a0001c0001t0002g0189a0001c0001t0004g0079a0001c0001t0004g0098others(12): Show | 15 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.703+7845G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20732126 | ||||||
| chr2:20732127
|
G | A | 17 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0202others(14): Show | 17 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.703+7844C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20732127 | ||||||
| chr2:20732201
|
C | T | 16 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0202others(13): Show | 16 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.703+7770G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20732201 | ||||||
| chr2:20732296
|
T | C | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+7675A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20732296 | ||||||
| chr2:20732463
|
G | A | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+7508C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20732463 | ||||||
| chr2:20732518
|
T | C | 73 | a0001c0001t0001g0012a0001c0001t0001g0117a0001c0001t0001g0133others(70): Show | 73 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.703+7453A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20732518 | ||||||
| chr2:20732636
|
G | C | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+7335C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20732636 | ||||||
| chr2:20732636
|
G | T | 4 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0003g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+7335C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20732636 | ||||||
| chr2:20732729
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.703+7242T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20732729 | ||||||
| chr2:20732812
|
T | C | 74 | a0001c0001t0001g0012a0001c0001t0001g0117a0001c0001t0001g0133others(71): Show | 74 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.703+7159A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20732812 | ||||||
| chr2:20732875
|
A | AT | 4 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(1): Show | 4 | HG02647.hp2 HG03710.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+7095dupA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20732875 | ||||||
| chr2:20732894
|
GGTCTCAC others(3): Show |
G | 48 | a0001c0001t0001g0042a0001c0001t0001g0068a0001c0001t0001g0100others(45): Show | 49 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.703+7067_703+7076d others(12): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20732894 | ||||||
| chr2:20732983
|
G | T | 2 | a0001c0001t0004g0043a0001c0001t0004g0157 | 2 | HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.703+6988C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20732983 | ||||||
| chr2:20733145
|
A | AT | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+6825dupA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20733145 | ||||||
| chr2:20733251
|
G | T | 4 | a0001c0001t0004g0043a0001c0001t0004g0114a0001c0001t0004g0157others(1): Show | 4 | HG01261.hp1 HG01515.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+6720C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20733251 | ||||||
| chr2:20733373
|
C | T | 7 | a0001c0001t0001g0006a0001c0001t0006g0242a0001c0002t0001g0191others(4): Show | 7 | HG03471.hp2 HG03688.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+6598G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20733373 | ||||||
| chr2:20733380
|
T | C | 75 | a0001c0001t0001g0012a0001c0001t0001g0117a0001c0001t0001g0133others(72): Show | 75 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.703+6591A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20733380 | ||||||
| chr2:20733383
|
C | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+6588G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20733383 | ||||||
| chr2:20733397
|
A | AT | 104 | a0001c0001t0001g0023a0001c0001t0001g0033a0001c0001t0001g0042others(101): Show | 105 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(102): Show |
intron_variant | MODIFIER | c.703+6573dupA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20733397 | ||||||
| chr2:20733397
|
A | ATT | 17 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0138others(14): Show | 17 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.703+6572_703+6573d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20733397 | ||||||
| chr2:20733397
|
AT | A | 5 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0003g0067others(2): Show | 5 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+6573delA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20733397 | ||||||
| chr2:20733433
|
T | A | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+6538A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20733433 | ||||||
| chr2:20733487
|
C | G | 1 | a0001c0001t0001g0042 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.703+6484G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20733487 | ||||||
| chr2:20733552
|
C | T | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+6419G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20733552 | ||||||
| chr2:20733686
|
G | A | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+6285C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20733686 | ||||||
| chr2:20733842
|
C | T | 2 | a0001c0001t0003g0204a0001c0001t0003g0205 | 2 | HG00639.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.703+6129G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20733842 | ||||||
| chr2:20733899
|
G | C | 1 | a0001c0001t0005g0046 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.703+6072C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20733899 | ||||||
| chr2:20733975
|
A | G | 1 | a0001c0001t0001g0092 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.703+5996T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20733975 | ||||||
| chr2:20733976
|
C | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+5995G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20733976 | ||||||
| chr2:20733985
|
C | G | 2 | a0001c0001t0003g0253a0001c0001t0003g0254 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.703+5986G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20733985 | ||||||
| chr2:20734047
|
A | G | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+5924T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20734047 | ||||||
| chr2:20734062
|
G | A | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+5909C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20734062 | ||||||
| chr2:20734099
|
T | C | 2 | a0001c0001t0005g0045a0001c0001t0005g0048 | 2 | HG00099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.703+5872A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20734099 | ||||||
| chr2:20734127
|
T | C | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+5844A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20734127 | ||||||
| chr2:20734376
|
A | G | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+5595T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20734376 | ||||||
| chr2:20734378
|
TC | T | 7 | a0001c0001t0001g0006a0001c0001t0006g0242a0001c0002t0001g0191others(4): Show | 7 | HG03471.hp2 HG03688.hp1 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.703+5592delG | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20734378 | ||||||
| chr2:20734505
|
G | C | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+5466C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20734505 | ||||||
| chr2:20734593
|
G | A | 1 | a0001c0001t0006g0242 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.703+5378C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20734593 | ||||||
| chr2:20734747
|
A | G | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+5224T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20734747 | ||||||
| chr2:20734781
|
G | A | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+5190C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20734781 | ||||||
| chr2:20734863
|
T | C | 64 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0042others(61): Show | 65 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.703+5108A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20734863 | ||||||
| chr2:20734890
|
C | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+5081G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20734890 | ||||||
| chr2:20734892
|
C | T | 18 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(15): Show | 18 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.703+5079G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20734892 | ||||||
| chr2:20734937
|
G | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+5034C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20734937 | ||||||
| chr2:20735089
|
G | A | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+4882C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20735089 | ||||||
| chr2:20735134
|
A | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+4837T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20735134 | ||||||
| chr2:20735283
|
T | C | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+4688A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20735283 | ||||||
| chr2:20735307
|
T | C | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.703+4664A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20735307 | ||||||
| chr2:20735309
|
C | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+4662G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20735309 | ||||||
| chr2:20735318
|
G | T | 41 | a0001c0001t0001g0042a0001c0001t0001g0100a0001c0001t0001g0109others(38): Show | 41 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.703+4653C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20735318 | ||||||
| chr2:20735602
|
G | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+4369C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20735602 | ||||||
| chr2:20735741
|
C | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+4230G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20735741 | ||||||
| chr2:20735979
|
C | T | 9 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+3992G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20735979 | ||||||
| chr2:20736011
|
C | G | 41 | a0001c0001t0001g0042a0001c0001t0001g0100a0001c0001t0001g0109others(38): Show | 41 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.703+3960G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20736011 | ||||||
| chr2:20736094
|
A | G | 16 | a0001c0001t0001g0006a0001c0001t0001g0041a0001c0001t0001g0202others(13): Show | 16 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.703+3877T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20736094 | ||||||
| chr2:20736403
|
C | G | 1 | a0001c0001t0014g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.703+3568G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20736403 | ||||||
| chr2:20736411
|
T | C | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+3560A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20736411 | ||||||
| chr2:20736482
|
A | G | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+3489T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20736482 | ||||||
| chr2:20736500
|
T | C | 129 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0042others(126): Show | 130 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.703+3471A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20736500 | ||||||
| chr2:20736592
|
A | G | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+3379T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20736592 | ||||||
| chr2:20736707
|
T | C | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+3264A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20736707 | ||||||
| chr2:20736756
|
A | G | 75 | a0001c0001t0001g0012a0001c0001t0001g0117a0001c0001t0001g0133others(72): Show | 75 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.703+3215T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20736756 | ||||||
| chr2:20736763
|
C | A | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+3208G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20736763 | ||||||
| chr2:20736770
|
C | CTT | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+3199_703+3200d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20736770 | ||||||
| chr2:20736819
|
T | C | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+3152A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20736819 | ||||||
| chr2:20736880
|
T | C | 74 | a0001c0001t0001g0012a0001c0001t0001g0117a0001c0001t0001g0133others(71): Show | 74 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.703+3091A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20736880 | ||||||
| chr2:20736912
|
A | G | 8 | a0001c0001t0004g0001a0001c0001t0004g0073a0001c0001t0004g0074others(5): Show | 9 | HG00099.hp2 HG00741.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.703+3059T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20736912 | ||||||
| chr2:20736999
|
C | G | 7 | a0001c0001t0001g0068a0001c0001t0001g0221a0001c0001t0001g0222others(4): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.703+2972G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20736999 | ||||||
| chr2:20737002
|
A | G | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+2969T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20737002 | ||||||
| chr2:20737115
|
T | C | 41 | a0001c0001t0001g0042a0001c0001t0001g0100a0001c0001t0001g0109others(38): Show | 41 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.703+2856A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20737115 | ||||||
| chr2:20737145
|
A | G | 1 | a0001c0001t0005g0227 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.703+2826T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20737145 | ||||||
| chr2:20737146
|
T | C | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+2825A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20737146 | ||||||
| chr2:20737169
|
A | G | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+2802T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20737169 | ||||||
| chr2:20737334
|
G | A | 2 | a0001c0001t0002g0153a0001c0001t0002g0174 | 2 | NA18953.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.703+2637C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20737334 | ||||||
| chr2:20737340
|
G | A | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+2631C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20737340 | ||||||
| chr2:20737361
|
A | T | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+2610T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20737361 | ||||||
| chr2:20737707
|
T | C | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+2264A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20737707 | ||||||
| chr2:20737721
|
A | T | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+2250T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20737721 | ||||||
| chr2:20737768
|
T | G | 43 | a0001c0001t0001g0018a0001c0001t0001g0033a0001c0001t0001g0121others(40): Show | 44 | HG00099.hp2 HG00438.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.703+2203A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20737768 | ||||||
| chr2:20737826
|
C | A | 1 | a0001c0001t0004g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.703+2145G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20737826 | ||||||
| chr2:20737975
|
C | G | 1 | a0001c0001t0005g0119 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.703+1996G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20737975 | ||||||
| chr2:20737990
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.703+1981T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20737990 | ||||||
| chr2:20738024
|
C | T | 2 | a0001c0001t0003g0253a0001c0001t0003g0254 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.703+1947G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738024 | ||||||
| chr2:20738035
|
C | T | 1 | a0001c0001t0005g0051 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.703+1936G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738035 | ||||||
| chr2:20738065
|
T | A | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+1906A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738065 | ||||||
| chr2:20738086
|
TA | T | 41 | a0001c0001t0001g0042a0001c0001t0001g0100a0001c0001t0001g0109others(38): Show | 41 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.703+1884delT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738086 | ||||||
| chr2:20738184
|
G | A | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+1787C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738184 | ||||||
| chr2:20738208
|
C | T | 7 | a0001c0001t0001g0068a0001c0001t0001g0221a0001c0001t0001g0222others(4): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.703+1763G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738208 | ||||||
| chr2:20738253
|
A | AAAT | 24 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0068others(21): Show | 24 | HG00438.hp2 HG01168.hp2 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.703+1715_703+1717d others(5): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738253 | ||||||
| chr2:20738253
|
A | AAATAAT | 10 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(7): Show | 10 | HG01346.hp2 HG02559.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+1712_703+1717d others(8): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738253 | ||||||
| chr2:20738253
|
A | AAATAATA others(2): Show |
30 | a0001c0001t0001g0033a0001c0001t0001g0121a0001c0001t0001g0122others(27): Show | 31 | HG00099.hp2 HG00639.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.703+1709_703+1717d others(11): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738253 | ||||||
| chr2:20738253
|
A | AAATAATA others(5): Show |
15 | a0001c0001t0001g0023a0001c0001t0001g0151a0001c0001t0001g0219others(12): Show | 15 | HG01081.hp2 HG01261.hp2 HG01496.hp1 others(12): Show |
intron_variant | MODIFIER | c.703+1706_703+1717d others(14): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738253 | ||||||
| chr2:20738253
|
AAAT | A | 43 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(40): Show | 44 | HG00140.hp2 HG00673.hp1 HG01069.hp1 others(41): Show |
intron_variant | MODIFIER | c.703+1715_703+1717d others(5): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738253 | ||||||
| chr2:20738253
|
AAATAATA others(5): Show |
A | 73 | a0001c0001t0001g0012a0001c0001t0001g0117a0001c0001t0001g0133others(70): Show | 73 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.703+1706_703+1717d others(14): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738253 | ||||||
| chr2:20738361
|
T | TCTCCATA others(349): Show |
1 | a0001c0001t0003g0067 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.703+1609_703+1610i others(358): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738361 | ||||||
| chr2:20738361
|
T | TCTCCATA others(356): Show |
1 | a0001c0001t0001g0041 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.703+1609_703+1610i others(365): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738361 | ||||||
| chr2:20738361
|
T | TCTCCATA others(352): Show |
1 | a0001c0001t0001g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.703+1609_703+1610i others(361): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738361 | ||||||
| chr2:20738361
|
T | TCTCCATA others(330): Show |
2 | a0001c0001t0006g0239a0001c0001t0006g0242 | 2 | HG02559.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.703+1609_703+1610i others(339): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738361 | ||||||
| chr2:20738374
|
A | ATATATAT others(347): Show |
1 | a0001c0001t0003g0201 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.703+1596_703+1597i others(356): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738374 | ||||||
| chr2:20738374
|
A | ATATATAT others(345): Show |
2 | a0001c0001t0003g0200a0001c0001t0007g0203 | 2 | HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.703+1596_703+1597i others(354): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738374 | ||||||
| chr2:20738374
|
A | ATATATAT others(346): Show |
1 | a0001c0001t0001g0202 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.703+1596_703+1597i others(355): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738374 | ||||||
| chr2:20738374
|
A | ATATATAT others(344): Show |
1 | a0001c0001t0003g0218 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.703+1596_703+1597i others(353): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738374 | ||||||
| chr2:20738374
|
A | T | 5 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0003g0067others(2): Show | 5 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+1597T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738374 | ||||||
| chr2:20738380
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.703+1591T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738380 | ||||||
| chr2:20738526
|
C | T | 1 | a0001c0002t0001g0193 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.703+1445G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738526 | ||||||
| chr2:20738614
|
C | T | 6 | a0001c0001t0003g0069a0001c0001t0003g0152a0001c0001t0006g0144others(3): Show | 6 | HG02615.hp1 HG02717.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.703+1357G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738614 | ||||||
| chr2:20738758
|
G | A | 16 | a0001c0001t0001g0042a0001c0001t0001g0100a0001c0001t0001g0110others(13): Show | 16 | HG01081.hp1 HG01346.hp1 HG01358.hp2 others(13): Show |
intron_variant | MODIFIER | c.703+1213C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738758 | ||||||
| chr2:20738758
|
G | GA | 88 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0041others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.703+1212dupT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20738758 | ||||||
| chr2:20739000
|
T | C | 7 | a0001c0001t0001g0068a0001c0001t0001g0221a0001c0001t0001g0222others(4): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.703+971A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20739000 | ||||||
| chr2:20739084
|
C | T | 1 | a0001c0001t0005g0107 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.703+887G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20739084 | ||||||
| chr2:20739303
|
C | T | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+668G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20739303 | ||||||
| chr2:20739613
|
T | G | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+358A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20739613 | ||||||
| chr2:20739629
|
C | T | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+342G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20739629 | ||||||
| chr2:20739710
|
G | A | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+261C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20739710 | ||||||
| chr2:20739713
|
G | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 5 | HG02572.hp1 HG02717.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+258C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20739713 | ||||||
| chr2:20739867
|
C | T | 1 | a0002c0003t0004g0235 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.703+104G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20739867 | ||||||
| chr2:20739946
|
T | C | 54 | a0001c0001t0001g0012a0001c0001t0001g0133a0001c0001t0001g0139others(51): Show | 54 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.703+25A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20739946 | ||||||
| chr2:20739948
|
C | T | 91 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0041others(88): Show | 91 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.703+23G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 5/6 | chr2 | 20739948 | ||||||
| chr2:20740246
|
A | T | 1 | a0001c0001t0003g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.469-41T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20740246 | ||||||
| chr2:20740360
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.469-155G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20740360 | ||||||
| chr2:20740407
|
C | A | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-202G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20740407 | ||||||
| chr2:20740589
|
G | A | 2 | a0003c0004t0002g0127a0003c0004t0002g0128 | 2 | HG02523.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.469-384C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20740589 | ||||||
| chr2:20740659
|
G | A | 2 | a0001c0001t0005g0252a0001c0006t0001g0240 | 2 | HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.469-454C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20740659 | ||||||
