Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6652 |
|---|---|
| ensemblid | ENSG00000140263.15 |
| hgncid | 11184 |
| symbol | SORD |
| name | sorbitol dehydrogenase |
| refseq_nuc | NM_003104.6 |
| refseq_prot | NP_003095.2 |
| ensembl_nuc | ENST00000267814.14 |
| ensembl_prot | ENSP00000267814.9 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 45023195 |
| end | 45077185 |
| strand | + |
| ver | v1.2 |
| region | chr15:45023195-45077185 |
| region5000 | chr15:45018195-45082185 |
| regionname0 | SORD_chr15_45023195_45077185 |
| regionname5000 | SORD_chr15_45018195_45082185 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 357 | 196 | 18 | 44 | 94 | 9 | 30 | 67 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002 | 0/0 | 357 | 79 | 52 | 12 | 14 | 1 | 0 | 11 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0003 | 1/0 | 357 | 23 | 14 | 6 | 2 | 0 | 0 | 2 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0004 | 0/0 | 357 | 8 | 7 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0005 | 0/0 | 357 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0006 | 0/0 | 357 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 1074 | 190 | 16 | 43 | 92 | 9 | 29 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| c0002 | 0/0 | 1074 | 63 | 47 | 12 | 3 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| c0003 | 1/0 | 1074 | 23 | 14 | 6 | 2 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| c0004 | 0/0 | 1074 | 12 | 1 | 0 | 11 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| c0005 | 0/0 | 1074 | 4 | 3 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| c0006 | 0/0 | 1074 | 4 | 4 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| c0007 | 0/0 | 1074 | 4 | 4 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| c0008 | 0/0 | 1074 | 3 | 1 | 1 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| c0009 | 0/0 | 1074 | 2 | 0 | 0 | 2 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| c0010 | 0/0 | 1074 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| c0011 | 0/0 | 1074 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| c0012 | 0/0 | 1074 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| 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 | 1/1 | 3745 | 179 | 17 | 42 | 85 | 10 | 23 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0002 | 0/0 | 3742 | 19 | 19 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0003 | 0/0 | 3742 | 17 | 16 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0004 | 0/0 | 3744 | 14 | 0 | 0 | 14 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0005 | 0/0 | 3744 | 10 | 5 | 4 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0006 | 0/0 | 3744 | 5 | 5 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0007 | 0/0 | 3745 | 5 | 4 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0008 | 0/0 | 3745 | 5 | 4 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0009 | 0/0 | 3745 | 4 | 0 | 0 | 4 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0010 | 0/0 | 3742 | 4 | 4 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0011 | 0/0 | 3744 | 3 | 3 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0012 | 0/0 | 3744 | 3 | 2 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0013 | 0/0 | 3742 | 3 | 0 | 3 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0014 | 0/0 | 3745 | 2 | 2 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0015 | 0/0 | 3744 | 2 | 0 | 2 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0016 | 0/0 | 3744 | 2 | 0 | 0 | 0 | 0 | 2 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0017 | 0/0 | 3745 | 2 | 2 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0018 | 0/0 | 3745 | 2 | 0 | 0 | 0 | 0 | 2 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0019 | 0/0 | 3745 | 2 | 0 | 1 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0020 | 0/0 | 3744 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0021 | 0/0 | 3745 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0022 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0023 | 0/0 | 3742 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0024 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0025 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0026 | 0/0 | 3744 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0027 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0028 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0029 | 0/0 | 3745 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0030 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0031 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0032 | 0/0 | 3745 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0033 | 0/0 | 3745 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0034 | 0/0 | 3745 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0035 | 0/0 | 3745 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0036 | 0/0 | 3745 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0037 | 0/0 | 3742 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0038 | 0/0 | 3743 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0039 | 0/0 | 3742 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0040 | 0/0 | 3742 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0041 | 0/0 | 3742 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0042 | 0/0 | 3742 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0043 | 0/0 | 3743 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| t0044 | 0/0 | 3742 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| 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 | 3 | 2 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0161 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0167 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1074 | 190 | 16 | 43 | 92 | 9 | 29 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0008 | 0/0 | 1074 | 3 | 1 | 1 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0009 | 0/0 | 1074 | 2 | 0 | 0 | 2 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0010 | 0/0 | 1074 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0002 | 0/0 | 1074 | 63 | 47 | 12 | 3 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0004 | 0/0 | 1074 | 12 | 1 | 0 | 11 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0007 | 0/0 | 1074 | 4 | 4 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0003c0003 | 1/0 | 1074 | 23 | 14 | 6 | 2 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0004c0005 | 0/0 | 1074 | 4 | 3 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0004c0006 | 0/0 | 1074 | 4 | 4 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0005c0012 | 0/0 | 1074 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0006c0011 | 0/0 | 1074 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4818 | 154 | 6 | 36 | 80 | 9 | 22 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0004 | 0/0 | 4817 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0005 | 0/0 | 4817 | 3 | 1 | 1 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0007 | 0/0 | 4818 | 3 | 2 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0008 | 0/0 | 4818 | 2 | 2 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0009 | 0/0 | 4818 | 3 | 0 | 0 | 3 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0014 | 0/0 | 4818 | 2 | 2 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0016 | 0/0 | 4817 | 2 | 0 | 0 | 0 | 0 | 2 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0017 | 0/0 | 4818 | 2 | 2 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0018 | 0/0 | 4818 | 2 | 0 | 0 | 0 | 0 | 2 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0019 | 0/0 | 4818 | 2 | 0 | 1 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0022 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0025 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0026 | 0/0 | 4817 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0027 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0028 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0029 | 0/0 | 4818 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0030 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0031 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0032 | 0/0 | 4818 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0033 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0034 | 0/0 | 4818 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0036 | 0/0 | 4818 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0038 | 0/0 | 4816 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0001t0042 | 0/0 | 4815 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0008t0001 | 0/0 | 4818 | 2 | 0 | 1 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0008t0007 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0009t0001 | 0/0 | 4818 | 2 | 0 | 0 | 2 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0001c0010t0001 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0002t0001 | 0/0 | 4818 | 7 | 1 | 5 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0002t0002 | 0/0 | 4815 | 17 | 17 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0002t0003 | 0/0 | 4815 | 17 | 16 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0002t0004 | 0/0 | 4817 | 2 | 0 | 0 | 2 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0002t0006 | 0/0 | 4817 | 5 | 5 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0002t0007 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0002t0011 | 0/0 | 4817 | 2 | 2 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0002t0012 | 0/0 | 4817 | 2 | 1 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0002t0013 | 0/0 | 4815 | 3 | 0 | 3 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0002t0020 | 0/0 | 4817 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0002t0021 | 0/0 | 4818 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0002t0023 | 0/0 | 4815 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0002t0037 | 0/0 | 4815 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0002t0040 | 0/0 | 4815 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0002t0043 | 0/0 | 4816 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0002t0044 | 0/0 | 4815 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0004t0001 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0004t0004 | 0/0 | 4817 | 10 | 0 | 0 | 10 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0004t0009 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0002c0007t0010 | 0/0 | 4815 | 4 | 4 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0003c0003t0001 | 1/0 | 4818 | 9 | 6 | 0 | 2 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0003c0003t0005 | 0/0 | 4817 | 7 | 4 | 3 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0003c0003t0008 | 0/0 | 4818 | 3 | 2 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0003c0003t0015 | 0/0 | 4817 | 2 | 0 | 2 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0003c0003t0035 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0003c0003t0041 | 0/0 | 4815 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0004c0005t0001 | 0/0 | 4818 | 2 | 2 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0004c0005t0004 | 0/0 | 4817 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0004c0005t0024 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0004c0006t0002 | 0/0 | 4815 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0004c0006t0011 | 0/0 | 4817 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0004c0006t0012 | 0/0 | 4817 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0004c0006t0039 | 0/0 | 4815 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0005c0012t0002 | 0/0 | 4815 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| a0006c0011t0001 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | copy fasta | chr15 | 45018195 | 45082185 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0167 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0005g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0008g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0008g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0009g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0009g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0009g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0014g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0014g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0016g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0016g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0017g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0017g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0018g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0018g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0019g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0019g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0022g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0025g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0026g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0027g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0028g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0029g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0030g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0031g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0032g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0033g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0034g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0036g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0038g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0001t0042g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0008t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0008t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0008t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0009t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0001c0010t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0003g0001 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0004g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0011g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0011g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0012g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0012g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0013g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0013g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0013g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0020g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0021g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0023g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0037g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0040g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0043g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0002t0044g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0004t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0004t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0004t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0004t0004g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0004t0004g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0004t0004g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0004t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0004t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0004t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0004t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0004t0009g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0007t0010g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0007t0010g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0007t0010g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0002c0007t0010g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0001g0161 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0005g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0005g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0005g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0005g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0008g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0008g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0008g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0015g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0035g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0003c0003t0041g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0004c0005t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0004c0005t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0004c0005t0024g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0004c0006t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0004c0006t0011g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0004c0006t0012g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0004c0006t0039g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0005c0012t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| a0006c0011t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | GBR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0187 | EUR | GBR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0131 | EUR | FIN | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0072 | EUR | FIN | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00438 | hp1 | a0002 | c0004 | t0004 | g0020 | EAS | CHS | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00558 | hp2 | a0004 | c0005 | t0004 | g0021 | EAS | CHS | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | CHS | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0216 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00639 | hp2 | a0001 | c0001 | t0038 | g0144 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00642 | hp2 | a0002 | c0002 | t0003 | g0001 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0218 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01070 | hp2 | a0003 | c0003 | t0015 | g0009 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01071 | hp2 | a0003 | c0003 | t0015 | g0009 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01074 | hp2 | a0001 | c0001 | t0042 | g0249 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01099 | hp1 | a0002 | c0002 | t0021 | g0274 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01099 | hp2 | a0001 | c0008 | t0001 | g0048 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0219 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01109 | hp1 | a0002 | c0002 | t0023 | g0273 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01243 | hp1 | a0001 | c0001 | t0032 | g0277 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01255 | hp2 | a0003 | c0003 | t0008 | g0263 | AMR | CLM | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01361 | hp1 | a0001 | c0001 | t0036 | g0163 | AMR | CLM | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01433 | hp1 | a0001 | c0001 | t0019 | g0172 | AMR | CLM | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01496 | hp2 | a0002 | c0002 | t0012 | g0260 | AMR | CLM | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | IBS | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01884 | hp1 | a0003 | c0003 | t0001 | g0275 | AFR | ACB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0099 | AFR | ACB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01891 | hp1 | a0002 | c0002 | t0003 | g0113 | AFR | ACB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01891 | hp2 | a0004 | c0006 | t0002 | g0295 | AFR | ACB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01928 | hp1 | a0002 | c0002 | t0013 | g0031 | AMR | PEL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01934 | hp1 | a0003 | c0003 | t0005 | g0093 | AMR | PEL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01943 | hp1 | a0003 | c0003 | t0005 | g0095 | AMR | PEL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01978 | hp2 | a0002 | c0002 | t0013 | g0030 | AMR | PEL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01981 | hp1 | a0001 | c0001 | t0005 | g0139 | AMR | PEL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01981 | hp2 | a0001 | c0001 | t0034 | g0121 | AMR | PEL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02004 | hp1 | a0003 | c0003 | t0005 | g0094 | AMR | PEL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02056 | hp1 | a0002 | c0004 | t0004 | g0017 | EAS | KHV | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02074 | hp2 | a0001 | c0001 | t0033 | g0012 | EAS | KHV | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02083 | hp1 | a0002 | c0004 | t0004 | g0015 | EAS | KHV | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02083 | hp2 | a0006 | c0011 | t0001 | g0224 | EAS | KHV | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02145 | hp1 | a0002 | c0002 | t0003 | g0114 | AFR | ACB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02145 | hp2 | a0003 | c0003 | t0001 | g0296 | AFR | ACB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02148 | hp2 | a0002 | c0002 | t0013 | g0029 | AMR | PEL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02257 | hp1 | a0003 | c0003 | t0008 | g0225 | AFR | ACB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02280 | hp1 | a0002 | c0002 | t0040 | g0261 | AFR | ACB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0074 | AFR | ACB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02293 | hp1 | a0002 | c0002 | t0001 | g0221 | AMR | PEL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0217 | AMR | PEL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02572 | hp1 | a0001 | c0001 | t0008 | g0108 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02572 | hp2 | a0004 | c0005 | t0024 | g0234 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02615 | hp1 | a0002 | c0002 | t0003 | g0027 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02615 | hp2 | a0002 | c0002 | t0006 | g0241 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02622 | hp1 | a0002 | c0002 | t0002 | g0116 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02622 | hp2 | a0003 | c0003 | t0001 | g0024 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0086 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02630 | hp2 | a0002 | c0002 | t0003 | g0252 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02647 | hp2 | a0002 | c0002 | t0003 | g0091 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02717 | hp1 | a0002 | c0002 | t0003 | g0292 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02717 | hp2 | a0002 | c0002 | t0011 | g0293 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02735 | hp2 | a0001 | c0001 | t0018 | g0066 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02738 | hp1 | a0001 | c0001 | t0018 | g0069 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02809 | hp2 | a0004 | c0006 | t0011 | g0250 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02818 | hp1 | a0002 | c0002 | t0003 | g0281 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0177 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02886 | hp1 | a0002 | c0007 | t0010 | g0087 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0100 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0026 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02895 | hp2 | a0002 | c0007 | t0010 | g0097 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02896 | hp1 | a0001 | c0001 | t0014 | g0271 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02896 | hp2 | a0004 | c0005 | t0001 | g0006 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02897 | hp1 | a0004 | c0005 | t0001 | g0006 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02897 | hp2 | a0002 | c0007 | t0010 | g0098 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02922 | hp1 | a0002 | c0002 | t0002 | g0238 | AFR | ESN | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02922 | hp2 | a0003 | c0003 | t0005 | g0259 | AFR | ESN | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02965 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | ESN | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02965 | hp2 | a0004 | c0006 | t0039 | g0118 | AFR | ESN | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02970 | hp1 | a0002 | c0002 | t0003 | g0001 | AFR | ESN | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02970 | hp2 | a0001 | c0001 | t0017 | g0083 | AFR | ESN | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0073 | AFR | ESN | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0255 | AFR | ESN | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03017 | hp2 | a0001 | c0001 | t0029 | g0284 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03041 | hp1 | a0003 | c0003 | t0005 | g0256 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03041 | hp2 | a0004 | c0006 | t0012 | g0267 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0076 | AFR | MSL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03098 | hp2 | a0002 | c0002 | t0003 | g0115 | AFR | MSL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03130 | hp1 | a0003 | c0003 | t0041 | g0253 | AFR | ESN | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0235 | AFR | ESN | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03139 | hp1 | a0001 | c0001 | t0017 | g0084 | AFR | ESN | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03195 | hp1 | a0003 | c0003 | t0035 | g0120 | AFR | ESN | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03195 | hp2 | a0003 | c0003 | t0001 | g0025 | AFR | ESN | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03209 | hp1 | a0002 | c0004 | t0001 | g0119 | AFR | MSL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03209 | hp2 | a0002 | c0002 | t0007 | g0226 | AFR | MSL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | MSL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03225 | hp2 | a0005 | c0012 | t0002 | g0103 | AFR | MSL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03453 | hp1 | a0002 | c0002 | t0011 | g0251 | AFR | MSL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03453 | hp2 | a0002 | c0002 | t0003 | g0111 | AFR | MSL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0236 | AFR | MSL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03486 | hp2 | a0002 | c0002 | t0006 | g0246 | AFR | MSL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03516 | hp1 | a0003 | c0003 | t0005 | g0257 | AFR | ESN | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0075 | AFR | ESN | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03540 | hp1 | a0002 | c0002 | t0003 | g0112 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03540 | hp2 | a0002 | c0002 | t0003 | g0280 | AFR | GWD | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03579 | hp1 | a0003 | c0003 | t0005 | g0254 | AFR | MSL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03579 | hp2 | a0002 | c0007 | t0010 | g0278 | AFR | MSL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0285 | SAS | BEB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG04115 | hp1 | a0001 | c0008 | t0001 | g0283 | SAS | STU | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | STU | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | BEB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG04184 | hp2 | a0001 | c0001 | t0016 | g0282 | SAS | BEB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | STU | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | STU | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18522 | hp1 | a0002 | c0002 | t0006 | g0239 | AFR | YRI | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | YRI | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18612 | hp1 | a0001 | c0001 | t0030 | g0154 | EAS | CHB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CHB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18906 | hp1 | a0002 | c0002 | t0002 | g0077 | AFR | YRI | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18906 | hp2 | a0001 | c0001 | t0022 | g0272 | AFR | YRI | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18951 | hp1 | a0002 | c0002 | t0004 | g0014 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18953 | hp2 | a0001 | c0001 | t0009 | g0034 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18957 | hp1 | a0002 | c0002 | t0043 | g0223 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0080 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18967 | hp1 | a0002 | c0002 | t0004 | g0013 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18971 | hp2 | a0001 | c0001 | t0007 | g0208 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18973 | hp1 | a0002 | c0004 | t0009 | g0023 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18977 | hp2 | a0001 | c0001 | t0025 | g0047 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18982 | hp1 | a0002 | c0004 | t0004 | g0018 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18982 | hp2 | a0001 | c0001 | t0009 | g0200 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18983 | hp2 | a0001 | c0001 | t0027 | g0149 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18989 | hp1 | a0002 | c0004 | t0004 | g0016 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18989 | hp2 | a0001 | c0001 | t0009 | g0182 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18990 | hp2 | a0002 | c0004 | t0004 | g0022 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18992 | hp1 | a0001 | c0009 | t0001 | g0008 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18992 | hp2 | a0001 | c0001 | t0031 | g0061 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18993 | hp2 | a0003 | c0003 | t0001 | g0038 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19012 | hp2 | a0002 | c0004 | t0004 | g0067 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19030 | hp1 | a0001 | c0001 | t0008 | g0107 | AFR | LWK | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0243 | AFR | LWK | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0101 | AFR | LWK | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19043 | hp2 | a0001 | c0008 | t0007 | g0214 | AFR | LWK | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19056 | hp2 | a0001 | c0001 | t0026 | g0134 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19065 | hp1 | a0001 | c0001 | t0028 | g0060 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19068 | hp1 | a0001 | c0009 | t0001 | g0008 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19068 | hp2 | a0002 | c0004 | t0004 | g0004 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19078 | hp1 | a0002 | c0004 | t0004 | g0019 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19078 | hp2 | a0003 | c0003 | t0001 | g0039 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19085 | hp1 | a0002 | c0004 | t0004 | g0004 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19240 | hp1 | a0002 | c0002 | t0003 | g0262 | AFR | YRI | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0276 | AFR | YRI | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA20129 | hp1 | a0002 | c0002 | t0003 | g0279 | AFR | ASW | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA20129 | hp2 | a0002 | c0002 | t0037 | g0117 | AFR | ASW | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0287 | EUR | TSI | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | TSI | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0229 | EUR | TSI | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | TSI | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA20905 | hp1 | a0001 | c0001 | t0019 | g0193 | SAS | GIH | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA20905 | hp2 | a0001 | c0001 | t0016 | g0159 | SAS | GIH | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02109 | hp1 | a0002 | c0002 | t0020 | g0269 | AFR | ACB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02109 | hp2 | a0003 | c0003 | t0001 | g0110 | AFR | ACB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02486 | hp1 | a0002 | c0002 | t0006 | g0242 | AFR | ACB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02486 | hp2 | a0001 | c0010 | t0001 | g0184 | AFR | ACB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02559 | hp1 | a0002 | c0002 | t0012 | g0268 | AFR | ACB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG02559 | hp2 | a0002 | c0002 | t0006 | g0240 | AFR | ACB | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03471 | hp1 | a0002 | c0002 | t0003 | g0001 | AFR | MSL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG03471 | hp2 | a0001 | c0001 | t0014 | g0270 | AFR | MSL | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG06807 | hp1 | a0002 | c0002 | t0003 | g0237 | AFR | USA | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| HG06807 | hp2 | a0003 | c0003 | t0008 | g0288 | AFR | USA | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0227 | AFR | USA | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA20300 | hp2 | a0003 | c0003 | t0001 | g0294 | AFR | USA | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0215 | AFR | LWK | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| NA21309 | hp2 | a0002 | c0002 | t0044 | g0258 | AFR | LWK | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0167 | REF | REF | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| homoSapiens_grch38 | hp1 | a0003 | c0003 | t0001 | g0161 | REF | REF | SORD_chr15_45018195_45082185 | SORD | chr15 | 45018195 | 45082185 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:45061072
|
C | T | 1 | a0005 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.271C>T | p.Arg91Cys | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/9 | 360/4818 | 271/1074 | 91/357 | chr15 | 45061072 | ||
| chr15:45068947
|
G | C | 1 | a0006 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.681G>C | p.Glu227Asp | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/9 | 770/4818 | 681/1074 | 227/357 | chr15 | 45068947 | ||
| chr15:45068982
|
A | T | 3 | a0002a0004a0005 | 88 | HG00438.hp1 HG00558.hp2 HG00639.hp1 others(85): Show |
missense_variant | MODERATE | c.716A>T | p.Gln239Leu | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/9 | 805/4818 | 716/1074 | 239/357 | chr15 | 45068982 | ||
| chr15:45072336
|
A | C | 4 | a0001a0002a0005others(1): Show | 277 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(274): Show |
missense_variant | MODERATE | c.806A>C | p.Asn269Thr | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/9 | 895/4818 | 806/1074 | 269/357 | chr15 | 45072336 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:45061167
|
G | A | 1 | a0001c0010 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.366G>A | p.Thr122Thr | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/9 | 455/4818 | 366/1074 | 122/357 | chr15 | 45061167 | ||
| chr15:45065301
|
C | T | 1 | a0001c0009 | 2 | NA18992.hp1 NA19068.hp1 |
synonymous_variant | LOW | c.456C>T | p.Gly152Gly | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/9 | 545/4818 | 456/1074 | 152/357 | chr15 | 45065301 | ||
| chr15:45065349
|
C | T | 1 | a0002c0007 | 4 | HG02886.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
synonymous_variant | LOW | c.504C>T | p.Gly168Gly | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/9 | 593/4818 | 504/1074 | 168/357 | chr15 | 45065349 | ||
| chr15:45069043
|
G | A | 3 | a0001c0008a0002c0004a0004c0005 | 19 | HG00438.hp1 HG00558.hp2 HG01099.hp2 others(16): Show |
synonymous_variant | LOW | c.777G>A | p.Ala259Ala | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/9 | 866/4818 | 777/1074 | 259/357 | chr15 | 45069043 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:45023203
|
G | A | 5 | a0001c0001t0014a0001c0001t0022a0002c0002t0020others(2): Show | 6 | HG01099.hp1 HG01109.hp1 HG02109.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-81G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/9 | 81 | chr15 | 45023203 | |||||
| chr15:45073555
|
CCA | C | 15 | a0001c0001t0038a0001c0001t0042a0002c0002t0002others(12): Show | 52 | HG00639.hp2 HG00642.hp2 HG01074.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*28_*29delCA | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 28 | INFO_REALIGN_3_PRIME | chr15 | 45073555 | ||||
| chr15:45073564
|
T | C | 28 | a0001c0001t0004a0001c0001t0005a0001c0001t0038others(25): Show | 90 | HG00438.hp1 HG00558.hp2 HG00639.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*34T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 34 | chr15 | 45073564 | |||||
| chr15:45073581
|
A | G | 2 | a0002c0002t0013a0002c0002t0044 | 4 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*51A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 51 | chr15 | 45073581 | |||||
| chr15:45073592
|
T | G | 11 | a0001c0001t0004a0001c0001t0005a0002c0002t0004others(8): Show | 35 | HG00438.hp1 HG00558.hp2 HG01070.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*62T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 62 | chr15 | 45073592 | |||||
| chr15:45073621
|
T | A | 4 | a0002c0002t0006a0002c0002t0011a0002c0002t0020others(1): Show | 9 | HG02109.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*91T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 91 | chr15 | 45073621 | |||||
| chr15:45073671
|
A | C | 13 | a0001c0001t0042a0002c0002t0002a0002c0002t0003others(10): Show | 50 | HG00642.hp2 HG01074.hp2 HG01109.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*141A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 141 | chr15 | 45073671 | |||||
| chr15:45073702
|
A | G | 2 | a0002c0002t0013a0002c0002t0044 | 4 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*172A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 172 | chr15 | 45073702 | |||||
| chr15:45073817
|
G | A | 1 | a0002c0002t0044 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*287G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 287 | chr15 | 45073817 | |||||
| chr15:45073878
|
A | G | 1 | a0001c0001t0036 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*348A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 348 | chr15 | 45073878 | |||||
| chr15:45073881
|
G | A | 1 | a0002c0002t0021 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*351G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 351 | chr15 | 45073881 | |||||
| chr15:45074291
|
G | C | 30 | a0001c0001t0004a0001c0001t0005a0001c0001t0009others(27): Show | 94 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*761G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 761 | chr15 | 45074291 | |||||
| chr15:45074304
|
C | T | 28 | a0001c0001t0004a0001c0001t0005a0001c0001t0042others(25): Show | 90 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*774C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 774 | chr15 | 45074304 | |||||
| chr15:45074306
|
T | C | 28 | a0001c0001t0004a0001c0001t0005a0001c0001t0042others(25): Show | 90 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*776T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 776 | chr15 | 45074306 | |||||
| chr15:45074328
|
C | T | 2 | a0001c0001t0008a0003c0003t0008 | 5 | HG01255.hp2 HG02257.hp1 HG02572.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*798C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 798 | chr15 | 45074328 | |||||
| chr15:45074414
|
C | G | 8 | a0001c0001t0009a0001c0001t0042a0002c0002t0012others(5): Show | 14 | HG01074.hp2 HG01496.hp2 HG02559.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*884C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 884 | chr15 | 45074414 | |||||
| chr15:45074453
|
T | G | 1 | a0004c0006t0039 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*923T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 923 | chr15 | 45074453 | |||||
| chr15:45074459
|
G | A | 1 | a0003c0003t0015 | 2 | HG01070.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*929G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 929 | chr15 | 45074459 | |||||
| chr15:45074565
|
C | G | 1 | a0003c0003t0035 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1035C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 1035 | chr15 | 45074565 | |||||
| chr15:45074614
|
A | G | 27 | a0001c0001t0004a0001c0001t0005a0001c0001t0042others(24): Show | 89 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*1084A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 1084 | chr15 | 45074614 | |||||
| chr15:45074624
|
C | T | 2 | a0001c0001t0018a0001c0001t0019 | 4 | HG01433.hp1 HG02735.hp2 HG02738.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1094C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 1094 | chr15 | 45074624 | |||||
| chr15:45074652
|
C | T | 2 | a0002c0002t0012a0004c0006t0012 | 3 | HG01496.hp2 HG02559.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1122C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 1122 | chr15 | 45074652 | |||||
| chr15:45074701
|
A | G | 1 | a0001c0001t0034 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1171A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 1171 | chr15 | 45074701 | |||||
| chr15:45074793
|
C | T | 1 | a0001c0001t0017 | 2 | HG02970.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1263C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 1263 | chr15 | 45074793 | |||||
| chr15:45075323
|
T | A | 27 | a0001c0001t0004a0001c0001t0005a0001c0001t0016others(24): Show | 90 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1793T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 1793 | chr15 | 45075323 | |||||
| chr15:45075330
|
C | A | 1 | a0001c0001t0025 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1800C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 1800 | chr15 | 45075330 | |||||
| chr15:45075367
|
TC | T | 28 | a0001c0001t0004a0001c0001t0005a0001c0001t0016others(25): Show | 91 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1839delC | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 1839 | INFO_REALIGN_3_PRIME | chr15 | 45075367 | ||||
| chr15:45075368
|
C | T | 1 | a0001c0001t0019 | 2 | HG01433.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1838C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 1838 | chr15 | 45075368 | |||||
| chr15:45075461
|
G | C | 11 | a0001c0001t0004a0001c0001t0027a0002c0002t0003others(8): Show | 42 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*1931G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 1931 | chr15 | 45075461 | |||||
| chr15:45075567
|
C | G | 1 | a0001c0001t0033 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2037C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2037 | chr15 | 45075567 | |||||
| chr15:45075595
|
G | A | 1 | a0001c0001t0028 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2065G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2065 | chr15 | 45075595 | |||||
| chr15:45075631
|
G | C | 3 | a0002c0002t0003a0002c0002t0040a0004c0006t0039 | 19 | HG00642.hp2 HG01891.hp1 HG02145.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2101G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2101 | chr15 | 45075631 | |||||
| chr15:45075635
|
A | G | 3 | a0002c0002t0003a0002c0002t0040a0004c0006t0039 | 19 | HG00642.hp2 HG01891.hp1 HG02145.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2105A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2105 | chr15 | 45075635 | |||||
| chr15:45075639
|
C | T | 3 | a0002c0002t0003a0002c0002t0040a0004c0006t0039 | 19 | HG00642.hp2 HG01891.hp1 HG02145.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2109C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2109 | chr15 | 45075639 | |||||
| chr15:45075640
|
T | C | 3 | a0002c0002t0003a0002c0002t0040a0004c0006t0039 | 19 | HG00642.hp2 HG01891.hp1 HG02145.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2110T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2110 | chr15 | 45075640 | |||||
| chr15:45075641
|
G | A | 3 | a0002c0002t0003a0002c0002t0040a0004c0006t0039 | 19 | HG00642.hp2 HG01891.hp1 HG02145.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2111G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2111 | chr15 | 45075641 | |||||
| chr15:45075648
|
T | G | 27 | a0001c0001t0004a0001c0001t0005a0001c0001t0007others(24): Show | 90 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*2118T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2118 | chr15 | 45075648 | |||||
| chr15:45075660
|
T | G | 8 | a0002c0002t0002a0002c0002t0003a0002c0002t0023others(5): Show | 40 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2130T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2130 | chr15 | 45075660 | |||||
| chr15:45075669
|
T | A | 8 | a0002c0002t0002a0002c0002t0003a0002c0002t0023others(5): Show | 40 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*2139T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2139 | chr15 | 45075669 | |||||
| chr15:45075729
|
C | T | 1 | a0002c0002t0021 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2199C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2199 | chr15 | 45075729 | |||||
| chr15:45075750
|
T | C | 3 | a0002c0002t0003a0002c0002t0040a0004c0006t0039 | 19 | HG00642.hp2 HG01891.hp1 HG02145.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2220T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2220 | chr15 | 45075750 | |||||
| chr15:45075752
|
T | C | 3 | a0002c0002t0003a0002c0002t0040a0004c0006t0039 | 19 | HG00642.hp2 HG01891.hp1 HG02145.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2222T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2222 | chr15 | 45075752 | |||||
| chr15:45075812
|
T | C | 3 | a0002c0002t0003a0002c0002t0040a0004c0006t0039 | 19 | HG00642.hp2 HG01891.hp1 HG02145.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2282T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2282 | chr15 | 45075812 | |||||
| chr15:45075927
|
G | A | 2 | a0001c0001t0025a0003c0003t0041 | 2 | HG03130.hp1 NA18977.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2397G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2397 | chr15 | 45075927 | |||||
| chr15:45075996
|
G | A | 2 | a0002c0002t0013a0002c0002t0044 | 4 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2466G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2466 | chr15 | 45075996 | |||||
| chr15:45076007
|
G | A | 3 | a0002c0002t0003a0002c0002t0040a0004c0006t0039 | 19 | HG00642.hp2 HG01891.hp1 HG02145.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*2477G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2477 | chr15 | 45076007 | |||||
| chr15:45076248
|
G | T | 2 | a0002c0002t0012a0004c0006t0012 | 3 | HG01496.hp2 HG02559.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2718G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2718 | chr15 | 45076248 | |||||
| chr15:45076292
|
C | G | 2 | a0001c0001t0022a0001c0001t0032 | 2 | HG01243.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2762C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 2762 | chr15 | 45076292 | |||||
| chr15:45076604
|
G | A | 1 | a0002c0002t0006 | 5 | HG02486.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3074G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 3074 | chr15 | 45076604 | |||||
| chr15:45076694
|
C | T | 2 | a0002c0002t0013a0002c0002t0044 | 4 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3164C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 3164 | chr15 | 45076694 | |||||
| chr15:45076896
|
C | A | 1 | a0004c0005t0024 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3366C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 3366 | chr15 | 45076896 | |||||
| chr15:45076980
|
G | A | 12 | a0001c0001t0029a0002c0002t0002a0002c0002t0003others(9): Show | 49 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*3450G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 3450 | chr15 | 45076980 | |||||
| chr15:45077079
|
G | A | 1 | a0001c0001t0030 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3549G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 3549 | chr15 | 45077079 | |||||
| chr15:45077177
|
T | C | 1 | a0001c0001t0031 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3647T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 9/9 | 3647 | chr15 | 45077177 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:45023546
|
C | T | 4 | a0002c0002t0011g0293a0003c0003t0001g0294a0003c0003t0001g0296others(1): Show | 4 | HG01891.hp2 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+197C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45023546 | ||||||
| chr15:45023556
|
C | T | 2 | a0001c0001t0001g0291a0002c0002t0003g0292 | 2 | HG02647.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.66+207C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45023556 | ||||||
| chr15:45023640
|
C | T | 3 | a0001c0001t0001g0289a0001c0001t0001g0290a0003c0003t0008g0288 | 3 | HG06807.hp2 NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.66+291C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45023640 | ||||||
| chr15:45023694
|
T | C | 1 | a0002c0002t0002g0010 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.66+345T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45023694 | ||||||
| chr15:45023740
|
G | C | 2 | a0001c0001t0001g0011a0001c0001t0033g0012 | 2 | HG02074.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.66+391G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45023740 | ||||||
| chr15:45023853
|
C | T | 1 | a0002c0002t0001g0287 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.66+504C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45023853 | ||||||
| chr15:45023865
|
G | A | 2 | a0002c0002t0004g0013a0002c0002t0004g0014 | 2 | NA18951.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.66+516G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45023865 | ||||||
| chr15:45023909
|
C | T | 12 | a0001c0001t0001g0286a0001c0001t0005g0285a0001c0001t0016g0282others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.66+560C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45023909 | ||||||
| chr15:45023962
|
C | T | 12 | a0001c0001t0001g0286a0001c0001t0005g0285a0001c0001t0016g0282others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.66+613C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45023962 | ||||||
| chr15:45023967
|
G | C | 10 | a0002c0004t0004g0004a0002c0004t0004g0015a0002c0004t0004g0016others(7): Show | 11 | HG00438.hp1 HG00558.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.66+618G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45023967 | ||||||
| chr15:45024144
|
A | C | 9 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0014g0270others(6): Show | 9 | HG01099.hp1 HG01109.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+795A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45024144 | ||||||
| chr15:45024269
|
A | G | 2 | a0002c0002t0012g0268a0004c0006t0012g0267 | 2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.66+920A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45024269 | ||||||
| chr15:45024393
|
A | C | 6 | a0001c0001t0014g0270a0001c0001t0014g0271a0001c0001t0022g0272others(3): Show | 6 | HG01099.hp1 HG01109.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+1044A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45024393 | ||||||
| chr15:45024408
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.66+1059C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45024408 | ||||||
| chr15:45024417
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.66+1068C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45024417 | ||||||
| chr15:45024466
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.66+1117C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45024466 | ||||||
| chr15:45024551
|
C | A | 4 | a0001c0001t0007g0026a0002c0002t0003g0027a0003c0003t0001g0024others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+1202C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45024551 | ||||||
| chr15:45024646
|
T | C | 69 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(66): Show | 71 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.66+1297T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45024646 | ||||||
| chr15:45024777
|
A | G | 102 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(99): Show | 105 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.66+1428A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45024777 | ||||||
| chr15:45024852
|
G | A | 18 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0014g0270others(15): Show | 19 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(16): Show |
intron_variant | MODIFIER | c.66+1503G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45024852 | ||||||
| chr15:45024899
|
GC | G | 12 | a0001c0001t0001g0286a0001c0001t0005g0285a0001c0001t0016g0282others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.66+1553delC | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45024899 | |||||
| chr15:45025205
|
G | C | 10 | a0002c0004t0004g0004a0002c0004t0004g0015a0002c0004t0004g0016others(7): Show | 11 | HG00438.hp1 HG00558.hp2 HG02056.hp1 others(8): Show |
intron_variant | MODIFIER | c.66+1856G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45025205 | ||||||
| chr15:45025252
|
C | G | 7 | a0002c0002t0002g0255a0002c0002t0012g0260a0002c0002t0044g0258others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.66+1903C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45025252 | ||||||
| chr15:45025283
|
C | T | 3 | a0002c0002t0003g0252a0002c0002t0011g0251a0004c0006t0011g0250 | 3 | HG02630.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.66+1934C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45025283 | ||||||
| chr15:45025313
|
G | A | 2 | a0001c0001t0017g0083a0001c0001t0017g0084 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.66+1964G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45025313 | ||||||
| chr15:45025338
|
G | C | 1 | a0001c0001t0001g0085 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.66+1989G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45025338 | ||||||
| chr15:45025534
|
G | T | 1 | a0001c0001t0042g0249 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.66+2185G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45025534 | ||||||
| chr15:45025583
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.66+2234C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45025583 | ||||||
| chr15:45025605
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.66+2256A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45025605 | ||||||
| chr15:45025624
|
C | CA | 22 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(19): Show | 22 | HG01255.hp2 HG01934.hp1 HG01943.hp1 others(19): Show |
intron_variant | MODIFIER | c.66+2295dupA | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45025624 | |||||
| chr15:45025624
|
CA | C | 27 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0001g0082others(24): Show | 27 | HG01099.hp1 HG01109.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.66+2295delA | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45025624 | |||||
| chr15:45025625
|
A | T | 1 | a0001c0001t0001g0247 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.66+2276A>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45025625 | ||||||
| chr15:45025698
|
G | A | 7 | a0002c0002t0002g0255a0002c0002t0012g0260a0002c0002t0044g0258others(4): Show | 8 | HG01070.hp2 HG01071.hp2 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.66+2349G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45025698 | ||||||
| chr15:45025717
|
A | C | 33 | a0001c0001t0001g0286a0001c0001t0001g0289a0001c0001t0001g0290others(30): Show | 34 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.66+2368A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45025717 | ||||||
| chr15:45025780
|
G | A | 9 | a0001c0001t0001g0102a0001c0001t0005g0086a0002c0002t0002g0099others(6): Show | 9 | HG01884.hp2 HG02630.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.66+2431G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45025780 | ||||||