| chr2:20740662
|
G | A | 1 | a0001c0002t0001g0191 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.469-457C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20740662 | ||||||
| chr2:20740713
|
T | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-508A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20740713 | ||||||
| chr2:20740746
|
A | G | 91 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0041others(88): Show | 91 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.469-541T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20740746 | ||||||
| chr2:20740785
|
C | A | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-580G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20740785 | ||||||
| chr2:20740825
|
C | T | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-620G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20740825 | ||||||
| chr2:20740832
|
T | A | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-627A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20740832 | ||||||
| chr2:20740988
|
C | T | 5 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0003g0067others(2): Show | 5 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-783G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20740988 | ||||||
| chr2:20741024
|
T | C | 3 | a0001c0001t0003g0200a0001c0001t0003g0201a0001c0001t0007g0203 | 3 | HG01346.hp2 HG02965.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.469-819A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20741024 | ||||||
| chr2:20741040
|
C | T | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-835G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20741040 | ||||||
| chr2:20741150
|
T | C | 1 | a0001c0001t0005g0065 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.469-945A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20741150 | ||||||
| chr2:20741276
|
C | T | 1 | a0001c0001t0006g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.469-1071G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20741276 | ||||||
| chr2:20741277
|
A | G | 139 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0041others(136): Show | 140 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.469-1072T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20741277 | ||||||
| chr2:20741323
|
T | C | 1 | a0001c0001t0005g0165 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.469-1118A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20741323 | ||||||
| chr2:20741338
|
A | G | 4 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0003g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.469-1133T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20741338 | ||||||
| chr2:20741538
|
C | T | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1333G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20741538 | ||||||
| chr2:20741565
|
A | C | 1 | a0001c0001t0004g0164 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.469-1360T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20741565 | ||||||
| chr2:20741568
|
G | C | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1363C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20741568 | ||||||
| chr2:20741672
|
A | G | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1467T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20741672 | ||||||
| chr2:20741761
|
A | G | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1556T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20741761 | ||||||
| chr2:20741790
|
C | G | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-1585G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20741790 | ||||||
| chr2:20741805
|
CT | C | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-1601delA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20741805 | ||||||
| chr2:20741856
|
C | A | 1 | a0001c0001t0001g0196 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.469-1651G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20741856 | ||||||
| chr2:20741995
|
T | C | 140 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0041others(137): Show | 141 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.469-1790A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20741995 | ||||||
| chr2:20742031
|
A | G | 1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.469-1826T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20742031 | ||||||
| chr2:20742050
|
A | G | 1 | a0001c0001t0003g0126 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.469-1845T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20742050 | ||||||
| chr2:20742407
|
A | C | 73 | a0001c0001t0001g0012a0001c0001t0001g0117a0001c0001t0001g0133others(70): Show | 73 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.469-2202T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20742407 | ||||||
| chr2:20742436
|
C | T | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.469-2231G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20742436 | ||||||
| chr2:20742511
|
T | C | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-2306A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20742511 | ||||||
| chr2:20742545
|
G | A | 4 | a0001c0001t0001g0060a0001c0001t0008g0061a0001c0001t0008g0093others(1): Show | 4 | HG02080.hp1 HG02129.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-2340C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20742545 | ||||||
| chr2:20742550
|
T | G | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-2345A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20742550 | ||||||
| chr2:20742562
|
T | C | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-2357A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20742562 | ||||||
| chr2:20742710
|
G | A | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-2505C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20742710 | ||||||
| chr2:20742793
|
C | CT | 7 | a0001c0001t0001g0023a0001c0001t0001g0229a0001c0001t0001g0230others(4): Show | 8 | HG00741.hp1 HG01258.hp2 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.469-2589dupA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20742793 | ||||||
| chr2:20742793
|
C | CTTT | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-2591_469-2589d others(5): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20742793 | ||||||
| chr2:20742793
|
CT | C | 122 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0100others(119): Show | 123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.469-2589delA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20742793 | ||||||
| chr2:20742904
|
C | A | 5 | a0001c0001t0001g0068a0001c0001t0001g0221a0001c0001t0001g0222others(2): Show | 5 | HG01884.hp2 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-2699G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20742904 | ||||||
| chr2:20742906
|
C | A | 5 | a0001c0001t0001g0068a0001c0001t0001g0221a0001c0001t0001g0222others(2): Show | 5 | HG01884.hp2 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-2701G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20742906 | ||||||
| chr2:20742948
|
A | T | 80 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0117others(77): Show | 80 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.469-2743T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20742948 | ||||||
| chr2:20742969
|
T | C | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-2764A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20742969 | ||||||
| chr2:20743020
|
G | C | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-2815C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20743020 | ||||||
| chr2:20743062
|
C | T | 1 | a0001c0001t0005g0166 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.469-2857G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20743062 | ||||||
| chr2:20743125
|
C | T | 2 | a0001c0001t0002g0029a0001c0001t0002g0158 | 2 | HG00642.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.469-2920G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20743125 | ||||||
| chr2:20743241
|
TA | T | 6 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(3): Show | 6 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-3037delT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20743241 | ||||||
| chr2:20743292
|
T | G | 3 | a0001c0001t0004g0043a0001c0001t0004g0114a0001c0001t0004g0157 | 3 | HG01261.hp1 HG01515.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.469-3087A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20743292 | ||||||
| chr2:20743301
|
TCCAAGTC others(105): Show |
T | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-3208_469-3097d others(2): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20743301 | ||||||
| chr2:20743311
|
C | CT | 24 | a0001c0001t0001g0023a0001c0001t0001g0138a0001c0001t0001g0221others(21): Show | 24 | HG00438.hp2 HG01261.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.469-3107dupA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20743311 | ||||||
| chr2:20743311
|
C | CTT | 16 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(13): Show | 17 | HG01106.hp2 HG01192.hp1 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.469-3108_469-3107d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20743311 | ||||||
| chr2:20743311
|
CT | C | 25 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0056others(22): Show | 25 | HG00140.hp2 HG00639.hp2 HG00673.hp1 others(22): Show |
intron_variant | MODIFIER | c.469-3107delA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20743311 | ||||||
| chr2:20743311
|
CTT | C | 41 | a0001c0001t0001g0042a0001c0001t0001g0100a0001c0001t0001g0109others(38): Show | 41 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.469-3108_469-3107d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20743311 | ||||||
| chr2:20743338
|
A | G | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.469-3133T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20743338 | ||||||
| chr2:20743370
|
T | C | 1 | a0001c0001t0002g0134 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.469-3165A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20743370 | ||||||
| chr2:20743373
|
G | C | 80 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0117others(77): Show | 80 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.469-3168C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20743373 | ||||||
| chr2:20743404
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.469-3199G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20743404 | ||||||
| chr2:20743525
|
C | G | 74 | a0001c0001t0001g0012a0001c0001t0001g0117a0001c0001t0001g0133others(71): Show | 74 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.469-3320G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20743525 | ||||||
| chr2:20743582
|
A | G | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-3377T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20743582 | ||||||
| chr2:20743603
|
A | T | 9 | a0001c0001t0001g0202a0001c0001t0001g0233a0001c0001t0003g0067others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.469-3398T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20743603 | ||||||
| chr2:20743982
|
A | G | 43 | a0001c0001t0001g0018a0001c0001t0001g0033a0001c0001t0001g0121others(40): Show | 44 | HG00099.hp2 HG00438.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.469-3777T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20743982 | ||||||
| chr2:20744005
|
C | G | 9 | a0001c0001t0001g0202a0001c0001t0001g0233a0001c0001t0003g0067others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.469-3800G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20744005 | ||||||
| chr2:20744199
|
T | C | 1 | a0002c0003t0004g0235 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.469-3994A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20744199 | ||||||
| chr2:20744223
|
AT | A | 24 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(21): Show | 24 | HG00280.hp1 HG00639.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.469-4019delA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20744223 | ||||||
| chr2:20744223
|
ATT | A | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 109 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.469-4020_469-4019d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20744223 | ||||||
| chr2:20744223
|
ATTT | A | 49 | a0001c0001t0001g0006a0001c0001t0001g0042a0001c0001t0001g0100others(46): Show | 49 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.469-4021_469-4019d others(5): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20744223 | ||||||
| chr2:20744676
|
A | G | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-4471T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20744676 | ||||||
| chr2:20744865
|
C | G | 73 | a0001c0001t0001g0012a0001c0001t0001g0117a0001c0001t0001g0133others(70): Show | 73 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.469-4660G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20744865 | ||||||
| chr2:20745014
|
T | C | 2 | a0001c0001t0002g0076a0001c0006t0001g0240 | 2 | HG03225.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.469-4809A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20745014 | ||||||
| chr2:20745111
|
T | C | 194 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0018others(191): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.469-4906A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20745111 | ||||||
| chr2:20745113
|
T | G | 1 | a0001c0001t0001g0179 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.469-4908A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20745113 | ||||||
| chr2:20745152
|
C | A | 1 | a0001c0001t0002g0132 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.469-4947G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20745152 | ||||||
| chr2:20745253
|
T | C | 9 | a0001c0001t0001g0202a0001c0001t0001g0233a0001c0001t0003g0067others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.469-5048A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20745253 | ||||||
| chr2:20745390
|
A | G | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 120 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.469-5185T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20745390 | ||||||
| chr2:20745530
|
T | C | 9 | a0001c0001t0001g0202a0001c0001t0001g0233a0001c0001t0003g0067others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.469-5325A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20745530 | ||||||
| chr2:20745579
|
A | G | 9 | a0001c0001t0001g0202a0001c0001t0001g0233a0001c0001t0003g0067others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.469-5374T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20745579 | ||||||
| chr2:20745737
|
T | C | 138 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0042others(135): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.469-5532A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20745737 | ||||||
| chr2:20745761
|
G | T | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.469-5556C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20745761 | ||||||
| chr2:20745951
|
G | A | 1 | a0001c0001t0004g0043 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.469-5746C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20745951 | ||||||
| chr2:20746002
|
G | A | 48 | a0001c0001t0001g0042a0001c0001t0001g0068a0001c0001t0001g0100others(45): Show | 49 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.469-5797C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20746002 | ||||||
| chr2:20746091
|
G | T | 9 | a0001c0001t0001g0202a0001c0001t0001g0233a0001c0001t0003g0067others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.469-5886C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20746091 | ||||||
| chr2:20746112
|
T | G | 1 | a0001c0001t0002g0088 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.469-5907A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20746112 | ||||||
| chr2:20746198
|
G | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-5993C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20746198 | ||||||
| chr2:20746252
|
G | C | 1 | a0001c0001t0009g0118 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.469-6047C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20746252 | ||||||
| chr2:20746279
|
T | C | 9 | a0001c0001t0001g0202a0001c0001t0001g0233a0001c0001t0003g0067others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.469-6074A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20746279 | ||||||
| chr2:20746319
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.469-6114T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20746319 | ||||||
| chr2:20746320
|
T | A | 1 | a0001c0001t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.469-6115A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20746320 | ||||||
| chr2:20746342
|
T | C | 9 | a0001c0001t0001g0202a0001c0001t0001g0233a0001c0001t0003g0067others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.469-6137A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20746342 | ||||||
| chr2:20746466
|
C | T | 52 | a0001c0001t0001g0018a0001c0001t0001g0033a0001c0001t0001g0121others(49): Show | 53 | HG00099.hp2 HG00438.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.469-6261G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20746466 | ||||||
| chr2:20746468
|
T | A | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-6263A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20746468 | ||||||
| chr2:20746471
|
C | T | 9 | a0001c0001t0001g0202a0001c0001t0001g0233a0001c0001t0003g0067others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.469-6266G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20746471 | ||||||
| chr2:20746637
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.469-6432A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20746637 | ||||||
| chr2:20746685
|
A | C | 1 | a0001c0001t0001g0245 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.469-6480T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20746685 | ||||||
| chr2:20746764
|
C | T | 2 | a0001c0001t0001g0219a0001c0001t0001g0231 | 2 | HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.469-6559G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20746764 | ||||||
| chr2:20746849
|
C | T | 5 | a0001c0001t0001g0068a0001c0001t0001g0221a0001c0001t0001g0222others(2): Show | 5 | HG01884.hp2 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-6644G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20746849 | ||||||
| chr2:20747046
|
T | C | 138 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0042others(135): Show | 139 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.469-6841A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20747046 | ||||||
| chr2:20747091
|
G | T | 1 | a0001c0001t0006g0242 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.469-6886C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20747091 | ||||||
| chr2:20747437
|
T | C | 91 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0041others(88): Show | 91 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.469-7232A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20747437 | ||||||
| chr2:20747545
|
A | C | 1 | a0001c0001t0001g0154 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.469-7340T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20747545 | ||||||
| chr2:20747549
|
C | A | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-7344G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20747549 | ||||||
| chr2:20747567
|
T | C | 1 | a0001c0001t0004g0098 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.469-7362A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20747567 | ||||||
| chr2:20747638
|
A | C | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-7433T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20747638 | ||||||
| chr2:20747671
|
T | C | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-7466A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20747671 | ||||||
| chr2:20747795
|
C | T | 254 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.469-7590G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20747795 | ||||||
| chr2:20747854
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.469-7649G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20747854 | ||||||
| chr2:20747969
|
G | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0147a0001c0001t0001g0179 | 3 | HG02129.hp2 HG02523.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.469-7764C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20747969 | ||||||
| chr2:20747973
|
A | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0147a0001c0001t0001g0179 | 3 | HG02129.hp2 HG02523.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.469-7768T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20747973 | ||||||
| chr2:20748049
|
G | T | 1 | a0001c0001t0006g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.469-7844C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20748049 | ||||||
| chr2:20748095
|
A | G | 1 | a0001c0001t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.469-7890T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20748095 | ||||||
| chr2:20748332
|
C | T | 2 | a0001c0001t0003g0253a0001c0001t0003g0254 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.469-8127G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20748332 | ||||||
| chr2:20748525
|
A | C | 1 | a0001c0001t0003g0083 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.469-8320T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20748525 | ||||||
| chr2:20748566
|
C | G | 169 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0018others(166): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.469-8361G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20748566 | ||||||
| chr2:20748679
|
G | A | 6 | a0001c0001t0003g0069a0001c0001t0003g0152a0001c0001t0006g0144others(3): Show | 6 | HG02615.hp1 HG02717.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-8474C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20748679 | ||||||
| chr2:20748778
|
A | T | 169 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0018others(166): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.469-8573T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20748778 | ||||||
| chr2:20748919
|
C | A | 232 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.469-8714G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20748919 | ||||||
| chr2:20748960
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.469-8755G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20748960 | ||||||
| chr2:20749368
|
T | A | 4 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(1): Show | 4 | HG01934.hp2 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.469-9163A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20749368 | ||||||
| chr2:20749587
|
T | C | 1 | a0001c0001t0005g0046 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.469-9382A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20749587 | ||||||
| chr2:20749646
|
T | C | 4 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0003g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.469-9441A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20749646 | ||||||
| chr2:20749942
|
C | A | 1 | a0001c0001t0006g0242 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.469-9737G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20749942 | ||||||
| chr2:20750023
|
C | CT | 98 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0117others(95): Show | 98 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.469-9819dupA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20750023 | ||||||
| chr2:20750023
|
C | CTT | 14 | a0001c0001t0001g0023a0001c0001t0001g0148a0001c0001t0001g0229others(11): Show | 14 | HG01261.hp2 HG01496.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.469-9820_469-9819d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20750023 | ||||||
| chr2:20750023
|
CT | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(26): Show | 29 | HG00140.hp2 HG00673.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.469-9819delA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20750023 | ||||||
| chr2:20750023
|
CTTTT | C | 7 | a0001c0001t0004g0001a0001c0001t0004g0073a0001c0001t0004g0074others(4): Show | 8 | HG00099.hp2 HG00741.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.469-9822_469-9819d others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20750023 | ||||||
| chr2:20750023
|
CTTTTTT | C | 10 | a0001c0001t0001g0041a0001c0001t0001g0202a0001c0001t0001g0233others(7): Show | 10 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-9824_469-9819d others(8): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20750023 | ||||||
| chr2:20750151
|
T | C | 47 | a0001c0001t0001g0042a0001c0001t0001g0068a0001c0001t0001g0100others(44): Show | 48 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.469-9946A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20750151 | ||||||
| chr2:20750179
|
T | C | 137 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0041others(134): Show | 138 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.469-9974A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20750179 | ||||||
| chr2:20750246
|
G | A | 1 | a0001c0001t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.469-10041C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20750246 | ||||||
| chr2:20750643
|
T | G | 1 | a0001c0001t0006g0242 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.469-10438A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20750643 | ||||||
| chr2:20750956
|
T | C | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.469-10751A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20750956 | ||||||
| chr2:20751005
|
T | C | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.469-10800A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20751005 | ||||||
| chr2:20751075
|
C | T | 1 | a0001c0001t0001g0138 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.469-10870G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20751075 | ||||||
| chr2:20751086
|
A | G | 169 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0018others(166): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.469-10881T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20751086 | ||||||
| chr2:20751198
|
T | G | 5 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0003g0067others(2): Show | 5 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-10993A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20751198 | ||||||
| chr2:20751220
|
T | C | 40 | a0001c0001t0001g0042a0001c0001t0001g0100a0001c0001t0001g0109others(37): Show | 40 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.469-11015A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20751220 | ||||||
| chr2:20751276
|
G | T | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-11071C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20751276 | ||||||
| chr2:20751286
|
A | G | 1 | a0002c0003t0004g0235 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.469-11081T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20751286 | ||||||
| chr2:20751346
|
A | G | 1 | a0001c0001t0003g0105 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.469-11141T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20751346 | ||||||
| chr2:20751415
|
T | C | 6 | a0001c0001t0001g0060a0001c0001t0001g0182a0001c0001t0002g0089others(3): Show | 6 | HG02080.hp1 HG02129.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-11210A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20751415 | ||||||
| chr2:20751487
|
C | T | 2 | a0002c0003t0001g0237a0002c0003t0004g0238 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.469-11282G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20751487 | ||||||
| chr2:20751572
|
A | G | 169 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0018others(166): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.469-11367T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20751572 | ||||||
| chr2:20751684
|
C | A | 169 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0018others(166): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.469-11479G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20751684 | ||||||
| chr2:20751927
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.469-11722C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20751927 | ||||||
| chr2:20751960
|
C | T | 9 | a0001c0001t0001g0202a0001c0001t0001g0233a0001c0001t0003g0067others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.469-11755G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20751960 | ||||||
| chr2:20751980
|
C | T | 19 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(16): Show | 19 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.469-11775G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20751980 | ||||||
| chr2:20752167
|
C | T | 3 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215 | 3 | HG01952.hp1 HG02293.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.469-11962G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20752167 | ||||||
| chr2:20752206
|
TA | T | 179 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(176): Show | 181 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.469-12002delT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20752206 | ||||||
| chr2:20752218
|
T | A | 1 | a0001c0001t0002g0134 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.469-12013A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20752218 | ||||||
| chr2:20752253
|
C | T | 9 | a0001c0001t0001g0202a0001c0001t0001g0233a0001c0001t0003g0067others(6): Show | 9 | HG01346.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.469-12048G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20752253 | ||||||
| chr2:20752423
|
A | G | 2 | a0001c0001t0003g0204a0001c0001t0003g0205 | 2 | HG00639.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.469-12218T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20752423 | ||||||
| chr2:20752681
|
T | C | 1 | a0001c0001t0004g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.469-12476A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20752681 | ||||||
| chr2:20752722
|
T | C | 1 | a0001c0001t0006g0242 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.469-12517A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20752722 | ||||||
| chr2:20752753
|
T | C | 2 | a0001c0001t0001g0092a0001c0001t0002g0058 | 2 | NA18999.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.469-12548A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20752753 | ||||||
| chr2:20752802
|
T | C | 61 | a0001c0001t0001g0006a0001c0001t0001g0042a0001c0001t0001g0068others(58): Show | 62 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.469-12597A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20752802 | ||||||
| chr2:20752956
|
T | C | 2 | a0002c0003t0001g0237a0002c0003t0004g0238 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.469-12751A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20752956 | ||||||
| chr2:20752974
|
C | T | 1 | a0001c0001t0005g0045 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.469-12769G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20752974 | ||||||
| chr2:20752975
|
GACA | G | 232 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.469-12773_469-1277 others(7): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20752975 | ||||||
| chr2:20753104
|
C | A | 2 | a0001c0001t0003g0008a0001c0001t0003g0030 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.469-12899G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20753104 | ||||||
| chr2:20753330
|
G | C | 125 | a0001c0001t0001g0012a0001c0001t0001g0042a0001c0001t0001g0068others(122): Show | 126 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.469-13125C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20753330 | ||||||
| chr2:20753364
|
G | A | 11 | a0001c0001t0001g0023a0001c0001t0001g0229a0001c0001t0001g0230others(8): Show | 11 | HG01261.hp2 HG01496.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.469-13159C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20753364 | ||||||
| chr2:20753428
|
T | C | 136 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0042others(133): Show | 137 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.469-13223A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20753428 | ||||||
| chr2:20753482
|
C | T | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-13277G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20753482 | ||||||
| chr2:20753664
|
A | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-13459T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20753664 | ||||||
| chr2:20753699
|
A | C | 85 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0117others(82): Show | 85 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.469-13494T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20753699 | ||||||
| chr2:20753844
|
C | A | 11 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(8): Show | 11 | HG01255.hp1 HG02109.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.469-13639G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20753844 | ||||||
| chr2:20753863
|
T | C | 3 | a0001c0001t0001g0233a0001c0001t0003g0067a0001c0001t0006g0239 | 3 | HG02145.hp2 HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.469-13658A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20753863 | ||||||
| chr2:20753932
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.469-13727C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20753932 | ||||||
| chr2:20754020
|
T | C | 1 | a0001c0001t0005g0059 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.469-13815A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20754020 | ||||||
| chr2:20754163
|
C | T | 3 | a0001c0001t0001g0071a0001c0001t0001g0181a0001c0001t0003g0180 | 3 | HG02280.hp2 HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.469-13958G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20754163 | ||||||
| chr2:20754202
|
C | T | 1 | a0001c0001t0003g0167 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.469-13997G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20754202 | ||||||
| chr2:20754213
|
C | T | 168 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0018others(165): Show | 169 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.469-14008G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20754213 | ||||||
| chr2:20754305
|
C | T | 2 | a0001c0001t0002g0084a0001c0001t0005g0123 | 2 | HG01168.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.469-14100G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20754305 | ||||||
| chr2:20754329
|
A | C | 1 | a0001c0001t0001g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.469-14124T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20754329 | ||||||
| chr2:20754333
|
A | T | 2 | a0001c0001t0002g0102a0001c0006t0001g0240 | 2 | HG03225.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.469-14128T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20754333 | ||||||
| chr2:20754442
|
G | C | 1 | a0001c0001t0002g0129 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.469-14237C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20754442 | ||||||
| chr2:20754475
|
A | G | 7 | a0001c0001t0001g0068a0001c0001t0001g0221a0001c0001t0001g0222others(4): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.469-14270T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20754475 | ||||||
| chr2:20754487
|
A | C | 1 | a0001c0001t0001g0023 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.469-14282T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20754487 | ||||||
| chr2:20754500
|
C | CA | 13 | a0001c0001t0001g0169a0001c0001t0001g0233a0001c0001t0002g0055others(10): Show | 13 | HG01255.hp2 HG02451.hp2 HG02647.hp2 others(10): Show |
intron_variant | MODIFIER | c.469-14296dupT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20754500 | ||||||
| chr2:20754500
|
C | CAA | 7 | a0001c0001t0001g0004a0001c0001t0003g0101a0001c0001t0004g0217others(4): Show | 7 | HG02015.hp2 HG02922.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.469-14297_469-1429 others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20754500 | ||||||
| chr2:20754500
|
C | CAAA | 67 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0019others(64): Show | 68 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.469-14298_469-1429 others(7): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20754500 | ||||||
| chr2:20754500
|
C | CAAAA | 42 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0041others(39): Show | 42 | HG00438.hp2 HG01081.hp2 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.469-14299_469-1429 others(8): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20754500 | ||||||
| chr2:20754500
|
CA | C | 49 | a0001c0001t0001g0042a0001c0001t0001g0100a0001c0001t0001g0109others(46): Show | 50 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.469-14296delT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20754500 | ||||||
| chr2:20754667
|
C | G | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.469-14462G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20754667 | ||||||
| chr2:20754955
|
A | G | 1 | a0001c0001t0003g0105 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.469-14750T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20754955 | ||||||
| chr2:20755041
|
C | T | 2 | a0002c0003t0001g0237a0002c0003t0004g0238 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.469-14836G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755041 | ||||||
| chr2:20755123
|
C | CTG | 10 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0232others(7): Show | 10 | HG01496.hp1 HG01884.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-14920_469-1491 others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755123 | ||||||
| chr2:20755123
|
C | CTGTG | 6 | a0001c0001t0001g0006a0001c0001t0001g0179a0001c0001t0001g0249others(3): Show | 6 | HG01934.hp2 HG02523.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.469-14922_469-1491 others(8): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755123 | ||||||
| chr2:20755123
|
CTGTGTT | C | 10 | a0001c0001t0001g0071a0001c0001t0001g0181a0001c0001t0003g0180others(7): Show | 10 | HG00639.hp2 HG02280.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.469-14924_469-1491 others(10): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755123 | ||||||
| chr2:20755123
|
CTGTGTTT others(1): Show |
C | 7 | a0001c0001t0001g0041a0001c0001t0003g0069a0001c0001t0003g0152others(4): Show | 7 | HG01081.hp2 HG02615.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.469-14926_469-1491 others(12): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755123 | ||||||
| chr2:20755125
|
GTGTT | G | 59 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(56): Show | 60 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.469-14924_469-1492 others(8): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755125 | ||||||
| chr2:20755127
|
GTT | G | 15 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(12): Show | 15 | HG01255.hp1 HG01433.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.469-14924_469-1492 others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755127 | ||||||
| chr2:20755129
|
T | G | 34 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0023others(31): Show | 34 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.469-14924A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755129 | ||||||
| chr2:20755129
|
T | TTG | 44 | a0001c0001t0001g0042a0001c0001t0001g0100a0001c0001t0001g0109others(41): Show | 44 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.469-14926_469-1492 others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755129 | ||||||
| chr2:20755129
|
T | TTGTGTGT others(9): Show |
1 | a0001c0001t0001g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.469-14940_469-1492 others(20): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755129 | ||||||
| chr2:20755129
|
TTG | T | 5 | a0001c0001t0002g0055a0001c0001t0002g0064a0001c0001t0002g0106others(2): Show | 5 | HG02559.hp1 HG03471.hp1 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-14926_469-1492 others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755129 | ||||||
| chr2:20755129
|
TTGTG | T | 56 | a0001c0001t0001g0012a0001c0001t0001g0068a0001c0001t0001g0133others(53): Show | 57 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.469-14928_469-1492 others(8): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755129 | ||||||
| chr2:20755272
|
AG | A | 14 | a0001c0001t0001g0018a0001c0001t0001g0121a0001c0001t0001g0122others(11): Show | 14 | HG00438.hp2 HG01106.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.469-15068delC | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755272 | ||||||
| chr2:20755383
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.469-15178T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755383 | ||||||
| chr2:20755431
|
G | A | 1 | a0001c0001t0005g0017 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.469-15226C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755431 | ||||||
| chr2:20755565
|
C | A | 12 | a0001c0001t0001g0018a0001c0001t0001g0138a0001c0001t0001g0147others(9): Show | 12 | HG00438.hp2 HG02129.hp2 HG02523.hp1 others(9): Show |
intron_variant | MODIFIER | c.469-15360G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755565 | ||||||
| chr2:20755573
|
A | C | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.469-15368T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755573 | ||||||
| chr2:20755607
|
G | A | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.469-15402C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755607 | ||||||
| chr2:20755677
|
G | A | 1 | a0002c0003t0004g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.469-15472C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755677 | ||||||
| chr2:20755707
|
C | A | 1 | a0001c0001t0002g0106 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.469-15502G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755707 | ||||||
| chr2:20755712
|
G | A | 3 | a0001c0001t0001g0233a0001c0001t0003g0067a0001c0001t0006g0239 | 3 | HG02145.hp2 HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.469-15507C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755712 | ||||||
| chr2:20755731
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.469-15526C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755731 | ||||||
| chr2:20755883
|
G | T | 1 | a0001c0001t0001g0196 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.469-15678C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20755883 | ||||||
| chr2:20756039
|
C | CT | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.469-15835dupA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20756039 | ||||||
| chr2:20756055
|
G | A | 1 | a0001c0001t0006g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.469-15850C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20756055 | ||||||
| chr2:20756092
|
C | T | 7 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(4): Show | 7 | HG00639.hp2 HG01346.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.469-15887G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20756092 | ||||||
| chr2:20756106
|
C | T | 2 | a0001c0001t0003g0206a0001c0001t0003g0207 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.469-15901G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20756106 | ||||||
| chr2:20756191
|
T | C | 2 | a0001c0002t0001g0192a0001c0002t0001g0193 | 2 | HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.469-15986A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20756191 | ||||||
| chr2:20756356
|
G | A | 3 | a0001c0001t0001g0233a0001c0001t0003g0067a0001c0001t0006g0239 | 3 | HG02145.hp2 HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.469-16151C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20756356 | ||||||
| chr2:20756402
|
A | C | 73 | a0001c0001t0001g0012a0001c0001t0001g0117a0001c0001t0001g0133others(70): Show | 73 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.469-16197T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20756402 | ||||||
| chr2:20756702
|
G | A | 10 | a0001c0001t0001g0023a0001c0001t0001g0229a0001c0001t0001g0230others(7): Show | 10 | HG01261.hp2 HG01496.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.469-16497C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20756702 | ||||||
| chr2:20757206
|
T | C | 1 | a0001c0001t0003g0083 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.469-17001A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20757206 | ||||||
| chr2:20757439
|
T | C | 1 | a0001c0001t0006g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.469-17234A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20757439 | ||||||
| chr2:20757442
|
C | A | 7 | a0001c0001t0001g0068a0001c0001t0001g0221a0001c0001t0001g0222others(4): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.469-17237G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20757442 | ||||||
| chr2:20757511
|
T | G | 1 | a0001c0001t0006g0242 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.468+17299A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20757511 | ||||||
| chr2:20757639
|
G | T | 40 | a0001c0001t0001g0042a0001c0001t0001g0100a0001c0001t0001g0109others(37): Show | 40 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.468+17171C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20757639 | ||||||
| chr2:20757698
|
G | A | 1 | a0001c0001t0003g0104 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.468+17112C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20757698 | ||||||
| chr2:20757703
|
C | G | 1 | a0002c0003t0004g0235 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.468+17107G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20757703 | ||||||
| chr2:20757832
|
T | G | 77 | a0001c0001t0001g0012a0001c0001t0001g0117a0001c0001t0001g0133others(74): Show | 78 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.468+16978A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20757832 | ||||||
| chr2:20757844
|
C | T | 3 | a0001c0001t0001g0233a0001c0001t0003g0067a0001c0001t0006g0239 | 3 | HG02145.hp2 HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.468+16966G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20757844 | ||||||
| chr2:20757966
|
T | C | 6 | a0001c0001t0001g0072a0001c0001t0003g0008a0001c0001t0003g0030others(3): Show | 6 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+16844A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20757966 | ||||||
| chr2:20758033
|
A | G | 1 | a0001c0001t0006g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.468+16777T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20758033 | ||||||
| chr2:20758182
|
T | C | 1 | a0001c0001t0003g0101 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.468+16628A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20758182 | ||||||
| chr2:20758218
|
T | C | 1 | a0001c0001t0009g0118 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.468+16592A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20758218 | ||||||
| chr2:20758344
|
G | C | 1 | a0001c0001t0004g0160 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.468+16466C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20758344 | ||||||
| chr2:20758350
|
A | G | 2 | a0001c0001t0001g0219a0001c0001t0001g0231 | 2 | HG02109.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.468+16460T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20758350 | ||||||
| chr2:20758377
|
C | T | 1 | a0005c0007t0001g0062 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.468+16433G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20758377 | ||||||
| chr2:20758626
|
G | A | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.468+16184C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20758626 | ||||||
| chr2:20758885
|
C | T | 1 | a0001c0001t0003g0104 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.468+15925G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20758885 | ||||||
| chr2:20758926
|
C | T | 1 | a0001c0001t0003g0067 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.468+15884G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20758926 | ||||||
| chr2:20759137
|
A | G | 1 | a0001c0001t0003g0170 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.468+15673T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20759137 | ||||||
| chr2:20759155
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.468+15655C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20759155 | ||||||
| chr2:20759226
|
A | G | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG02630.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.468+15584T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20759226 | ||||||
| chr2:20759305
|
T | G | 5 | a0001c0001t0003g0008a0001c0001t0003g0030a0001c0001t0003g0101others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+15505A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20759305 | ||||||
| chr2:20759507
|
T | C | 1 | a0001c0001t0003g0016 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.468+15303A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20759507 | ||||||