| chr15:45025797
|
A | G | 12 | a0001c0001t0001g0286a0001c0001t0005g0285a0001c0001t0016g0282others(9): Show | 12 | HG01243.hp1 HG01884.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.66+2448A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45025797 | ||||||
| chr15:45025833
|
G | A | 9 | a0001c0001t0001g0286a0001c0001t0005g0285a0001c0001t0016g0282others(6): Show | 9 | HG01243.hp1 HG01884.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.66+2484G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45025833 | ||||||
| chr15:45025855
|
G | A | 1 | a0001c0001t0001g0104 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.66+2506G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45025855 | ||||||
| chr15:45025951
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.66+2602G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45025951 | ||||||
| chr15:45026053
|
G | C | 9 | a0001c0001t0001g0102a0001c0001t0005g0086a0002c0002t0002g0099others(6): Show | 9 | HG01884.hp2 HG02630.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.66+2704G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45026053 | ||||||
| chr15:45026115
|
G | A | 1 | a0002c0007t0010g0087 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.66+2766G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45026115 | ||||||
| chr15:45026374
|
A | G | 112 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(109): Show | 115 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.66+3025A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45026374 | ||||||
| chr15:45026560
|
G | T | 1 | a0001c0001t0001g0286 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.66+3211G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45026560 | ||||||
| chr15:45026593
|
C | T | 3 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233 | 3 | HG00597.hp2 HG02523.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.66+3244C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45026593 | ||||||
| chr15:45026640
|
T | C | 1 | a0001c0001t0001g0028 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.66+3291T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45026640 | ||||||
| chr15:45026643
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.66+3294G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45026643 | ||||||
| chr15:45026662
|
T | C | 2 | a0003c0003t0005g0254a0003c0003t0041g0253 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.66+3313T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45026662 | ||||||
| chr15:45026700
|
C | G | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | HG02735.hp1 HG03239.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.66+3351C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45026700 | ||||||
| chr15:45026777
|
G | A | 4 | a0002c0002t0011g0293a0003c0003t0001g0294a0003c0003t0001g0296others(1): Show | 4 | HG01891.hp2 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+3428G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45026777 | ||||||
| chr15:45026873
|
CT | C | 145 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(142): Show | 151 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.66+3526delT | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45026873 | |||||
| chr15:45026913
|
A | G | 2 | a0003c0003t0005g0254a0003c0003t0041g0253 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.66+3564A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45026913 | ||||||
| chr15:45026990
|
A | C | 2 | a0002c0004t0001g0119a0003c0003t0035g0120 | 2 | HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.66+3641A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45026990 | ||||||
| chr15:45027155
|
G | A | 6 | a0001c0001t0014g0270a0001c0001t0014g0271a0001c0001t0022g0272others(3): Show | 6 | HG01099.hp1 HG01109.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+3806G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45027155 | ||||||
| chr15:45027236
|
A | C | 1 | a0001c0001t0001g0078 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.66+3887A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45027236 | ||||||
| chr15:45027448
|
G | A | 1 | a0001c0001t0034g0121 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.66+4099G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45027448 | ||||||
| chr15:45027452
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.66+4103G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45027452 | ||||||
| chr15:45027475
|
T | C | 25 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0286others(22): Show | 26 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.66+4126T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45027475 | ||||||
| chr15:45027539
|
C | T | 5 | a0001c0001t0014g0270a0001c0001t0014g0271a0001c0001t0022g0272others(2): Show | 5 | HG01099.hp1 HG01109.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.66+4190C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45027539 | ||||||
| chr15:45027741
|
T | C | 2 | a0001c0001t0008g0108a0004c0005t0024g0234 | 2 | HG02572.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.66+4392T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45027741 | ||||||
| chr15:45027742
|
G | A | 1 | a0004c0005t0024g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.66+4393G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45027742 | ||||||
| chr15:45027767
|
T | C | 12 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(9): Show | 13 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(10): Show |
intron_variant | MODIFIER | c.66+4418T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45027767 | ||||||
| chr15:45027784
|
A | C | 94 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(91): Show | 98 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.66+4435A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45027784 | ||||||
| chr15:45027790
|
T | C | 75 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(72): Show | 81 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.66+4441T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45027790 | ||||||
| chr15:45027835
|
C | T | 9 | a0001c0001t0008g0107a0001c0001t0022g0272a0002c0002t0012g0260others(6): Show | 10 | HG01070.hp2 HG01071.hp2 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.66+4486C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45027835 | ||||||
| chr15:45027868
|
C | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.66+4519C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45027868 | ||||||
| chr15:45027882
|
A | G | 93 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(90): Show | 96 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(93): Show |
intron_variant | MODIFIER | c.66+4533A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45027882 | ||||||
| chr15:45027892
|
T | A | 21 | a0001c0001t0001g0064a0001c0001t0001g0072a0002c0002t0002g0010others(18): Show | 22 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.66+4543T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45027892 | ||||||
| chr15:45027917
|
A | T | 13 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0092others(10): Show | 13 | HG01934.hp1 HG01943.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.66+4568A>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45027917 | ||||||
| chr15:45027957
|
G | A | 11 | a0001c0001t0001g0123a0001c0001t0016g0282a0001c0001t0029g0284others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.66+4608G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45027957 | ||||||
| chr15:45028177
|
A | C | 2 | a0003c0003t0005g0254a0003c0003t0041g0253 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.66+4828A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028177 | ||||||
| chr15:45028198
|
AC | A | 4 | a0003c0003t0005g0254a0003c0003t0008g0263a0003c0003t0008g0288others(1): Show | 4 | HG01255.hp2 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+4850delC | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028198 | ||||||
| chr15:45028200
|
A | T | 4 | a0003c0003t0005g0254a0003c0003t0008g0263a0003c0003t0008g0288others(1): Show | 4 | HG01255.hp2 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+4851A>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028200 | ||||||
| chr15:45028201
|
A | G | 4 | a0003c0003t0005g0254a0003c0003t0008g0263a0003c0003t0008g0288others(1): Show | 4 | HG01255.hp2 HG03130.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+4852A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028201 | ||||||
| chr15:45028235
|
C | T | 2 | a0003c0003t0005g0254a0003c0003t0041g0253 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.66+4886C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028235 | ||||||
| chr15:45028250
|
T | C | 2 | a0003c0003t0005g0254a0003c0003t0041g0253 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.66+4901T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028250 | ||||||
| chr15:45028251
|
G | A | 2 | a0003c0003t0005g0254a0003c0003t0041g0253 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.66+4902G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028251 | ||||||
| chr15:45028275
|
C | T | 13 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(10): Show | 14 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.66+4926C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028275 | ||||||
| chr15:45028276
|
A | G | 14 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(11): Show | 15 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.66+4927A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028276 | ||||||
| chr15:45028283
|
T | C | 13 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(10): Show | 14 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.66+4934T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028283 | ||||||
| chr15:45028284
|
G | A | 13 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(10): Show | 14 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.66+4935G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028284 | ||||||
| chr15:45028295
|
G | C | 13 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(10): Show | 14 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.66+4946G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028295 | ||||||
| chr15:45028299
|
C | T | 1 | a0002c0002t0003g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.66+4950C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028299 | ||||||
| chr15:45028300
|
G | C | 13 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(10): Show | 14 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(11): Show |
intron_variant | MODIFIER | c.66+4951G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028300 | ||||||
| chr15:45028598
|
G | A | 12 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0291others(9): Show | 12 | HG01934.hp1 HG01943.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.66+5249G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028598 | ||||||
| chr15:45028736
|
G | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0081others(8): Show | 12 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.66+5387G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028736 | ||||||
| chr15:45028810
|
G | A | 11 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0081others(8): Show | 12 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.66+5461G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028810 | ||||||
| chr15:45028833
|
G | T | 1 | a0002c0002t0003g0262 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.66+5484G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028833 | ||||||
| chr15:45028931
|
T | G | 55 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(52): Show | 57 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.66+5582T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028931 | ||||||
| chr15:45028984
|
G | C | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.66+5635G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028984 | ||||||
| chr15:45028985
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0001g0128 | 2 | HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.66+5636G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45028985 | ||||||
| chr15:45029182
|
A | C | 25 | a0001c0001t0001g0028a0001c0001t0001g0064a0001c0001t0001g0065others(22): Show | 26 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.66+5833A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45029182 | ||||||
| chr15:45029352
|
T | G | 4 | a0002c0002t0003g0262a0002c0002t0040g0261a0003c0003t0008g0263others(1): Show | 4 | HG01255.hp2 HG02280.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+6003T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45029352 | ||||||
| chr15:45029395
|
G | A | 24 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(21): Show | 25 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.66+6046G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45029395 | ||||||
| chr15:45029656
|
T | G | 4 | a0002c0002t0003g0262a0002c0002t0040g0261a0003c0003t0008g0263others(1): Show | 4 | HG01255.hp2 HG02280.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+6307T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45029656 | ||||||
| chr15:45029678
|
T | A | 4 | a0002c0002t0003g0262a0002c0002t0040g0261a0003c0003t0008g0263others(1): Show | 4 | HG01255.hp2 HG02280.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+6329T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45029678 | ||||||
| chr15:45029679
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.66+6330G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45029679 | ||||||
| chr15:45029730
|
C | T | 2 | a0001c0001t0017g0083a0001c0001t0017g0084 | 2 | HG02970.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.66+6381C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45029730 | ||||||
| chr15:45029832
|
T | G | 7 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(4): Show | 7 | HG00621.hp1 HG00673.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.66+6483T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45029832 | ||||||
| chr15:45030026
|
T | C | 11 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0081others(8): Show | 12 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.66+6677T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45030026 | ||||||
| chr15:45030067
|
A | G | 4 | a0001c0001t0001g0102a0002c0002t0002g0100a0002c0002t0002g0101others(1): Show | 4 | HG02886.hp2 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+6718A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45030067 | ||||||
| chr15:45030069
|
C | T | 4 | a0001c0001t0001g0102a0002c0002t0002g0100a0002c0002t0002g0101others(1): Show | 4 | HG02886.hp2 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+6720C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45030069 | ||||||
| chr15:45030070
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.66+6721G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45030070 | ||||||
| chr15:45030131
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.66+6782C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45030131 | ||||||
| chr15:45030343
|
C | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(21): Show | 25 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.66+6994C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45030343 | ||||||
| chr15:45030561
|
G | A | 17 | a0001c0001t0001g0109a0001c0001t0001g0264a0001c0001t0017g0083others(14): Show | 20 | HG00642.hp2 HG01891.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.66+7212G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45030561 | ||||||
| chr15:45030759
|
T | A | 4 | a0002c0002t0003g0262a0002c0002t0040g0261a0003c0003t0008g0263others(1): Show | 4 | HG01255.hp2 HG02280.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+7410T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45030759 | ||||||
| chr15:45030812
|
GCCTGGTG others(5): Show |
G | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7464_66+7475del others(12): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45030812 | ||||||
| chr15:45030859
|
A | G | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7510A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45030859 | ||||||
| chr15:45030911
|
C | T | 1 | a0006c0011t0001g0224 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.66+7562C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45030911 | ||||||
| chr15:45030929
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.66+7580G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45030929 | ||||||
| chr15:45030999
|
C | A | 25 | a0001c0001t0001g0028a0001c0001t0001g0064a0001c0001t0001g0065others(22): Show | 26 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.66+7650C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45030999 | ||||||
| chr15:45031024
|
G | A | 2 | a0002c0002t0003g0279a0003c0003t0001g0275 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.66+7675G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031024 | ||||||
| chr15:45031046
|
GC | G | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7698delC | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031046 | ||||||
| chr15:45031048
|
A | G | 4 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031others(1): Show | 4 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.66+7699A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031048 | ||||||
| chr15:45031050
|
C | G | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7701C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031050 | ||||||
| chr15:45031066
|
C | T | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7717C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031066 | ||||||
| chr15:45031128
|
C | T | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7779C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031128 | ||||||
| chr15:45031133
|
C | T | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7784C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031133 | ||||||
| chr15:45031134
|
T | G | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7785T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031134 | ||||||
| chr15:45031138
|
A | C | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7789A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031138 | ||||||
| chr15:45031146
|
T | C | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7797T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031146 | ||||||
| chr15:45031147
|
G | A | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7798G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031147 | ||||||
| chr15:45031158
|
A | C | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7809A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031158 | ||||||
| chr15:45031175
|
G | A | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7826G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031175 | ||||||
| chr15:45031224
|
A | G | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7875A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031224 | ||||||
| chr15:45031233
|
G | A | 6 | a0001c0001t0007g0026a0002c0002t0013g0029a0002c0002t0013g0030others(3): Show | 6 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.66+7884G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031233 | ||||||
| chr15:45031240
|
C | T | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7891C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031240 | ||||||
| chr15:45031276
|
C | T | 8 | a0001c0001t0001g0220a0001c0001t0001g0222a0002c0002t0001g0216others(5): Show | 8 | HG00639.hp1 HG01069.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.66+7927C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031276 | ||||||
| chr15:45031309
|
TAAAACAA others(11): Show |
T | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7965_66+7982del others(18): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45031309 | |||||
| chr15:45031326
|
C | CA | 9 | a0001c0001t0001g0092a0001c0001t0014g0270a0001c0001t0014g0271others(6): Show | 9 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+7990dupA | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45031326 | |||||
| chr15:45031326
|
C | CAA | 15 | a0001c0001t0007g0026a0001c0001t0008g0107a0002c0002t0002g0227others(12): Show | 15 | HG02486.hp1 HG02559.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.66+7989_66+7990dup others(2): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45031326 | |||||
| chr15:45031326
|
CA | C | 23 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(20): Show | 24 | HG01884.hp1 HG02630.hp1 HG02976.hp2 others(21): Show |
intron_variant | MODIFIER | c.66+7990delA | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45031326 | |||||
| chr15:45031339
|
A | C | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7990A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031339 | ||||||
| chr15:45031340
|
C | A | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7991C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031340 | ||||||
| chr15:45031347
|
G | A | 21 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 22 | HG01884.hp1 HG02630.hp1 HG02976.hp2 others(19): Show |
intron_variant | MODIFIER | c.66+7998G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031347 | ||||||
| chr15:45031347
|
G | T | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+7998G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031347 | ||||||
| chr15:45031356
|
G | A | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+8007G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031356 | ||||||
| chr15:45031367
|
C | T | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+8018C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031367 | ||||||
| chr15:45031377
|
C | T | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+8028C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031377 | ||||||
| chr15:45031626
|
A | T | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+8277A>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031626 | ||||||
| chr15:45031656
|
C | T | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+8307C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031656 | ||||||
| chr15:45031702
|
C | CT | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+8354dupT | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45031702 | |||||
| chr15:45031730
|
C | T | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+8381C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031730 | ||||||
| chr15:45031732
|
C | A | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+8383C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031732 | ||||||
| chr15:45031733
|
C | T | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+8384C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031733 | ||||||
| chr15:45031747
|
C | T | 7 | a0001c0001t0001g0245a0002c0002t0003g0027a0002c0002t0003g0091others(4): Show | 7 | HG02257.hp1 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.66+8398C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031747 | ||||||
| chr15:45031765
|
C | A | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+8416C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031765 | ||||||
| chr15:45031803
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.66+8454G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031803 | ||||||
| chr15:45031822
|
T | C | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+8473T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031822 | ||||||
| chr15:45031826
|
T | A | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+8477T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031826 | ||||||
| chr15:45031863
|
C | T | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.66+8514C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031863 | ||||||
| chr15:45031940
|
T | C | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.67-8468T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031940 | ||||||
| chr15:45031945
|
T | TAA | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.67-8461_67-8460dup others(2): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45031945 | |||||
| chr15:45031954
|
C | A | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.67-8454C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031954 | ||||||
| chr15:45031964
|
T | C | 21 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 22 | HG01884.hp1 HG02630.hp1 HG02976.hp2 others(19): Show |
intron_variant | MODIFIER | c.67-8444T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031964 | ||||||
| chr15:45031968
|
G | A | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.67-8440G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031968 | ||||||
| chr15:45031995
|
G | A | 1 | a0001c0001t0001g0289 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.67-8413G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45031995 | ||||||
| chr15:45032192
|
C | T | 21 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(18): Show | 22 | HG01884.hp1 HG02630.hp1 HG02976.hp2 others(19): Show |
intron_variant | MODIFIER | c.67-8216C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032192 | ||||||
| chr15:45032195
|
G | A | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.67-8213G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032195 | ||||||
| chr15:45032201
|
A | C | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.67-8207A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032201 | ||||||
| chr15:45032216
|
A | G | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.67-8192A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032216 | ||||||
| chr15:45032219
|
G | C | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.67-8189G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032219 | ||||||
| chr15:45032239
|
G | GAATATAG others(2): Show |
3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.67-8166_67-8158dup others(9): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45032239 | |||||
| chr15:45032285
|
TG | T | 12 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0291others(9): Show | 12 | HG01934.hp1 HG01943.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.67-8121delG | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45032285 | |||||
| chr15:45032290
|
A | G | 6 | a0001c0001t0007g0215a0001c0008t0007g0214a0002c0002t0007g0226others(3): Show | 6 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.67-8118A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032290 | ||||||
| chr15:45032341
|
G | C | 1 | a0004c0006t0039g0118 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.67-8067G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032341 | ||||||
| chr15:45032345
|
G | A | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.67-8063G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032345 | ||||||
| chr15:45032350
|
A | G | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.67-8058A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032350 | ||||||
| chr15:45032361
|
T | A | 1 | a0001c0001t0001g0228 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.67-8047T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032361 | ||||||
| chr15:45032397
|
T | A | 2 | a0003c0003t0005g0254a0003c0003t0041g0253 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.67-8011T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032397 | ||||||
| chr15:45032400
|
A | G | 1 | a0003c0003t0035g0120 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.67-8008A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032400 | ||||||
| chr15:45032455
|