| chr2:20760052
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG01106.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.468+14758T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20760052 | ||||||
| chr2:20760151
|
G | C | 26 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(23): Show | 26 | HG00140.hp2 HG00673.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.468+14659C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20760151 | ||||||
| chr2:20760234
|
G | C | 1 | a0001c0001t0003g0067 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.468+14576C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20760234 | ||||||
| chr2:20760439
|
T | A | 1 | a0001c0001t0001g0181 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.468+14371A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20760439 | ||||||
| chr2:20760563
|
G | C | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.468+14247C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20760563 | ||||||
| chr2:20760619
|
T | C | 1 | a0001c0001t0006g0242 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.468+14191A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20760619 | ||||||
| chr2:20760701
|
C | G | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.468+14109G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20760701 | ||||||
| chr2:20760819
|
C | T | 1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.468+13991G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20760819 | ||||||
| chr2:20760885
|
T | C | 1 | a0001c0001t0002g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.468+13925A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20760885 | ||||||
| chr2:20761086
|
T | TC | 4 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0003g0067others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+13723dupG | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20761086 | ||||||
| chr2:20761139
|
A | G | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+13671T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20761139 | ||||||
| chr2:20761387
|
TA | T | 180 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 182 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.468+13422delT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20761387 | ||||||
| chr2:20761502
|
T | G | 1 | a0001c0001t0001g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.468+13308A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20761502 | ||||||
| chr2:20761553
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.468+13257T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20761553 | ||||||
| chr2:20761830
|
C | T | 47 | a0001c0001t0001g0042a0001c0001t0001g0068a0001c0001t0001g0100others(44): Show | 48 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(45): Show |
intron_variant | MODIFIER | c.468+12980G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20761830 | ||||||
| chr2:20761919
|
T | G | 7 | a0001c0001t0001g0068a0001c0001t0001g0221a0001c0001t0001g0222others(4): Show | 8 | HG01884.hp2 HG02451.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.468+12891A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20761919 | ||||||
| chr2:20762026
|
T | C | 2 | a0001c0001t0003g0253a0001c0001t0003g0254 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.468+12784A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20762026 | ||||||
| chr2:20762140
|
C | G | 7 | a0001c0001t0004g0079a0001c0001t0004g0116a0001c0001t0004g0120others(4): Show | 7 | HG00140.hp1 HG01123.hp1 HG01258.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+12670G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20762140 | ||||||
| chr2:20762309
|
C | G | 52 | a0001c0001t0001g0042a0001c0001t0001g0068a0001c0001t0001g0100others(49): Show | 53 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.468+12501G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20762309 | ||||||
| chr2:20762540
|
T | TAA | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+12268_468+1226 others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20762540 | ||||||
| chr2:20762609
|
TTAAG | T | 4 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(1): Show | 4 | HG01934.hp2 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.468+12197_468+1220 others(8): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20762609 | ||||||
| chr2:20762658
|
G | T | 3 | a0001c0001t0001g0233a0001c0001t0003g0067a0001c0001t0006g0239 | 3 | HG02145.hp2 HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.468+12152C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20762658 | ||||||
| chr2:20762806
|
C | T | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+12004G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20762806 | ||||||
| chr2:20762910
|
C | T | 55 | a0001c0001t0001g0042a0001c0001t0001g0068a0001c0001t0001g0100others(52): Show | 56 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(53): Show |
intron_variant | MODIFIER | c.468+11900G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20762910 | ||||||
| chr2:20763330
|
G | A | 2 | a0002c0003t0001g0237a0002c0003t0004g0238 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.468+11480C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20763330 | ||||||
| chr2:20763508
|
T | C | 2 | a0002c0003t0001g0237a0002c0003t0004g0238 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.468+11302A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20763508 | ||||||
| chr2:20763546
|
G | A | 3 | a0001c0001t0002g0102a0001c0001t0003g0063a0001c0001t0003g0167 | 3 | NA18977.hp1 NA18999.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.468+11264C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20763546 | ||||||
| chr2:20763879
|
T | A | 40 | a0001c0001t0001g0042a0001c0001t0001g0100a0001c0001t0001g0109others(37): Show | 40 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.468+10931A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20763879 | ||||||
| chr2:20763965
|
AT | A | 82 | a0001c0001t0001g0006a0001c0001t0001g0042a0001c0001t0001g0068others(79): Show | 83 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(80): Show |
intron_variant | MODIFIER | c.468+10844delA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20763965 | ||||||
| chr2:20763965
|
ATT | A | 73 | a0001c0001t0001g0012a0001c0001t0001g0023a0001c0001t0001g0117others(70): Show | 73 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.468+10843_468+1084 others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20763965 | ||||||
| chr2:20764011
|
T | A | 1 | a0001c0001t0002g0146 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.468+10799A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20764011 | ||||||
| chr2:20764177
|
A | ATG | 106 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(103): Show | 106 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.468+10631_468+1063 others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20764177 | ||||||
| chr2:20764258
|
A | G | 2 | a0001c0001t0005g0002a0001c0001t0005g0224 | 3 | HG02451.hp1 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.468+10552T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20764258 | ||||||
| chr2:20764411
|
T | G | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.468+10399A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20764411 | ||||||
| chr2:20764456
|
C | T | 1 | a0001c0001t0010g0115 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.468+10354G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20764456 | ||||||
| chr2:20764496
|
T | C | 2 | a0001c0001t0003g0253a0001c0001t0003g0254 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.468+10314A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20764496 | ||||||
| chr2:20764552
|
T | C | 6 | a0001c0001t0001g0006a0001c0002t0001g0191a0001c0002t0001g0192others(3): Show | 6 | HG03688.hp1 HG03704.hp2 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.468+10258A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20764552 | ||||||
| chr2:20764594
|
T | A | 1 | a0001c0001t0003g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.468+10216A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20764594 | ||||||
| chr2:20764608
|
T | G | 3 | a0001c0001t0001g0236a0002c0003t0001g0237a0002c0003t0004g0238 | 3 | HG02257.hp2 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.468+10202A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20764608 | ||||||
| chr2:20764639
|
CTG | C | 5 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(2): Show | 5 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+10169_468+1017 others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20764639 | ||||||
| chr2:20764893
|
A | T | 1 | a0001c0001t0005g0252 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.468+9917T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20764893 | ||||||
| chr2:20764924
|
G | A | 1 | a0001c0001t0004g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.468+9886C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20764924 | ||||||
| chr2:20764969
|
T | C | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.468+9841A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20764969 | ||||||
| chr2:20765037
|
C | G | 18 | a0001c0001t0001g0041a0001c0001t0001g0117a0001c0001t0001g0139others(15): Show | 18 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.468+9773G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20765037 | ||||||
| chr2:20765042
|
A | G | 1 | a0001c0001t0006g0242 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.468+9768T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20765042 | ||||||
| chr2:20765049
|
A | G | 1 | a0001c0001t0002g0036 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.468+9761T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20765049 | ||||||
| chr2:20765295
|
C | T | 3 | a0001c0001t0004g0250a0001c0002t0001g0191a0001c0002t0001g0194 | 3 | HG03688.hp1 HG04228.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.468+9515G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20765295 | ||||||
| chr2:20765406
|
C | T | 2 | a0001c0001t0001g0169a0001c0001t0002g0168 | 2 | HG01255.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.468+9404G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20765406 | ||||||
| chr2:20765507
|
A | G | 1 | a0001c0001t0003g0218 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.468+9303T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20765507 | ||||||
| chr2:20765547
|
C | T | 7 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(4): Show | 7 | HG02109.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+9263G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20765547 | ||||||
| chr2:20765576
|
C | T | 1 | a0001c0001t0004g0185 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.468+9234G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20765576 | ||||||
| chr2:20765606
|
C | A | 19 | a0001c0001t0001g0071a0001c0001t0001g0196a0001c0001t0001g0202others(16): Show | 20 | HG01167.hp1 HG01346.hp2 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.468+9204G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20765606 | ||||||
| chr2:20765607
|
T | A | 18 | a0001c0001t0001g0071a0001c0001t0001g0196a0001c0001t0001g0202others(15): Show | 19 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.468+9203A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20765607 | ||||||
| chr2:20766020
|
C | A | 1 | a0001c0001t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.468+8790G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20766020 | ||||||
| chr2:20766072
|
C | CT | 8 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0001g0236others(5): Show | 8 | HG02165.hp2 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+8737dupA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20766072 | ||||||
| chr2:20766269
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG01106.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.468+8541G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20766269 | ||||||
| chr2:20766776
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.468+8034G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20766776 | ||||||
| chr2:20766823
|
C | G | 3 | a0001c0001t0001g0068a0001c0001t0002g0066a0001c0001t0003g0067 | 3 | HG01884.hp2 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.468+7987G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20766823 | ||||||
| chr2:20766873
|
G | C | 3 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0004g0246 | 3 | HG02451.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.468+7937C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20766873 | ||||||
| chr2:20766919
|
C | T | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 8 | HG02451.hp1 HG02886.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+7891G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20766919 | ||||||
| chr2:20766927
|
C | T | 1 | a0001c0001t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.468+7883G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20766927 | ||||||
| chr2:20767029
|
C | T | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.468+7781G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20767029 | ||||||
| chr2:20767096
|
G | C | 2 | a0001c0001t0001g0208a0001c0001t0001g0215 | 2 | HG01952.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.468+7714C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20767096 | ||||||
| chr2:20767330
|
T | TC | 22 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(19): Show | 22 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.468+7479dupG | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20767330 | ||||||
| chr2:20767628
|
G | C | 1 | a0001c0001t0004g0099 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.468+7182C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20767628 | ||||||
| chr2:20767634
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.468+7176G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20767634 | ||||||
| chr2:20767638
|
G | A | 22 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(19): Show | 22 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.468+7172C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20767638 | ||||||
| chr2:20767650
|
G | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG01106.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.468+7160C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20767650 | ||||||
| chr2:20768048
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.468+6762G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20768048 | ||||||
| chr2:20768091
|
C | T | 1 | a0001c0001t0005g0103 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.468+6719G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20768091 | ||||||
| chr2:20768123
|
C | T | 7 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(4): Show | 7 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+6687G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20768123 | ||||||
| chr2:20768224
|
G | A | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.468+6586C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20768224 | ||||||
| chr2:20768383
|
G | A | 1 | a0001c0001t0004g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.468+6427C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20768383 | ||||||
| chr2:20768521
|
A | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0233 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.468+6289T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20768521 | ||||||
| chr2:20768527
|
AC | A | 5 | a0001c0001t0003g0083a0001c0001t0003g0124a0001c0001t0003g0125others(2): Show | 5 | HG00735.hp2 HG01168.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.468+6282delG | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20768527 | ||||||
| chr2:20768602
|
T | C | 2 | a0001c0001t0003g0206a0001c0001t0003g0207 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.468+6208A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20768602 | ||||||
| chr2:20768960
|
C | T | 4 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(1): Show | 4 | HG01167.hp2 HG03710.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+5850G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20768960 | ||||||
| chr2:20769052
|
C | T | 5 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(2): Show | 5 | HG01934.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.468+5758G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20769052 | ||||||
| chr2:20769063
|
C | T | 1 | a0001c0001t0003g0173 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.468+5747G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20769063 | ||||||
| chr2:20769109
|
C | T | 3 | a0001c0001t0004g0011a0001c0001t0004g0114a0001c0001t0004g0176 | 3 | HG02630.hp2 HG03139.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.468+5701G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20769109 | ||||||
| chr2:20769173
|
C | G | 1 | a0001c0001t0004g0160 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.468+5637G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20769173 | ||||||
| chr2:20769312
|
G | A | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0003g0218 | 3 | HG02630.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.468+5498C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20769312 | ||||||
| chr2:20769321
|
T | G | 1 | a0001c0001t0002g0112 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.468+5489A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20769321 | ||||||
| chr2:20769448
|
T | C | 1 | a0001c0001t0002g0178 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.468+5362A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20769448 | ||||||
| chr2:20769776
|
A | G | 10 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(7): Show | 10 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+5034T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20769776 | ||||||
| chr2:20769947
|
T | C | 1 | a0001c0001t0004g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.468+4863A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20769947 | ||||||
| chr2:20769986
|
A | T | 1 | a0001c0001t0004g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.468+4824T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20769986 | ||||||
| chr2:20770009
|
C | T | 1 | a0001c0001t0006g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.468+4801G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20770009 | ||||||
| chr2:20770104
|
A | G | 1 | a0001c0001t0006g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.468+4706T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20770104 | ||||||
| chr2:20770178
|
A | T | 5 | a0001c0001t0001g0233a0001c0001t0001g0244a0001c0001t0001g0245others(2): Show | 5 | HG02451.hp2 HG02630.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.468+4632T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20770178 | ||||||
| chr2:20770293
|
G | A | 103 | a0001c0001t0001g0012a0001c0001t0001g0133a0001c0001t0001g0138others(100): Show | 105 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.468+4517C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20770293 | ||||||
| chr2:20770485
|
G | A | 8 | a0001c0001t0003g0014a0001c0001t0003g0015a0001c0001t0003g0016others(5): Show | 8 | HG03688.hp1 HG03710.hp1 HG03710.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+4325C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20770485 | ||||||
| chr2:20770820
|
G | A | 4 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(1): Show | 4 | HG02886.hp1 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.468+3990C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20770820 | ||||||
| chr2:20770839
|
C | CAGGCAGA others(1): Show |
5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.468+3963_468+3970d others(10): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20770839 | ||||||
| chr2:20770874
|
T | A | 1 | a0001c0001t0001g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.468+3936A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20770874 | ||||||
| chr2:20771367
|
C | A | 1 | a0001c0001t0005g0113 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.468+3443G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20771367 | ||||||
| chr2:20771570
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.468+3240G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20771570 | ||||||
| chr2:20771739
|
C | T | 22 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(19): Show | 22 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.468+3071G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20771739 | ||||||
| chr2:20771755
|
A | G | 1 | a0001c0001t0006g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.468+3055T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20771755 | ||||||
| chr2:20771758
|
TTTTGGAC others(35): Show |
T | 243 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(240): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.468+3010_468+3051d others(44): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20771758 | ||||||
| chr2:20771835
|
T | C | 22 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(19): Show | 22 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.468+2975A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20771835 | ||||||
| chr2:20771873
|
A | G | 22 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(19): Show | 22 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.468+2937T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20771873 | ||||||
| chr2:20771921
|
G | A | 254 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.468+2889C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20771921 | ||||||
| chr2:20772190
|
C | G | 22 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(19): Show | 22 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.468+2620G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20772190 | ||||||
| chr2:20772249
|
G | T | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 8 | HG02451.hp1 HG02886.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+2561C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20772249 | ||||||
| chr2:20772422
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.468+2388T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20772422 | ||||||
| chr2:20772644
|
A | C | 7 | a0001c0001t0003g0101a0001c0001t0004g0099a0001c0006t0001g0240others(4): Show | 7 | HG02257.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+2166T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20772644 | ||||||
| chr2:20772646
|
C | T | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0003g0218 | 3 | HG02630.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.468+2164G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20772646 | ||||||
| chr2:20772721
|
C | T | 1 | a0001c0001t0006g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.468+2089G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20772721 | ||||||
| chr2:20772907
|
A | G | 29 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(26): Show | 29 | HG00140.hp2 HG00673.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.468+1903T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20772907 | ||||||
| chr2:20772964
|
A | C | 1 | a0001c0001t0004g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.468+1846T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20772964 | ||||||
| chr2:20773024
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.468+1786A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20773024 | ||||||
| chr2:20773140
|
T | C | 1 | a0001c0001t0005g0166 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.468+1670A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20773140 | ||||||
| chr2:20773166
|
A | G | 7 | a0001c0001t0003g0101a0001c0001t0004g0099a0001c0006t0001g0240others(4): Show | 7 | HG02257.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+1644T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20773166 | ||||||
| chr2:20773177
|
C | T | 10 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(7): Show | 10 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+1633G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20773177 | ||||||
| chr2:20773326
|
AG | A | 12 | a0001c0001t0003g0101a0001c0001t0004g0099a0001c0002t0001g0191others(9): Show | 12 | HG02257.hp1 HG02647.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.468+1483delC | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20773326 | ||||||
| chr2:20773327
|
G | A | 10 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(7): Show | 10 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.468+1483C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20773327 | ||||||
| chr2:20773475
|
A | G | 3 | a0001c0001t0001g0241a0001c0001t0006g0242a0004c0005t0013g0243 | 3 | HG02486.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.468+1335T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20773475 | ||||||
| chr2:20773649
|
C | T | 5 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(2): Show | 5 | HG01934.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.468+1161G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20773649 | ||||||
| chr2:20773829
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.468+981G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20773829 | ||||||
| chr2:20773838
|
T | C | 1 | a0001c0001t0004g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.468+972A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20773838 | ||||||
| chr2:20773861
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.468+949C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20773861 | ||||||
| chr2:20773924
|
C | G | 1 | a0001c0001t0001g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.468+886G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20773924 | ||||||
| chr2:20774108
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.468+702A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20774108 | ||||||
| chr2:20774127
|
G | T | 22 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(19): Show | 22 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.468+683C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20774127 | ||||||
| chr2:20774162
|
A | AT | 7 | a0001c0001t0003g0101a0001c0001t0004g0099a0001c0006t0001g0240others(4): Show | 7 | HG02257.hp1 HG02647.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.468+647dupA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20774162 | ||||||
| chr2:20774246
|
C | T | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.468+564G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20774246 | ||||||
| chr2:20774360
|
TA | T | 12 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(9): Show | 13 | HG02451.hp1 HG02451.hp2 HG02630.hp1 others(10): Show |
intron_variant | MODIFIER | c.468+449delT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20774360 | ||||||
| chr2:20774442
|
A | G | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 8 | HG02451.hp1 HG02886.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.468+368T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 4/6 | chr2 | 20774442 | ||||||
| chr2:20775072
|
T | C | 4 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(1): Show | 4 | HG02886.hp1 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-93A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20775072 | ||||||
| chr2:20775169
|
CCTTCA | C | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-195_299-191del others(5): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20775169 | ||||||
| chr2:20775303
|
A | G | 2 | a0001c0001t0005g0002a0001c0001t0005g0224 | 3 | HG02451.hp1 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.299-324T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20775303 | ||||||
| chr2:20775327
|
G | A | 5 | a0001c0001t0004g0099a0002c0003t0001g0237a0002c0003t0004g0234others(2): Show | 5 | HG02257.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-348C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20775327 | ||||||
| chr2:20775795
|
C | T | 3 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0005g0035 | 3 | HG00741.hp2 HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.299-816G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20775795 | ||||||
| chr2:20775913
|
T | C | 5 | a0001c0001t0004g0099a0002c0003t0001g0237a0002c0003t0004g0234others(2): Show | 5 | HG02257.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-934A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20775913 | ||||||
| chr2:20775958
|
T | C | 3 | a0001c0001t0003g0253a0001c0001t0003g0254a0001c0001t0005g0252 | 3 | HG02559.hp1 HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.299-979A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20775958 | ||||||
| chr2:20776037
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.299-1058A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20776037 | ||||||
| chr2:20776161
|
G | A | 1 | a0001c0001t0004g0026 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.299-1182C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20776161 | ||||||
| chr2:20776223
|
T | G | 13 | a0001c0001t0001g0041a0001c0001t0001g0221a0001c0001t0001g0222others(10): Show | 14 | HG02451.hp1 HG02451.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.299-1244A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20776223 | ||||||
| chr2:20776236
|
T | G | 1 | a0001c0001t0005g0166 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.299-1257A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20776236 | ||||||
| chr2:20776304
|
G | T | 1 | a0001c0001t0003g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.299-1325C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20776304 | ||||||
| chr2:20776532
|
A | G | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.299-1553T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20776532 | ||||||
| chr2:20776643
|
G | A | 1 | a0001c0001t0001g0139 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.299-1664C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20776643 | ||||||
| chr2:20776714
|
T | C | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.299-1735A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20776714 | ||||||
| chr2:20776786
|
T | C | 29 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(26): Show | 29 | HG00140.hp2 HG00673.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.299-1807A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20776786 | ||||||
| chr2:20776931
|
G | T | 1 | a0001c0001t0001g0133 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.299-1952C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20776931 | ||||||
| chr2:20777248
|
A | T | 1 | a0001c0001t0001g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.299-2269T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20777248 | ||||||
| chr2:20777314
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.299-2335T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20777314 | ||||||
| chr2:20777392
|
G | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0004g0246 | 3 | HG02451.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.299-2413C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20777392 | ||||||
| chr2:20777400
|
A | G | 3 | a0001c0001t0001g0041a0001c0001t0001g0233a0001c0001t0004g0246 | 3 | HG02451.hp2 HG02976.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.299-2421T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20777400 | ||||||
| chr2:20777510
|
C | T | 21 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(18): Show | 21 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.299-2531G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20777510 | ||||||
| chr2:20777694
|
A | G | 22 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(19): Show | 22 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.299-2715T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20777694 | ||||||
| chr2:20777773
|
T | C | 102 | a0001c0001t0001g0012a0001c0001t0001g0041a0001c0001t0001g0133others(99): Show | 104 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.299-2794A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20777773 | ||||||
| chr2:20777778
|
A | G | 1 | a0001c0001t0004g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.299-2799T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20777778 | ||||||
| chr2:20777944
|
T | C | 3 | a0001c0001t0001g0241a0001c0001t0006g0242a0004c0005t0013g0243 | 3 | HG02486.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.299-2965A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20777944 | ||||||
| chr2:20778088
|
GGAAA | G | 5 | a0001c0001t0004g0099a0002c0003t0001g0237a0002c0003t0004g0234others(2): Show | 5 | HG02257.hp1 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-3113_299-3110d others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20778088 | ||||||
| chr2:20778214
|
C | T | 1 | a0001c0001t0003g0069 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.299-3235G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20778214 | ||||||
| chr2:20778298
|
C | T | 5 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(2): Show | 5 | HG01934.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-3319G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20778298 | ||||||
| chr2:20778331
|
CACA | C | 10 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(7): Show | 10 | HG02071.hp2 HG02074.hp2 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.299-3355_299-3353d others(5): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20778331 | ||||||
| chr2:20778336
|
C | A | 3 | a0001c0001t0003g0253a0001c0001t0003g0254a0001c0001t0005g0252 | 3 | HG02559.hp1 HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.299-3357G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20778336 | ||||||
| chr2:20778403
|
C | T | 1 | a0001c0001t0004g0142 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.299-3424G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20778403 | ||||||
| chr2:20778420
|
CCA | C | 3 | a0001c0001t0001g0241a0001c0001t0006g0242a0004c0005t0013g0243 | 3 | HG02486.hp1 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.299-3443_299-3442d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20778420 | ||||||
| chr2:20778855
|
T | C | 1 | a0001c0001t0005g0097 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.299-3876A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20778855 | ||||||
| chr2:20778922
|
C | CAT | 18 | a0001c0001t0001g0169a0001c0001t0001g0236a0001c0001t0002g0159others(15): Show | 18 | HG01255.hp2 HG01361.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.299-3945_299-3944d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20778922 | ||||||
| chr2:20778922
|
C | CATAT | 4 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(1): Show | 4 | HG01934.hp2 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.299-3947_299-3944d others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20778922 | ||||||
| chr2:20778922
|
CAT | C | 129 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(126): Show | 131 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.299-3945_299-3944d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20778922 | ||||||
| chr2:20779021
|
T | C | 1 | a0001c0001t0005g0163 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.299-4042A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20779021 | ||||||
| chr2:20779258
|
C | G | 2 | a0001c0001t0004g0099a0002c0003t0004g0234 | 2 | HG02257.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.299-4279G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20779258 | ||||||
| chr2:20779438
|
G | A | 2 | a0001c0001t0001g0184a0001c0001t0001g0186 | 2 | HG00140.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.299-4459C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20779438 | ||||||
| chr2:20779551
|
CATATATA others(3): Show |
C | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0003g0218 | 3 | HG02630.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.299-4582_299-4573d others(12): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20779551 | ||||||
| chr2:20779593
|
T | C | 1 | a0001c0001t0014g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.299-4614A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20779593 | ||||||
| chr2:20779701
|
T | C | 7 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0003g0200others(4): Show | 7 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.299-4722A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20779701 | ||||||
| chr2:20779741
|
A | T | 40 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(37): Show | 41 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(38): Show |
intron_variant | MODIFIER | c.299-4762T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20779741 | ||||||
| chr2:20779754
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.299-4775A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20779754 | ||||||
| chr2:20779800
|
T | TA | 11 | a0001c0001t0004g0099a0001c0002t0001g0191a0001c0002t0001g0192others(8): Show | 11 | HG02257.hp1 HG02647.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.299-4822dupT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20779800 | ||||||
| chr2:20779976
|
G | T | 21 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(18): Show | 21 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.299-4997C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20779976 | ||||||
| chr2:20779993
|
G | A | 49 | a0001c0001t0001g0012a0001c0001t0001g0133a0001c0001t0001g0138others(46): Show | 50 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.299-5014C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20779993 | ||||||
| chr2:20780165
|
A | T | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-5186T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20780165 | ||||||
| chr2:20780192
|
T | C | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-5213A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20780192 | ||||||
| chr2:20780205
|
A | C | 7 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(4): Show | 7 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.299-5226T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20780205 | ||||||
| chr2:20780294
|
A | G | 3 | a0001c0001t0002g0038a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | NA18945.hp2 NA18951.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.299-5315T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20780294 | ||||||
| chr2:20780420
|
A | T | 2 | a0001c0001t0002g0153a0001c0001t0002g0174 | 2 | NA18953.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.299-5441T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20780420 | ||||||
| chr2:20780539
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.299-5560C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20780539 | ||||||
| chr2:20780630
|
A | G | 1 | a0001c0001t0001g0241 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.299-5651T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20780630 | ||||||
| chr2:20780703
|
C | T | 2 | a0001c0001t0002g0029a0001c0001t0003g0030 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.299-5724G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20780703 | ||||||
| chr2:20780766
|
C | T | 1 | a0001c0001t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.299-5787G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20780766 | ||||||
| chr2:20780900
|
C | T | 3 | a0001c0001t0004g0078a0001c0001t0004g0079a0001c0001t0004g0188 | 3 | HG01081.hp2 HG01258.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.299-5921G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20780900 | ||||||
| chr2:20781045
|
T | C | 4 | a0001c0001t0001g0241a0001c0001t0006g0242a0001c0006t0001g0240others(1): Show | 4 | HG02486.hp1 HG03225.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.299-6066A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20781045 | ||||||
| chr2:20781048
|
T | C | 1 | a0001c0001t0002g0158 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.299-6069A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20781048 | ||||||
| chr2:20781150
|
T | C | 14 | a0001c0001t0001g0041a0001c0001t0001g0221a0001c0001t0001g0222others(11): Show | 15 | HG02451.hp1 HG02451.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-6171A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20781150 | ||||||
| chr2:20781191
|
T | C | 3 | a0001c0001t0003g0253a0001c0001t0003g0254a0001c0001t0005g0252 | 3 | HG02559.hp1 HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.299-6212A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20781191 | ||||||
| chr2:20781494
|
T | C | 11 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(8): Show | 11 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.299-6515A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20781494 | ||||||
| chr2:20781945
|
A | G | 1 | a0001c0001t0004g0011 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.299-6966T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20781945 | ||||||
| chr2:20782073
|
T | C | 5 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(2): Show | 5 | HG01934.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-7094A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20782073 | ||||||
| chr2:20782083
|
C | G | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.299-7104G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20782083 | ||||||
| chr2:20782511
|
C | T | 14 | a0001c0001t0001g0041a0001c0001t0001g0221a0001c0001t0001g0222others(11): Show | 15 | HG02451.hp1 HG02451.hp2 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.299-7532G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20782511 | ||||||
| chr2:20782631
|
T | C | 60 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(57): Show | 61 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.298+7624A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20782631 | ||||||
| chr2:20782711
|
C | G | 2 | a0001c0001t0004g0099a0002c0003t0004g0234 | 2 | HG02257.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.298+7544G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20782711 | ||||||
| chr2:20782716
|
C | T | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.298+7539G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20782716 | ||||||
| chr2:20782727
|
C | T | 2 | a0001c0001t0004g0099a0002c0003t0004g0234 | 2 | HG02257.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.298+7528G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20782727 | ||||||
| chr2:20782752
|
T | C | 14 | a0001c0001t0001g0241a0001c0001t0001g0247a0001c0001t0001g0248others(11): Show | 14 | HG01934.hp2 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.298+7503A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20782752 | ||||||
| chr2:20782754
|
A | C | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+7501T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20782754 | ||||||
| chr2:20782958
|
C | G | 7 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0003g0200others(4): Show | 7 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.298+7297G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20782958 | ||||||
| chr2:20783007
|
A | G | 1 | a0001c0001t0002g0087 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.298+7248T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20783007 | ||||||
| chr2:20783114
|
A | T | 3 | a0001c0001t0001g0068a0001c0001t0002g0066a0001c0001t0003g0067 | 3 | HG01884.hp2 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.298+7141T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20783114 | ||||||
| chr2:20783234
|
C | T | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.298+7021G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20783234 | ||||||
| chr2:20783235
|
G | A | 49 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0133others(46): Show | 50 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(47): Show |
intron_variant | MODIFIER | c.298+7020C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20783235 | ||||||
| chr2:20783333
|
A | T | 1 | a0001c0001t0003g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.298+6922T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20783333 | ||||||
| chr2:20783490
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.298+6765T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20783490 | ||||||
| chr2:20783523
|
A | T | 1 | a0001c0001t0001g0019 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.298+6732T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20783523 | ||||||
| chr2:20783563
|
C | G | 34 | a0001c0001t0001g0006a0001c0001t0001g0042a0001c0001t0001g0100others(31): Show | 34 | HG00099.hp1 HG00642.hp2 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.298+6692G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20783563 | ||||||
| chr2:20783690
|
TTTTG | T | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+6561_298+6564d others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20783690 | ||||||
| chr2:20783780
|
C | T | 6 | a0001c0001t0001g0236a0001c0001t0004g0099a0002c0003t0001g0237others(3): Show | 6 | HG02257.hp1 HG02257.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.298+6475G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20783780 | ||||||
| chr2:20783885
|
T | C | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 8 | HG02451.hp1 HG02886.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+6370A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20783885 | ||||||
| chr2:20783900
|
T | A | 115 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0041others(112): Show | 117 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.298+6355A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20783900 | ||||||
| chr2:20783956
|
G | A | 1 | a0001c0001t0002g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.298+6299C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20783956 | ||||||
| chr2:20783961
|
C | T | 1 | a0001c0001t0002g0132 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.298+6294G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20783961 | ||||||
| chr2:20784174
|
G | A | 64 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0133others(61): Show | 65 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.298+6081C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20784174 | ||||||
| chr2:20784403
|
T | C | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 8 | HG02451.hp1 HG02886.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+5852A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20784403 | ||||||
| chr2:20784405
|
T | A | 1 | a0001c0001t0001g0034 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.298+5850A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20784405 | ||||||
| chr2:20784483
|
T | C | 1 | a0001c0001t0005g0048 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.298+5772A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20784483 | ||||||
| chr2:20784519
|
C | A | 12 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0247others(9): Show | 12 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.298+5736G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20784519 | ||||||
| chr2:20784532
|
G | A | 8 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0003g0069others(5): Show | 8 | HG02280.hp2 HG02615.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.298+5723C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20784532 | ||||||
| chr2:20784786
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.298+5469G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20784786 | ||||||
| chr2:20784834
|
C | G | 1 | a0001c0001t0006g0144 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.298+5421G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20784834 | ||||||
| chr2:20785185
|
C | T | 2 | a0001c0001t0004g0044a0001c0001t0005g0017 | 2 | HG00735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.298+5070G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20785185 | ||||||
| chr2:20785560
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.298+4695G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20785560 | ||||||
| chr2:20785654
|
T | C | 6 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0005g0045others(3): Show | 6 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+4601A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20785654 | ||||||
| chr2:20785694
|
C | G | 1 | a0001c0001t0003g0170 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.298+4561G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20785694 | ||||||
| chr2:20785695
|
T | A | 6 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0005g0045others(3): Show | 6 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.298+4560A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20785695 | ||||||
| chr2:20785726
|
C | T | 1 | a0001c0001t0002g0028 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.298+4529G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20785726 | ||||||
| chr2:20785762
|
C | T | 4 | a0001c0001t0001g0053a0001c0001t0001g0090a0001c0001t0002g0040others(1): Show | 4 | HG00438.hp1 HG00673.hp1 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.298+4493G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20785762 | ||||||