T | C | 23 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(20): Show | 24 | HG01884.hp1 HG02630.hp1 HG02976.hp2 others(21): Show |
intron_variant | MODIFIER | c.67-7953T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032455 | ||||||
| chr15:45032461
|
G | A | 2 | a0002c0002t0003g0262a0002c0002t0040g0261 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.67-7947G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032461 | ||||||
| chr15:45032569
|
A | G | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.67-7839A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032569 | ||||||
| chr15:45032574
|
G | A | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.67-7834G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032574 | ||||||
| chr15:45032647
|
C | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0026g0134 | 3 | NA19056.hp2 NA19060.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.67-7761C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032647 | ||||||
| chr15:45032720
|
C | T | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.67-7688C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032720 | ||||||
| chr15:45032734
|
G | C | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.67-7674G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032734 | ||||||
| chr15:45032780
|
A | G | 4 | a0001c0001t0007g0026a0002c0002t0013g0029a0002c0002t0013g0030others(1): Show | 4 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-7628A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032780 | ||||||
| chr15:45032818
|
G | A | 13 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0123others(10): Show | 13 | HG01884.hp1 HG02630.hp1 HG02976.hp2 others(10): Show |
intron_variant | MODIFIER | c.67-7590G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032818 | ||||||
| chr15:45032871
|
G | A | 25 | a0001c0001t0001g0028a0001c0001t0001g0064a0001c0001t0001g0065others(22): Show | 26 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(23): Show |
intron_variant | MODIFIER | c.67-7537G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45032871 | ||||||
| chr15:45033006
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.67-7402C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45033006 | ||||||
| chr15:45033325
|
C | G | 3 | a0001c0001t0001g0003a0001c0001t0001g0212a0001c0001t0001g0213 | 5 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-7083C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45033325 | ||||||
| chr15:45033325
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0031g0061 | 2 | NA18992.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.67-7083C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45033325 | ||||||
| chr15:45033421
|
G | A | 7 | a0001c0001t0014g0270a0001c0001t0014g0271a0001c0001t0022g0272others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-6987G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45033421 | ||||||
| chr15:45033495
|
A | T | 1 | a0002c0002t0003g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67-6913A>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45033495 | ||||||
| chr15:45033742
|
A | G | 120 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(117): Show | 125 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.67-6666A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45033742 | ||||||
| chr15:45033936
|
T | G | 11 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0081others(8): Show | 12 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(9): Show |
intron_variant | MODIFIER | c.67-6472T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45033936 | ||||||
| chr15:45033964
|
A | G | 2 | a0001c0001t0008g0107a0004c0006t0039g0118 | 2 | HG02965.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.67-6444A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45033964 | ||||||
| chr15:45034086
|
G | C | 24 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(21): Show | 25 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.67-6322G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45034086 | ||||||
| chr15:45034091
|
G | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(21): Show | 25 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.67-6317G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45034091 | ||||||
| chr15:45034108
|
A | G | 24 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(21): Show | 25 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.67-6300A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45034108 | ||||||
| chr15:45034145
|
T | C | 4 | a0002c0002t0003g0262a0002c0002t0040g0261a0003c0003t0008g0263others(1): Show | 4 | HG01255.hp2 HG02280.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-6263T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45034145 | ||||||
| chr15:45034160
|
T | C | 51 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(48): Show | 53 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.67-6248T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45034160 | ||||||
| chr15:45034187
|
C | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(21): Show | 25 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.67-6221C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45034187 | ||||||
| chr15:45034201
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.67-6207T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45034201 | ||||||
| chr15:45034302
|
A | G | 1 | a0001c0001t0001g0211 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.67-6106A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45034302 | ||||||
| chr15:45034522
|
T | C | 14 | a0001c0001t0007g0026a0002c0002t0002g0227a0002c0002t0002g0236others(11): Show | 14 | HG02486.hp1 HG02559.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.67-5886T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45034522 | ||||||
| chr15:45034565
|
C | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(23): Show | 27 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.67-5843C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45034565 | ||||||
| chr15:45034567
|
G | A | 26 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(23): Show | 27 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.67-5841G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45034567 | ||||||
| chr15:45034568
|
C | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(23): Show | 27 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.67-5840C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45034568 | ||||||
| chr15:45034607
|
G | A | 2 | a0002c0002t0021g0274a0002c0002t0023g0273 | 2 | HG01099.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.67-5801G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45034607 | ||||||
| chr15:45034630
|
G | A | 7 | a0001c0001t0001g0102a0002c0002t0002g0100a0002c0002t0002g0101others(4): Show | 7 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-5778G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45034630 | ||||||
| chr15:45034633
|
C | G | 11 | a0002c0002t0002g0227a0002c0002t0002g0236a0002c0002t0002g0238others(8): Show | 11 | HG02486.hp1 HG02559.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.67-5775C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45034633 | ||||||
| chr15:45034925
|
A | G | 27 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(24): Show | 28 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(25): Show |
intron_variant | MODIFIER | c.67-5483A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45034925 | ||||||
| chr15:45035040
|
G | C | 1 | a0002c0002t0003g0279 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.67-5368G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45035040 | ||||||
| chr15:45035113
|
T | C | 26 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(23): Show | 27 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.67-5295T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45035113 | ||||||
| chr15:45035136
|
T | G | 18 | a0001c0001t0001g0028a0001c0001t0001g0064a0001c0001t0001g0065others(15): Show | 19 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(16): Show |
intron_variant | MODIFIER | c.67-5272T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45035136 | ||||||
| chr15:45035215
|
T | C | 1 | a0003c0003t0001g0025 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.67-5193T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45035215 | ||||||
| chr15:45035301
|
G | A | 1 | a0001c0001t0008g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.67-5107G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45035301 | ||||||
| chr15:45035416
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.67-4992G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45035416 | ||||||
| chr15:45035428
|
T | C | 1 | a0002c0002t0002g0235 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.67-4980T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45035428 | ||||||
| chr15:45035464
|
T | G | 5 | a0001c0001t0001g0109a0001c0001t0017g0083a0001c0001t0017g0084others(2): Show | 6 | HG02109.hp2 HG02257.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.67-4944T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45035464 | ||||||
| chr15:45035465
|
G | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02015.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.67-4943G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45035465 | ||||||
| chr15:45035465
|
G | T | 5 | a0001c0001t0005g0086a0002c0002t0002g0255a0002c0002t0002g0276others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-4943G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45035465 | ||||||
| chr15:45035522
|
C | T | 1 | a0005c0012t0002g0103 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.67-4886C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45035522 | ||||||
| chr15:45035596
|
T | A | 48 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(45): Show | 50 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.67-4812T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45035596 | ||||||
| chr15:45035647
|
G | A | 10 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0123others(7): Show | 10 | HG03017.hp2 HG03130.hp1 HG03579.hp1 others(7): Show |
intron_variant | MODIFIER | c.67-4761G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45035647 | ||||||
| chr15:45035809
|
G | A | 6 | a0002c0004t0004g0015a0002c0004t0004g0016a0002c0004t0004g0017others(3): Show | 6 | HG00438.hp1 HG02056.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-4599G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45035809 | ||||||
| chr15:45035814
|
G | A | 5 | a0001c0001t0005g0086a0002c0002t0002g0255a0002c0002t0002g0276others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-4594G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45035814 | ||||||
| chr15:45036001
|
G | A | 7 | a0001c0001t0014g0270a0001c0001t0014g0271a0001c0001t0022g0272others(4): Show | 7 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-4407G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45036001 | ||||||
| chr15:45036199
|
T | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.67-4209T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45036199 | ||||||
| chr15:45036230
|
A | T | 1 | a0001c0001t0007g0215 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.67-4178A>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45036230 | ||||||
| chr15:45036357
|
T | C | 2 | a0002c0004t0001g0119a0003c0003t0035g0120 | 2 | HG03195.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.67-4051T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45036357 | ||||||
| chr15:45036412
|
C | G | 4 | a0002c0002t0003g0262a0002c0002t0040g0261a0003c0003t0008g0263others(1): Show | 4 | HG01255.hp2 HG02280.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-3996C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45036412 | ||||||
| chr15:45036518
|
T | C | 26 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(23): Show | 27 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.67-3890T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45036518 | ||||||
| chr15:45036558
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.67-3850G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45036558 | ||||||
| chr15:45036585
|
T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(16): Show | 20 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.67-3823T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45036585 | ||||||
| chr15:45036783
|
T | C | 8 | a0001c0001t0001g0220a0001c0001t0001g0222a0002c0002t0001g0216others(5): Show | 8 | HG00639.hp1 HG01069.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.67-3625T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45036783 | ||||||
| chr15:45036794
|
G | GA | 7 | a0001c0001t0001g0041a0001c0001t0001g0138a0001c0001t0001g0140others(4): Show | 7 | HG01109.hp2 HG01123.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-3606dupA | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45036794 | |||||
| chr15:45036822
|
G | C | 1 | a0003c0003t0035g0120 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.67-3586G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45036822 | ||||||
| chr15:45036922
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.67-3486T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45036922 | ||||||
| chr15:45037122
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.67-3286A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45037122 | ||||||
| chr15:45037200
|
C | T | 12 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0291others(9): Show | 12 | HG01934.hp1 HG01943.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.67-3208C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45037200 | ||||||
| chr15:45037234
|
C | T | 2 | a0003c0003t0008g0263a0003c0003t0008g0288 | 2 | HG01255.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.67-3174C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45037234 | ||||||
| chr15:45037269
|
C | G | 1 | a0001c0001t0001g0210 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.67-3139C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45037269 | ||||||
| chr15:45037293
|
G | A | 17 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0068others(14): Show | 18 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.67-3115G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45037293 | ||||||
| chr15:45037312
|
T | C | 2 | a0002c0002t0003g0262a0002c0002t0040g0261 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.67-3096T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45037312 | ||||||
| chr15:45037356
|
C | A | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | HG02735.hp1 HG03239.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.67-3052C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45037356 | ||||||
| chr15:45037528
|
G | A | 4 | a0002c0002t0003g0262a0002c0002t0040g0261a0003c0003t0008g0263others(1): Show | 4 | HG01255.hp2 HG02280.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-2880G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45037528 | ||||||
| chr15:45037530
|
G | C | 24 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(21): Show | 25 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.67-2878G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45037530 | ||||||
| chr15:45037635
|
G | A | 3 | a0001c0001t0001g0070a0001c0001t0001g0143a0001c0001t0038g0144 | 3 | HG00639.hp2 HG01081.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.67-2773G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45037635 | ||||||
| chr15:45037663
|
A | G | 24 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(21): Show | 25 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.67-2745A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45037663 | ||||||
| chr15:45037698
|
G | A | 4 | a0002c0002t0002g0227a0002c0002t0002g0238a0002c0002t0002g0243others(1): Show | 4 | HG02922.hp1 HG06807.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-2710G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45037698 | ||||||
| chr15:45037721
|
T | G | 3 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0078 | 3 | NA18971.hp1 NA18986.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.67-2687T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45037721 | ||||||
| chr15:45037722
|
G | A | 16 | a0001c0001t0001g0088a0001c0001t0001g0138a0001c0001t0001g0140others(13): Show | 16 | HG00597.hp1 HG01109.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.67-2686G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45037722 | ||||||
| chr15:45037781
|
T | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(16): Show | 20 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.67-2627T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45037781 | ||||||
| chr15:45037793
|
G | T | 1 | a0002c0002t0003g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.67-2615G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45037793 | ||||||
| chr15:45037962
|
TA | T | 27 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(24): Show | 28 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(25): Show |
intron_variant | MODIFIER | c.67-2431delA | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45037962 | |||||
| chr15:45037983
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.67-2425G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45037983 | ||||||
| chr15:45037998
|
G | C | 26 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(23): Show | 27 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.67-2410G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45037998 | ||||||
| chr15:45038004
|
T | A | 1 | a0001c0001t0001g0105 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.67-2404T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038004 | ||||||
| chr15:45038102
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.67-2306G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038102 | ||||||
| chr15:45038126
|
C | CCCTT | 32 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0041others(29): Show | 32 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.67-2216_67-2213dup others(4): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45038126 | |||||
| chr15:45038126
|
C | CCCTTCCT others(1): Show |
9 | a0001c0001t0001g0011a0001c0001t0001g0035a0001c0001t0001g0062others(6): Show | 9 | HG01109.hp2 HG01433.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.67-2220_67-2213dup others(8): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45038126 | |||||
| chr15:45038126
|
CCCTT | C | 64 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0051others(61): Show | 66 | HG00140.hp2 HG00597.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.67-2216_67-2213del others(4): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45038126 | |||||
| chr15:45038126
|
CCCTTCCT others(1): Show |
C | 48 | a0001c0001t0001g0002a0001c0001t0001g0044a0001c0001t0001g0070others(45): Show | 50 | HG00558.hp1 HG00735.hp2 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.67-2220_67-2213del others(8): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45038126 | |||||
| chr15:45038126
|
CCCTTCCT others(5): Show |
C | 44 | a0001c0001t0001g0028a0001c0001t0001g0072a0001c0001t0001g0122others(41): Show | 48 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.67-2224_67-2213del others(12): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45038126 | |||||
| chr15:45038126
|
CCCTTCCT others(9): Show |
C | 23 | a0001c0001t0001g0065a0001c0001t0001g0088a0001c0001t0001g0109others(20): Show | 25 | HG00140.hp1 HG01884.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.67-2228_67-2213del others(16): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45038126 | |||||
| chr15:45038126
|
CCCTTCCT others(13): Show |
C | 5 | a0001c0001t0001g0265a0001c0001t0001g0290a0002c0002t0002g0010others(2): Show | 5 | HG01099.hp1 HG01123.hp2 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-2232_67-2213del others(20): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45038126 | |||||
| chr15:45038126
|
CCCTTCCT others(17): Show |
C | 1 | a0001c0001t0001g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.67-2236_67-2213del others(24): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45038126 | |||||
| chr15:45038126
|
CCCTTCCT others(21): Show |
C | 8 | a0001c0001t0001g0096a0001c0001t0001g0291a0002c0002t0003g0292others(5): Show | 8 | HG01934.hp1 HG02004.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.67-2240_67-2213del others(28): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45038126 | |||||
| chr15:45038126
|
CCCTTCCT others(25): Show |
C | 4 | a0001c0001t0001g0092a0002c0002t0012g0268a0003c0003t0005g0095others(1): Show | 4 | HG01943.hp1 HG02559.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-2244_67-2213del others(32): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45038126 | |||||
| chr15:45038128
|
C | CTTCCTTC others(5): Show |
2 | a0001c0001t0001g0081a0002c0002t0013g0031 | 2 | HG01928.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.67-2269_67-2268ins others(12): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45038128 | |||||
| chr15:45038128
|
C | CTTCCTTC others(17): Show |
1 | a0002c0002t0013g0029 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.67-2269_67-2268ins others(24): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45038128 | |||||
| chr15:45038132
|
C | CTTCCTTC others(13): Show |
2 | a0002c0002t0004g0013a0002c0002t0004g0014 | 2 | NA18951.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.67-2269_67-2268ins others(20): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45038132 | |||||
| chr15:45038134
|
T | C | 1 | a0001c0001t0001g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.67-2274T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038134 | ||||||
| chr15:45038136
|
C | CTTCTTTC others(9): Show |
4 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0004g0080others(1): Show | 5 | HG01978.hp2 NA18945.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-2269_67-2268ins others(16): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45038136 | |||||
| chr15:45038140
|
C | T | 8 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0081others(5): Show | 8 | HG01928.hp1 HG03130.hp1 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.67-2268C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038140 | ||||||
| chr15:45038144
|
C | T | 3 | a0001c0001t0005g0086a0001c0001t0029g0284a0001c0008t0001g0283 | 3 | HG02630.hp1 HG03017.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.67-2264C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038144 | ||||||
| chr15:45038148
|
C | T | 5 | a0001c0001t0001g0123a0002c0002t0002g0255a0002c0002t0002g0276others(2): Show | 5 | HG01884.hp1 HG02976.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-2260C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038148 | ||||||
| chr15:45038152
|
C | T | 7 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0286others(4): Show | 7 | HG03130.hp1 HG03927.hp1 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-2256C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038152 | ||||||
| chr15:45038156
|
C | T | 2 | a0001c0001t0029g0284a0001c0008t0001g0283 | 2 | HG03017.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.67-2252C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038156 | ||||||
| chr15:45038204
|
C | G | 19 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(16): Show | 20 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.67-2204C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038204 | ||||||
| chr15:45038512
|
A | G | 26 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(23): Show | 27 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.67-1896A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038512 | ||||||
| chr15:45038533
|
C | G | 2 | a0001c0001t0026g0134a0002c0002t0012g0268 | 2 | HG02559.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.67-1875C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038533 | ||||||
| chr15:45038534
|
G | C | 1 | a0002c0004t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.67-1874G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038534 | ||||||
| chr15:45038622
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.67-1786A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038622 | ||||||
| chr15:45038626
|
A | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.67-1782A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038626 | ||||||
| chr15:45038642
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.67-1766A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038642 | ||||||
| chr15:45038651
|
C | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.67-1757C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038651 | ||||||
| chr15:45038662
|
A | G | 23 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0068others(20): Show | 24 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(21): Show |
intron_variant | MODIFIER | c.67-1746A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038662 | ||||||
| chr15:45038871
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.67-1537G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038871 | ||||||
| chr15:45038876
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.67-1532G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038876 | ||||||
| chr15:45038918
|
C | G | 1 | a0002c0002t0012g0260 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.67-1490C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45038918 | ||||||
| chr15:45039128
|
T | A | 19 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(16): Show | 20 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.67-1280T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45039128 | ||||||
| chr15:45039133
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.67-1275T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45039133 | ||||||
| chr15:45039135
|
C | CT | 45 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(42): Show | 47 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.67-1262dupT | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr15 | 45039135 | |||||
| chr15:45039149
|
G | C | 4 | a0002c0002t0003g0262a0002c0002t0040g0261a0003c0003t0008g0263others(1): Show | 4 | HG01255.hp2 HG02280.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-1259G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45039149 | ||||||
| chr15:45039197
|
G | T | 16 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0068others(13): Show | 17 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.67-1211G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45039197 | ||||||
| chr15:45039265
|
A | G | 7 | a0001c0001t0001g0102a0002c0002t0002g0100a0002c0002t0002g0101others(4): Show | 7 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-1143A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45039265 | ||||||
| chr15:45039273
|
C | T | 1 | a0002c0002t0012g0268 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.67-1135C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45039273 | ||||||
| chr15:45039290
|
G | C | 7 | a0001c0001t0001g0102a0002c0002t0002g0100a0002c0002t0002g0101others(4): Show | 7 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-1118G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45039290 | ||||||
| chr15:45039370
|
C | T | 7 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(4): Show | 7 | HG00621.hp1 HG00673.hp1 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.67-1038C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45039370 | ||||||
| chr15:45039371
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.67-1037G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45039371 | ||||||