| chr2:20785768
|
C | T | 107 | a0001c0001t0001g0012a0001c0001t0001g0133a0001c0001t0001g0138others(104): Show | 109 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.298+4487G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20785768 | ||||||
| chr2:20785803
|
G | C | 1 | a0001c0001t0003g0170 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.298+4452C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20785803 | ||||||
| chr2:20785820
|
AT | A | 9 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0229others(6): Show | 9 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.298+4434delA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20785820 | ||||||
| chr2:20785997
|
T | A | 30 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(27): Show | 30 | HG00140.hp2 HG00438.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.298+4258A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20785997 | ||||||
| chr2:20786001
|
T | C | 1 | a0001c0001t0004g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.298+4254A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20786001 | ||||||
| chr2:20786344
|
C | G | 1 | a0001c0001t0004g0160 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.298+3911G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20786344 | ||||||
| chr2:20786351
|
G | A | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0003g0218 | 3 | HG02630.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.298+3904C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20786351 | ||||||
| chr2:20786382
|
G | T | 1 | a0001c0001t0003g0173 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.298+3873C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20786382 | ||||||
| chr2:20786391
|
C | T | 1 | a0001c0001t0003g0172 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.298+3864G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20786391 | ||||||
| chr2:20786678
|
T | G | 1 | a0001c0001t0006g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.298+3577A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20786678 | ||||||
| chr2:20786835
|
T | A | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(9): Show | 12 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.298+3420A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20786835 | ||||||
| chr2:20786899
|
A | T | 1 | a0001c0001t0002g0129 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.298+3356T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20786899 | ||||||
| chr2:20786923
|
C | A | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+3332G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20786923 | ||||||
| chr2:20787342
|
GGA | G | 107 | a0001c0001t0001g0012a0001c0001t0001g0133a0001c0001t0001g0138others(104): Show | 109 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.298+2911_298+2912d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20787342 | ||||||
| chr2:20787612
|
C | T | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.298+2643G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20787612 | ||||||
| chr2:20787694
|
T | C | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+2561A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20787694 | ||||||
| chr2:20787761
|
A | G | 1 | a0001c0001t0004g0075 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.298+2494T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20787761 | ||||||
| chr2:20787818
|
T | A | 1 | a0001c0002t0001g0191 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.298+2437A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20787818 | ||||||
| chr2:20787963
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.298+2292C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20787963 | ||||||
| chr2:20787979
|
G | A | 60 | a0001c0001t0001g0012a0001c0001t0001g0133a0001c0001t0001g0138others(57): Show | 61 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.298+2276C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20787979 | ||||||
| chr2:20787986
|
A | G | 1 | a0001c0001t0002g0131 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.298+2269T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20787986 | ||||||
| chr2:20788099
|
A | G | 3 | a0001c0001t0003g0253a0001c0001t0003g0254a0001c0001t0005g0252 | 3 | HG02559.hp1 HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.298+2156T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20788099 | ||||||
| chr2:20788547
|
A | G | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 8 | HG02451.hp1 HG02886.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.298+1708T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20788547 | ||||||
| chr2:20788639
|
T | C | 114 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0041others(111): Show | 116 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.298+1616A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20788639 | ||||||
| chr2:20788652
|
A | C | 1 | a0003c0004t0002g0127 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.298+1603T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20788652 | ||||||
| chr2:20788979
|
A | G | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.298+1276T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20788979 | ||||||
| chr2:20789102
|
C | A | 5 | a0001c0001t0003g0253a0001c0001t0003g0254a0001c0001t0004g0246others(2): Show | 5 | HG02486.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.298+1153G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20789102 | ||||||
| chr2:20789108
|
T | C | 1 | a0001c0001t0004g0099 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.298+1147A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20789108 | ||||||
| chr2:20789132
|
T | A | 10 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(7): Show | 10 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.298+1123A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20789132 | ||||||
| chr2:20789202
|
T | C | 1 | a0001c0001t0002g0064 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.298+1053A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20789202 | ||||||
| chr2:20789430
|
C | G | 3 | a0001c0001t0003g0211a0001c0001t0003g0212a0001c0001t0003g0213 | 3 | HG01358.hp1 HG01981.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.298+825G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20789430 | ||||||
| chr2:20789774
|
A | T | 59 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0202others(56): Show | 60 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.298+481T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20789774 | ||||||
| chr2:20789791
|
T | C | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+464A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20789791 | ||||||
| chr2:20790240
|
T | C | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.298+15A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 3/6 | chr2 | 20790240 | ||||||
| chr2:20790407
|
A | G | 26 | a0001c0001t0001g0041a0001c0001t0001g0219a0001c0001t0001g0221others(23): Show | 27 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.155-9T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20790407 | ||||||
| chr2:20790475
|
G | A | 1 | a0002c0003t0004g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.155-77C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20790475 | ||||||
| chr2:20790553
|
C | A | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.155-155G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20790553 | ||||||
| chr2:20790641
|
G | A | 3 | a0001c0001t0003g0253a0001c0001t0003g0254a0001c0001t0005g0252 | 3 | HG02559.hp1 HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.155-243C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20790641 | ||||||
| chr2:20790840
|
T | C | 2 | a0001c0001t0001g0041a0001c0001t0001g0233 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.155-442A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20790840 | ||||||
| chr2:20790945
|
A | G | 7 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0003g0200others(4): Show | 7 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.155-547T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20790945 | ||||||
| chr2:20791002
|
T | C | 1 | a0001c0001t0001g0215 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.155-604A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20791002 | ||||||
| chr2:20791219
|
G | A | 1 | a0001c0001t0001g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.155-821C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20791219 | ||||||
| chr2:20791339
|
T | C | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(9): Show | 12 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.155-941A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20791339 | ||||||
| chr2:20791588
|
G | T | 29 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(26): Show | 29 | HG00140.hp2 HG00438.hp1 HG00673.hp1 others(26): Show |
intron_variant | MODIFIER | c.155-1190C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20791588 | ||||||
| chr2:20791768
|
T | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG01106.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.155-1370A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20791768 | ||||||
| chr2:20791913
|
C | T | 15 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(12): Show | 15 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.155-1515G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20791913 | ||||||
| chr2:20791972
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0006g0242 | 2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.155-1574G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20791972 | ||||||
| chr2:20792050
|
T | C | 3 | a0001c0001t0003g0211a0001c0001t0003g0212a0001c0001t0003g0213 | 3 | HG01358.hp1 HG01981.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.155-1652A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20792050 | ||||||
| chr2:20792520
|
G | A | 1 | a0001c0001t0005g0119 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.155-2122C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20792520 | ||||||
| chr2:20792540
|
C | T | 2 | a0001c0001t0002g0102a0001c0001t0003g0167 | 2 | NA18977.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.155-2142G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20792540 | ||||||
| chr2:20792720
|
G | A | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.155-2322C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20792720 | ||||||
| chr2:20792824
|
A | T | 1 | a0001c0001t0003g0173 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.155-2426T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20792824 | ||||||
| chr2:20793017
|
T | C | 4 | a0002c0003t0001g0237a0002c0003t0004g0234a0002c0003t0004g0235others(1): Show | 4 | HG02647.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-2619A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20793017 | ||||||
| chr2:20793035
|
T | A | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.155-2637A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20793035 | ||||||
| chr2:20793199
|
A | T | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(9): Show | 12 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.155-2801T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20793199 | ||||||
| chr2:20793426
|
A | G | 5 | a0001c0001t0001g0236a0002c0003t0001g0237a0002c0003t0004g0234others(2): Show | 5 | HG02257.hp2 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-3028T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20793426 | ||||||
| chr2:20793560
|
G | A | 5 | a0001c0001t0001g0236a0002c0003t0001g0237a0002c0003t0004g0234others(2): Show | 5 | HG02257.hp2 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.155-3162C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20793560 | ||||||
| chr2:20793610
|
C | G | 9 | a0001c0001t0001g0041a0001c0001t0001g0221a0001c0001t0001g0222others(6): Show | 10 | HG02451.hp1 HG02451.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.155-3212G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20793610 | ||||||
| chr2:20793644
|
C | G | 7 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0003g0200others(4): Show | 7 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.155-3246G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20793644 | ||||||
| chr2:20793747
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.155-3349G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20793747 | ||||||
| chr2:20793773
|
T | TAAAC | 60 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0202others(57): Show | 61 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.155-3379_155-3376d others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20793773 | ||||||
| chr2:20793957
|
A | G | 1 | a0001c0001t0001g0208 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.155-3559T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20793957 | ||||||
| chr2:20794006
|
T | C | 58 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0202others(55): Show | 59 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.155-3608A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20794006 | ||||||
| chr2:20794055
|
G | A | 2 | a0001c0001t0005g0002a0001c0001t0005g0224 | 3 | HG02451.hp1 HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.155-3657C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20794055 | ||||||
| chr2:20794057
|
GGT | G | 58 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0202others(55): Show | 59 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.155-3661_155-3660d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20794057 | ||||||
| chr2:20794061
|
T | G | 58 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0202others(55): Show | 59 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.155-3663A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20794061 | ||||||
| chr2:20794062
|
C | T | 58 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0202others(55): Show | 59 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.155-3664G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20794062 | ||||||
| chr2:20794063
|
A | G | 58 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0202others(55): Show | 59 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.155-3665T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20794063 | ||||||
| chr2:20794119
|
G | A | 1 | a0001c0001t0005g0051 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.155-3721C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20794119 | ||||||
| chr2:20794472
|
C | T | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.155-4074G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20794472 | ||||||
| chr2:20794545
|
C | T | 1 | a0001c0002t0001g0194 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.155-4147G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20794545 | ||||||
| chr2:20794576
|
T | C | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.155-4178A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20794576 | ||||||
| chr2:20794598
|
A | G | 1 | a0001c0001t0003g0101 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.155-4200T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20794598 | ||||||
| chr2:20794642
|
C | A | 8 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(5): Show | 9 | HG02451.hp1 HG02451.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.155-4244G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20794642 | ||||||
| chr2:20794659
|
G | A | 4 | a0002c0003t0001g0237a0002c0003t0004g0234a0002c0003t0004g0235others(1): Show | 4 | HG02647.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.155-4261C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20794659 | ||||||
| chr2:20794958
|
T | C | 58 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0202others(55): Show | 59 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.155-4560A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20794958 | ||||||
| chr2:20795066
|
T | A | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.155-4668A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20795066 | ||||||
| chr2:20795169
|
A | C | 1 | a0001c0001t0003g0024 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.155-4771T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20795169 | ||||||
| chr2:20795305
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.155-4907G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20795305 | ||||||
| chr2:20795306
|
G | A | 12 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0247others(9): Show | 12 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.155-4908C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20795306 | ||||||
| chr2:20795548
|
G | C | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0003g0218 | 3 | HG02630.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.155-5150C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20795548 | ||||||
| chr2:20795927
|
T | C | 2 | a0001c0001t0002g0088a0001c0001t0004g0026 | 2 | HG00639.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.154+5383A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20795927 | ||||||
| chr2:20795945
|
C | CCA | 7 | a0001c0001t0001g0053a0001c0001t0001g0249a0001c0001t0004g0250others(4): Show | 7 | HG01934.hp2 HG02647.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+5363_154+5364d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20795945 | ||||||
| chr2:20795945
|
CCA | C | 40 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0072others(37): Show | 41 | HG00741.hp2 HG01070.hp2 HG01071.hp1 others(38): Show |
intron_variant | MODIFIER | c.154+5363_154+5364d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20795945 | ||||||
| chr2:20795945
|
CCACA | C | 127 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0018others(124): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(125): Show |
intron_variant | MODIFIER | c.154+5361_154+5364d others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20795945 | ||||||
| chr2:20795945
|
CCACACA | C | 7 | a0001c0001t0002g0129a0001c0001t0003g0167a0001c0001t0003g0253others(4): Show | 7 | HG02559.hp1 HG02622.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.154+5359_154+5364d others(8): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20795945 | ||||||
| chr2:20795945
|
CCACACAC others(3): Show |
C | 3 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0006t0001g0240 | 3 | HG00140.hp2 HG01516.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.154+5355_154+5364d others(12): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20795945 | ||||||
| chr2:20795945
|
CCACACAC others(5): Show |
C | 1 | a0001c0001t0003g0201 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.154+5353_154+5364d others(14): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20795945 | ||||||
| chr2:20795951
|
A | C | 1 | a0001c0001t0005g0097 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.154+5359T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20795951 | ||||||
| chr2:20795982
|
CACA | C | 3 | a0001c0001t0001g0100a0001c0001t0003g0170a0001c0001t0004g0078 | 3 | HG01081.hp1 HG01081.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.154+5325_154+5327d others(5): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20795982 | ||||||
| chr2:20796057
|
T | C | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0003g0218 | 3 | HG02630.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.154+5253A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20796057 | ||||||
| chr2:20796227
|
G | C | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.154+5083C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20796227 | ||||||
| chr2:20796323
|
G | A | 2 | a0002c0003t0001g0237a0002c0003t0004g0238 | 2 | HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.154+4987C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20796323 | ||||||
| chr2:20796472
|
A | G | 1 | a0001c0001t0002g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.154+4838T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20796472 | ||||||
| chr2:20796579
|
G | T | 1 | a0001c0001t0005g0065 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.154+4731C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20796579 | ||||||
| chr2:20796866
|
A | G | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.154+4444T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20796866 | ||||||
| chr2:20796878
|
G | C | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+4432C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20796878 | ||||||
| chr2:20797026
|
A | G | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 8 | HG02451.hp1 HG02886.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+4284T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20797026 | ||||||
| chr2:20797279
|
G | C | 2 | a0001c0001t0001g0241a0001c0001t0006g0242 | 2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.154+4031C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20797279 | ||||||
| chr2:20797470
|
A | G | 1 | a0001c0001t0002g0084 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.154+3840T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20797470 | ||||||
| chr2:20797493
|
T | C | 1 | a0001c0001t0005g0065 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.154+3817A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20797493 | ||||||
| chr2:20797527
|
G | A | 1 | a0001c0001t0004g0120 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.154+3783C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20797527 | ||||||
| chr2:20797591
|
T | C | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.154+3719A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20797591 | ||||||
| chr2:20797618
|
G | A | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0003g0218 | 3 | HG02630.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.154+3692C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20797618 | ||||||
| chr2:20797839
|
AAAAC | A | 9 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0229others(6): Show | 9 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.154+3467_154+3470d others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20797839 | ||||||
| chr2:20797844
|
A | T | 1 | a0001c0001t0004g0156 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.154+3466T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20797844 | ||||||
| chr2:20797849
|
G | A | 1 | a0001c0001t0003g0167 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.154+3461C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20797849 | ||||||
| chr2:20797922
|
C | A | 2 | a0001c0001t0001g0121a0001c0001t0001g0122 | 2 | HG01106.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.154+3388G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20797922 | ||||||
| chr2:20798054
|
T | G | 5 | a0001c0001t0001g0236a0002c0003t0001g0237a0002c0003t0004g0234others(2): Show | 5 | HG02257.hp2 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+3256A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20798054 | ||||||
| chr2:20798418
|
A | C | 4 | a0002c0003t0001g0237a0002c0003t0004g0234a0002c0003t0004g0235others(1): Show | 4 | HG02647.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.154+2892T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20798418 | ||||||
| chr2:20798530
|
C | T | 3 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0005g0035 | 3 | HG00741.hp2 HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.154+2780G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20798530 | ||||||
| chr2:20798555
|
GTATAA | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 5 | HG01261.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.154+2750_154+2754d others(7): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20798555 | ||||||
| chr2:20798566
|
T | TTAATA | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(9): Show | 12 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.154+2739_154+2743d others(7): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20798566 | ||||||
| chr2:20798672
|
A | G | 12 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0247others(9): Show | 12 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.154+2638T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20798672 | ||||||
| chr2:20798694
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.154+2616A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20798694 | ||||||
| chr2:20798764
|
GATA | G | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0003g0218 | 3 | HG02630.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.154+2543_154+2545d others(5): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20798764 | ||||||
| chr2:20798836
|
C | A | 1 | a0001c0001t0005g0123 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.154+2474G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20798836 | ||||||
| chr2:20798901
|
C | G | 1 | a0001c0001t0004g0044 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.154+2409G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20798901 | ||||||
| chr2:20799086
|
G | T | 1 | a0001c0001t0004g0142 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.154+2224C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20799086 | ||||||
| chr2:20799388
|
T | C | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.154+1922A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20799388 | ||||||
| chr2:20799407
|
C | T | 1 | a0001c0001t0004g0075 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.154+1903G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20799407 | ||||||
| chr2:20799408
|
G | A | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(9): Show | 12 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.154+1902C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20799408 | ||||||
| chr2:20799760
|
T | A | 4 | a0001c0001t0003g0083a0001c0001t0003g0124a0001c0001t0003g0125others(1): Show | 4 | HG00735.hp2 HG01168.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+1550A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20799760 | ||||||
| chr2:20800086
|
C | T | 3 | a0001c0001t0005g0225a0001c0001t0005g0226a0001c0001t0005g0227 | 3 | HG01884.hp1 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.154+1224G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20800086 | ||||||
| chr2:20800167
|
G | C | 1 | a0001c0001t0003g0008 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.154+1143C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20800167 | ||||||
| chr2:20800270
|
A | T | 57 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0208others(54): Show | 58 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.154+1040T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20800270 | ||||||
| chr2:20800397
|
A | C | 26 | a0001c0001t0001g0041a0001c0001t0001g0219a0001c0001t0001g0221others(23): Show | 27 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.154+913T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20800397 | ||||||
| chr2:20800530
|
C | G | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.154+780G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20800530 | ||||||
| chr2:20800603
|
A | C | 1 | a0001c0001t0004g0099 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.154+707T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20800603 | ||||||
| chr2:20800611
|
ATTTTTAT others(8): Show |
A | 16 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(13): Show | 16 | HG00280.hp1 HG00639.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.154+684_154+698del others(15): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20800611 | ||||||
| chr2:20800766
|
T | C | 1 | a0001c0001t0004g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.154+544A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20800766 | ||||||
| chr2:20801087
|
A | AAC | 44 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0202others(41): Show | 45 | HG00639.hp2 HG01167.hp1 HG01255.hp1 others(42): Show |
intron_variant | MODIFIER | c.154+221_154+222dup others(2): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20801087 | ||||||
| chr2:20801087
|
A | AACAC | 3 | a0001c0001t0001g0236a0002c0003t0004g0234a0002c0003t0004g0235 | 3 | HG02257.hp2 HG02647.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.154+219_154+222dup others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20801087 | ||||||
| chr2:20801089
|
C | CAT | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(9): Show | 12 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.154+220_154+221ins others(2): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 2/6 | chr2 | 20801089 | ||||||
| chr2:20801470
|
A | G | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 8 | HG02451.hp1 HG02886.hp1 HG03130.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.-2-5T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20801470 | ||||||
| chr2:20801666
|
T | C | 3 | a0001c0001t0001g0154a0001c0001t0002g0153a0001c0001t0002g0174 | 3 | NA18953.hp1 NA18990.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.-2-201A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20801666 | ||||||
| chr2:20801930
|
A | ATG | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0003g0161others(3): Show | 6 | HG01433.hp1 HG02572.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-467_-2-466dupCA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20801930 | ||||||
| chr2:20801930
|
ATG | A | 11 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0003g0083others(8): Show | 11 | HG00735.hp2 HG01168.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2-467_-2-466delCA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20801930 | ||||||
| chr2:20801930
|
ATGTG | A | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 8 | HG02451.hp1 HG02451.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-469_-2-466delCA others(2): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20801930 | ||||||
| chr2:20801930
|
ATGTGTGT others(7): Show |
A | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-479_-2-466delCA others(12): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20801930 | ||||||
| chr2:20801954
|
G | GTA | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(9): Show | 12 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-490_-2-489insTA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20801954 | ||||||
| chr2:20801956
|
G | GTGTGTA | 4 | a0002c0003t0001g0237a0002c0003t0004g0234a0002c0003t0004g0235others(1): Show | 4 | HG02647.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-492_-2-491insTA others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20801956 | ||||||
| chr2:20801958
|
A | ATG | 4 | a0001c0001t0001g0068a0001c0001t0002g0066a0001c0001t0003g0067others(1): Show | 4 | HG01884.hp2 HG02145.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-495_-2-494dupCA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20801958 | ||||||
| chr2:20801958
|
A | G | 17 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(14): Show | 17 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.-2-493T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20801958 | ||||||
| chr2:20801958
|
ATGTG | A | 14 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0241others(11): Show | 14 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.-2-497_-2-494delCA others(2): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20801958 | ||||||
| chr2:20802000
|
A | G | 6 | a0001c0001t0001g0236a0001c0001t0002g0096a0002c0003t0001g0237others(3): Show | 6 | HG00673.hp2 HG02257.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-535T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20802000 | ||||||
| chr2:20802023
|
C | T | 12 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0247others(9): Show | 12 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-558G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20802023 | ||||||
| chr2:20802039
|
ATATC | A | 7 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(4): Show | 8 | HG02451.hp1 HG02886.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-578_-2-575delGA others(2): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20802039 | ||||||
| chr2:20802074
|
G | A | 55 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0208others(52): Show | 56 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.-2-609C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20802074 | ||||||
| chr2:20802095
|
C | T | 16 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(13): Show | 16 | HG00280.hp1 HG00639.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.-2-630G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20802095 | ||||||
| chr2:20802171
|
T | G | 1 | a0001c0001t0004g0250 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-2-706A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20802171 | ||||||
| chr2:20802312
|
G | A | 9 | a0001c0001t0001g0041a0001c0001t0001g0071a0001c0001t0001g0072others(6): Show | 9 | HG02280.hp2 HG02615.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2-847C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20802312 | ||||||
| chr2:20802434
|
T | C | 1 | a0001c0001t0006g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-2-969A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20802434 | ||||||
| chr2:20802477
|
A | G | 2 | a0001c0001t0003g0206a0001c0001t0003g0207 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-2-1012T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20802477 | ||||||
| chr2:20802507
|
C | G | 1 | a0001c0001t0002g0084 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-2-1042G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20802507 | ||||||
| chr2:20802648
|
C | T | 2 | a0001c0001t0004g0160a0001c0001t0004g0175 | 2 | NA18942.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.-2-1183G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20802648 | ||||||
| chr2:20802671
|
C | G | 1 | a0001c0002t0001g0192 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-2-1206G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20802671 | ||||||
| chr2:20802709
|
T | C | 3 | a0001c0001t0001g0169a0001c0001t0002g0159a0001c0001t0002g0168 | 3 | HG01255.hp2 HG01361.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.-2-1244A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20802709 | ||||||
| chr2:20802968
|
T | C | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(9): Show | 12 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-1503A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20802968 | ||||||
| chr2:20803206
|
G | A | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-1741C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20803206 | ||||||
| chr2:20803855
|
C | A | 1 | a0001c0001t0006g0199 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-2-2390G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20803855 | ||||||
| chr2:20803930
|
T | C | 5 | a0001c0001t0001g0236a0002c0003t0001g0237a0002c0003t0004g0234others(2): Show | 5 | HG02257.hp2 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-2465A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20803930 | ||||||
| chr2:20804135
|
T | C | 13 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0229others(10): Show | 13 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-2-2670A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20804135 | ||||||
| chr2:20804479
|
A | C | 1 | a0001c0001t0001g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-2-3014T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20804479 | ||||||
| chr2:20804491
|
T | C | 15 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(12): Show | 15 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.-2-3026A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20804491 | ||||||
| chr2:20805019
|
T | C | 1 | a0001c0001t0001g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-2-3554A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20805019 | ||||||
| chr2:20805066
|
C | T | 10 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0003g0200others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-3601G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20805066 | ||||||
| chr2:20805159
|
T | C | 60 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0208others(57): Show | 61 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.-2-3694A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20805159 | ||||||
| chr2:20805204
|
T | C | 1 | a0001c0001t0002g0087 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-2-3739A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20805204 | ||||||
| chr2:20805216
|
G | A | 60 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0208others(57): Show | 61 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.-2-3751C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20805216 | ||||||
| chr2:20805232
|
T | C | 1 | a0001c0001t0002g0183 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-2-3767A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20805232 | ||||||
| chr2:20805264
|
CAAAT | C | 3 | a0001c0001t0003g0211a0001c0001t0003g0212a0001c0001t0003g0213 | 3 | HG01358.hp1 HG01981.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-2-3803_-2-3800del others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20805264 | ||||||
| chr2:20805277
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-2-3812G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20805277 | ||||||
| chr2:20805498
|
G | C | 4 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(1): Show | 4 | HG01934.hp2 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-4033C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20805498 | ||||||
| chr2:20805550
|
C | T | 1 | a0001c0001t0004g0142 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-2-4085G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20805550 | ||||||
| chr2:20805551
|
G | A | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-4086C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20805551 | ||||||
| chr2:20805636
|
C | A | 1 | a0001c0001t0001g0071 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-2-4171G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20805636 | ||||||
| chr2:20805649
|
T | C | 254 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.-2-4184A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20805649 | ||||||
| chr2:20805816
|
T | C | 50 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0133others(47): Show | 51 | HG00099.hp2 HG00280.hp2 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.-2-4351A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20805816 | ||||||
| chr2:20805898
|
A | ATACT | 62 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0202others(59): Show | 63 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(60): Show |
intron_variant | MODIFIER | c.-2-4434_-2-4433ins others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20805898 | ||||||
| chr2:20806316
|
C | A | 1 | a0001c0001t0004g0142 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-2-4851G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20806316 | ||||||
| chr2:20806344
|
C | T | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-2-4879G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20806344 | ||||||
| chr2:20806629
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-2-5164A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20806629 | ||||||
| chr2:20806825
|
A | G | 1 | a0001c0001t0002g0028 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-2-5360T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20806825 | ||||||
| chr2:20806917
|
A | G | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(9): Show | 12 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-5452T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20806917 | ||||||
| chr2:20807065
|
C | G | 9 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(6): Show | 10 | HG02451.hp1 HG02451.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-5600G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20807065 | ||||||
| chr2:20807160
|
A | G | 1 | a0001c0001t0002g0095 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-2-5695T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20807160 | ||||||
| chr2:20807305
|
A | C | 1 | a0001c0001t0009g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-2-5840T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20807305 | ||||||
| chr2:20807637
|
A | G | 9 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0229others(6): Show | 9 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2-6172T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20807637 | ||||||
| chr2:20807853
|
A | C | 121 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(118): Show | 122 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.-2-6388T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20807853 | ||||||
| chr2:20807935
|
C | T | 1 | a0001c0001t0002g0159 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-2-6470G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20807935 | ||||||
| chr2:20807935
|
CA | C | 45 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0202others(42): Show | 46 | HG00438.hp1 HG00639.hp2 HG01070.hp1 others(43): Show |
intron_variant | MODIFIER | c.-2-6471delT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20807935 | ||||||
| chr2:20807942
|
A | G | 5 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(2): Show | 5 | HG01934.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-6477T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20807942 | ||||||
| chr2:20808115
|
A | G | 5 | a0001c0001t0001g0236a0002c0003t0001g0237a0002c0003t0004g0234others(2): Show | 5 | HG02257.hp2 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-6650T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20808115 | ||||||
| chr2:20808286
|
A | C | 17 | a0001c0001t0001g0219a0001c0001t0001g0228a0001c0001t0001g0229others(14): Show | 17 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-2-6821T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20808286 | ||||||
| chr2:20808507
|
C | T | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(9): Show | 12 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-7042G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20808507 | ||||||
| chr2:20808644
|
A | C | 21 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(18): Show | 21 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.-2-7179T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20808644 | ||||||
| chr2:20808657
|
C | CA | 6 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0033others(3): Show | 6 | HG01175.hp2 HG02622.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-7193dupT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20808657 | ||||||
| chr2:20808657
|
CA | C | 58 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0196others(55): Show | 59 | HG00639.hp2 HG01167.hp1 HG01168.hp1 others(56): Show |
intron_variant | MODIFIER | c.-2-7193delT | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20808657 | ||||||
| chr2:20808729
|
T | C | 1 | a0001c0001t0002g0155 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-2-7264A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20808729 | ||||||
| chr2:20808966
|
T | G | 2 | a0001c0001t0001g0041a0001c0001t0001g0233 | 2 | HG02451.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-2-7501A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20808966 | ||||||
| chr2:20808997
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0006g0242 | 2 | HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-2-7532G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20808997 | ||||||
| chr2:20809118
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-2-7653C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20809118 | ||||||
| chr2:20809235
|
C | CAAAAAA | 18 | a0001c0001t0001g0196a0001c0001t0001g0219a0001c0001t0001g0228others(15): Show | 18 | HG01167.hp1 HG01255.hp1 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2-7776_-2-7771dup others(6): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20809235 | ||||||
| chr2:20809235
|
C | CAAAAAAA | 35 | a0001c0001t0001g0041a0001c0001t0001g0068a0001c0001t0001g0071others(32): Show | 35 | HG00639.hp2 HG01070.hp2 HG01346.hp2 others(32): Show |
intron_variant | MODIFIER | c.-2-7777_-2-7771dup others(7): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20809235 | ||||||
| chr2:20809235
|
C | CAAAAAAA others(1): Show |
15 | a0001c0001t0001g0072a0001c0001t0001g0215a0001c0001t0001g0244others(12): Show | 16 | HG01934.hp2 HG02280.hp1 HG02293.hp1 others(13): Show |
intron_variant | MODIFIER | c.-2-7778_-2-7771dup others(8): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20809235 | ||||||
| chr2:20809331
|
G | A | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0003g0069others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-7866C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20809331 | ||||||
| chr2:20809385
|
G | C | 4 | a0002c0003t0001g0237a0002c0003t0004g0234a0002c0003t0004g0235others(1): Show | 4 | HG02647.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-2-7920C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20809385 | ||||||
| chr2:20809578
|
A | AAT | 5 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(2): Show | 5 | HG01934.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-8115_-2-8114dup others(2): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20809578 | ||||||
| chr2:20809727
|
G | A | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(9): Show | 12 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-8262C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20809727 | ||||||
| chr2:20809762
|
A | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 5 | HG01261.hp2 HG02572.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-2-8297T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20809762 | ||||||
| chr2:20809838
|
G | A | 15 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0247others(12): Show | 15 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-8373C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20809838 | ||||||
| chr2:20810470
|
T | C | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-9005A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20810470 | ||||||
| chr2:20810819
|
A | C | 10 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0003g0200others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-9354T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20810819 | ||||||
| chr2:20810822
|
T | C | 1 | a0001c0001t0009g0145 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-2-9357A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20810822 | ||||||
| chr2:20810884
|
C | T | 62 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0202others(59): Show | 63 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(60): Show |
intron_variant | MODIFIER | c.-2-9419G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20810884 | ||||||
| chr2:20810918
|
AAC | A | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-9455_-2-9454del others(2): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20810918 | ||||||
| chr2:20810943
|
T | C | 62 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0202others(59): Show | 63 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(60): Show |
intron_variant | MODIFIER | c.-2-9478A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20810943 | ||||||
| chr2:20810986
|
T | G | 67 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0202others(64): Show | 68 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.-2-9521A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20810986 | ||||||
| chr2:20811104
|
A | G | 62 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0202others(59): Show | 63 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(60): Show |
intron_variant | MODIFIER | c.-2-9639T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20811104 | ||||||
| chr2:20811135
|
A | G | 62 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0202others(59): Show | 63 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(60): Show |
intron_variant | MODIFIER | c.-2-9670T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20811135 | ||||||
| chr2:20811139
|
T | A | 1 | a0001c0001t0002g0146 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-2-9674A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20811139 | ||||||
| chr2:20811178
|
C | T | 1 | a0001c0001t0006g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-2-9713G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20811178 | ||||||
| chr2:20811209
|
G | A | 11 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(8): Show | 11 | HG02523.hp1 HG03831.hp2 HG06807.hp1 others(8): Show |
intron_variant | MODIFIER | c.-2-9744C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20811209 | ||||||
| chr2:20811300
|
G | A | 1 | a0001c0001t0004g0075 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-2-9835C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20811300 | ||||||
| chr2:20811367
|
CTAATCTC others(6): Show |