| chr15:45039491
|
C | G | 187 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(184): Show | 194 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(191): Show |
intron_variant | MODIFIER | c.67-917C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45039491 | ||||||
| chr15:45039529
|
T | C | 2 | a0003c0003t0008g0263a0003c0003t0008g0288 | 2 | HG01255.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.67-879T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45039529 | ||||||
| chr15:45039638
|
G | C | 9 | a0001c0001t0008g0107a0002c0002t0002g0010a0002c0002t0002g0073others(6): Show | 9 | HG01884.hp2 HG02280.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.67-770G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45039638 | ||||||
| chr15:45039870
|
G | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.67-538G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45039870 | ||||||
| chr15:45040150
|
A | G | 19 | a0001c0001t0005g0086a0001c0001t0007g0026a0002c0002t0002g0227others(16): Show | 19 | HG01884.hp1 HG02486.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.67-258A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45040150 | ||||||
| chr15:45040233
|
G | A | 1 | a0001c0001t0001g0171 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.67-175G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45040233 | ||||||
| chr15:45040246
|
T | A | 1 | a0001c0001t0001g0133 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.67-162T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45040246 | ||||||
| chr15:45040267
|
A | C | 5 | a0001c0001t0005g0086a0002c0002t0002g0255a0002c0002t0002g0276others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-141A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45040267 | ||||||
| chr15:45040316
|
T | A | 26 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(23): Show | 27 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.67-92T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 1/8 | chr15 | 45040316 | ||||||
| chr15:45040471
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.100+30T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45040471 | ||||||
| chr15:45040473
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.100+32A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45040473 | ||||||
| chr15:45040679
|
C | T | 5 | a0001c0001t0005g0086a0002c0002t0002g0255a0002c0002t0002g0276others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+238C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45040679 | ||||||
| chr15:45040824
|
C | G | 2 | a0003c0003t0008g0263a0003c0003t0008g0288 | 2 | HG01255.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.100+383C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45040824 | ||||||
| chr15:45041183
|
C | T | 17 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0068others(14): Show | 18 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.100+742C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45041183 | ||||||
| chr15:45041194
|
G | A | 1 | a0001c0001t0019g0193 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.100+753G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45041194 | ||||||
| chr15:45041248
|
G | A | 14 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0291others(11): Show | 14 | HG01934.hp1 HG01943.hp1 HG01981.hp1 others(11): Show |
intron_variant | MODIFIER | c.100+807G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45041248 | ||||||
| chr15:45041306
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.100+865A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45041306 | ||||||
| chr15:45041312
|
A | G | 4 | a0002c0002t0003g0262a0002c0002t0040g0261a0003c0003t0008g0263others(1): Show | 4 | HG01255.hp2 HG02280.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+871A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45041312 | ||||||
| chr15:45041421
|
T | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0212a0001c0001t0001g0213 | 5 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+980T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45041421 | ||||||
| chr15:45041495
|
G | A | 48 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(45): Show | 50 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.100+1054G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45041495 | ||||||
| chr15:45041722
|
C | T | 1 | a0001c0001t0001g0290 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.100+1281C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45041722 | ||||||
| chr15:45041747
|
C | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.100+1306C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45041747 | ||||||
| chr15:45041762
|
G | A | 1 | a0002c0002t0021g0274 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.100+1321G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45041762 | ||||||
| chr15:45041805
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.100+1364G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45041805 | ||||||
| chr15:45041814
|
T | A | 1 | a0001c0001t0001g0194 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.100+1373T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45041814 | ||||||
| chr15:45041862
|
C | A | 2 | a0001c0001t0022g0272a0001c0001t0032g0277 | 2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.101-1395C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45041862 | ||||||
| chr15:45041882
|
A | G | 7 | a0001c0001t0001g0289a0001c0001t0001g0290a0001c0001t0005g0086others(4): Show | 7 | HG01884.hp1 HG02630.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.101-1375A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45041882 | ||||||
| chr15:45041906
|
G | C | 3 | a0001c0001t0007g0215a0001c0008t0007g0214a0002c0002t0007g0226 | 3 | HG03209.hp2 NA19043.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.101-1351G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45041906 | ||||||
| chr15:45041939
|
C | A | 9 | a0001c0001t0001g0264a0002c0002t0002g0116a0002c0002t0002g0235others(6): Show | 11 | HG00642.hp2 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.101-1318C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45041939 | ||||||
| chr15:45042130
|
G | C | 50 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(47): Show | 52 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.101-1127G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042130 | ||||||
| chr15:45042139
|
A | T | 1 | a0003c0003t0005g0095 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.101-1118A>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042139 | ||||||
| chr15:45042180
|
G | A | 3 | a0003c0003t0005g0256a0003c0003t0005g0257a0003c0003t0005g0259 | 3 | HG02922.hp2 HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.101-1077G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042180 | ||||||
| chr15:45042188
|
T | A | 17 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0068others(14): Show | 18 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.101-1069T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042188 | ||||||
| chr15:45042321
|
G | A | 1 | a0001c0001t0005g0139 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.101-936G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042321 | ||||||
| chr15:45042361
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0248 | 2 | HG02602.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.101-896G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042361 | ||||||
| chr15:45042462
|
A | G | 1 | a0001c0001t0009g0034 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.101-795A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042462 | ||||||
| chr15:45042499
|
A | AAAAT | 7 | a0001c0001t0001g0041a0001c0001t0001g0133a0001c0001t0001g0135others(4): Show | 7 | HG01175.hp1 HG03195.hp1 NA18990.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-730_101-727dup others(4): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr15 | 45042499 | |||||
| chr15:45042499
|
A | AAAATAAA others(5): Show |
2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.101-738_101-727dup others(12): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr15 | 45042499 | |||||
| chr15:45042499
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.101-758A>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042499 | ||||||
| chr15:45042519
|
TAAATAAA others(5): Show |
T | 19 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(16): Show | 20 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.101-737_101-726del others(12): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042519 | ||||||
| chr15:45042523
|
T | G | 2 | a0002c0002t0002g0255a0002c0002t0002g0276 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.101-734T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042523 | ||||||
| chr15:45042523
|
T | TAAAGAAA others(5): Show |
2 | a0002c0002t0003g0279a0003c0003t0001g0275 | 2 | HG01884.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.101-731_101-730ins others(12): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr15 | 45042523 | |||||
| chr15:45042527
|
T | G | 4 | a0002c0002t0002g0255a0002c0002t0002g0276a0002c0002t0003g0279others(1): Show | 4 | HG01884.hp1 HG02976.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-730T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042527 | ||||||
| chr15:45042527
|
T | TAAAGAAA others(5): Show |
1 | a0001c0001t0005g0086 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.101-726_101-725ins others(12): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr15 | 45042527 | |||||
| chr15:45042574
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.101-683C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042574 | ||||||
| chr15:45042608
|
T | G | 2 | a0002c0002t0003g0262a0002c0002t0040g0261 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.101-649T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042608 | ||||||
| chr15:45042631
|
C | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(23): Show | 27 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.101-626C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042631 | ||||||
| chr15:45042726
|
A | G | 2 | a0003c0003t0005g0254a0003c0003t0041g0253 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.101-531A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042726 | ||||||
| chr15:45042728
|
A | G | 2 | a0003c0003t0005g0254a0003c0003t0041g0253 | 2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.101-529A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042728 | ||||||
| chr15:45042730
|
A | C | 58 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(55): Show | 60 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.101-527A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042730 | ||||||
| chr15:45042752
|
T | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(57): Show | 62 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.101-505T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042752 | ||||||
| chr15:45042798
|
T | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(57): Show | 62 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.101-459T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042798 | ||||||
| chr15:45042802
|
T | C | 60 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(57): Show | 62 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.101-455T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042802 | ||||||
| chr15:45042876
|
C | G | 45 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(42): Show | 47 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(44): Show |
intron_variant | MODIFIER | c.101-381C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042876 | ||||||
| chr15:45042902
|
C | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(55): Show | 60 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.101-355C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042902 | ||||||
| chr15:45042970
|
G | A | 1 | a0001c0001t0019g0172 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.101-287G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45042970 | ||||||
| chr15:45043003
|
C | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(23): Show | 27 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(24): Show |
intron_variant | MODIFIER | c.101-254C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45043003 | ||||||
| chr15:45043064
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(16): Show | 20 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.101-193C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45043064 | ||||||
| chr15:45043074
|
C | T | 19 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(16): Show | 20 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.101-183C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45043074 | ||||||
| chr15:45043079
|
T | C | 9 | a0001c0001t0001g0264a0002c0002t0002g0116a0002c0002t0002g0235others(6): Show | 11 | HG00642.hp2 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.101-178T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45043079 | ||||||
| chr15:45043116
|
T | C | 19 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(16): Show | 20 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(17): Show |
intron_variant | MODIFIER | c.101-141T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45043116 | ||||||
| chr15:45043166
|
C | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(21): Show | 25 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.101-91C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45043166 | ||||||
| chr15:45043168
|
A | C | 88 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(85): Show | 90 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.101-89A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45043168 | ||||||
| chr15:45043252
|
A | G | 1 | a0001c0001t0008g0108 | 1 | HG02572.hp1 | splice_region_variant&intron_variant | LOW | c.101-5A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 2/8 | chr15 | 45043252 | ||||||
| chr15:45043582
|
C | G | 31 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(28): Show | 32 | HG00140.hp2 HG00735.hp2 HG01517.hp1 others(29): Show |
intron_variant | MODIFIER | c.265+161C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45043582 | ||||||
| chr15:45043815
|
C | A | 59 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(56): Show | 61 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.265+394C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45043815 | ||||||
| chr15:45043838
|
C | G | 1 | a0002c0002t0037g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.265+417C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45043838 | ||||||
| chr15:45043842
|
C | T | 4 | a0001c0001t0001g0102a0002c0002t0002g0100a0002c0002t0002g0101others(1): Show | 4 | HG02886.hp2 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+421C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45043842 | ||||||
| chr15:45043891
|
C | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(21): Show | 25 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.265+470C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45043891 | ||||||
| chr15:45043967
|
C | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.265+546C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45043967 | ||||||
| chr15:45044023
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.265+602A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044023 | ||||||
| chr15:45044104
|
G | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.265+683G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044104 | ||||||
| chr15:45044107
|
T | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.265+686T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044107 | ||||||
| chr15:45044132
|
T | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.265+711T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044132 | ||||||
| chr15:45044331
|
G | T | 13 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0291others(10): Show | 13 | HG01934.hp1 HG01943.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.265+910G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044331 | ||||||
| chr15:45044376
|
C | T | 24 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(21): Show | 25 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.265+955C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044376 | ||||||
| chr15:45044460
|
T | C | 9 | a0001c0001t0008g0107a0002c0002t0002g0010a0002c0002t0002g0073others(6): Show | 9 | HG01884.hp2 HG02280.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.265+1039T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044460 | ||||||
| chr15:45044702
|
CT | C | 268 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(265): Show | 279 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.265+1297delT | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 45044702 | |||||
| chr15:45044741
|
C | G | 4 | a0002c0002t0011g0293a0003c0003t0001g0294a0003c0003t0001g0296others(1): Show | 4 | HG01891.hp2 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+1320C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044741 | ||||||
| chr15:45044751
|
T | G | 5 | a0001c0001t0005g0086a0002c0002t0002g0255a0002c0002t0002g0276others(2): Show | 5 | HG01884.hp1 HG02630.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+1330T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044751 | ||||||
| chr15:45044823
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0133a0001c0001t0001g0196 | 5 | HG00558.hp1 NA18945.hp2 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+1402G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044823 | ||||||
| chr15:45044898
|
G | A | 47 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0032others(44): Show | 49 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.265+1477G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044898 | ||||||
| chr15:45044936
|
G | T | 1 | a0002c0002t0037g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.265+1515G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044936 | ||||||
| chr15:45044938
|
T | A | 1 | a0002c0002t0037g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.265+1517T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044938 | ||||||
| chr15:45044939
|
C | T | 1 | a0002c0002t0037g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.265+1518C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044939 | ||||||
| chr15:45044944
|
C | T | 1 | a0002c0002t0037g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.265+1523C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044944 | ||||||
| chr15:45044950
|
T | G | 1 | a0002c0002t0037g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.265+1529T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044950 | ||||||
| chr15:45044955
|
C | T | 1 | a0002c0002t0037g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.265+1534C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044955 | ||||||
| chr15:45044961
|
C | G | 1 | a0002c0002t0037g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.265+1540C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044961 | ||||||
| chr15:45044963
|
G | T | 1 | a0002c0002t0037g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.265+1542G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044963 | ||||||
| chr15:45044968
|
G | A | 1 | a0002c0002t0037g0117 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.265+1547G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45044968 | ||||||
| chr15:45045049
|
T | C | 1 | a0001c0001t0005g0285 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.265+1628T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45045049 | ||||||
| chr15:45045305
|
T | C | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(267): Show | 281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.265+1884T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45045305 | ||||||
| chr15:45045332
|
G | A | 2 | a0003c0003t0001g0038a0003c0003t0001g0039 | 2 | NA18993.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.265+1911G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45045332 | ||||||
| chr15:45045544
|
CAA | C | 9 | a0001c0001t0001g0146a0001c0001t0001g0151a0001c0001t0001g0220others(6): Show | 9 | HG01884.hp1 HG02074.hp2 HG02148.hp1 others(6): Show |
intron_variant | MODIFIER | c.265+2147_265+2148d others(4): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 45045544 | |||||
| chr15:45045544
|
CAAA | C | 183 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(180): Show | 190 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.265+2146_265+2148d others(5): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 45045544 | |||||
| chr15:45045544
|
CAAAA | C | 64 | a0001c0001t0001g0044a0001c0001t0001g0059a0001c0001t0001g0092others(61): Show | 67 | HG00642.hp2 HG01099.hp1 HG01109.hp1 others(64): Show |
intron_variant | MODIFIER | c.265+2145_265+2148d others(6): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 45045544 | |||||
| chr15:45045544
|
CAAAAA | C | 19 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0068others(16): Show | 20 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.265+2144_265+2148d others(7): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 45045544 | |||||
| chr15:45045583
|
A | G | 3 | a0002c0004t0004g0004a0002c0004t0004g0022a0002c0004t0009g0023 | 4 | NA18973.hp1 NA18990.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+2162A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45045583 | ||||||
| chr15:45045591
|
A | G | 13 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0291others(10): Show | 13 | HG01934.hp1 HG01943.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.265+2170A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45045591 | ||||||
| chr15:45045744
|
C | A | 8 | a0001c0001t0001g0041a0001c0001t0001g0106a0001c0001t0001g0132others(5): Show | 8 | NA18970.hp1 NA18990.hp1 NA18997.hp1 others(5): Show |
intron_variant | MODIFIER | c.265+2323C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45045744 | ||||||
| chr15:45045769
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.265+2348C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45045769 | ||||||
| chr15:45045858
|
G | A | 2 | a0002c0002t0002g0255a0002c0002t0002g0276 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.265+2437G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45045858 | ||||||
| chr15:45045926
|
A | G | 9 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0081others(6): Show | 10 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.265+2505A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45045926 | ||||||
| chr15:45046046
|
G | C | 6 | a0001c0001t0001g0158a0001c0001t0001g0205a0001c0001t0001g0206others(3): Show | 6 | HG02056.hp2 NA18747.hp2 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.265+2625G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45046046 | ||||||
| chr15:45046133
|
G | C | 23 | a0001c0001t0001g0011a0001c0001t0001g0129a0001c0001t0001g0135others(20): Show | 23 | HG00639.hp1 HG01069.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.265+2712G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45046133 | ||||||
| chr15:45046273
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.265+2852C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45046273 | ||||||
| chr15:45046431
|
A | C | 4 | a0002c0002t0003g0262a0002c0002t0040g0261a0003c0003t0008g0263others(1): Show | 4 | HG01255.hp2 HG02280.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+3010A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45046431 | ||||||
| chr15:45046514
|
T | A | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(267): Show | 281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.265+3093T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45046514 | ||||||
| chr15:45046626
|
C | A | 1 | a0001c0001t0007g0215 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.265+3205C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45046626 | ||||||
| chr15:45046640
|
C | T | 1 | a0002c0002t0003g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.265+3219C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45046640 | ||||||
| chr15:45046741
|
G | T | 1 | a0002c0002t0002g0101 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.265+3320G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45046741 | ||||||
| chr15:45046879
|
G | A | 1 | a0001c0001t0005g0086 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.265+3458G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45046879 | ||||||
| chr15:45046885
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.265+3464G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45046885 | ||||||
| chr15:45047308
|
T | C | 9 | a0001c0001t0001g0264a0002c0002t0002g0116a0002c0002t0002g0235others(6): Show | 11 | HG00642.hp2 HG01891.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.265+3887T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45047308 | ||||||
| chr15:45047313
|
T | C | 9 | a0001c0001t0001g0264a0002c0002t0002g0116a0002c0002t0002g0235others(6): Show | 11 | HG00642.hp2 HG01891.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.265+3892T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45047313 | ||||||
| chr15:45047316
|
T | G | 9 | a0001c0001t0001g0264a0002c0002t0002g0116a0002c0002t0002g0235others(6): Show | 11 | HG00642.hp2 HG01891.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.265+3895T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45047316 | ||||||
| chr15:45047401
|
C | T | 2 | a0002c0002t0003g0111a0002c0004t0004g0022 | 2 | HG03453.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.265+3980C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45047401 | ||||||
| chr15:45047909
|
G | A | 2 | a0001c0001t0001g0232a0001c0001t0001g0233 | 2 | HG02523.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.265+4488G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45047909 | ||||||
| chr15:45047982
|
A | G | 1 | a0001c0001t0001g0064 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.265+4561A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45047982 | ||||||
| chr15:45048044
|
C | T | 1 | a0004c0005t0001g0006 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.265+4623C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45048044 | ||||||
| chr15:45048232
|
C | T | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(244): Show | 257 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(254): Show |
intron_variant | MODIFIER | c.265+4811C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45048232 | ||||||
| chr15:45048483
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.265+5062A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45048483 | ||||||
| chr15:45048648
|
G | A | 7 | a0001c0001t0001g0178a0001c0001t0001g0191a0001c0001t0001g0192others(4): Show | 7 | HG00642.hp1 HG01074.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.265+5227G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45048648 | ||||||
| chr15:45048668
|
G | A | 1 | a0002c0002t0004g0013 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.265+5247G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45048668 | ||||||
| chr15:45048778
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.265+5357C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45048778 | ||||||
| chr15:45048893
|
T | C | 4 | a0002c0002t0002g0227a0002c0002t0002g0238a0002c0002t0002g0243others(1): Show | 4 | HG02922.hp1 HG06807.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+5472T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45048893 | ||||||
| chr15:45048956
|
G | A | 4 | a0002c0002t0003g0262a0002c0002t0040g0261a0003c0003t0008g0263others(1): Show | 4 | HG01255.hp2 HG02280.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+5535G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45048956 | ||||||
| chr15:45049060
|
G | A | 1 | a0001c0001t0001g0191 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.265+5639G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45049060 | ||||||
| chr15:45049063
|
G | C | 1 | a0002c0004t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.265+5642G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45049063 | ||||||
| chr15:45049073
|
T | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.265+5652T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45049073 | ||||||
| chr15:45049183
|
C | A | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(267): Show | 281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.265+5762C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45049183 | ||||||
| chr15:45049411
|
C | T | 247 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(244): Show | 257 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(254): Show |
intron_variant | MODIFIER | c.265+5990C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45049411 | ||||||
| chr15:45049520
|
A | C | 249 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(246): Show | 259 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(256): Show |
intron_variant | MODIFIER | c.265+6099A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45049520 | ||||||
| chr15:45049565
|
T | C | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(268): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.265+6144T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45049565 | ||||||
| chr15:45049676
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.265+6255T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45049676 | ||||||
| chr15:45049684
|
T | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0065 | 2 | HG00140.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.265+6263T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45049684 | ||||||
| chr15:45049773
|
T | G | 1 | a0003c0003t0005g0254 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.265+6352T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45049773 | ||||||
| chr15:45050144
|
G | A | 1 | a0002c0002t0003g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.265+6723G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45050144 | ||||||
| chr15:45050358
|
C | T | 3 | a0001c0001t0001g0088a0001c0001t0001g0151a0001c0001t0030g0154 | 3 | NA18612.hp1 NA19007.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.265+6937C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45050358 | ||||||
| chr15:45050363
|
G | A | 13 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0291others(10): Show | 13 | HG01934.hp1 HG01943.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.265+6942G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45050363 | ||||||
| chr15:45050372
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0131a0001c0001t0001g0157others(1): Show | 5 | HG00323.hp1 HG01106.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.265+6951C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45050372 | ||||||
| chr15:45050382
|
T | A | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(267): Show | 281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.265+6961T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45050382 | ||||||
| chr15:45050924
|
C | T | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(269): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.265+7503C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45050924 | ||||||
| chr15:45050958
|
C | T | 13 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0291others(10): Show | 13 | HG01934.hp1 HG01943.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.265+7537C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45050958 | ||||||
| chr15:45051238
|
T | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.265+7817T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45051238 | ||||||
| chr15:45051245
|
T | C | 1 | a0001c0001t0001g0032 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.265+7824T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45051245 | ||||||
| chr15:45051309
|
C | T | 3 | a0001c0001t0001g0003a0001c0001t0001g0212a0001c0001t0001g0213 | 5 | HG00738.hp2 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.265+7888C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45051309 | ||||||
| chr15:45051497
|
G | A | 1 | a0001c0001t0025g0047 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.265+8076G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45051497 | ||||||
| chr15:45051521
|
A | C | 3 | a0001c0001t0007g0026a0003c0003t0001g0024a0003c0003t0001g0025 | 3 | HG02622.hp2 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.265+8100A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45051521 | ||||||
| chr15:45051580
|
C | T | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(272): Show | 286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.265+8159C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45051580 | ||||||
| chr15:45051631
|
A | G | 1 | a0001c0001t0001g0188 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.265+8210A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45051631 | ||||||
| chr15:45051744
|
G | C | 1 | a0001c0001t0001g0085 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.265+8323G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45051744 | ||||||
| chr15:45051888
|
T | C | 236 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(233): Show | 246 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(243): Show |
intron_variant | MODIFIER | c.265+8467T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45051888 | ||||||
| chr15:45052023
|
T | C | 249 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(246): Show | 259 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(256): Show |
intron_variant | MODIFIER | c.265+8602T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45052023 | ||||||
| chr15:45052028
|
T | A | 249 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(246): Show | 259 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(256): Show |
intron_variant | MODIFIER | c.265+8607T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45052028 | ||||||
| chr15:45052115
|
A | C | 4 | a0001c0001t0001g0102a0002c0002t0002g0100a0002c0002t0002g0101others(1): Show | 4 | HG02886.hp2 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.265+8694A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45052115 | ||||||
| chr15:45052385
|
T | C | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG02015.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.266-8682T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45052385 | ||||||
| chr15:45052414
|
G | C | 1 | a0001c0001t0008g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.266-8653G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45052414 | ||||||
| chr15:45052438
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.266-8629G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45052438 | ||||||
| chr15:45052650
|
T | C | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(269): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.266-8417T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45052650 | ||||||
| chr15:45052671
|
T | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.266-8396T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45052671 | ||||||
| chr15:45052745
|
C | T | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | HG02735.hp1 HG03239.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.266-8322C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45052745 | ||||||
| chr15:45052860
|
G | T | 1 | a0002c0002t0003g0111 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.266-8207G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45052860 | ||||||
| chr15:45052864
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.266-8203G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45052864 | ||||||
| chr15:45053120
|
A | C | 1 | a0002c0002t0012g0268 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.266-7947A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45053120 | ||||||
| chr15:45053324
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.266-7743G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45053324 | ||||||
| chr15:45053543
|
C | T | 8 | a0001c0001t0001g0041a0001c0001t0001g0106a0001c0001t0001g0132others(5): Show | 8 | NA18970.hp1 NA18990.hp1 NA18997.hp1 others(5): Show |
intron_variant | MODIFIER | c.266-7524C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45053543 | ||||||
| chr15:45053754
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.266-7313A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45053754 | ||||||
| chr15:45053809
|
C | A | 275 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(272): Show | 286 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.266-7258C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45053809 | ||||||
| chr15:45053824
|
G | A | 5 | a0002c0002t0006g0239a0002c0002t0006g0240a0002c0002t0006g0241others(2): Show | 5 | HG02486.hp1 HG02559.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.266-7243G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45053824 | ||||||
| chr15:45053924
|
C | T | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(269): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.266-7143C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45053924 | ||||||
| chr15:45054015
|
C | G | 1 | a0001c0001t0008g0108 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.266-7052C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45054015 | ||||||
| chr15:45054062
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.266-7005G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45054062 | ||||||
| chr15:45054093
|
T | C | 273 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(270): Show | 284 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.266-6974T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45054093 | ||||||
| chr15:45054233
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.266-6834G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45054233 | ||||||
| chr15:45054290
|
A | G | 1 | a0002c0004t0004g0020 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.266-6777A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45054290 | ||||||
| chr15:45054292
|
T | C | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(269): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.266-6775T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45054292 | ||||||
| chr15:45054299
|
A | C | 3 | a0001c0001t0001g0096a0002c0007t0010g0097a0002c0007t0010g0098 | 3 | HG02895.hp2 HG02897.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.266-6768A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45054299 | ||||||
| chr15:45054363
|
T | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.266-6704T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45054363 | ||||||
| chr15:45054472
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.266-6595G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45054472 | ||||||
| chr15:45054496
|
G | C | 1 | a0001c0001t0001g0157 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.266-6571G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45054496 | ||||||
| chr15:45054906
|
C | T | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(267): Show | 281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.266-6161C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45054906 | ||||||
| chr15:45054932
|
G | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.266-6135G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45054932 | ||||||
| chr15:45054938
|
C | T | 11 | a0001c0001t0001g0102a0002c0002t0002g0100a0002c0002t0002g0101others(8): Show | 11 | HG01891.hp2 HG02145.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.266-6129C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45054938 | ||||||
| chr15:45054940
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.266-6127A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45054940 | ||||||
| chr15:45054963
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.266-6104T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45054963 | ||||||
| chr15:45054967
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.266-6100A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45054967 | ||||||
| chr15:45054992
|
T | C | 1 | a0003c0003t0035g0120 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.266-6075T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45054992 | ||||||
| chr15:45055015
|
T | C | 1 | a0001c0001t0001g0126 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.266-6052T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45055015 | ||||||
| chr15:45055018
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.266-6049T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45055018 | ||||||
| chr15:45055045
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.266-6022G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45055045 | ||||||
| chr15:45055077
|
C | T | 1 | a0001c0001t0001g0174 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.266-5990C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45055077 | ||||||
| chr15:45055107
|
T | C | 1 | a0001c0001t0001g0174 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.266-5960T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45055107 | ||||||
| chr15:45055128
|
G | C | 1 | a0001c0001t0001g0174 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.266-5939G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45055128 | ||||||
| chr15:45055159
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.266-5908A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45055159 | ||||||
| chr15:45055179
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.266-5888A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45055179 | ||||||
| chr15:45055316
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.266-5751C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45055316 | ||||||
| chr15:45055579
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | NA18985.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.266-5488C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45055579 | ||||||
| chr15:45055620
|
A | G | 21 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0068others(18): Show | 22 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(19): Show |
intron_variant | MODIFIER | c.266-5447A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45055620 | ||||||
| chr15:45055642
|
A | G | 3 | a0002c0002t0003g0252a0002c0002t0011g0251a0004c0006t0011g0250 | 3 | HG02630.hp2 HG02809.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.266-5425A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45055642 | ||||||
| chr15:45055662
|
C | T | 4 | a0002c0002t0003g0262a0002c0002t0040g0261a0003c0003t0008g0263others(1): Show | 4 | HG01255.hp2 HG02280.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-5405C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45055662 | ||||||
| chr15:45055774
|
T | G | 249 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(246): Show | 259 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(256): Show |
intron_variant | MODIFIER | c.266-5293T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45055774 | ||||||
| chr15:45055839
|
G | A | 4 | a0002c0002t0003g0262a0002c0002t0040g0261a0003c0003t0008g0263others(1): Show | 4 | HG01255.hp2 HG02280.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-5228G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45055839 | ||||||
| chr15:45055891
|
C | T | 17 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0068others(14): Show | 18 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.266-5176C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45055891 | ||||||
| chr15:45055892
|
G | A | 2 | a0001c0001t0001g0059a0001c0001t0025g0047 | 2 | NA18955.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.266-5175G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45055892 | ||||||
| chr15:45056104
|
A | G | 17 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0068others(14): Show | 18 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.266-4963A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45056104 | ||||||
| chr15:45056239
|
T | A | 1 | a0001c0001t0001g0041 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.266-4828T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45056239 | ||||||
| chr15:45056240
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.266-4827C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45056240 | ||||||
| chr15:45056242
|
C | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.266-4825C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45056242 | ||||||
| chr15:45056278
|
C | G | 270 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(267): Show | 281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.266-4789C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45056278 | ||||||
| chr15:45056443
|
C | T | 2 | a0002c0002t0003g0262a0002c0002t0040g0261 | 2 | HG02280.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.266-4624C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45056443 | ||||||
| chr15:45056563
|
C | A | 22 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0033others(19): Show | 23 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(20): Show |
intron_variant | MODIFIER | c.266-4504C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45056563 | ||||||
| chr15:45056593
|
T | A | 4 | a0001c0001t0001g0102a0002c0002t0002g0100a0002c0002t0002g0101others(1): Show | 4 | HG02886.hp2 HG03139.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-4474T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45056593 | ||||||
| chr15:45057523
|
G | A | 3 | a0001c0001t0007g0026a0003c0003t0001g0024a0003c0003t0001g0025 | 3 | HG02622.hp2 HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.266-3544G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45057523 | ||||||
| chr15:45057612
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.266-3455G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45057612 | ||||||
| chr15:45057639
|
C | T | 3 | a0002c0002t0002g0010a0002c0002t0002g0077a0002c0002t0002g0099 | 3 | HG01884.hp2 HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.266-3428C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45057639 | ||||||
| chr15:45057667
|
C | T | 21 | a0001c0001t0001g0005a0001c0001t0001g0032a0001c0001t0001g0079others(18): Show | 22 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(19): Show |
intron_variant | MODIFIER | c.266-3400C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45057667 | ||||||
| chr15:45057698
|
G | A | 2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG02004.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.266-3369G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45057698 | ||||||
| chr15:45057782
|
C | CA | 7 | a0001c0001t0001g0102a0002c0002t0002g0100a0002c0002t0002g0101others(4): Show | 7 | HG02630.hp2 HG02809.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.266-3277dupA | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 45057782 | |||||
| chr15:45057793
|
AAAAG | A | 3 | a0001c0001t0001g0286a0001c0001t0005g0285a0001c0008t0001g0283 | 3 | HG03927.hp1 HG04115.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.266-3258_266-3255d others(6): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 45057793 | |||||
| chr15:45058218
|
G | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.266-2849G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45058218 | ||||||
| chr15:45058218
|
G | T | 267 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(264): Show | 278 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.266-2849G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45058218 | ||||||
| chr15:45058360
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.266-2707G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45058360 | ||||||
| chr15:45058384
|
C | A | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.266-2683C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45058384 | ||||||
| chr15:45058449
|
C | T | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | HG02735.hp1 HG03239.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.266-2618C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45058449 | ||||||
| chr15:45058763
|
C | A | 271 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(268): Show | 282 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.266-2304C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45058763 | ||||||
| chr15:45058925
|
C | A | 1 | a0001c0001t0008g0108 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.266-2142C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45058925 | ||||||
| chr15:45058948
|
C | T | 3 | a0002c0002t0011g0293a0003c0003t0001g0275a0004c0006t0002g0295 | 3 | HG01884.hp1 HG01891.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.266-2119C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45058948 | ||||||
| chr15:45059166
|
T | C | 17 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0068others(14): Show | 18 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.266-1901T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45059166 | ||||||
| chr15:45059171
|
G | A | 17 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0068others(14): Show | 18 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.266-1896G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45059171 | ||||||
| chr15:45059349
|
C | A | 11 | a0002c0002t0002g0227a0002c0002t0002g0236a0002c0002t0002g0238others(8): Show | 11 | HG02486.hp1 HG02559.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.266-1718C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45059349 | ||||||
| chr15:45059374
|
A | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.266-1693A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45059374 | ||||||
| chr15:45059465
|
A | G | 1 | a0002c0002t0003g0280 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.266-1602A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45059465 | ||||||
| chr15:45059542
|
G | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.266-1525G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45059542 | ||||||
| chr15:45059551
|
T | C | 4 | a0002c0002t0003g0262a0002c0002t0040g0261a0003c0003t0008g0263others(1): Show | 4 | HG01255.hp2 HG02280.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-1516T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45059551 | ||||||
| chr15:45059589
|
G | C | 272 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(269): Show | 283 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.266-1478G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45059589 | ||||||
| chr15:45059663
|
A | T | 17 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0068others(14): Show | 18 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.266-1404A>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45059663 | ||||||
| chr15:45059715
|
T | G | 4 | a0002c0002t0011g0293a0003c0003t0001g0294a0003c0003t0001g0296others(1): Show | 4 | HG01891.hp2 HG02145.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-1352T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45059715 | ||||||
| chr15:45059725
|
T | C | 4 | a0002c0002t0003g0262a0002c0002t0040g0261a0003c0003t0008g0263others(1): Show | 4 | HG01255.hp2 HG02280.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-1342T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45059725 | ||||||
| chr15:45059810
|
A | G | 1 | a0001c0001t0029g0284 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.266-1257A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45059810 | ||||||
| chr15:45059836
|
C | T | 17 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0068others(14): Show | 18 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.266-1231C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45059836 | ||||||
| chr15:45060095
|
T | C | 1 | a0003c0003t0001g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.266-972T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45060095 | ||||||
| chr15:45060206
|
A | G | 3 | a0002c0002t0013g0029a0002c0002t0013g0030a0002c0002t0013g0031 | 3 | HG01928.hp1 HG01978.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.266-861A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45060206 | ||||||
| chr15:45060236
|
T | TA | 4 | a0002c0002t0003g0262a0002c0002t0040g0261a0003c0003t0008g0263others(1): Show | 4 | HG01255.hp2 HG02280.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.266-830dupA | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 45060236 | |||||
| chr15:45060273
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.266-794G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45060273 | ||||||
| chr15:45060301
|
C | T | 3 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233 | 3 | HG00597.hp2 HG02523.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.266-766C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45060301 | ||||||
| chr15:45060743
|
A | AG | 266 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(263): Show | 277 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.266-321dupG | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr15 | 45060743 | |||||
| chr15:45060848
|
A | G | 3 | a0001c0001t0005g0086a0002c0002t0002g0255a0002c0002t0002g0276 | 3 | HG02630.hp1 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.266-219A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45060848 | ||||||
| chr15:45060867
|
G | A | 17 | a0001c0001t0001g0028a0001c0001t0001g0065a0001c0001t0001g0068others(14): Show | 18 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.266-200G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45060867 | ||||||
| chr15:45061011
|
C | T | 1 | a0002c0004t0004g0020 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.266-56C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45061011 | ||||||
| chr15:45061032
|
C | T | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(247): Show | 260 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(257): Show |
intron_variant | MODIFIER | c.266-35C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 3/8 | chr15 | 45061032 | ||||||
| chr15:45061272
|
T | A | 3 | a0001c0001t0005g0086a0002c0002t0002g0255a0002c0002t0002g0276 | 3 | HG02630.hp1 HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.425+46T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45061272 | ||||||
| chr15:45061439
|
T | C | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG03239.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.425+213T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45061439 | ||||||
| chr15:45061508
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.425+282G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45061508 | ||||||
| chr15:45061565
|
C | G | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG03239.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.425+339C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45061565 | ||||||
| chr15:45061566
|
GTCATAAC others(303): Show |
G | 2 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | HG03239.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.425+341_425+650del | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45061566 | ||||||
| chr15:45061585
|