C | 10 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0003g0200others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-9915_-2-9903del others(13): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20811367 | ||||||
| chr2:20811396
|
T | C | 1 | a0001c0001t0001g0006 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-2-9931A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20811396 | ||||||
| chr2:20811461
|
A | G | 1 | a0001c0001t0005g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-2-9996T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20811461 | ||||||
| chr2:20811484
|
GT | G | 14 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(11): Show | 15 | HG02451.hp1 HG02886.hp1 HG03130.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-10020delA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20811484 | ||||||
| chr2:20811484
|
GTT | G | 54 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0202others(51): Show | 54 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.-2-10021_-2-10020d others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20811484 | ||||||
| chr2:20811622
|
C | G | 1 | a0001c0001t0003g0082 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-2-10157G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20811622 | ||||||
| chr2:20811699
|
C | T | 1 | a0001c0001t0011g0081 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-2-10234G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20811699 | ||||||
| chr2:20811736
|
G | A | 1 | a0001c0001t0005g0216 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-2-10271C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20811736 | ||||||
| chr2:20811910
|
T | C | 10 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0003g0200others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-10445A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20811910 | ||||||
| chr2:20812063
|
G | T | 1 | a0001c0001t0002g0158 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-2-10598C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20812063 | ||||||
| chr2:20812073
|
A | G | 7 | a0001c0001t0004g0078a0001c0001t0004g0079a0001c0001t0004g0080others(4): Show | 7 | HG01081.hp2 HG01258.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-10608T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20812073 | ||||||
| chr2:20812162
|
G | C | 1 | a0001c0001t0006g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-2-10697C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20812162 | ||||||
| chr2:20812181
|
C | G | 1 | a0001c0001t0005g0035 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-2-10716G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20812181 | ||||||
| chr2:20812224
|
C | A | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-10759G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20812224 | ||||||
| chr2:20812391
|
G | A | 1 | a0001c0001t0001g0249 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-3+10646C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20812391 | ||||||
| chr2:20812439
|
T | C | 24 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0222others(21): Show | 25 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-3+10598A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20812439 | ||||||
| chr2:20812441
|
G | C | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+10596C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20812441 | ||||||
| chr2:20812512
|
T | C | 1 | a0001c0001t0002g0155 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.-3+10525A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20812512 | ||||||
| chr2:20812548
|
T | C | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(9): Show | 12 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+10489A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20812548 | ||||||
| chr2:20812691
|
C | T | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(9): Show | 12 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+10346G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20812691 | ||||||
| chr2:20812820
|
G | T | 1 | a0001c0001t0005g0077 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-3+10217C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20812820 | ||||||
| chr2:20813148
|
T | C | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-3+9889A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20813148 | ||||||
| chr2:20813235
|
A | G | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(9): Show | 12 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+9802T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20813235 | ||||||
| chr2:20813288
|
T | A | 3 | a0001c0001t0001g0241a0001c0001t0006g0239a0001c0001t0006g0242 | 3 | HG02559.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-3+9749A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20813288 | ||||||
| chr2:20813320
|
G | A | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+9717C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20813320 | ||||||
| chr2:20813329
|
G | A | 4 | a0002c0003t0001g0237a0002c0003t0004g0234a0002c0003t0004g0235others(1): Show | 4 | HG02647.hp2 HG02809.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+9708C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20813329 | ||||||
| chr2:20813383
|
C | T | 1 | a0001c0001t0002g0076 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-3+9654G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20813383 | ||||||
| chr2:20813704
|
C | G | 4 | a0001c0001t0004g0001a0001c0001t0004g0073a0001c0001t0004g0074others(1): Show | 5 | HG00099.hp2 HG00741.hp1 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-3+9333G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20813704 | ||||||
| chr2:20813714
|
G | C | 5 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(2): Show | 5 | HG01934.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+9323C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20813714 | ||||||
| chr2:20814064
|
T | C | 32 | a0001c0001t0001g0041a0001c0001t0001g0219a0001c0001t0001g0221others(29): Show | 33 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.-3+8973A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20814064 | ||||||
| chr2:20814174
|
C | T | 4 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(1): Show | 4 | HG01934.hp2 HG02280.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-3+8863G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20814174 | ||||||
| chr2:20814229
|
TG | T | 139 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0012others(136): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.-3+8807delC | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20814229 | ||||||
| chr2:20814229
|
TGG | T | 38 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0020others(35): Show | 38 | HG00280.hp1 HG00438.hp1 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.-3+8806_-3+8807del others(2): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20814229 | ||||||
| chr2:20814230
|
G | GA | 7 | a0001c0001t0001g0041a0001c0001t0001g0219a0001c0001t0001g0236others(4): Show | 7 | HG02109.hp1 HG02257.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-3+8806_-3+8807ins others(1): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20814230 | ||||||
| chr2:20814231
|
G | A | 21 | a0001c0001t0001g0221a0001c0001t0001g0222a0001c0001t0001g0223others(18): Show | 22 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.-3+8806C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20814231 | ||||||
| chr2:20814231
|
G | C | 1 | a0001c0001t0001g0190 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-3+8806C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20814231 | ||||||
| chr2:20814293
|
C | A | 4 | a0001c0001t0001g0202a0001c0001t0003g0200a0001c0001t0003g0201others(1): Show | 4 | HG01346.hp2 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+8744G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20814293 | ||||||
| chr2:20814348
|
C | G | 1 | a0001c0001t0005g0051 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-3+8689G>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20814348 | ||||||
| chr2:20814417
|
A | G | 1 | a0001c0001t0012g0007 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-3+8620T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20814417 | ||||||
| chr2:20814603
|
G | A | 1 | a0001c0001t0004g0176 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-3+8434C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20814603 | ||||||
| chr2:20814883
|
T | C | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0003g0218 | 3 | HG02630.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-3+8154A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20814883 | ||||||
| chr2:20814901
|
G | A | 34 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0222others(31): Show | 35 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.-3+8136C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20814901 | ||||||
| chr2:20814945
|
G | A | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-3+8092C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20814945 | ||||||
| chr2:20815034
|
A | G | 2 | a0001c0001t0003g0049a0001c0001t0003g0050 | 2 | NA18955.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.-3+8003T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20815034 | ||||||
| chr2:20815123
|
C | T | 254 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.-3+7914G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20815123 | ||||||
| chr2:20815193
|
G | C | 3 | a0001c0001t0002g0038a0001c0001t0002g0177a0001c0001t0002g0178 | 3 | NA18945.hp2 NA18951.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.-3+7844C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20815193 | ||||||
| chr2:20815289
|
T | C | 10 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0003g0200others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3+7748A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20815289 | ||||||
| chr2:20815314
|
C | T | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+7723G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20815314 | ||||||
| chr2:20815506
|
A | G | 6 | a0001c0001t0004g0043a0001c0001t0004g0044a0001c0001t0005g0045others(3): Show | 6 | HG00099.hp1 HG00642.hp2 HG00735.hp1 others(3): Show |
intron_variant | MODIFIER | c.-3+7531T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20815506 | ||||||
| chr2:20815722
|
C | T | 15 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0247others(12): Show | 15 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+7315G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20815722 | ||||||
| chr2:20815845
|
G | A | 62 | a0001c0001t0001g0041a0001c0001t0001g0196a0001c0001t0001g0202others(59): Show | 63 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(60): Show |
intron_variant | MODIFIER | c.-3+7192C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20815845 | ||||||
| chr2:20815851
|
T | C | 1 | a0004c0005t0013g0243 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-3+7186A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20815851 | ||||||
| chr2:20815901
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-3+7136T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20815901 | ||||||
| chr2:20816003
|
G | A | 193 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.-3+7034C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20816003 | ||||||
| chr2:20816047
|
A | G | 1 | a0001c0001t0002g0040 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-3+6990T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20816047 | ||||||
| chr2:20816367
|
T | G | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+6670A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20816367 | ||||||
| chr2:20816447
|
A | T | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0003g0218 | 3 | HG02630.hp1 HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-3+6590T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20816447 | ||||||
| chr2:20816499
|
A | G | 1 | a0001c0001t0010g0039 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-3+6538T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20816499 | ||||||
| chr2:20816515
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-3+6522A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20816515 | ||||||
| chr2:20816613
|
C | A | 66 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0208others(63): Show | 67 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.-3+6424G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20816613 | ||||||
| chr2:20816633
|
C | T | 66 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0208others(63): Show | 67 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.-3+6404G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20816633 | ||||||
| chr2:20816682
|
C | A | 3 | a0001c0001t0001g0241a0001c0001t0006g0239a0001c0001t0006g0242 | 3 | HG02559.hp2 HG03471.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-3+6355G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20816682 | ||||||
| chr2:20816749
|
T | C | 2 | a0001c0001t0001g0181a0001c0001t0003g0180 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-3+6288A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20816749 | ||||||
| chr2:20816818
|
C | A | 1 | a0001c0001t0001g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-3+6219G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20816818 | ||||||
| chr2:20816905
|
A | T | 31 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0222others(28): Show | 32 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.-3+6132T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20816905 | ||||||
| chr2:20816948
|
A | G | 15 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0247others(12): Show | 15 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+6089T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20816948 | ||||||
| chr2:20817059
|
A | T | 254 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(251): Show | 256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.-3+5978T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20817059 | ||||||
| chr2:20817624
|
C | A | 15 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0247others(12): Show | 15 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(12): Show |
intron_variant | MODIFIER | c.-3+5413G>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20817624 | ||||||
| chr2:20817987
|
A | C | 1 | a0001c0001t0002g0038 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-3+5050T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20817987 | ||||||
| chr2:20818162
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-3+4875C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20818162 | ||||||
| chr2:20818330
|
A | G | 3 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0005g0035 | 3 | HG00741.hp2 HG03704.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-3+4707T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20818330 | ||||||
| chr2:20818570
|
C | CT | 18 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(15): Show | 18 | HG00280.hp1 HG00639.hp1 HG01069.hp1 others(15): Show |
intron_variant | MODIFIER | c.-3+4466dupA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20818570 | ||||||
| chr2:20818570
|
CT | C | 15 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(12): Show | 15 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.-3+4466delA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20818570 | ||||||
| chr2:20818862
|
C | T | 1 | a0001c0006t0001g0240 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-3+4175G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20818862 | ||||||
| chr2:20818952
|
C | T | 3 | a0001c0001t0003g0253a0001c0001t0003g0254a0001c0001t0005g0252 | 3 | HG02559.hp1 HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-3+4085G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20818952 | ||||||
| chr2:20819214
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-3+3823G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20819214 | ||||||
| chr2:20819216
|
AT | A | 61 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0208others(58): Show | 62 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.-3+3820delA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20819216 | ||||||
| chr2:20819536
|
G | C | 1 | a0001c0001t0002g0183 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-3+3501C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20819536 | ||||||
| chr2:20819559
|
G | A | 30 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0222others(27): Show | 31 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.-3+3478C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20819559 | ||||||
| chr2:20819614
|
C | T | 2 | a0001c0001t0003g0206a0001c0001t0003g0207 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-3+3423G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20819614 | ||||||
| chr2:20819740
|
C | T | 1 | a0001c0001t0006g0239 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-3+3297G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20819740 | ||||||
| chr2:20819870
|
G | A | 66 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0208others(63): Show | 67 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.-3+3167C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20819870 | ||||||
| chr2:20820022
|
A | G | 5 | a0001c0002t0001g0191a0001c0002t0001g0192a0001c0002t0001g0193others(2): Show | 5 | HG03688.hp1 HG03710.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+3015T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20820022 | ||||||
| chr2:20820030
|
C | T | 61 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0208others(58): Show | 62 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.-3+3007G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20820030 | ||||||
| chr2:20820246
|
T | C | 66 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0208others(63): Show | 67 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.-3+2791A>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20820246 | ||||||
| chr2:20820247
|
G | A | 10 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0003g0200others(7): Show | 10 | HG00639.hp2 HG01167.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.-3+2790C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20820247 | ||||||
| chr2:20820283
|
C | T | 1 | a0001c0001t0005g0017 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-3+2754G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20820283 | ||||||
| chr2:20820402
|
G | T | 6 | a0001c0001t0001g0233a0001c0001t0001g0236a0002c0003t0001g0237others(3): Show | 6 | HG02257.hp2 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+2635C>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20820402 | ||||||
| chr2:20820419
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-3+2618T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20820419 | ||||||
| chr2:20820643
|
A | T | 20 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0222others(17): Show | 21 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-3+2394T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20820643 | ||||||
| chr2:20820737
|
A | G | 4 | a0001c0001t0003g0013a0001c0001t0003g0014a0001c0001t0003g0015others(1): Show | 4 | HG01167.hp2 HG03710.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+2300T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20820737 | ||||||
| chr2:20820913
|
T | G | 2 | a0001c0001t0003g0204a0001c0001t0003g0205 | 2 | HG00639.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-3+2124A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20820913 | ||||||
| chr2:20820923
|
AAAAC | A | 3 | a0001c0001t0001g0184a0001c0001t0001g0186a0001c0001t0004g0185 | 3 | HG00140.hp2 HG01175.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.-3+2110_-3+2113del others(4): Show |
LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20820923 | ||||||
| chr2:20821071
|
T | A | 1 | a0001c0001t0004g0246 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-3+1966A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20821071 | ||||||
| chr2:20821143
|
C | T | 67 | a0001c0001t0001g0012a0001c0001t0001g0196a0001c0001t0001g0202others(64): Show | 68 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(65): Show |
intron_variant | MODIFIER | c.-3+1894G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20821143 | ||||||
| chr2:20821145
|
G | A | 1 | a0001c0001t0004g0187 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-3+1892C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20821145 | ||||||
| chr2:20821472
|
T | G | 1 | a0001c0001t0004g0188 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-3+1565A>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20821472 | ||||||
| chr2:20821509
|
C | T | 27 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0208others(24): Show | 27 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.-3+1528G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20821509 | ||||||
| chr2:20821604
|
C | T | 1 | a0001c0001t0003g0218 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-3+1433G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20821604 | ||||||
| chr2:20821799
|
C | T | 1 | a0001c0001t0004g0011 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-3+1238G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20821799 | ||||||
| chr2:20822013
|
A | T | 1 | a0001c0001t0003g0008 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-3+1024T>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20822013 | ||||||
| chr2:20822129
|
CT | C | 253 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(250): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.-3+907delA | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20822129 | ||||||
| chr2:20822178
|
G | A | 5 | a0001c0001t0001g0247a0001c0001t0001g0248a0001c0001t0001g0249others(2): Show | 5 | HG01934.hp2 HG02280.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+859C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20822178 | ||||||
| chr2:20822268
|
G | A | 2 | a0001c0001t0001g0190a0001c0001t0002g0189 | 2 | HG03831.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-3+769C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20822268 | ||||||
| chr2:20822329
|
A | G | 61 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0208others(58): Show | 62 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.-3+708T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20822329 | ||||||
| chr2:20822432
|
G | C | 66 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0208others(63): Show | 67 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(64): Show |
intron_variant | MODIFIER | c.-3+605C>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20822432 | ||||||
| chr2:20822453
|
A | G | 1 | a0001c0001t0012g0007 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-3+584T>C | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20822453 | ||||||
| chr2:20822598
|
G | A | 61 | a0001c0001t0001g0196a0001c0001t0001g0202a0001c0001t0001g0208others(58): Show | 62 | HG00639.hp2 HG01070.hp2 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.-3+439C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20822598 | ||||||
| chr2:20822618
|
A | C | 1 | a0001c0001t0001g0006 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-3+419T>G | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20822618 | ||||||
| chr2:20822662
|
G | A | 3 | a0001c0001t0003g0253a0001c0001t0003g0254a0001c0001t0005g0252 | 3 | HG02559.hp1 HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-3+375C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20822662 | ||||||
| chr2:20822730
|
C | T | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(9): Show | 12 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+307G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20822730 | ||||||
| chr2:20822810
|
T | A | 12 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0215others(9): Show | 12 | HG01070.hp2 HG01358.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-3+227A>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20822810 | ||||||
| chr2:20822934
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005 | 3 | NA18975.hp1 NA18984.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-3+103G>A | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20822934 | ||||||
| chr2:20823025
|
G | A | 39 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0222others(36): Show | 40 | HG01255.hp1 HG01496.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.-3+12C>T | LDAH | ENSG00000118961.15 | transcript | ENST00000237822.8 | protein_coding | 1/6 | chr2 | 20823025 |