C | T | 5 | a0001c0001t0001g0106a0001c0001t0001g0123a0001c0001t0001g0162others(2): Show | 5 | HG03654.hp1 NA19001.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.425+359C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45061585 | ||||||
| chr15:45061663
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.425+437C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45061663 | ||||||
| chr15:45061668
|
C | A | 1 | a0001c0001t0001g0032 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.425+442C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45061668 | ||||||
| chr15:45061829
|
A | C | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.425+603A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45061829 | ||||||
| chr15:45061837
|
C | G | 1 | a0002c0002t0001g0218 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.425+611C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45061837 | ||||||
| chr15:45061863
|
C | T | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | NA18969.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.425+637C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45061863 | ||||||
| chr15:45061926
|
C | T | 3 | a0001c0001t0001g0245a0002c0007t0010g0278a0003c0003t0008g0225 | 3 | HG02257.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.425+700C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45061926 | ||||||
| chr15:45061969
|
C | T | 28 | a0001c0001t0001g0003a0001c0001t0001g0058a0001c0001t0001g0070others(25): Show | 30 | HG00140.hp2 HG00639.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.425+743C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45061969 | ||||||
| chr15:45061988
|
C | G | 2 | a0001c0001t0001g0141a0001c0001t0001g0265 | 2 | HG01123.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.425+762C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45061988 | ||||||
| chr15:45062006
|
T | A | 21 | a0001c0001t0001g0005a0001c0001t0001g0058a0001c0001t0001g0079others(18): Show | 22 | HG01496.hp2 HG01928.hp1 HG01978.hp2 others(19): Show |
intron_variant | MODIFIER | c.425+780T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062006 | ||||||
| chr15:45062018
|
T | G | 62 | a0001c0001t0001g0005a0001c0001t0001g0058a0001c0001t0001g0068others(59): Show | 64 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(61): Show |
intron_variant | MODIFIER | c.425+792T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062018 | ||||||
| chr15:45062023
|
C | A | 11 | a0001c0001t0001g0058a0001c0001t0001g0168a0001c0001t0001g0174others(8): Show | 11 | NA18747.hp2 NA18951.hp2 NA18957.hp1 others(8): Show |
intron_variant | MODIFIER | c.425+797C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062023 | ||||||
| chr15:45062035
|
A | C | 29 | a0001c0001t0001g0005a0001c0001t0001g0036a0001c0001t0001g0037others(26): Show | 30 | HG00621.hp1 HG00673.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.425+809A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062035 | ||||||
| chr15:45062040
|
G | C | 2 | a0001c0001t0001g0147a0001c0001t0027g0149 | 2 | NA18964.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.425+814G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062040 | ||||||
| chr15:45062050
|
A | C | 1 | a0001c0001t0001g0173 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.425+824A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062050 | ||||||
| chr15:45062111
|
G | A | 25 | a0001c0001t0001g0179a0001c0001t0008g0107a0002c0002t0002g0116others(22): Show | 28 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.425+885G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062111 | ||||||
| chr15:45062128
|
TG | T | 38 | a0001c0001t0001g0005a0001c0001t0001g0058a0001c0001t0001g0079others(35): Show | 39 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.425+904delG | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr15 | 45062128 | |||||
| chr15:45062134
|
G | A | 38 | a0001c0001t0001g0005a0001c0001t0001g0058a0001c0001t0001g0079others(35): Show | 39 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.425+908G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062134 | ||||||
| chr15:45062135
|
C | A | 38 | a0001c0001t0001g0005a0001c0001t0001g0058a0001c0001t0001g0079others(35): Show | 39 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.425+909C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062135 | ||||||
| chr15:45062135
|
C | T | 1 | a0001c0001t0001g0032 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.425+909C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062135 | ||||||
| chr15:45062140
|
T | C | 38 | a0001c0001t0001g0005a0001c0001t0001g0058a0001c0001t0001g0079others(35): Show | 39 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.425+914T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062140 | ||||||
| chr15:45062142
|
C | T | 38 | a0001c0001t0001g0005a0001c0001t0001g0058a0001c0001t0001g0079others(35): Show | 39 | HG01099.hp1 HG01109.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.425+916C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062142 | ||||||
| chr15:45062171
|
C | G | 216 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(213): Show | 225 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(222): Show |
intron_variant | MODIFIER | c.425+945C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062171 | ||||||
| chr15:45062185
|
G | A | 31 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0081others(28): Show | 32 | HG01099.hp1 HG01109.hp1 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.425+959G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062185 | ||||||
| chr15:45062188
|
A | T | 41 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0001g0081others(38): Show | 42 | HG01099.hp1 HG01109.hp1 HG01891.hp2 others(39): Show |
intron_variant | MODIFIER | c.425+962A>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062188 | ||||||
| chr15:45062256
|
G | A | 1 | a0002c0002t0023g0273 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.425+1030G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062256 | ||||||
| chr15:45062309
|
G | A | 6 | a0001c0001t0001g0167a0001c0001t0005g0139a0001c0001t0016g0159others(3): Show | 6 | HG01934.hp1 HG01981.hp1 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.425+1083G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062309 | ||||||
| chr15:45062310
|
A | G | 1 | a0001c0001t0022g0272 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.425+1084A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062310 | ||||||
| chr15:45062315
|
C | T | 1 | a0003c0003t0015g0009 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.425+1089C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062315 | ||||||
| chr15:45062373
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.425+1147G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062373 | ||||||
| chr15:45062470
|
C | T | 23 | a0001c0001t0001g0043a0001c0001t0001g0046a0001c0001t0001g0057others(20): Show | 24 | HG00735.hp2 HG01081.hp2 HG01934.hp2 others(21): Show |
intron_variant | MODIFIER | c.425+1244C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062470 | ||||||
| chr15:45062506
|
G | A | 47 | a0001c0001t0001g0005a0001c0001t0001g0033a0001c0001t0001g0096others(44): Show | 48 | HG00438.hp1 HG00558.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.425+1280G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062506 | ||||||
| chr15:45062605
|
G | A | 6 | a0001c0001t0008g0107a0001c0001t0017g0083a0001c0001t0017g0084others(3): Show | 6 | HG02572.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.425+1379G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062605 | ||||||
| chr15:45062706
|
C | G | 143 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(140): Show | 150 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.425+1480C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062706 | ||||||
| chr15:45062734
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.425+1508C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062734 | ||||||
| chr15:45062735
|
G | A | 30 | a0001c0001t0001g0065a0001c0001t0001g0289a0001c0001t0005g0139others(27): Show | 32 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.425+1509G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062735 | ||||||
| chr15:45062778
|
T | C | 1 | a0004c0005t0024g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.425+1552T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062778 | ||||||
| chr15:45062810
|
G | A | 152 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0035others(149): Show | 160 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.425+1584G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062810 | ||||||
| chr15:45062866
|
G | A | 183 | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0011others(180): Show | 192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.425+1640G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062866 | ||||||
| chr15:45062950
|
A | G | 24 | a0001c0001t0001g0070a0001c0001t0007g0215a0002c0002t0002g0116others(21): Show | 27 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.425+1724A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062950 | ||||||
| chr15:45062951
|
A | C | 1 | a0001c0001t0001g0211 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.425+1725A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062951 | ||||||
| chr15:45062951
|
A | G | 24 | a0001c0001t0001g0070a0001c0001t0007g0215a0002c0002t0002g0116others(21): Show | 27 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.425+1725A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062951 | ||||||
| chr15:45062954
|
C | T | 1 | a0002c0004t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.425+1728C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062954 | ||||||
| chr15:45062969
|
C | T | 14 | a0002c0002t0002g0116a0002c0002t0002g0227a0002c0002t0002g0235others(11): Show | 17 | HG00642.hp2 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.425+1743C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062969 | ||||||
| chr15:45062986
|
A | T | 16 | a0001c0001t0001g0058a0001c0001t0001g0105a0001c0001t0001g0148others(13): Show | 16 | HG00597.hp1 HG00621.hp2 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.425+1760A>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062986 | ||||||
| chr15:45062990
|
C | G | 12 | a0001c0001t0001g0166a0002c0002t0012g0268a0002c0004t0001g0119others(9): Show | 13 | HG01255.hp2 HG02074.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.425+1764C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45062990 | ||||||
| chr15:45063002
|
G | C | 1 | a0001c0001t0001g0162 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.425+1776G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063002 | ||||||
| chr15:45063072
|
T | C | 10 | a0002c0002t0003g0001a0002c0002t0003g0111a0002c0002t0003g0112others(7): Show | 12 | HG00642.hp2 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.425+1846T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063072 | ||||||
| chr15:45063106
|
G | A | 7 | a0002c0002t0012g0268a0002c0004t0001g0119a0003c0003t0008g0225others(4): Show | 8 | HG01255.hp2 HG02257.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.425+1880G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063106 | ||||||
| chr15:45063302
|
T | C | 3 | a0001c0001t0001g0131a0001c0001t0001g0169a0001c0001t0001g0228 | 3 | HG00323.hp1 HG03239.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.426-1969T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063302 | ||||||
| chr15:45063330
|
C | G | 5 | a0002c0004t0001g0119a0003c0003t0008g0225a0003c0003t0008g0263others(2): Show | 6 | HG01255.hp2 HG02257.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.426-1941C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063330 | ||||||
| chr15:45063395
|
G | T | 2 | a0001c0001t0022g0272a0001c0001t0032g0277 | 2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.426-1876G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063395 | ||||||
| chr15:45063396
|
G | T | 4 | a0001c0001t0001g0138a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG01109.hp2 HG01123.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.426-1875G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063396 | ||||||
| chr15:45063508
|
C | T | 1 | a0002c0002t0044g0258 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.426-1763C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063508 | ||||||
| chr15:45063525
|
A | G | 35 | a0001c0001t0001g0002a0001c0001t0001g0096a0001c0001t0001g0102others(32): Show | 40 | HG00558.hp1 HG00642.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.426-1746A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063525 | ||||||
| chr15:45063562
|
C | T | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(291): Show | 306 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.426-1709C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063562 | ||||||
| chr15:45063592
|
G | C | 1 | a0002c0004t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.426-1679G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063592 | ||||||
| chr15:45063707
|
G | A | 1 | a0004c0005t0024g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.426-1564G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063707 | ||||||
| chr15:45063715
|
A | G | 3 | a0003c0003t0008g0225a0003c0003t0008g0263a0003c0003t0008g0288 | 3 | HG01255.hp2 HG02257.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.426-1556A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063715 | ||||||
| chr15:45063751
|
G | A | 6 | a0002c0002t0011g0293a0002c0004t0001g0119a0003c0003t0008g0225others(3): Show | 7 | HG01255.hp2 HG02257.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.426-1520G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063751 | ||||||
| chr15:45063765
|
G | T | 1 | a0003c0003t0035g0120 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.426-1506G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063765 | ||||||
| chr15:45063789
|
A | C | 1 | a0001c0001t0001g0247 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.426-1482A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063789 | ||||||
| chr15:45063797
|
C | T | 1 | a0001c0001t0001g0035 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.426-1474C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063797 | ||||||
| chr15:45063867
|
G | A | 12 | a0001c0001t0001g0291a0001c0001t0008g0107a0002c0002t0004g0013others(9): Show | 12 | HG01884.hp1 HG01928.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.426-1404G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063867 | ||||||
| chr15:45063920
|
G | A | 5 | a0002c0002t0004g0013a0002c0002t0004g0014a0002c0002t0013g0029others(2): Show | 5 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.426-1351G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45063920 | ||||||
| chr15:45064038
|
G | T | 6 | a0002c0002t0004g0013a0002c0002t0004g0014a0002c0002t0013g0029others(3): Show | 6 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.426-1233G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45064038 | ||||||
| chr15:45064045
|
T | C | 17 | a0002c0002t0003g0001a0002c0002t0003g0027a0002c0002t0003g0091others(14): Show | 19 | HG00642.hp2 HG01891.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.426-1226T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45064045 | ||||||
| chr15:45064063
|
G | A | 2 | a0002c0002t0012g0268a0004c0006t0012g0267 | 2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.426-1208G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45064063 | ||||||
| chr15:45064134
|
C | G | 228 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(225): Show | 239 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.426-1137C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45064134 | ||||||
| chr15:45064235
|
G | A | 20 | a0002c0002t0006g0239a0002c0002t0006g0240a0002c0002t0006g0241others(17): Show | 21 | HG00438.hp1 HG00558.hp2 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.426-1036G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45064235 | ||||||
| chr15:45064269
|
G | T | 4 | a0002c0007t0010g0087a0002c0007t0010g0097a0002c0007t0010g0098others(1): Show | 4 | HG02886.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.426-1002G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45064269 | ||||||
| chr15:45064275
|
G | A | 1 | a0001c0001t0034g0121 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.426-996G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45064275 | ||||||
| chr15:45064373
|
C | T | 10 | a0002c0004t0001g0119a0002c0007t0010g0087a0002c0007t0010g0097others(7): Show | 11 | HG01255.hp2 HG02257.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.426-898C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45064373 | ||||||
| chr15:45064429
|
C | T | 1 | a0003c0003t0015g0009 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.426-842C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45064429 | ||||||
| chr15:45064653
|
T | C | 20 | a0002c0002t0003g0001a0002c0002t0003g0027a0002c0002t0003g0091others(17): Show | 22 | HG00642.hp2 HG01891.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.426-618T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45064653 | ||||||
| chr15:45064654
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.426-617G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45064654 | ||||||
| chr15:45064938
|
T | C | 6 | a0002c0004t0001g0119a0003c0003t0008g0225a0003c0003t0008g0263others(3): Show | 7 | HG01255.hp2 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.426-333T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45064938 | ||||||
| chr15:45064972
|
T | G | 13 | a0002c0002t0004g0013a0002c0002t0004g0014a0002c0002t0013g0029others(10): Show | 14 | HG01255.hp2 HG01928.hp1 HG01978.hp2 others(11): Show |
intron_variant | MODIFIER | c.426-299T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45064972 | ||||||
| chr15:45065013
|
T | C | 4 | a0002c0007t0010g0087a0002c0007t0010g0097a0002c0007t0010g0098others(1): Show | 4 | HG02886.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.426-258T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45065013 | ||||||
| chr15:45065014
|
G | C | 4 | a0002c0007t0010g0087a0002c0007t0010g0097a0002c0007t0010g0098others(1): Show | 4 | HG02886.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.426-257G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45065014 | ||||||
| chr15:45065016
|
T | C | 4 | a0002c0007t0010g0087a0002c0007t0010g0097a0002c0007t0010g0098others(1): Show | 4 | HG02886.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.426-255T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45065016 | ||||||
| chr15:45065042
|
G | A | 7 | a0002c0002t0002g0116a0002c0002t0002g0227a0002c0002t0002g0235others(4): Show | 7 | HG01891.hp2 HG02622.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.426-229G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45065042 | ||||||
| chr15:45065055
|
T | G | 1 | a0001c0001t0001g0220 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.426-216T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45065055 | ||||||
| chr15:45065211
|
A | T | 5 | a0001c0001t0001g0065a0001c0001t0001g0070a0001c0001t0001g0164others(2): Show | 5 | HG00140.hp1 HG01123.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.426-60A>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45065211 | ||||||
| chr15:45065212
|
T | G | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(171): Show | 181 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.426-59T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45065212 | ||||||
| chr15:45065250
|
G | A | 5 | a0001c0001t0001g0291a0001c0001t0008g0107a0003c0003t0001g0024others(2): Show | 5 | HG01884.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.426-21G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 4/8 | chr15 | 45065250 | ||||||
| chr15:45065453
|
A | G | 4 | a0002c0002t0002g0116a0002c0002t0002g0227a0002c0002t0037g0117others(1): Show | 4 | HG01891.hp2 HG02622.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.544+64A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45065453 | ||||||
| chr15:45065493
|
C | T | 1 | a0002c0002t0043g0223 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.544+104C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45065493 | ||||||
| chr15:45065648
|
A | T | 1 | a0004c0005t0024g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.544+259A>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45065648 | ||||||
| chr15:45065856
|
G | A | 4 | a0002c0002t0012g0260a0003c0003t0005g0256a0003c0003t0005g0257others(1): Show | 4 | HG01496.hp2 HG02922.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.544+467G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45065856 | ||||||
| chr15:45066016
|
G | C | 2 | a0001c0001t0001g0151a0001c0001t0030g0154 | 2 | NA18612.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.544+627G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45066016 | ||||||
| chr15:45066105
|
G | A | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(165): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.544+716G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45066105 | ||||||
| chr15:45066108
|
G | T | 1 | a0002c0002t0044g0258 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.544+719G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45066108 | ||||||
| chr15:45066223
|
T | C | 5 | a0001c0001t0001g0291a0001c0001t0008g0107a0003c0003t0001g0024others(2): Show | 5 | HG01884.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.544+834T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45066223 | ||||||
| chr15:45066244
|
C | CA | 26 | a0001c0001t0001g0072a0001c0001t0001g0124a0001c0001t0001g0167others(23): Show | 28 | HG00323.hp2 HG00642.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.544+874dupA | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr15 | 45066244 | |||||
| chr15:45066244
|
CA | C | 9 | a0001c0001t0001g0065a0001c0001t0001g0070a0001c0001t0001g0164others(6): Show | 9 | HG00140.hp1 HG01123.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.544+874delA | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr15 | 45066244 | |||||
| chr15:45066374
|
C | T | 1 | a0001c0001t0014g0270 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.544+985C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45066374 | ||||||
| chr15:45066523
|
G | A | 4 | a0002c0007t0010g0087a0002c0007t0010g0097a0002c0007t0010g0098others(1): Show | 4 | HG02886.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.544+1134G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45066523 | ||||||
| chr15:45066595
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.544+1206C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45066595 | ||||||
| chr15:45066648
|
C | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(170): Show | 180 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.544+1259C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45066648 | ||||||
| chr15:45066677
|
G | A | 12 | a0002c0002t0003g0001a0002c0002t0003g0111a0002c0002t0003g0112others(9): Show | 14 | HG00642.hp2 HG01891.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.544+1288G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45066677 | ||||||
| chr15:45066758
|
C | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(162): Show | 172 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.544+1369C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45066758 | ||||||
| chr15:45066960
|
G | A | 1 | a0004c0005t0001g0006 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.545-1221G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45066960 | ||||||
| chr15:45066999
|
G | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0062 | 2 | HG00621.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.545-1182G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45066999 | ||||||
| chr15:45067102
|
C | T | 20 | a0002c0002t0006g0239a0002c0002t0006g0240a0002c0002t0006g0241others(17): Show | 21 | HG00438.hp1 HG00558.hp2 HG02056.hp1 others(18): Show |
intron_variant | MODIFIER | c.545-1079C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45067102 | ||||||
| chr15:45067127
|
T | C | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(170): Show | 180 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.545-1054T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45067127 | ||||||
| chr15:45067244
|
C | G | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(165): Show | 175 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.545-937C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45067244 | ||||||
| chr15:45067294
|
G | A | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(170): Show | 180 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.545-887G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45067294 | ||||||
| chr15:45067408
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.545-773G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45067408 | ||||||
| chr15:45067569
|
G | A | 1 | a0003c0003t0035g0120 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.545-612G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45067569 | ||||||
| chr15:45067719
|
C | A | 4 | a0002c0007t0010g0087a0002c0007t0010g0097a0002c0007t0010g0098others(1): Show | 4 | HG02886.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.545-462C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45067719 | ||||||
| chr15:45067792
|
A | C | 1 | a0002c0002t0044g0258 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.545-389A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45067792 | ||||||
| chr15:45067794
|
A | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(170): Show | 180 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.545-387A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45067794 | ||||||
| chr15:45067834
|
C | T | 2 | a0002c0002t0037g0117a0004c0006t0002g0295 | 2 | HG01891.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.545-347C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45067834 | ||||||
| chr15:45067896
|
G | C | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(170): Show | 180 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.545-285G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45067896 | ||||||
| chr15:45067926
|
A | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(170): Show | 180 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.545-255A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45067926 | ||||||
| chr15:45067980
|
G | A | 1 | a0001c0001t0029g0284 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.545-201G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45067980 | ||||||
| chr15:45068152
|
G | C | 4 | a0002c0007t0010g0087a0002c0007t0010g0097a0002c0007t0010g0098others(1): Show | 4 | HG02886.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.545-29G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 5/8 | chr15 | 45068152 | ||||||
| chr15:45068328
|
T | C | 2 | a0001c0001t0001g0160a0003c0003t0041g0253 | 2 | HG03130.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.610+82T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068328 | ||||||
| chr15:45068376
|
A | G | 1 | a0001c0001t0026g0134 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.610+130A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068376 | ||||||
| chr15:45068384
|
A | G | 1 | a0001c0001t0026g0134 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.610+138A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068384 | ||||||
| chr15:45068385
|
G | A | 1 | a0001c0001t0008g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.610+139G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068385 | ||||||
| chr15:45068389
|
G | T | 291 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(288): Show | 303 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(300): Show |
intron_variant | MODIFIER | c.610+143G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068389 | ||||||
| chr15:45068421
|
C | G | 1 | a0002c0002t0002g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.610+175C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068421 | ||||||
| chr15:45068436
|
T | A | 1 | a0001c0001t0001g0286 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.610+190T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068436 | ||||||
| chr15:45068437
|
T | G | 1 | a0001c0001t0001g0286 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.610+191T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068437 | ||||||
| chr15:45068439
|
G | T | 1 | a0001c0001t0001g0286 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.610+193G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068439 | ||||||
| chr15:45068442
|
TGA | T | 16 | a0001c0001t0001g0183a0001c0001t0017g0083a0001c0001t0017g0084others(13): Show | 16 | HG00673.hp2 HG02056.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.610+202_610+203del others(2): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 45068442 | |||||
| chr15:45068444
|
A | T | 1 | a0001c0001t0001g0286 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.610+198A>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068444 | ||||||
| chr15:45068446
|
AGAGTGT | A | 21 | a0001c0001t0001g0007a0001c0001t0001g0058a0001c0001t0001g0105others(18): Show | 22 | HG00323.hp1 HG00558.hp2 HG00597.hp1 others(19): Show |
intron_variant | MODIFIER | c.610+202_610+207del others(6): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 45068446 | |||||
| chr15:45068448
|
A | AGAGT | 6 | a0002c0004t0001g0119a0003c0003t0008g0225a0003c0003t0008g0263others(3): Show | 7 | HG01255.hp2 HG02257.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.610+203_610+204ins others(4): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 45068448 | |||||
| chr15:45068448
|
A | T | 1 | a0003c0003t0001g0296 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.610+202A>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068448 | ||||||
| chr15:45068450
|
T | A | 60 | a0001c0001t0001g0003a0001c0001t0001g0212a0001c0001t0001g0213others(57): Show | 65 | HG00438.hp1 HG00642.hp2 HG00738.hp2 others(62): Show |
intron_variant | MODIFIER | c.610+204T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068450 | ||||||
| chr15:45068452
|
T | A | 30 | a0002c0002t0002g0010a0002c0002t0002g0073a0002c0002t0002g0074others(27): Show | 31 | HG00438.hp1 HG01099.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.610+206T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068452 | ||||||
| chr15:45068454
|
T | A | 1 | a0002c0002t0002g0074 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.610+208T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068454 | ||||||
| chr15:45068463
|
GTC | G | 8 | a0001c0001t0001g0210a0002c0002t0012g0260a0002c0002t0012g0268others(5): Show | 8 | HG01081.hp1 HG01496.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.610+219_610+220del others(2): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 45068463 | |||||
| chr15:45068465
|
C | G | 129 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(126): Show | 137 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.610+219C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068465 | ||||||
| chr15:45068507
|
T | TAGAGC | 10 | a0001c0001t0001g0209a0002c0002t0002g0236a0002c0002t0004g0013others(7): Show | 10 | HG01928.hp1 HG01978.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.610+264_610+268dup others(5): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 45068507 | |||||
| chr15:45068785
|
A | G | 69 | a0002c0002t0002g0010a0002c0002t0002g0073a0002c0002t0002g0074others(66): Show | 73 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.611-92A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068785 | ||||||
| chr15:45068795
|
T | C | 8 | a0001c0001t0001g0079a0001c0001t0001g0081a0001c0001t0004g0080others(5): Show | 8 | HG01496.hp2 HG02148.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.611-82T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068795 | ||||||
| chr15:45068813
|
C | T | 165 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(162): Show | 172 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.611-64C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068813 | ||||||
| chr15:45068841
|
TG | T | 3 | a0002c0002t0012g0260a0002c0002t0012g0268a0004c0006t0012g0267 | 3 | HG01496.hp2 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.611-35delG | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068841 | ||||||
| chr15:45068846
|
G | T | 1 | a0001c0001t0030g0154 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.611-31G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | chr15 | 45068846 | ||||||
| chr15:45068848
|
A | AT | 25 | a0001c0001t0001g0291a0001c0001t0005g0086a0001c0001t0008g0107others(22): Show | 25 | HG01099.hp1 HG01109.hp1 HG01255.hp2 others(22): Show |
splice_region_variant&intron_variant | LOW | c.611-9dupT | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 45068848 | |||||
| chr15:45068848
|
A | ATT | 6 | a0002c0007t0010g0087a0002c0007t0010g0097a0002c0007t0010g0098others(3): Show | 6 | HG01884.hp1 HG02886.hp1 HG02895.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.611-10_611-9dupTT | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 45068848 | |||||
| chr15:45068848
|
AT | A | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(208): Show | 222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.611-9delT | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr15 | 45068848 | |||||
| chr15:45069087
|
A | G | 2 | a0001c0001t0001g0033a0002c0002t0004g0014 | 2 | NA18951.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.786+35A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45069087 | ||||||
| chr15:45069089
|
A | AGGGGAGT others(15): Show |
1 | a0003c0003t0035g0120 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.786+38_786+59dupGG others(20): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr15 | 45069089 | |||||
| chr15:45069181
|
A | C | 77 | a0001c0001t0001g0143a0002c0002t0002g0010a0002c0002t0002g0073others(74): Show | 81 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.786+129A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45069181 | ||||||
| chr15:45069194
|
C | CT | 44 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0046others(41): Show | 45 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.786+172dupT | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr15 | 45069194 | |||||
| chr15:45069194
|
CT | C | 13 | a0001c0001t0001g0028a0001c0001t0001g0053a0001c0001t0001g0054others(10): Show | 13 | HG00639.hp2 HG01070.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.786+172delT | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr15 | 45069194 | |||||
| chr15:45069194
|
CTT | C | 9 | a0002c0002t0003g0027a0002c0002t0006g0241a0002c0004t0004g0017others(6): Show | 9 | HG02056.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.786+171_786+172del others(2): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr15 | 45069194 | |||||
| chr15:45069194
|
CTTT | C | 62 | a0002c0002t0002g0010a0002c0002t0002g0073a0002c0002t0002g0074others(59): Show | 66 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.786+170_786+172del others(3): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr15 | 45069194 | |||||
| chr15:45069200
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.786+148T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45069200 | ||||||
| chr15:45069205
|
T | C | 1 | a0004c0005t0024g0234 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.786+153T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45069205 | ||||||
| chr15:45069206
|
T | C | 6 | a0002c0002t0003g0027a0002c0002t0006g0241a0002c0004t0004g0017others(3): Show | 6 | HG02056.hp1 HG02615.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+154T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45069206 | ||||||
| chr15:45069207
|
T | C | 62 | a0002c0002t0002g0010a0002c0002t0002g0073a0002c0002t0002g0074others(59): Show | 66 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.786+155T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45069207 | ||||||
| chr15:45069263
|
G | A | 1 | a0001c0008t0001g0283 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.786+211G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45069263 | ||||||
| chr15:45069269
|
C | G | 1 | a0001c0001t0001g0052 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.786+217C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45069269 | ||||||
| chr15:45069347
|
C | T | 76 | a0002c0002t0002g0010a0002c0002t0002g0073a0002c0002t0002g0074others(73): Show | 80 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.786+295C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45069347 | ||||||
| chr15:45069792
|
T | C | 1 | a0001c0001t0001g0165 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.786+740T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45069792 | ||||||
| chr15:45069890
|
C | T | 6 | a0002c0002t0004g0013a0002c0002t0004g0014a0002c0002t0013g0029others(3): Show | 6 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.786+838C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45069890 | ||||||
| chr15:45069893
|
G | A | 1 | a0001c0001t0001g0002 | 3 | HG00558.hp1 NA18970.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.786+841G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45069893 | ||||||
| chr15:45069976
|
G | A | 3 | a0002c0002t0012g0260a0002c0002t0012g0268a0004c0006t0012g0267 | 3 | HG01496.hp2 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.786+924G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45069976 | ||||||
| chr15:45070029
|
C | T | 76 | a0001c0001t0004g0080a0002c0002t0002g0010a0002c0002t0002g0073others(73): Show | 80 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.786+977C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45070029 | ||||||
| chr15:45070074
|
A | G | 1 | a0001c0001t0001g0132 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.786+1022A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45070074 | ||||||
| chr15:45070099
|
A | G | 22 | a0002c0002t0003g0001a0002c0002t0003g0027a0002c0002t0003g0091others(19): Show | 24 | HG00642.hp2 HG01891.hp1 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.786+1047A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45070099 | ||||||
| chr15:45070329
|
C | T | 3 | a0002c0004t0001g0119a0004c0005t0001g0006a0004c0005t0024g0234 | 4 | HG02572.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.786+1277C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45070329 | ||||||
| chr15:45070372
|
C | T | 69 | a0001c0001t0004g0080a0002c0002t0002g0010a0002c0002t0002g0073others(66): Show | 73 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.786+1320C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45070372 | ||||||
| chr15:45070461
|
C | T | 294 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(291): Show | 306 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(303): Show |
intron_variant | MODIFIER | c.786+1409C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45070461 | ||||||
| chr15:45070543
|
G | C | 5 | a0001c0001t0001g0185a0002c0007t0010g0087a0002c0007t0010g0097others(2): Show | 5 | HG02129.hp2 HG02886.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+1491G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45070543 | ||||||
| chr15:45070696
|
G | A | 3 | a0002c0004t0001g0119a0004c0005t0001g0006a0004c0005t0024g0234 | 4 | HG02572.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-1621G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45070696 | ||||||
| chr15:45070833
|
G | A | 3 | a0002c0002t0012g0260a0002c0002t0012g0268a0004c0006t0012g0267 | 3 | HG01496.hp2 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.787-1484G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45070833 | ||||||
| chr15:45070914
|
G | T | 2 | a0001c0001t0019g0172a0001c0001t0019g0193 | 2 | HG01433.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.787-1403G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45070914 | ||||||
| chr15:45070945
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0054 | 2 | NA18973.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.787-1372C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45070945 | ||||||
| chr15:45070973
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.787-1344G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45070973 | ||||||
| chr15:45070973
|
G | T | 1 | a0001c0001t0001g0220 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.787-1344G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45070973 | ||||||
| chr15:45071063
|
A | G | 3 | a0002c0002t0012g0260a0002c0002t0012g0268a0004c0006t0012g0267 | 3 | HG01496.hp2 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.787-1254A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45071063 | ||||||
| chr15:45071143
|
G | A | 72 | a0001c0001t0004g0080a0002c0002t0002g0010a0002c0002t0002g0073others(69): Show | 76 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.787-1174G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45071143 | ||||||
| chr15:45071173
|
C | T | 6 | a0002c0004t0004g0015a0002c0004t0004g0016a0002c0004t0004g0017others(3): Show | 6 | HG00438.hp1 HG02056.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.787-1144C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45071173 | ||||||
| chr15:45071199
|
G | T | 23 | a0002c0002t0003g0001a0002c0002t0003g0113a0002c0002t0003g0115others(20): Show | 25 | HG00642.hp2 HG01891.hp1 HG01928.hp1 others(22): Show |
intron_variant | MODIFIER | c.787-1118G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45071199 | ||||||
| chr15:45071226
|
C | T | 167 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(164): Show | 174 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.787-1091C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45071226 | ||||||
| chr15:45071306
|
A | T | 1 | a0001c0001t0001g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.787-1011A>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45071306 | ||||||
| chr15:45071383
|
C | A | 4 | a0001c0001t0001g0291a0003c0003t0001g0024a0003c0003t0001g0025others(1): Show | 4 | HG01884.hp1 HG02622.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-934C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45071383 | ||||||
| chr15:45071420
|
G | C | 6 | a0002c0002t0004g0013a0002c0002t0004g0014a0002c0002t0013g0029others(3): Show | 6 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-897G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45071420 | ||||||
| chr15:45071435
|
C | CCTT | 6 | a0002c0002t0004g0013a0002c0002t0004g0014a0002c0002t0013g0029others(3): Show | 6 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-881_787-880ins others(3): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr15 | 45071435 | |||||
| chr15:45071455
|
A | G | 6 | a0002c0002t0004g0013a0002c0002t0004g0014a0002c0002t0013g0029others(3): Show | 6 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-862A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45071455 | ||||||
| chr15:45071475
|
G | A | 6 | a0002c0002t0004g0013a0002c0002t0004g0014a0002c0002t0013g0029others(3): Show | 6 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-842G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45071475 | ||||||
| chr15:45071484
|
C | A | 6 | a0002c0002t0004g0013a0002c0002t0004g0014a0002c0002t0013g0029others(3): Show | 6 | HG01928.hp1 HG01978.hp2 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.787-833C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45071484 | ||||||
| chr15:45071531
|
C | T | 1 | a0001c0001t0042g0249 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.787-786C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45071531 | ||||||
| chr15:45071575
|
T | C | 3 | a0001c0001t0001g0212a0001c0001t0042g0249a0002c0004t0001g0119 | 3 | HG01074.hp2 HG01256.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.787-742T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45071575 | ||||||
| chr15:45071598
|
C | G | 2 | a0001c0001t0042g0249a0002c0002t0043g0223 | 2 | HG01074.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.787-719C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45071598 | ||||||
| chr15:45071809
|
A | C | 15 | a0001c0001t0001g0058a0001c0001t0001g0148a0001c0001t0001g0165others(12): Show | 15 | HG00597.hp1 HG00621.hp2 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.787-508A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45071809 | ||||||
| chr15:45071833
|
T | C | 248 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(245): Show | 258 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(255): Show |
intron_variant | MODIFIER | c.787-484T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45071833 | ||||||
| chr15:45071980
|
G | A | 1 | a0002c0002t0020g0269 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.787-337G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45071980 | ||||||
| chr15:45072059
|
C | T | 1 | a0001c0001t0028g0060 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.787-258C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45072059 | ||||||
| chr15:45072087
|
T | C | 1 | a0004c0006t0039g0118 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.787-230T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45072087 | ||||||
| chr15:45072092
|
G | T | 1 | a0003c0003t0001g0110 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.787-225G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45072092 | ||||||
| chr15:45072099
|
C | G | 22 | a0001c0001t0027g0149a0002c0002t0003g0001a0002c0002t0003g0027others(19): Show | 24 | HG00642.hp2 HG01496.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.787-218C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45072099 | ||||||
| chr15:45072119
|
C | G | 1 | a0002c0004t0001g0119 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.787-198C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45072119 | ||||||
| chr15:45072119
|
C | T | 169 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0032others(166): Show | 173 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.787-198C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45072119 | ||||||
| chr15:45072131
|
C | A | 4 | a0002c0007t0010g0087a0002c0007t0010g0097a0002c0007t0010g0098others(1): Show | 4 | HG02886.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-186C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45072131 | ||||||
| chr15:45072280
|
T | A | 1 | a0001c0001t0001g0085 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.787-37T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 7/8 | chr15 | 45072280 | ||||||
| chr15:45072449
|
C | T | 214 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(211): Show | 221 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.908+11C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072449 | ||||||
| chr15:45072451
|
T | C | 1 | a0003c0003t0035g0120 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.908+13T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072451 | ||||||
| chr15:45072496
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.908+58C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072496 | ||||||
| chr15:45072508
|
TG | T | 226 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(223): Show | 234 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.908+73delG | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr15 | 45072508 | |||||
| chr15:45072525
|
G | A | 1 | a0002c0002t0011g0293 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.908+87G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072525 | ||||||
| chr15:45072552
|
T | C | 1 | a0001c0001t0016g0159 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.908+114T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072552 | ||||||
| chr15:45072571
|
G | A | 6 | a0001c0001t0001g0178a0001c0001t0001g0191a0001c0001t0001g0192others(3): Show | 6 | HG00642.hp1 HG01081.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+133G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072571 | ||||||
| chr15:45072604
|
A | T | 21 | a0002c0002t0002g0010a0002c0002t0002g0073a0002c0002t0002g0074others(18): Show | 21 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.908+166A>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072604 | ||||||
| chr15:45072607
|
G | C | 24 | a0001c0001t0038g0144a0001c0001t0042g0249a0002c0002t0002g0010others(21): Show | 24 | HG00639.hp2 HG01074.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.908+169G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072607 | ||||||
| chr15:45072611
|
G | A | 24 | a0001c0001t0038g0144a0001c0001t0042g0249a0002c0002t0002g0010others(21): Show | 24 | HG00639.hp2 HG01074.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.908+173G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072611 | ||||||
| chr15:45072613
|
T | TAAAGAAT others(296): Show |
2 | a0002c0002t0002g0076a0002c0002t0002g0243 | 2 | HG03098.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.908+186_908+187ins others(303): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr15 | 45072613 | |||||
| chr15:45072613
|
T | TAAAGAAT others(297): Show |
22 | a0001c0001t0038g0144a0001c0001t0042g0249a0002c0002t0002g0010others(19): Show | 22 | HG00639.hp2 HG01074.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.908+186_908+187ins others(304): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr15 | 45072613 | |||||
| chr15:45072620
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.908+182T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072620 | ||||||
| chr15:45072641
|
T | G | 5 | a0001c0001t0007g0026a0002c0007t0010g0087a0002c0007t0010g0097others(2): Show | 5 | HG02886.hp1 HG02895.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.908+203T>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072641 | ||||||
| chr15:45072673
|
A | G | 20 | a0001c0001t0001g0096a0001c0001t0001g0109a0001c0001t0001g0125others(17): Show | 21 | HG01243.hp1 HG01255.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.908+235A>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072673 | ||||||
| chr15:45072674
|
G | C | 38 | a0001c0001t0001g0090a0001c0001t0001g0096a0001c0001t0001g0109others(35): Show | 39 | HG01099.hp1 HG01243.hp1 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.908+236G>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072674 | ||||||
| chr15:45072694
|
C | T | 52 | a0001c0001t0001g0186a0001c0001t0001g0228a0001c0001t0001g0229others(49): Show | 54 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(51): Show |
intron_variant | MODIFIER | c.908+256C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072694 | ||||||
| chr15:45072701
|
C | G | 56 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0183others(53): Show | 58 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.908+263C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072701 | ||||||
| chr15:45072705
|
C | T | 56 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0183others(53): Show | 58 | HG00639.hp2 HG00642.hp2 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.908+267C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072705 | ||||||
| chr15:45072712
|
CT | C | 53 | a0001c0001t0001g0128a0001c0001t0038g0144a0001c0001t0042g0249others(50): Show | 55 | HG00639.hp2 HG00642.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.908+280delT | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr15 | 45072712 | |||||
| chr15:45072717
|
T | A | 53 | a0001c0001t0001g0128a0001c0001t0038g0144a0001c0001t0042g0249others(50): Show | 55 | HG00639.hp2 HG00642.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.908+279T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072717 | ||||||
| chr15:45072724
|
T | A | 53 | a0001c0001t0001g0128a0001c0001t0038g0144a0001c0001t0042g0249others(50): Show | 55 | HG00639.hp2 HG00642.hp2 HG01074.hp2 others(52): Show |
intron_variant | MODIFIER | c.908+286T>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072724 | ||||||
| chr15:45072738
|
G | A | 8 | a0001c0001t0001g0028a0001c0001t0001g0128a0001c0001t0017g0083others(5): Show | 8 | HG00639.hp2 HG01070.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.908+300G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072738 | ||||||
| chr15:45072743
|
G | A | 2 | a0002c0002t0012g0260a0002c0002t0012g0268 | 2 | HG01496.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.908+305G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072743 | ||||||
| chr15:45072758
|
C | A | 6 | a0001c0001t0001g0063a0001c0001t0001g0128a0001c0001t0038g0144others(3): Show | 6 | HG00639.hp2 HG01074.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+320C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072758 | ||||||
| chr15:45072766
|
GGAA | G | 69 | a0001c0001t0004g0080a0002c0002t0002g0010a0002c0002t0002g0073others(66): Show | 72 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.908+333_908+335del others(3): Show |
SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr15 | 45072766 | |||||
| chr15:45072868
|
C | G | 20 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0062others(17): Show | 20 | HG00621.hp1 HG01256.hp2 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.908+430C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072868 | ||||||
| chr15:45072887
|
C | T | 38 | a0002c0002t0002g0010a0002c0002t0002g0073a0002c0002t0002g0074others(35): Show | 40 | HG00642.hp2 HG01109.hp1 HG01884.hp2 others(37): Show |
intron_variant | MODIFIER | c.908+449C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072887 | ||||||
| chr15:45072975
|
A | C | 97 | a0001c0001t0001g0065a0001c0001t0001g0070a0001c0001t0001g0160others(94): Show | 101 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.909-390A>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45072975 | ||||||
| chr15:45073096
|
T | C | 92 | a0001c0001t0001g0195a0001c0001t0001g0248a0001c0001t0004g0080others(89): Show | 96 | HG00438.hp1 HG00558.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.909-269T>C | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45073096 | ||||||
| chr15:45073126
|
C | A | 2 | a0001c0001t0001g0096a0001c0001t0001g0102 | 2 | HG03139.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.909-239C>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45073126 | ||||||
| chr15:45073155
|
G | T | 17 | a0002c0002t0003g0001a0002c0002t0003g0027a0002c0002t0003g0091others(14): Show | 19 | HG00642.hp2 HG01891.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.909-210G>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45073155 | ||||||
| chr15:45073170
|
G | A | 8 | a0001c0001t0005g0086a0001c0001t0005g0139a0001c0001t0005g0285others(5): Show | 9 | HG01070.hp2 HG01071.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.909-195G>A | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45073170 | ||||||
| chr15:45073177
|
C | G | 77 | a0001c0001t0004g0080a0001c0001t0005g0086a0001c0001t0005g0139others(74): Show | 81 | HG00438.hp1 HG00558.hp2 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.909-188C>G | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45073177 | ||||||
| chr15:45073278
|
C | T | 3 | a0002c0002t0012g0260a0002c0002t0012g0268a0004c0006t0012g0267 | 3 | HG01496.hp2 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.909-87C>T | SORD | ENSG00000140263.15 | transcript | ENST00000267814.14 | protein_coding | 8/8 | chr15 | 45073278 |